Endometriosis Is Associated with an Increased Risk of Coronary Artery Disease in Asian Women

This study was approved by the Institutional Review Board of China Medical University and the Hospital Research Ethics Committee (IRB permit number: CMUH-104-REC2-115) and is in compliance with institutional guidelines. Written informed consent from patients was waived due to low risk, and the study was approved by the institutional IRB of China Medical University and the Hospital Research Ethics Committee. This was a retrospective population-based cohort study. The data were retrieved from the Taiwan National Health Insurance Research Database (NHIRD). The purpose of creating the NHIRD was to generate reference data for medical and health policies and enhance medical research resources in Taiwan. The NHIRD includes numerous registration records of the general population in Taiwan, including clinical visits, hospitalizations, diagnoses, prescriptions, medical costs for reimbursement, and residential areas. All patient-related information was encrypted for confidentiality. The diagnoses in the NHIRD were coded by physicians in accordance with the International Classification of Disease, 9th Revision, Clinical Modification (ICD-9-CM) between 2000 and 2013. We selected 19,454 patients newly diagnosed with endometriosis, which were incident cases, (ICD-9-CM code: 617) between 2000 and 2012 from the Longitudinal Health Insurance. The comparison group (those without endometriosis; N = 77,816) were randomly selected from the NHIRD by matching the age frequency and the index year. Patients above 64 years old or diagnosed with CAD before the index date were eliminated. We followed up with the patients until the diagnosis of CAD, withdrawal from the National Health Insurance system, death, or the end of the study (31 December 2013). The outcome of interest was the incidence of CAD (ICD-9-CM codes: 410–414, A270, and A279) after the index date. The following conditions that are known to be associated with CAD were evaluated as a potential confounder including obesity (ICD-9-CM codes: 278 and A183), and risk factors of CAD including chronic kidney disease (ICD-9-CM codes: 585 and 586), hypertension (ICD-9-CM codes: 401–405, A260, and A269), hyperlipidemia (ICD-9-CM codes: 272.0–272.4), and diabetes mellitus (ICD-9-CM code: 250) [ 19 , 20 ]. We also considered the role of surgeries (including hysterectomy and oophorectomy) and medication (including hormone, statin, aspirin, antihypertensive therapy, diabetes medication, or insulin therapy) on the risk of CAD [ 21 ]. Categorical variables were compared using univariate analysis with the chi-square test. Continuous variables were compared by the Student’s t-test. We calculated person-years as the sum of the follow-up period for each individual. The incidence rate was calculated by the number of events and person-years. Univariate and multivariable estimated–hazard ratios (HRs) and 95% confidence intervals (CI) were calculated by the Cox proportional hazard model. Besides, we looked into the interaction between the potential confounders and endometriosis by including an interaction term into the multivariable model. The cumulative incidence of endometriosis to CAD was assessed by Kaplan–Meier analysis and the log-rank test. A two-tailed p -value of <0.05 and a 95% CI not including 1 were deemed statistically significant. All data were analyzed by SAS version 9.4 (SAS Institute Inc., Cary, NC, USA) for Windows 10.

Endometriosis is a systemic chronic inflammatory disease that affects 5–10% of the women of reproductive age in the United States [ 1 ]. The prevalence of endometriosis is higher in Asian women (approximately 6.8–15.7%) than in Caucasian women [ 2 , 3 ]. Endometriosis is characterized by the presence of endometrial tissues outside the uterus, leading to dysmenorrhea, dyspareunia, pelvic or abdominal pain, and infertility. The exact origin and pathogenesis of endometriosis remain unclear. The American Society for Reproductive Medicine (ASRM) criteria is mostly used to define the severity of endometriosis [ 4 ]. Based on endometriosis lesion’s location and size, