Statin in Combination with Xuezhikang Capsules Get More Lipid-Regulating Effects Than Statin Only: A Systematic Review and Meta-Analysis

Statin in Combination with Xuezhikang Capsules Get More Lipid-Regulating Effects Than Statin Only: A Systematic Review and Meta-Analysis | Research Square window.SnipcartSettings = { analytics: { enabled: false } }; (function() { var accessVector = localStorage.getItem('access_vector') || ''; window.dataLayer = window.dataLayer || []; if (accessVector) { window.dataLayer.push({ user: { profile: { profileInfo: { snid: accessVector } } } }); } })(); (function(w,d,s,l,i){w[l]=w[l]||[];w[l].push({'gtm.start':new Date().getTime(),event:'gtm.js'});var f=d.getElementsByTagName(s)[0],j=d.createElement(s),dl=l!='dataLayer'?'&l='+l:'';j.async=true;j.src='https://www.googletagmanager.com/gtm.js?id='+i+dl;f.parentNode.insertBefore(j,f);})(window,document,'script','dataLayer','GTM-K279D39R'); Browse Preprints In Review Journals COVID-19 Preprints AJE Video Bytes Research Tools Research Promotion AJE Professional Editing AJE Rubriq About Preprint Platform In Review Editorial Policies Our Team Advisory Board Help Center Sign In Submit a Preprint Cite Share Download PDF Research Statin in Combination with Xuezhikang Capsules Get More Lipid-Regulating Effects Than Statin Only: A Systematic Review and Meta-Analysis Dongxiong Chen, Huiyan Feng, Yigen Li, Jinzhu Huang This is a preprint; it has not been peer reviewed by a journal. https://doi.org/ 10.21203/rs.3.rs-1037189/v1 This work is licensed under a CC BY 4.0 License Status: Posted Version 1 posted You are reading this latest preprint version Abstract Background To compare the lipid-regulating effects and safety of statin combined with Xuezhikang capsules and statin used alone for hyperlipidemia. Methods CNKI, Wanfang database, VIP Chinese Journals, PubMed, Embase, and Cochrane library were searched to comprehensively collect and screen RCTs of Xuezhikang combined with statin compared with statin used alone for lipid modifying treatment in hyperlipidemia patients from the database built as of September 2021, and the Cochrane 5.1.0 quality evaluation form was used to evaluate the quality of the included literature and The Cochrane 5.1.0 quality assessment form was used to evaluate the quality of the included literature and bias analysis, extract basic study information, primary and secondary outcome indicators, and meta-analysis of the outcome indicators was performed using RevMan 5.3. Results A total of 14 studies with a total of 2042 patients were included, and the quality of the included studies was low to medium. ①Effectiveness rate: OR=3.63,95%CI[2.69,4.90]; Funnel plot: all within the funnel, but not in accordance with the principle of "aggregation at the top and dispersion at the bottom". ②Total cholesterol: MD=-0.61,95%CI[-0.84,-0.39], The forest plots of each subgroup are to the left. ③Triglycerides: MD=-0.30,95%CI[-0.41,-0.19], The forest plots of each subgroup are to the left,. ④ LDL: MD=-0.33,95%CI[-0.46,-0.20], The forest plots of each subgroup are to the left. ⑤ HDL: MD=0.23,95%CI[0.12,0.35], The forest plots of each subgroup are to the right. ⑥Adverse effects: OR=0.32, 95% CI[0.19,0.55]. Conclusion The combination of statin with Xuezhikang capsule has better effect on lipid regulation in patients with hyperlipidemia, and can effectively reduce the incidence of adverse events and has better safety. It is recommended that the treatment of Xuezhikang combined with statin can be used as a safer and more effective treatment for patients with hyperlipidemia. Integrative & Complementary Medicine Clinical Pharmacology Xuezhikang Capsule Statin Hyperlipidemia Meta-analysis Figures Figure 1 Figure 2 Figure 3 Figure 4 Figure 5 Figure 6 Figure 7 Figure 8 Figure 9 Introduction With the increasing standard of living of people, hyperlipidemia has become a common disease in modern society and has become a major risk factor for diseases such as atherosclerosis [1] . With childhood obesity becoming an epidemic in certain parts of the United States [2] , hyperlipidemia is either directly or indirectly affecting people's health. And the regulation and stabilization of lipid levels has become one of the health care behaviours in modern daily life [3] . Statins are the first-line of lipid-modifying therapy [4] , but their intensive use can have borderline effects [5] , and the relationship between benefits and risks and economic benefits still needs to be studied [6-8] . Xuezhikang Capsules(Xuezhikang) represent a natural statin lipid-lowering drug, whose main ingredient is red yeast, refined in a standard GMP process and containing 13 natural compound statins [9] and its toxicity is extremely low [10] . Compared with synthetic statins, Xuezhikang is not effective in the comprehensive regulation of blood lipids and reducing the incidence of adverse reactions, which not only can be used as a first-line clinical drug [11] , but also can improve the benefits [12] and reduce the risks of intensive statin use [13] . To further investigate the efficacy and adverse effects of statins combined with Xuezhikang in patients with hyperlipidemia, this study conducts a systematic review and meta-analysis of the relevant literature, with a view to provide evidence-based medicine for clinical application. 1 Materials And Methods 1.1 Search Strategy 1.1.1 Databases A systematic literature review was conducted by using the databases CNKI, Wanfang database, VIP Chinese Journals, PubMed/Medline, Embase, Cochrane Library. Furthermore, the reference list of the relevant articles was manually searched. 1.1.2 Search Time and language From the database built to September 2021 with no language restriction. 1.1.3 Search Strategy Take PubMed as an example: Title/ Abstract: Xuezhikang[Mesh] AND (statins[Mesh] OR atorvastatin[Title/Abstract] OR Lipitor[Title/Abstract] OR atrovastatin[Title/Abstract] OR atovastatin[Title/Abstract] OR rosuvastatin[Title/Abstract] OR Crestor[Title/Abstract] OR Rosuvastatin Calcium[Title/Abstract] OR Rosuvastatin[Title/Abstract] OR Simvastatin[Title/Abstract] OR Fluvastatin[Title/Abstract] OR pravastatin[Title /Abstract] OR Pravachol[Title/Abstract] OR provastatin[Title/Abstract] OR Mevalotin[Title/Abstract] OR fluvastatin[Title/Abstract]) AND ( hyperlipidemia[Mesh] OR hyperlipemia[Title/Abstract]) AND (Randomized controlled trial[Publication type] OR randomized[Title/Abstract] OR placebo[Title/Abstract]) 1.2 Registration Information This systematic review and meta-analysis complies with the PRISMA Statement [14] and is registered in PROSPERO(No. CRD42020200277). 1.3 Inclusion and Exclusion Criteria 1.3.1 Subjects ① Diagnostic criteria: Referring to Chinese guidelines for the prevention and treatment of dyslipidemia (revised 2016) [15] and Consensus Statement by the AACE and ACE on the Management of Dyslipidemia and Prevention of Cardiovascular Disease Algorithm [16] , inclusion in this study meets the following conditional hyperlipidemia population:a. TC≥6.2mmol/L(240mg/dl);b. TG≥2.3mmol/L(200mg/dl);c. HDLC≤1.0mmol/L( 40mg/dl);d.LDLC≥4.1mmol/L(160 mg/dl); e. Non-HDLC≥4.9mmol/L( 190mg/dl);f. Serum was examined after 12 – 14 h in 2 fasting within 2 weeks under a normal diet TC, TG, LDL-C, non-LDL-C indicators can be diagnosed as hyperlipidemia if one or more of the above criteria are met Disease; or the original history of hyperlipidemia, this blood lipid reached the above standards. ②Sex, age and comorbidities were not limited. 1.3.2 Intervention The trial group was treated with Xuezhikang capsules combined with statins, and the control group was treated with the same type and dose of statins as the trial group. 1.3.3 Outcome indicators Primary efficacy indicator: treatment efficiency. Secondary efficacy indicators: a.total cholesterol(TC); b. triglycerides(TG); c. low density lipoprotein(LDLC); d. high density lipoprotein(HDLC); e. number of adverse events. 1.3.4 Study Type Randomized controlled trial(RCT), no matter whether to adopt blinded or allocation concealment.. 1.3.5 Exclusion Criteria ① For patients who have taken other drugs affecting lipid metabolism concurrently during treatment. ② Literature for which complete data are not available. 1.4 Literature Screening and Data Extraction Two researchers(Chen and Feng) independently screened the literature according to the inclusion and exclusion criteria and cross-checked it, using a pre-designed data extraction form to extract information, including basic information about the study, study methods, observation of subjects, intervention and control measures, indicators, outcomes and occurrence of adverse effects. In case of disagreement, it was resolved in consultation with the third researcher(Li). If the information reported in the study was incomplete, further contact was made with the author to obtain it, and the study was excluded if relevant data were not eventually obtained. 1.5 Literature Evaluation The Cochrane 5.1.0 Quality Assessor's Manual is used to screen and assess the quality of the literature. Judgements of bias (selection bias, implementation bias, measurement bias, follow-up bias, reporting bias and other biases) were made as "low risk/uncertain/high risk". 1.6 Statistical Analysis Meta-analysis was performed by using RevMan 5. 3 software. The odds ratio(OR) was measured using the MH algorithm for count data and the mean difference(MD) was measured using the IV algorithm for continuous variable data with 95% confidence intervals(CI). Heterogeneity between the results of each included study was tested by Q-test and I 2 -test. We will use Cochrane manual thresholds to explain I 2 -test [17] and Q-test [18] . (I 2 :0~40%, may not be important;30%~60%, which may represent moderate heterogeneity; 50%~90%,may represent significant heterogeneity; 75%~100%,with considerable heterogeneity. P of Q-test:>0.1, low heterogeneity;0.1 or I 2 test: I 2 <50%, fixed effects model(FE) was used; if Q-test: P 50%, random-effects model(RE) was used, and sources of heterogeneity were identified by subgroup method or single-study exclusion method to reduce heterogeneity. P <0.05 for the combined effect indicator indicates a statistically significant difference. When the number of included studies was ≥10, an inverted funnel plot analysis was performed to detect publication bias, using the effect indicators of the included studies as horizontal coordinates and the inverse of the log standard error(SE) as vertical coordinates. Descriptive analysis was used when data heterogeneity due to other reasons was clearly not possible to combine for analysis. 2 Results 2.1 Literature Search Results A total of 992 papers were initially reviewed, and after reading the abstracts and full text, 14 RCTs [19-32] were eventually included, with the process shown in Figure 1. 2.2 Basic Characteristics of the Included Studies All the studies included 2042 patients, with 1022 in the trial group and 1020 in the control group. The statins involved included: atorvastatin, simvastatin, rosuvastatin and fluvastatin, all of which are at moderate doses according to guidelines. Study duration ranged from 4 to 12 weeks. All studies were funded by grants, as detailed in Table 1. 2.3 Quali ty Evaluation of Included Studies and Risk of Bias Assessment All studies were randomized. No sample size estimation or intentionality therapy analysis or blind method was performed. The methodological quality assessment of the included studies is described in detail in Table 2. The risk of bias of the included studies is assessed in Figures 2A and its summary in Figure 2B. 2.4 Meta-analysis 2.4.1 Effective Rate There was low heterogeneity between studies ( P =0.91, I 2 = 0%) and the combined effect size of FE model was used for analysis, showing that the treatment efficiency was significantly higher with the use of Xuezhikang (OR=3.63, 95%CI[2.69,4.90], P <0.00001), detailed in Figure 3. The publication bias was analyzed on the row funnel plot with the effective rate. The shape of the funnel plot was consistent with the inverted funnel type with narrow upper and wide lower shape, but the loose lower part and the graph were all hollow dots, suggesting the existence of publication bias. More details are shown in Figure 4. 2.4.2 TC All 14 studies reported data on TC with significant heterogeneity between studies ( P <0.00001, I 2 =95%). Using single study exclusion was not effective in reducing heterogeneity, while changing to subgroups with different statins was effective in reducing heterogeneity. Using MD as the effect size and combining effect sizes using the RE model, forest plot results showed that the addition of Xuezhikang all significantly reduced TC levels (MD=-0.61,95%CI[-0.84,-0.39], P <0.00001), Figure 5 for details. 2.4.3 TG 14 studies reported changes in TG with significant heterogeneity between studies ( P<0.00001 , I 2 =88%). Subgrouping with statins reduced heterogeneity, and forest plot results using the RE model with MD as the effect size showed that: the addition of Xuezhikang all significantly reduced TG levels (MD=-0.30,95%CI[-0.41,-0.19], P <0.00001), as detailed in Figure 6. 2.4.4 LDLC 11 studies [19,22-23,25-32] reported changes in LDLC levels, including 886 patients in the trial group and 884 patients in the control group, with significant heterogeneity between studies ( P <0.00001, I 2 =86%) and Heterogeneity was reduced by statins subgroup. The forest plot results show that the overall analysis results (MD=-0.33, 95%CI[-0.46,-0.20], P <0.00001) supported that the addition of Xuezhikang was more effective in reducing LDLC levels. However, in the subgroups, there was a statistically significant difference between the results of Xuezhikang combined with statins and statins used alone in the atorvastatin group and fluvastatin group ( P <0.00001), while there was no statistically significant difference in the simvastatin group, as detailed in Figure 7. 2.4.5 HDLC Changes in HDLC levels were reported in 13 studies [19-23,25-32] , including 1176 patients in the trial group and 1174 patients in the control group, with significant heterogeneity between studies ( P <0.00001, I 2 =96%). Heterogeneity was reduced by statins subgroup. With MD as the effect size, and using the RE model, the forest plot results show that the addition of Xuezhikang all significantly increased HDLC levels (MD= 0.23, 95%CI[0.12,0.35], P <0.00001), as detailed in Figure 8. 2.4.6 Adverse Event 8 studies [19,21,23,25,27,29,30,32] reported adverse events during and after the middle stage of the study, including bloating, nausea, vomiting and headache, with large heterogeneity between studies ( P =0.001, I 2 =71%). 8 studies were subclassified according to whether the number of cases was greater than 100, then we find out the heterogeneity was low in both subgroups(I 2 =0% in both). With OR as effect value, combined effect size of RE model was used for analysis. The results of forest plot showed that adding Xuezhikang could significantly reduce the number of adverse events happening, as detailed in Figure 9. 3 Discussion Blood lipids are the general term for cholesterol, triglycerides, and lipids in serum. Hyperlipidemia refers to plasma lipoprotein disorders. It is a metabolic disease, and its direct damage to the body is not obvious, and it generally does not have specific clinical discomfort symptoms [ 33 ] . Cholesterol is the total amount of cholesterol contained in various lipoproteins in the blood. It exists in the human body mainly in the form of free cholesterol and cholesteryl esters, and its level is related to the patient's age, gender, dietary habits and genetic factors, but its metabolic changes are relatively slow [ 34 ] and is less valuable than LDL for risk assessment [ 35 ] and prediction [ 36 ] of atherosclerotic cardiovascular disease. Triglycerides are formed when the three hydroxyl groups in the glycerol molecule are esterified by fatty acids and, similar to cholesterol, their levels are influenced by both genetics and the environment. However, unlike cholesterol, the metabolism of triglycerides is more influenced by diet and time, and triglyceride measurements may vary considerably within a short period of time in the same individual with dietary changes [ 37 ] . There was a study [ 38 ] suggested that elevated triglycerides are likely to have atherogenic effects by affecting the structure of lipoproteins, and that mild to moderate elevations in serum triglyceride levels may increase the risk of coronary heart disease in patients. LDL is the lipid core that makes up the atherosclerotic plaque and is also the initial and maintaining element of the chronic inflammatory response that is the pathological manifestation of atherosclerosis, so an increase in LDL is a major risk factor for the occurrence and development of atherosclerosis [ 39 ] . HDL is responsible for reverse cholesterol transport - transporting cholesterol from peripheral tissues to the liver for circulation or excretion in the form of bile acids, reducing cholesterol deposition in the vascular wall and acting as an anti-atherosclerotic agent [ 40 ] . Dyslipidemia, characterized by elevated LDL and cholesterol, is a noteworthy risk factor for atherosclerotic cardiovascular diseases(ASCVD). Other types of dyslipidemia, such as increased TG and decreased HDLC, are also associated with the development of ASCVD [ 41 ] . The ultimate treatment goal for dyslipidemia is to effectively reduce the risk of developing ASCVD [ 36 ] . In the 2016-edition of the Chinese Guidelines for the Prevention and Treatment of Dyslipidemia [ 42 ] , it is recommended that patients with dyslipidemia need to be assessed for residual risk of ASCVD. LDL and cholesterol levels can be independent predictors of the risk of ASCVD in individuals or groups of patients. Cholesterol accounts for 50% of LDL, and although the two levels are generally parallel, cholesterol is susceptible to HDL [ 43 ] , and LDL plays a central role in the development of ASCVD. So lowering LDL levels is the main target of intervention in the treatment of dyslipidemia in clinical practice. Although there is no clear evidence to support that lower lipid levels are associated with a lower risk of ASCVD, nor is there evidence of a specific lipid threshold for ASCVD risk reduction, current medication guidelines in most countries, mainly in China, support the setting of lipid-lowering targets rather than minimizing lipid levels [ 44 ] . Apart from considerations of improving patient compliance and facilitating physician assessment of lipid-lowering efficacy, the main reasons are that lipid modulation is a long-term treatment and intensive use has a borderline effect - a significant increase in adverse drug reactions [ 45 ] , a doubling of the patient's financial burden, a small but modest increase in lipid-lowering benefit, and no reduction in all-cause mortality [ 46 ] . Statins are clinically preferred and are Class I Recommendations and Class A Evidence in a variety of cardiovascular guidelines, including lovastatin, simvastatin, pravastatin, fluvastatin, atorvastatin, resuprastatin and pitavastatin. As inhibitors of HMG-COA reductase, statins inhibit cholesterol synthesis of the rate-limiting enzyme HMG-CoA reductase, reduce cholesterol synthesis and subsequently cells are upregulated to indicate LDL receptors, and accelerate serum LDL catabolism, while inhibiting very low-density lipoprotein synthesis, thereby regulating blood lipids to reduce coronary heart disease mortality [ 47 ] . A number of studies [ 48 – 51 ] have demonstrated that while regular doses of statins have a significant benefit in primary prevention in patients at high cardiovascular risk, further studies are needed to investigate the benefit in patients at low and intermediate risk. Similarly, there is no evidence to support that the benefits of intensive treatment with statins outweigh the risks, including (1) the benefits of short-term intensive intervention in the perioperative period in cardiovascular patients; (2) the benefits of long-term intensive intervention in patients with dyslipidemia-the proportional reduction in TC and LDLC, and the incidence of cardiovascular events and all-cause mortality; (3) the cost of medication to patients doubling may lead to reduced compliance; and (4) a significant increase in adverse reactions, predominantly abnormal liver function, but also including myalgia, headache, insomnia and various gastrointestinal symptoms. How are statin adverse reactions alleviated? Guidelines suggest switching to another statin, reducing dosage, decreasing the frequency of dosing or discontinuing the statin, but the latter three management options not only reduce the benefits of lipid modulation but may increase the risk of cardiovascular events. Xuezhikang, the only natural lipid regulator recognized by several authoritative guidelines in the cardiovascular field [including: ACC, AHA 2013 Guidelines for the Treatment of Blood Cholesterol to Reduce the Risk of Atherosclerosis in Adults, ESC, EAS 2011, 2016 Guidelines for the Management of Dyslipidemia, China 2007 Guidelines for the Diagnosis and Prevention of Chronic Stable Angina, 2016 Guidelines for the Prevention and Treatment of Dyslipidemia in Adults, 2018 Guidelines for the Rational Use of Drugs in Coronary Heart Disease. Guidelines, 2018 Guidelines for the Diagnosis and Treatment of Stable Coronary Heart Disease, 2018 Guidelines for the Diagnosis and Treatment of Acute Myocardial Infarction with Chinese and Western Medicine] is recognized as a natural lipid-regulating drug. Its main ingredient is monascus - which has been used for centuries in China as a food colouring and flavour enhancer [ 52 ] . It is refined through a modern GMP-standard process by adding special monascus to rice fermentation. It has a mechanism similar to that of statins, with 13 natural statin complexes as the main ingredients [ 53 ] . It is unique in reducing the risk of adverse reactions associated with the use of a single statin [ 54 ] . A number of RCTs [ 55 – 62 ] have demonstrated that Xuezhikang can lower cholesterol and LDL levels, reduce the incidence of adverse events, reduce the risk of cardiovascular events and recurrence, and significantly reduce coronary heart disease mortality and all-cause mortality. It is also inexpensive compared to synthetic statins. Based on the original lipid-lowering treatment with synthetic statins, the addition of Xuezhikang can be equivalent to intensify the effective of statin treatment and mitigate the risk of adverse reactions. To investigate the benefits and risks of intensifying statin therapy with Xuezhikang, this study included 2042 patients in 14 RCTs, with 1022 patients in the trial group (statin plus Xuezhikang) and 1020 patients in the control group (statin alone), and conducted a meta-analysis of the combined effect sizes of efficiency, TC, TG, LDLC, HDLC and adverse events. The results showed that compared with statins used alone, the addition of Xuezhikang intensive treatment could (i) significantly increase the effective rate, (ii) more effectively reduce TC, TG and LDLC levels and increase HDLC levels, (iii) significantly reduce the incidence of adverse events, and (iv) the lipid-regulating effect of simvastatin combined with Xuezhikang on LDLC was not significant. The 14 RCTs included in this study were low to moderate quality studies with obvious limitations, including: 1. All studies did not specify sample size estimates, which may affect test validity; 2. Although all included studies indicated that cases were randomly assigned to two groups, only eight studies clearly indicated the randomization method they used, while the remaining studies did not mention the specific randomization method and allocation concealment method, which is subject to unknowable selectivity bias. The remaining studies did not mention the specific randomization method and allocation concealment method, resulting in unknowable selectivity bias; 3. All cases did not mention whether they were blinded, either blinding of investigators and subjects or blinded evaluation of study outcomes, resulting in unknowable implementation bias and measurement bias; 4. Funnel plots of efficiency rates were found to be consistent with an inverted funnel shape with a narrow top and a wide bottom, but the lower part of the graph was lax and there are all hollow dots in the graphs, suggesting that there are insufficient large sample studies, low sample quality and publication bias; 5. Only 8 studies fully reported adverse events during the study period and follow-up, resulting in follow-up bias, Moreover, none of the three major systemic adverse reactions of statins - liver, muscle and digestive system - have been tracked and reported, which is not highly targeted; 6. In the study design, the effective rate of all studies took the proportion of cholesterol reduction as the threshold. TC and LDLC were equally important in lipid-regulating therapy, but only 11 RCTS reported LDLC levels; TG was reported in each RCTS. Since TG is easily affected by diet, only 10 RCTS mentioned whether to add therapeutic dietary intervention, which would cause unknown bias in this study. In summary, for the RCT study with statins combined with Xuezhikang as the intervention in the trial group, this analysis recommends: 1. The RCT should be designed more precisely before starting the study, for example, sample size estimation, clear randomization method, clear allocation method, application of blinding, and the number of adverse reactions and case shedding in the trial should be recorded based on facts; 2. Large sample clinical trials can be conducted to provide more comprehensive and objective clinical treatment; 3. The design of outcome indicators of the study should (1) if lipid-regulating efficacy is the study objective, the magnitude of lipid regulation of TC and LDLC should be the primary outcome indicator, and TG, HLDL and other lipoproteins should be secondary outcome indicators; (2) if safety is the study objective, the reporting of adverse effects should include liver, muscle and digestive system; (3) if TG is reported, whether to include dietary control should be considered. In Conclusion, the information extracted from the 14 RCTs included in this study was systematically evaluated and the results showed that Xuezhikang combined with statins had better and more stable modulation of cholesterol, triglyceride and LDL levels than statins used alone in terms of regulation of lipids in patients with hyperlipidemia, and there is a lower incidence rate of adverse events. The RCTs included in this study were of low to moderate quality and more high quality RCTs with large samples are needed to provide more reliable evidence. 4 Conclusion In conclusion, Xuezhikang capsule combined with statins in the treatment of hyperlipidemia can improve the clinical efficacy of patients, effectively reduce the levels of TG, TC and LDL-C, and increase the level of HDL-C, without serious adverse effects, which has certain guiding significance for clinical treatment. However, due to the influence of the quality of the included literature, the above results need to be verified by more high-quality studies with large sample size. Abbreviations Xuezhikang capsule: Xuezhikang; total cholesterol: TC; triglycerides: TG; low density lipoprotein: LDLC; high density lipoprotein: HDLC; Randomized controlled trial: RCT; odds ratio (OR); mean difference: MD; confidence intervals: CI; fixed effects model: FE; random-effects model: RE; standard error: SE; atherosclerotic cardiovascular diseases: ASCVD. Declarations Ethics approval and consent to participate Not applicable. Consent to publish Not applicable Availability of data and materials All data generated or analysed during this study are included in this published article [and its supplementary information files]. Competing interests All authors certify that they have no affiliations with or involvement in any organization or entity with any financial interest or non-financial interest in the subject matter or materials discussed in this manuscript. Funding The authors did not receive support from any organization for the submitted work. Authors' Contributions Chen and Feng contributed to literature search, data extraction, and data analysis. Li contributed to study conception and data analysis. Feng and Huang contributed to study conception, manuscript drafting, and data analysis. Chen critically revised the manuscript. All authors acknowledge the full responsibility for the analyses and interpretation of the report. Acknowledgements All authors acknowledge the full responsibility for the analyses and interpretation of the report. Author details 1 Guangzhou Hospital of Traditional Chinese Medicine, Cardiovascular Department, Guangzhou, Guangdong, China; 2 The Third Affiliated Hospital of Sun Yat-Sen University, Gynecology Department, Guangzhou, Guangdong, China; 3 Traditional Chinese Medicine Hospital of Guangdong Province, Endocrinology Department, Guangzhou, Guangdong, China; * Corresponding Author: e-mail address: dongxiong163@163com; ORCID Chen Dongxiong: https://orcid.org/0000-0003-4326-3188, Feng Huiyan: https://orcid.org/0000-0002-2805-7856, Li Yigen: https://orcid.org/0000-0002-1455-2258, Huang Jinzhu: https://orcid.org/0000-0002-4415-4349. References Libby P, Buring JE, Badimon L, Hansson GK, Deanfield J, Bittencourt MS, Tokgözoğlu L, Lewis EF. Atherosclerosis. Nat Rev Dis Primers. 2019 Aug 16;5(1):56. doi: 10.1038/s41572-019-0106-z. PMID: 31420554. Stewart J, McCallin T, Martinez J, Chacko S, Yusuf S. Hyperlipidemia. Pediatr Rev. 2020 Aug;41(8):393-402. doi: 10.1542/pir.2019-0053. PMID: 32737252. 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Ye P, Lu ZL, Du BM, Chen Z, Wu YF, Yu XH, Zhao YC; CCSPS Investigators. Effect of xuezhikang on cardiovascular events and mortality in elderly patients with a history of myocardial infarction: a subgroup analysis of elderly subjects from the China Coronary Secondary Prevention Study. J Am Geriatr Soc. 2007 Jul;55(7):1015-22. doi: 10.1111/j.1532-5415.2007.01230.x. PMID: 17608873. DU BM, Lu ZL, Chen Z, Wu YF. [The beneficial effects of lipid-lowering therapy with xuezhikang on cardiac events and total mortality in coronary heart disease patients with or without hypertension: a random, double-blinded, placebo controlled clinical trial]. Zhonghua Xin Xue Guan Bing Za Zhi. 2006 Oct;34(10):890-4. Chinese. PMID: 17217713. Li JJ, Lu ZL, Kou WR, Bolli R, Chen Z, Wu YF, Yu XH, Zhao YC. Impact of long-term Xuezhikang therapy on cardiovascular events in high-risk patients with nonspecific, preexisting abnormal liver tests: a post-hoc analysis from Chinese Coronary Secondary Prevention Study (CCSPS). Int J Cardiol. 2012 Feb 9;154(3):362-5. doi: 10.1016/j.ijcard.2011.11.005. Epub 2011 Dec 1. PMID: 22133469. Liu ZQ, Cui LQ, Wang Y. [Effect of Xuezhikang on cardiac function, serum C-reactive protein and blood lipid in patients with chronic heart failure]. Zhongguo Zhong Xi Yi Jie He Za Zhi. 2007 Mar;27(3):220-2. Chinese. PMID: 17432681. Supplementary Files Table1.xlsx Table 1 Clinical characteristics of 14 studies in the meta-analysis Table2.xlsx Table 2 Evaluation of Methodological Quality of 14 Studies Cite Share Download PDF Status: Posted Version 1 posted You are reading this latest preprint version Research Square lets you share your work early, gain feedback from the community, and start making changes to your manuscript prior to peer review in a journal. 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16:12:52","extension":"png","order_by":6,"title":"Figure 6","display":"","copyAsset":false,"role":"figure","size":49306,"visible":true,"origin":"","legend":"Comparison of TG between statin in combination with Xuezhikang and statin only in all 14 studies which were divided into 4 subgroup according to different statins. ","description":"","filename":"OKFig6TGforestdiagram.png","url":"https://assets-eu.researchsquare.com/files/rs-1037189/v1/246bae17e029b42a0fcb0a4c.png"},{"id":15828524,"identity":"ef5b8ec0-d06e-4b75-b51c-15f8b9099230","added_by":"auto","created_at":"2021-11-23 16:12:52","extension":"png","order_by":7,"title":"Figure 7","display":"","copyAsset":false,"role":"figure","size":42173,"visible":true,"origin":"","legend":"Comparison of LDLC between statin in combination with Xuezhikang and statin only in 11 studies which were divided into 3 subgroup according to different statins.","description":"","filename":"OKFig7LDLCforestdiagram.png","url":"https://assets-eu.researchsquare.com/files/rs-1037189/v1/0401fe150c2714d754187b34.png"},{"id":15827606,"identity":"6c713716-797b-4dea-86c2-fae69ac83275","added_by":"auto","created_at":"2021-11-23 16:09:52","extension":"png","order_by":8,"title":"Figure 8","display":"","copyAsset":false,"role":"figure","size":48329,"visible":true,"origin":"","legend":"Comparison of HDLC between statin in combination with Xuezhikang and statin only in 13 studies which were divided into 4 subgroup according to different statins.","description":"","filename":"OKFig8HDLCforestdiagram.png","url":"https://assets-eu.researchsquare.com/files/rs-1037189/v1/d73bb0aafc9d013f19ff3a4d.png"},{"id":15827605,"identity":"ead96e3f-5b65-40a0-acc6-c4f3ec2fe756","added_by":"auto","created_at":"2021-11-23 16:09:52","extension":"png","order_by":9,"title":"Figure 9","display":"","copyAsset":false,"role":"figure","size":31939,"visible":true,"origin":"","legend":"Adverse event of 8 studies in which statins combined with Xuezhikang were compared with statin alone were divided into 2 subgroups based on whether the patients included were more than 100.","description":"","filename":"OKFig9AdverseReactionsforestdiagram.png","url":"https://assets-eu.researchsquare.com/files/rs-1037189/v1/3520624dd2bdea87c40d9cd6.png"},{"id":15829277,"identity":"a739f88f-4c68-4127-882f-0734f84c1975","added_by":"auto","created_at":"2021-11-23 16:18:56","extension":"pdf","order_by":0,"title":"","display":"","copyAsset":false,"role":"manuscript-pdf","size":757460,"visible":true,"origin":"","legend":"","description":"","filename":"manuscript.pdf","url":"https://assets-eu.researchsquare.com/files/rs-1037189/v1/4789f7a0-a729-4492-8255-878127c15f95.pdf"},{"id":15827597,"identity":"88c620c5-f6bd-4f56-8bdd-a431df153255","added_by":"auto","created_at":"2021-11-23 16:09:52","extension":"xlsx","order_by":1,"title":"","display":"","copyAsset":false,"role":"supplement","size":12341,"visible":true,"origin":"","legend":"Table 1 Clinical characteristics of 14 studies in the meta-analysis","description":"","filename":"Table1.xlsx","url":"https://assets-eu.researchsquare.com/files/rs-1037189/v1/cda386784602a6e7a7d5f5a2.xlsx"},{"id":15829276,"identity":"652227f7-096c-4515-9137-7dfcc9b77631","added_by":"auto","created_at":"2021-11-23 16:18:52","extension":"xlsx","order_by":2,"title":"","display":"","copyAsset":false,"role":"supplement","size":10833,"visible":true,"origin":"","legend":"Table 2 Evaluation of Methodological Quality of 14 Studies ","description":"","filename":"Table2.xlsx","url":"https://assets-eu.researchsquare.com/files/rs-1037189/v1/0f6f439c0b62b1bf0169d5d2.xlsx"}],"financialInterests":"","formattedTitle":"\u003cp\u003eStatin in Combination with Xuezhikang Capsules Get More Lipid-Regulating Effects Than Statin Only: A Systematic Review and Meta-Analysis\u003c/p\u003e","fulltext":[{"header":"Introduction","content":"\u003cp\u003eWith the increasing standard of living of people, hyperlipidemia has become a common disease in modern society\u0026nbsp;and has become a major risk factor for diseases such as atherosclerosis\u003csup\u003e[1]\u003c/sup\u003e. With childhood obesity becoming an epidemic in certain parts of the United States\u003csup\u003e[2]\u003c/sup\u003e, hyperlipidemia is either directly or indirectly affecting people\u0026apos;s health. And the regulation and stabilization of lipid levels has become one of the health care behaviours in modern daily life\u003csup\u003e[3]\u003c/sup\u003e. Statins are the first-line of lipid-modifying therapy\u003csup\u003e[4]\u003c/sup\u003e, but their intensive use can have borderline effects\u003csup\u003e[5]\u003c/sup\u003e, and the relationship between benefits and risks and economic benefits still needs to be studied\u003csup\u003e[6-8]\u003c/sup\u003e. Xuezhikang Capsules(Xuezhikang) represent a natural statin lipid-lowering drug, whose main ingredient is red yeast, refined in a standard GMP process and containing 13 natural compound statins\u003csup\u003e[9]\u003c/sup\u003e and its toxicity is extremely low\u003csup\u003e[10]\u003c/sup\u003e. Compared with synthetic statins, Xuezhikang is not effective in the comprehensive regulation of blood lipids and reducing the incidence of adverse reactions, which not only can be used as a first-line clinical drug\u003csup\u003e[11]\u003c/sup\u003e, but also can improve the benefits\u003csup\u003e[12]\u003c/sup\u003e and reduce the risks of intensive statin use\u003csup\u003e[13]\u003c/sup\u003e. To further investigate the efficacy and adverse effects of statins combined with Xuezhikang in patients with hyperlipidemia, this study conducts a systematic review and meta-analysis of the relevant literature, with a view to provide evidence-based medicine for clinical application.\u003c/p\u003e"},{"header":"1 Materials And Methods","content":"\u003cp\u003e\u003cstrong\u003e1.1 Search Strategy\u003c/strong\u003e\u003c/p\u003e\n\u003cp\u003e\u003cstrong\u003e1.1.1 Databases\u003c/strong\u003e\u003c/p\u003e\n\u003cp\u003eA systematic literature review was conducted by using the databases CNKI, Wanfang database, VIP Chinese Journals, PubMed/Medline, Embase, Cochrane Library. Furthermore, the reference list of the relevant articles was manually searched.\u003c/p\u003e\n\u003cp\u003e\u003cstrong\u003e1.1.2 Search Time and language\u003c/strong\u003e\u003c/p\u003e\n\u003cp\u003eFrom the database built to September 2021 with no language restriction.\u003c/p\u003e\n\u003cp\u003e\u003cstrong\u003e1.1.3 Search Strategy\u003c/strong\u003e\u003c/p\u003e\n\u003cp\u003eTake PubMed as an example: Title/ Abstract: Xuezhikang[Mesh] AND (statins[Mesh] OR atorvastatin[Title/Abstract] OR Lipitor[Title/Abstract] OR atrovastatin[Title/Abstract] OR atovastatin[Title/Abstract] OR rosuvastatin[Title/Abstract] OR Crestor[Title/Abstract] OR Rosuvastatin Calcium[Title/Abstract] OR Rosuvastatin[Title/Abstract] OR Simvastatin[Title/Abstract] OR Fluvastatin[Title/Abstract] OR pravastatin[Title /Abstract] OR Pravachol[Title/Abstract] OR provastatin[Title/Abstract] OR Mevalotin[Title/Abstract] OR fluvastatin[Title/Abstract]) AND ( hyperlipidemia[Mesh] OR hyperlipemia[Title/Abstract]) AND (Randomized controlled trial[Publication type] OR randomized[Title/Abstract] OR placebo[Title/Abstract])\u003c/p\u003e\n\u003cp\u003e\u003cstrong\u003e1.2 Registration Information\u003c/strong\u003e\u003c/p\u003e\n\u003cp\u003eThis systematic review and meta-analysis complies with the PRISMA Statement\u003csup\u003e[14]\u003c/sup\u003e and is registered in PROSPERO(No. CRD42020200277).\u003c/p\u003e\n\u003cp\u003e\u003cstrong\u003e1.3 Inclusion and Exclusion Criteria\u003c/strong\u003e\u003c/p\u003e\n\u003cp\u003e\u003cstrong\u003e1.3.1 Subjects\u003c/strong\u003e\u003c/p\u003e\n\u003cp\u003e① Diagnostic criteria: Referring to \u003cem\u003eChinese guidelines for the prevention and treatment of dyslipidemia (revised 2016)\u003c/em\u003e\u003csup\u003e[15]\u003c/sup\u003e and \u003cem\u003eConsensus Statement by the AACE and ACE on the Management of Dyslipidemia and Prevention of Cardiovascular Disease Algorithm\u003c/em\u003e\u003csup\u003e[16]\u003c/sup\u003e, inclusion in this study meets the following conditional hyperlipidemia population:a. TC\u0026ge;6.2mmol/L(240mg/dl);b. TG\u0026ge;2.3mmol/L(200mg/dl);c. HDLC\u0026le;1.0mmol/L( 40mg/dl);d.LDLC\u0026ge;4.1mmol/L(160 mg/dl); e. Non-HDLC\u0026ge;4.9mmol/L( 190mg/dl);f. Serum was examined after 12 \u0026ndash; 14 h in 2 fasting within 2 weeks under a normal diet TC, TG, LDL-C, non-LDL-C indicators can be diagnosed as hyperlipidemia if one or more of the above criteria are met Disease; or the original history of hyperlipidemia, this blood lipid reached the above standards.\u0026nbsp;②Sex, age and comorbidities were not limited.\u003c/p\u003e\n\u003cp\u003e\u003cstrong\u003e1.3.2 Intervention\u003c/strong\u003e\u003c/p\u003e\n\u003cp\u003eThe trial group was treated with Xuezhikang capsules combined with statins, and the control group was treated with the same type and dose of statins as the trial group.\u003c/p\u003e\n\u003cp\u003e\u003cstrong\u003e1.3.3 Outcome indicators\u003c/strong\u003e\u0026nbsp;\u003c/p\u003e\n\u003cp\u003ePrimary efficacy indicator: treatment efficiency. Secondary efficacy indicators: a.total cholesterol(TC); b. triglycerides(TG); c. low density lipoprotein(LDLC); d. high density lipoprotein(HDLC); e. number of adverse events.\u003c/p\u003e\n\u003cp\u003e\u003cstrong\u003e1.3.4 Study Type\u003c/strong\u003e\u003c/p\u003e\n\u003cp\u003eRandomized controlled trial(RCT), no matter whether to adopt blinded or allocation concealment..\u003c/p\u003e\n\u003cp\u003e\u003cstrong\u003e1.3.5 Exclusion Criteria\u003c/strong\u003e\u0026nbsp;\u003c/p\u003e\n\u003cp\u003e① For patients who have taken other drugs affecting lipid metabolism concurrently during treatment.\u0026nbsp;② Literature for which complete data are not available.\u003c/p\u003e\n\u003cp\u003e\u003cstrong\u003e1.4 Literature Screening and Data Extraction\u003c/strong\u003e\u003c/p\u003e\n\u003cp\u003eTwo researchers(Chen and Feng) independently screened the literature according to the inclusion and exclusion criteria and cross-checked it, using a pre-designed data extraction form to extract information, including basic information about the study, study methods, observation of subjects, intervention and control measures, indicators, outcomes and occurrence of adverse effects. In case of disagreement, it was resolved in consultation with the third researcher(Li). If the information reported in the study was incomplete, further contact was made with the author to obtain it, and the study was excluded if relevant data were not eventually obtained.\u003c/p\u003e\n\u003cp\u003e\u003cstrong\u003e1.5 Literature Evaluation\u003c/strong\u003e\u003c/p\u003e\n\u003cp\u003eThe Cochrane 5.1.0 Quality Assessor\u0026apos;s Manual is used to screen and assess the quality of the literature. Judgements of bias (selection bias, implementation bias, measurement bias, follow-up bias, reporting bias and other biases) were made as \u0026quot;low risk/uncertain/high risk\u0026quot;.\u003c/p\u003e\n\u003cp\u003e\u003cstrong\u003e1.6 Statistical Analysis\u003c/strong\u003e\u003c/p\u003e\n\u003cp\u003eMeta-analysis was performed by using RevMan 5. 3 software. The odds ratio(OR) was measured using the MH algorithm for count data and the mean difference(MD) was measured using the IV algorithm for continuous variable data with 95% confidence intervals(CI). Heterogeneity between the results of each included study was tested by Q-test and I\u003csup\u003e2\u003c/sup\u003e-test. We will use Cochrane manual thresholds to explain I\u003csup\u003e2\u003c/sup\u003e-test\u003csup\u003e[17]\u003c/sup\u003eand Q-test\u003csup\u003e[18]\u003c/sup\u003e. (I\u003csup\u003e2\u003c/sup\u003e:0~40%, may not be important;30%~60%, which may represent moderate heterogeneity; 50%~90%,may represent significant heterogeneity; 75%~100%,with considerable heterogeneity. \u003cem\u003eP\u003c/em\u003e of Q-test:\u0026gt;0.1, low heterogeneity;\u0026lt;0.1, high heterogeneity.) If Q-est: \u003cem\u003eP\u003c/em\u003e\u0026gt;0.1 or I\u003csup\u003e2\u003c/sup\u003e test: I\u003csup\u003e2\u003c/sup\u003e\u0026lt;50%, fixed effects model(FE) was used; if Q-test: \u003cem\u003eP\u003c/em\u003e\u0026lt;0.1 or I\u003csup\u003e2\u003c/sup\u003e test: I\u003csup\u003e2\u003c/sup\u003e\u0026gt;50%, random-effects model(RE) was used, and sources of heterogeneity were identified by subgroup method or single-study exclusion method to reduce heterogeneity. \u003cem\u003eP\u003c/em\u003e\u0026lt;0.05 for the combined effect indicator indicates a statistically significant difference. When the number of included studies was \u0026ge;10, an inverted funnel plot analysis was performed to detect publication bias, using the effect indicators of the included studies as horizontal coordinates and the inverse of the log standard error(SE) as vertical coordinates. Descriptive analysis was used when data heterogeneity due to other reasons was clearly not possible to combine for analysis.\u003c/p\u003e"},{"header":"2 Results","content":"\u003cp\u003e\u003cstrong\u003e2.1 Literature Search Results\u003c/strong\u003e\u003c/p\u003e\n\u003cp\u003eA total of 992 papers were initially reviewed, and after reading the abstracts and full text, 14 RCTs\u003csup\u003e[19-32]\u003c/sup\u003e were eventually included, with the process shown in Figure 1.\u003c/p\u003e\n\u003cp\u003e\u003cstrong\u003e2.2 Basic Characteristics of the Included Studies\u003c/strong\u003e\u003c/p\u003e\n\u003cp\u003eAll the studies included 2042 patients, with 1022 in the trial group and 1020 in the control group. The statins involved included: atorvastatin, simvastatin, rosuvastatin and fluvastatin, all of which are at moderate doses according to guidelines. Study duration ranged from 4 to 12 weeks. All studies were funded by grants, as detailed in Table 1.\u003c/p\u003e\n\u003cp\u003e\u003cstrong\u003e2.3 Quali\u003c/strong\u003e\u003cstrong\u003ety Evaluation of Included Studies and Risk of Bias Assessment\u003c/strong\u003e\u003c/p\u003e\n\u003cp\u003eAll studies were randomized. No sample size estimation or intentionality therapy analysis or blind method was performed. The methodological quality assessment of the included studies is described in detail in Table 2. The risk of bias of the included studies is assessed in Figures 2A and its summary in Figure 2B.\u003c/p\u003e\n\u003cp\u003e\u003cstrong\u003e2.4 Meta-analysis\u003c/strong\u003e\u003c/p\u003e\n\u003cp\u003e\u003cstrong\u003e2.4.1 Effective Rate\u003c/strong\u003e\u003c/p\u003e\n\u003cp\u003eThere was low heterogeneity between studies (\u003cem\u003eP\u003c/em\u003e=0.91, I\u003cem\u003e\u003csup\u003e2\u0026nbsp;\u003c/sup\u003e\u003c/em\u003e= 0%) and the combined effect size of FE model was used for analysis, showing that the treatment efficiency was significantly higher with the use of Xuezhikang (OR=3.63, 95%CI[2.69,4.90], \u003cem\u003eP\u003c/em\u003e\u0026lt;0.00001), detailed in Figure 3. The publication bias was analyzed on the row funnel plot with the effective rate. The shape of the funnel plot was consistent with the inverted funnel type with narrow upper and wide lower shape, but the loose lower part and the graph were all hollow dots, suggesting the existence of publication bias. More details are shown in Figure 4.\u003c/p\u003e\n\u003cp\u003e\u003cstrong\u003e2.4.2 TC\u003c/strong\u003e\u003c/p\u003e\n\u003cp\u003eAll 14 studies reported data on TC with significant heterogeneity between studies (\u003cem\u003eP\u003c/em\u003e\u0026lt;0.00001, I\u003cem\u003e\u003csup\u003e2\u003c/sup\u003e\u0026nbsp;\u003c/em\u003e=95%). Using single study exclusion was not effective in reducing heterogeneity, while changing to subgroups with different statins was effective in reducing heterogeneity. Using MD as the effect size and combining effect sizes using the RE model, forest plot results showed that the addition of Xuezhikang all significantly reduced TC levels (MD=-0.61,95%CI[-0.84,-0.39],\u003cem\u003eP\u003c/em\u003e\u0026lt;0.00001), Figure 5 for details.\u003c/p\u003e\n\u003cp\u003e\u003cstrong\u003e2.4.3 TG\u003c/strong\u003e\u003c/p\u003e\n\u003cp\u003e14 studies reported changes in TG with significant heterogeneity between studies (\u003cem\u003eP\u0026lt;0.00001\u003c/em\u003e, I\u003cem\u003e\u003csup\u003e2\u003c/sup\u003e\u0026nbsp;\u003c/em\u003e=88%). Subgrouping with statins reduced heterogeneity, and forest plot results using the RE model with MD as the effect size showed that: the addition of Xuezhikang all significantly reduced TG levels (MD=-0.30,95%CI[-0.41,-0.19], \u003cem\u003eP\u003c/em\u003e\u0026lt;0.00001), as detailed in Figure 6.\u003c/p\u003e\n\u003cp\u003e\u003cstrong\u003e2.4.4 LDLC\u003c/strong\u003e\u003c/p\u003e\n\u003cp\u003e11 studies\u003csup\u003e[19,22-23,25-32]\u003c/sup\u003e reported changes in LDLC levels, including 886 patients in the trial group and 884 patients in the control group, with significant heterogeneity between studies (\u003cem\u003eP\u003c/em\u003e\u0026lt;0.00001, I\u003cem\u003e\u003csup\u003e2\u003c/sup\u003e\u003c/em\u003e=86%) and Heterogeneity was reduced by statins subgroup. The forest plot results show that the overall analysis results (MD=-0.33, 95%CI[-0.46,-0.20], \u003cem\u003eP\u003c/em\u003e\u0026lt;0.00001) supported that the addition of Xuezhikang was more effective in reducing LDLC levels. However, in the subgroups, there was a statistically significant difference between the results of Xuezhikang combined with statins and statins used alone in the atorvastatin group and fluvastatin group (\u003cem\u003eP\u003c/em\u003e\u0026lt;0.00001), while there was no statistically significant difference in the simvastatin group, as detailed in Figure 7.\u003c/p\u003e\n\u003cp\u003e\u003cstrong\u003e2.4.5 HDLC\u003c/strong\u003e\u003c/p\u003e\n\u003cp\u003eChanges in HDLC levels were reported in 13 studies\u003csup\u003e[19-23,25-32]\u003c/sup\u003e, including 1176 patients in the trial group and 1174 patients in the control group, with significant heterogeneity between studies (\u003cem\u003eP\u003c/em\u003e\u0026lt;0.00001, I\u003cem\u003e\u003csup\u003e2\u003c/sup\u003e\u003c/em\u003e=96%). Heterogeneity was reduced by statins subgroup. With MD as the effect size, and using the RE model, the forest plot results show that the addition of Xuezhikang all significantly increased HDLC levels (MD= 0.23, 95%CI[0.12,0.35], \u003cem\u003eP\u003c/em\u003e\u0026lt;0.00001), as detailed in Figure 8.\u003c/p\u003e\n\u003cp\u003e\u003cstrong\u003e2.4.6 Adverse Event\u003c/strong\u003e\u003c/p\u003e\n\u003cp\u003e8 studies\u003csup\u003e[19,21,23,25,27,29,30,32]\u003c/sup\u003e reported adverse events during and after the middle stage of the study, including bloating, nausea, vomiting and headache, with large heterogeneity between studies (\u003cem\u003eP\u003c/em\u003e=0.001, I\u003cem\u003e\u003csup\u003e2\u003c/sup\u003e\u003c/em\u003e=71%). 8 studies were subclassified according to whether the number of cases was greater than 100, then we find out the heterogeneity was low in both subgroups(I\u003cem\u003e\u003csup\u003e2\u003c/sup\u003e\u003c/em\u003e=0% in both). With OR as effect value, combined effect size of RE model was used for analysis. The results of forest plot showed that adding Xuezhikang could significantly reduce the number of adverse events happening, as detailed in Figure 9.\u003c/p\u003e"},{"header":"3 Discussion","content":"\u003cp\u003eBlood lipids are the general term for cholesterol, triglycerides, and lipids in serum. Hyperlipidemia refers to plasma lipoprotein disorders. It is a metabolic disease, and its direct damage to the body is not obvious, and it generally does not have specific clinical discomfort symptoms\u003csup\u003e[\u003cspan citationid=\"CR33\" class=\"CitationRef\"\u003e33\u003c/span\u003e]\u003c/sup\u003e. Cholesterol is the total amount of cholesterol contained in various lipoproteins in the blood. It exists in the human body mainly in the form of free cholesterol and cholesteryl esters, and its level is related to the patient's age, gender, dietary habits and genetic factors, but its metabolic changes are relatively slow\u003csup\u003e[\u003cspan citationid=\"CR34\" class=\"CitationRef\"\u003e34\u003c/span\u003e]\u003c/sup\u003e and is less valuable than LDL for risk assessment\u003csup\u003e[\u003cspan citationid=\"CR35\" class=\"CitationRef\"\u003e35\u003c/span\u003e]\u003c/sup\u003e and prediction\u003csup\u003e[\u003cspan citationid=\"CR36\" class=\"CitationRef\"\u003e36\u003c/span\u003e]\u003c/sup\u003e of atherosclerotic cardiovascular disease. Triglycerides are formed when the three hydroxyl groups in the glycerol molecule are esterified by fatty acids and, similar to cholesterol, their levels are influenced by both genetics and the environment. However, unlike cholesterol, the metabolism of triglycerides is more influenced by diet and time, and triglyceride measurements may vary considerably within a short period of time in the same individual with dietary changes\u003csup\u003e[\u003cspan citationid=\"CR37\" class=\"CitationRef\"\u003e37\u003c/span\u003e]\u003c/sup\u003e. There was a study\u003csup\u003e[\u003cspan citationid=\"CR38\" class=\"CitationRef\"\u003e38\u003c/span\u003e]\u003c/sup\u003e suggested that elevated triglycerides are likely to have atherogenic effects by affecting the structure of lipoproteins, and that mild to moderate elevations in serum triglyceride levels may increase the risk of coronary heart disease in patients. LDL is the lipid core that makes up the atherosclerotic plaque and is also the initial and maintaining element of the chronic inflammatory response that is the pathological manifestation of atherosclerosis, so an increase in LDL is a major risk factor for the occurrence and development of atherosclerosis\u003csup\u003e[\u003cspan citationid=\"CR39\" class=\"CitationRef\"\u003e39\u003c/span\u003e]\u003c/sup\u003e. HDL is responsible for reverse cholesterol transport - transporting cholesterol from peripheral tissues to the liver for circulation or excretion in the form of bile acids, reducing cholesterol deposition in the vascular wall and acting as an anti-atherosclerotic agent\u003csup\u003e[\u003cspan citationid=\"CR40\" class=\"CitationRef\"\u003e40\u003c/span\u003e]\u003c/sup\u003e.\u003c/p\u003e \u003cp\u003eDyslipidemia, characterized by elevated LDL and cholesterol, is a noteworthy risk factor for atherosclerotic cardiovascular diseases(ASCVD). Other types of dyslipidemia, such as increased TG and decreased HDLC, are also associated with the development of ASCVD\u003csup\u003e[\u003cspan citationid=\"CR41\" class=\"CitationRef\"\u003e41\u003c/span\u003e]\u003c/sup\u003e. The ultimate treatment goal for dyslipidemia is to effectively reduce the risk of developing ASCVD\u003csup\u003e[\u003cspan citationid=\"CR36\" class=\"CitationRef\"\u003e36\u003c/span\u003e]\u003c/sup\u003e. In the 2016-edition of the Chinese Guidelines for the Prevention and Treatment of Dyslipidemia\u003csup\u003e[\u003cspan citationid=\"CR42\" class=\"CitationRef\"\u003e42\u003c/span\u003e]\u003c/sup\u003e, it is recommended that patients with dyslipidemia need to be assessed for residual risk of ASCVD. LDL and cholesterol levels can be independent predictors of the risk of ASCVD in individuals or groups of patients. Cholesterol accounts for 50% of LDL, and although the two levels are generally parallel, cholesterol is susceptible to HDL\u003csup\u003e[\u003cspan citationid=\"CR43\" class=\"CitationRef\"\u003e43\u003c/span\u003e]\u003c/sup\u003e, and LDL plays a central role in the development of ASCVD. So lowering LDL levels is the main target of intervention in the treatment of dyslipidemia in clinical practice.\u003c/p\u003e \u003cp\u003eAlthough there is no clear evidence to support that lower lipid levels are associated with a lower risk of ASCVD, nor is there evidence of a specific lipid threshold for ASCVD risk reduction, current medication guidelines in most countries, mainly in China, support the setting of lipid-lowering targets rather than minimizing lipid levels\u003csup\u003e[\u003cspan citationid=\"CR44\" class=\"CitationRef\"\u003e44\u003c/span\u003e]\u003c/sup\u003e. Apart from considerations of improving patient compliance and facilitating physician assessment of lipid-lowering efficacy, the main reasons are that lipid modulation is a long-term treatment and intensive use has a borderline effect - a significant increase in adverse drug reactions\u003csup\u003e[\u003cspan citationid=\"CR45\" class=\"CitationRef\"\u003e45\u003c/span\u003e]\u003c/sup\u003e, a doubling of the patient's financial burden, a small but modest increase in lipid-lowering benefit, and no reduction in all-cause mortality\u003csup\u003e[\u003cspan citationid=\"CR46\" class=\"CitationRef\"\u003e46\u003c/span\u003e]\u003c/sup\u003e.\u003c/p\u003e \u003cp\u003eStatins are clinically preferred and are Class I Recommendations and Class A Evidence in a variety of cardiovascular guidelines, including lovastatin, simvastatin, pravastatin, fluvastatin, atorvastatin, resuprastatin and pitavastatin. As inhibitors of HMG-COA reductase, statins inhibit cholesterol synthesis of the rate-limiting enzyme HMG-CoA reductase, reduce cholesterol synthesis and subsequently cells are upregulated to indicate LDL receptors, and accelerate serum LDL catabolism, while inhibiting very low-density lipoprotein synthesis, thereby regulating blood lipids to reduce coronary heart disease mortality\u003csup\u003e[\u003cspan citationid=\"CR47\" class=\"CitationRef\"\u003e47\u003c/span\u003e]\u003c/sup\u003e. A number of studies\u003csup\u003e[\u003cspan additionalcitationids=\"CR49 CR50\" citationid=\"CR48\" class=\"CitationRef\"\u003e48\u003c/span\u003e\u0026ndash;\u003cspan citationid=\"CR51\" class=\"CitationRef\"\u003e51\u003c/span\u003e]\u003c/sup\u003e have demonstrated that while regular doses of statins have a significant benefit in primary prevention in patients at high cardiovascular risk, further studies are needed to investigate the benefit in patients at low and intermediate risk. Similarly, there is no evidence to support that the benefits of intensive treatment with statins outweigh the risks, including (1) the benefits of short-term intensive intervention in the perioperative period in cardiovascular patients; (2) the benefits of long-term intensive intervention in patients with dyslipidemia-the proportional reduction in TC and LDLC, and the incidence of cardiovascular events and all-cause mortality; (3) the cost of medication to patients doubling may lead to reduced compliance; and (4) a significant increase in adverse reactions, predominantly abnormal liver function, but also including myalgia, headache, insomnia and various gastrointestinal symptoms. How are statin adverse reactions alleviated? Guidelines suggest switching to another statin, reducing dosage, decreasing the frequency of dosing or discontinuing the statin, but the latter three management options not only reduce the benefits of lipid modulation but may increase the risk of cardiovascular events.\u003c/p\u003e \u003cp\u003eXuezhikang, the only natural lipid regulator recognized by several authoritative guidelines in the cardiovascular field [including: ACC, AHA 2013 Guidelines for the Treatment of Blood Cholesterol to Reduce the Risk of Atherosclerosis in Adults, ESC, EAS 2011, 2016 Guidelines for the Management of Dyslipidemia, China 2007 Guidelines for the Diagnosis and Prevention of Chronic Stable Angina, 2016 Guidelines for the Prevention and Treatment of Dyslipidemia in Adults, 2018 Guidelines for the Rational Use of Drugs in Coronary Heart Disease. Guidelines, 2018 Guidelines for the Diagnosis and Treatment of Stable Coronary Heart Disease, 2018 Guidelines for the Diagnosis and Treatment of Acute Myocardial Infarction with Chinese and Western Medicine] is recognized as a natural lipid-regulating drug. Its main ingredient is monascus - which has been used for centuries in China as a food colouring and flavour enhancer\u003csup\u003e[\u003cspan citationid=\"CR52\" class=\"CitationRef\"\u003e52\u003c/span\u003e]\u003c/sup\u003e. It is refined through a modern GMP-standard process by adding special monascus to rice fermentation. It has a mechanism similar to that of statins, with 13 natural statin complexes as the main ingredients\u003csup\u003e[\u003cspan citationid=\"CR53\" class=\"CitationRef\"\u003e53\u003c/span\u003e]\u003c/sup\u003e. It is unique in reducing the risk of adverse reactions associated with the use of a single statin\u003csup\u003e[\u003cspan citationid=\"CR54\" class=\"CitationRef\"\u003e54\u003c/span\u003e]\u003c/sup\u003e. A number of RCTs\u003csup\u003e[\u003cspan additionalcitationids=\"CR56 CR57 CR58 CR59 CR60 CR61\" citationid=\"CR55\" class=\"CitationRef\"\u003e55\u003c/span\u003e\u0026ndash;\u003cspan citationid=\"CR62\" class=\"CitationRef\"\u003e62\u003c/span\u003e]\u003c/sup\u003e have demonstrated that Xuezhikang can lower cholesterol and LDL levels, reduce the incidence of adverse events, reduce the risk of cardiovascular events and recurrence, and significantly reduce coronary heart disease mortality and all-cause mortality. It is also inexpensive compared to synthetic statins. Based on the original lipid-lowering treatment with synthetic statins, the addition of Xuezhikang can be equivalent to intensify the effective of statin treatment and mitigate the risk of adverse reactions.\u003c/p\u003e \u003cp\u003eTo investigate the benefits and risks of intensifying statin therapy with Xuezhikang, this study included 2042 patients in 14 RCTs, with 1022 patients in the trial group (statin plus Xuezhikang) and 1020 patients in the control group (statin alone), and conducted a meta-analysis of the combined effect sizes of efficiency, TC, TG, LDLC, HDLC and adverse events. The results showed that compared with statins used alone, the addition of Xuezhikang intensive treatment could (i) significantly increase the effective rate, (ii) more effectively reduce TC, TG and LDLC levels and increase HDLC levels, (iii) significantly reduce the incidence of adverse events, and (iv) the lipid-regulating effect of simvastatin combined with Xuezhikang on LDLC was not significant.\u003c/p\u003e \u003cp\u003eThe 14 RCTs included in this study were low to moderate quality studies with obvious limitations, including: 1. All studies did not specify sample size estimates, which may affect test validity; 2. Although all included studies indicated that cases were randomly assigned to two groups, only eight studies clearly indicated the randomization method they used, while the remaining studies did not mention the specific randomization method and allocation concealment method, which is subject to unknowable selectivity bias. The remaining studies did not mention the specific randomization method and allocation concealment method, resulting in unknowable selectivity bias; 3. All cases did not mention whether they were blinded, either blinding of investigators and subjects or blinded evaluation of study outcomes, resulting in unknowable implementation bias and measurement bias; 4. Funnel plots of efficiency rates were found to be consistent with an inverted funnel shape with a narrow top and a wide bottom, but the lower part of the graph was lax and there are all hollow dots in the graphs, suggesting that there are insufficient large sample studies, low sample quality and publication bias; 5. Only 8 studies fully reported adverse events during the study period and follow-up, resulting in follow-up bias, Moreover, none of the three major systemic adverse reactions of statins - liver, muscle and digestive system - have been tracked and reported, which is not highly targeted; 6. In the study design, the effective rate of all studies took the proportion of cholesterol reduction as the threshold. TC and LDLC were equally important in lipid-regulating therapy, but only 11 RCTS reported LDLC levels; TG was reported in each RCTS. Since TG is easily affected by diet, only 10 RCTS mentioned whether to add therapeutic dietary intervention, which would cause unknown bias in this study.\u003c/p\u003e \u003cp\u003eIn summary, for the RCT study with statins combined with Xuezhikang as the intervention in the trial group, this analysis recommends: 1. The RCT should be designed more precisely before starting the study, for example, sample size estimation, clear randomization method, clear allocation method, application of blinding, and the number of adverse reactions and case shedding in the trial should be recorded based on facts; 2. Large sample clinical trials can be conducted to provide more comprehensive and objective clinical treatment; 3. The design of outcome indicators of the study should (1) if lipid-regulating efficacy is the study objective, the magnitude of lipid regulation of TC and LDLC should be the primary outcome indicator, and TG, HLDL and other lipoproteins should be secondary outcome indicators; (2) if safety is the study objective, the reporting of adverse effects should include liver, muscle and digestive system; (3) if TG is reported, whether to include dietary control should be considered.\u003c/p\u003e \u003cp\u003eIn Conclusion, the information extracted from the 14 RCTs included in this study was systematically evaluated and the results showed that Xuezhikang combined with statins had better and more stable modulation of cholesterol, triglyceride and LDL levels than statins used alone in terms of regulation of lipids in patients with hyperlipidemia, and there is a lower incidence rate of adverse events. The RCTs included in this study were of low to moderate quality and more high quality RCTs with large samples are needed to provide more reliable evidence.\u003c/p\u003e"},{"header":"4 Conclusion","content":"\u003cp\u003eIn conclusion, Xuezhikang capsule combined with statins in the treatment of hyperlipidemia can improve the clinical efficacy of patients, effectively reduce the levels of TG, TC and LDL-C, and increase the level of HDL-C, without serious adverse effects, which has certain guiding significance for clinical treatment. However, due to the influence of the quality of the included literature, the above results need to be verified by more high-quality studies with large sample size.\u003c/p\u003e"},{"header":"Abbreviations","content":"\u003cp\u003eXuezhikang capsule: Xuezhikang; total cholesterol: TC; triglycerides: TG; low density lipoprotein: LDLC; high density lipoprotein: HDLC; Randomized controlled trial: RCT;\u0026nbsp;odds ratio (OR); mean difference: MD; confidence intervals: CI; fixed effects model: FE; random-effects model: RE; standard error: SE; atherosclerotic cardiovascular diseases: ASCVD.\u003c/p\u003e"},{"header":"Declarations","content":"\u003cp\u003e\u003cstrong\u003eEthics approval and consent to participate\u003c/strong\u003e\u003c/p\u003e\n\u003cp\u003eNot applicable.\u003c/p\u003e\n\u003cp\u003e\u003cstrong\u003eConsent to publish\u003c/strong\u003e\u003c/p\u003e\n\u003cp\u003eNot applicable\u003c/p\u003e\n\u003cp\u003e\u003cstrong\u003eAvailability of data and materials\u003c/strong\u003e\u003c/p\u003e\n\u003cp\u003eAll data generated or analysed during this study are included in this published article [and its supplementary information files].\u003c/p\u003e\n\u003cp\u003e\u003cstrong\u003eCompeting interests\u003c/strong\u003e\u003c/p\u003e\n\u003cp\u003eAll authors certify that they have no affiliations with or involvement in any organization or entity with any financial interest or non-financial interest in the subject matter or materials discussed in this manuscript.\u003c/p\u003e\n\u003cp\u003e\u003cstrong\u003eFunding\u003c/strong\u003e\u003c/p\u003e\n\u003cp\u003eThe authors did not receive support from any organization for the submitted work.\u003c/p\u003e\n\u003cp\u003e\u003cstrong\u003eAuthors\u0026apos; Contributions\u003c/strong\u003e\u003c/p\u003e\n\u003cp\u003eChen\u0026nbsp;and Feng\u0026nbsp;contributed to literature search, data extraction, and data analysis. Li contributed to study conception and data analysis. Feng and Huang contributed to study conception, manuscript drafting, and data analysis. Chen critically revised the manuscript. All authors acknowledge the full responsibility for the analyses and interpretation of the report.\u003cstrong\u003e\u003cbr\u003e\u0026nbsp;Acknowledgements\u003c/strong\u003e\u003c/p\u003e\n\u003cp\u003eAll authors acknowledge the full responsibility for the analyses and interpretation of the report.\u003c/p\u003e\n\u003cp\u003e\u003cstrong\u003eAuthor details\u003c/strong\u003e\u003c/p\u003e\n\u003cp\u003e\u003csup\u003e1\u0026nbsp;\u003c/sup\u003eGuangzhou Hospital of Traditional Chinese Medicine, Cardiovascular Department, Guangzhou, Guangdong, China; \u003csup\u003e2\u003c/sup\u003e The Third Affiliated Hospital of Sun Yat-Sen University, Gynecology Department, Guangzhou, Guangdong, China; \u003csup\u003e3\u003c/sup\u003e Traditional Chinese Medicine Hospital of Guangdong Province, Endocrinology Department, Guangzhou, Guangdong, China; * Corresponding Author: e-mail address: dongxiong163@163com;\u003c/p\u003e\n\u003cp\u003e\u003cstrong\u003eORCID\u003c/strong\u003e\u003c/p\u003e\n\u003cp\u003eChen Dongxiong: https://orcid.org/0000-0003-4326-3188, Feng Huiyan: https://orcid.org/0000-0002-2805-7856, Li Yigen: https://orcid.org/0000-0002-1455-2258, Huang Jinzhu: https://orcid.org/0000-0002-4415-4349.\u003c/p\u003e\n\u003cp\u003e\u0026nbsp;\u003c/p\u003e"},{"header":"References","content":"\u003col\u003e\n\u003cli\u003eLibby P, Buring JE, Badimon L, Hansson GK, Deanfield J, Bittencourt MS, Tokg\u0026ouml;zoğlu L, Lewis EF. 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PMID: 17432681.\u003c/li\u003e\n\u003c/ol\u003e"}],"fulltextSource":"","fullText":"","funders":[],"hasAdminPriorityOnWorkflow":false,"hasManuscriptDocX":true,"hasOptedInToPreprint":true,"hasPassedJournalQc":"","hasAnyPriority":false,"hideJournal":true,"highlight":"","institution":"","isAcceptedByJournal":false,"isAuthorSuppliedPdf":false,"isDeskRejected":"","isHiddenFromSearch":false,"isInQc":false,"isInWorkflow":false,"isPdf":false,"isPdfUpToDate":true,"isWithdrawnOrRetracted":false,"journal":{"display":true,"email":"[email protected]","identity":"researchsquare","isNatureJournal":false,"hasQc":true,"allowDirectSubmit":true,"externalIdentity":"","sideBox":"","snPcode":"","submissionUrl":"/submission","title":"Research Square","twitterHandle":"researchsquare","acdcEnabled":true,"dfaEnabled":false,"editorialSystem":"","reportingPortfolio":"","inReviewEnabled":false,"inReviewRevisionsEnabled":true},"keywords":"Xuezhikang Capsule, Statin, Hyperlipidemia, Meta-analysis","lastPublishedDoi":"10.21203/rs.3.rs-1037189/v1","lastPublishedDoiUrl":"https://doi.org/10.21203/rs.3.rs-1037189/v1","license":{"name":"CC BY 4.0","url":"https://creativecommons.org/licenses/by/4.0/"},"manuscriptAbstract":"\u003ch2\u003eBackground\u003c/h2\u003e \u003cp\u003eTo compare the lipid-regulating effects and safety of statin combined with Xuezhikang capsules and statin used alone for hyperlipidemia.\u003c/p\u003e\u003ch2\u003eMethods\u003c/h2\u003e \u003cp\u003eCNKI, Wanfang database, VIP Chinese Journals, PubMed, Embase, and Cochrane library were searched to comprehensively collect and screen RCTs of Xuezhikang combined with statin compared with statin used alone for lipid modifying treatment in hyperlipidemia patients from the database built as of September 2021, and the Cochrane 5.1.0 quality evaluation form was used to evaluate the quality of the included literature and The Cochrane 5.1.0 quality assessment form was used to evaluate the quality of the included literature and bias analysis, extract basic study information, primary and secondary outcome indicators, and meta-analysis of the outcome indicators was performed using RevMan 5.3.\u003c/p\u003e\u003ch2\u003eResults\u003c/h2\u003e \u003cp\u003eA total of 14 studies with a total of 2042 patients were included, and the quality of the included studies was low to medium. ①Effectiveness rate: OR=3.63,95%CI[2.69,4.90]; Funnel plot: all within the funnel, but not in accordance with the principle of \"aggregation at the top and dispersion at the bottom\". ②Total cholesterol: MD=-0.61,95%CI[-0.84,-0.39], The forest plots of each subgroup are to the left. ③Triglycerides: MD=-0.30,95%CI[-0.41,-0.19], The forest plots of each subgroup are to the left,. ④ LDL: MD=-0.33,95%CI[-0.46,-0.20], The forest plots of each subgroup are to the left. ⑤ HDL: MD=0.23,95%CI[0.12,0.35], The forest plots of each subgroup are to the right. ⑥Adverse effects: OR=0.32, 95% CI[0.19,0.55].\u003c/p\u003e\u003ch2\u003eConclusion\u003c/h2\u003e \u003cp\u003eThe combination of statin with Xuezhikang capsule has better effect on lipid regulation in patients with hyperlipidemia, and can effectively reduce the incidence of adverse events and has better safety. It is recommended that the treatment of Xuezhikang combined with statin can be used as a safer and more effective treatment for patients with hyperlipidemia.\u003c/p\u003e","manuscriptTitle":"Statin in Combination with Xuezhikang Capsules Get More Lipid-Regulating Effects Than Statin Only: A Systematic Review and Meta-Analysis","msid":"","msnumber":"","nonDraftVersions":[{"code":1,"date":"2021-11-23 16:09:50","doi":"10.21203/rs.3.rs-1037189/v1","editorialEvents":[{"type":"communityComments","content":0}],"status":"published","journal":{"display":true,"email":"[email protected]","identity":"researchsquare","isNatureJournal":false,"hasQc":true,"allowDirectSubmit":true,"externalIdentity":"","sideBox":"","snPcode":"","submissionUrl":"/submission","title":"Research Square","twitterHandle":"researchsquare","acdcEnabled":true,"dfaEnabled":false,"editorialSystem":"","reportingPortfolio":"","inReviewEnabled":false,"inReviewRevisionsEnabled":true}}],"origin":"","ownerIdentity":"cf64612f-c551-4a80-b3bb-9b6677476e5a","owner":[],"postedDate":"November 23rd, 2021","published":true,"recentEditorialEvents":[],"rejectedJournal":[],"revision":"","amendment":"","status":"posted","subjectAreas":[{"id":8687268,"name":"Integrative \u0026 Complementary Medicine"},{"id":8687269,"name":"Clinical Pharmacology"}],"tags":[],"updatedAt":"2021-11-23T16:09:52+00:00","versionOfRecord":[],"versionCreatedAt":"2021-11-23 16:09:50","video":"","vorDoi":"","vorDoiUrl":"","workflowStages":[]},"version":"v1","identity":"rs-1037189","journalConfig":"researchsquare"},"__N_SSP":true},"page":"/article/[identity]/[[...version]]","query":{"redirect":"/article/rs-1037189","identity":"rs-1037189","version":["v1"]},"buildId":"-HB7Z8yhvgn0wM9Nzuekk","isFallback":false,"isExperimentalCompile":false,"dynamicIds":[84888],"gssp":true,"scriptLoader":[]}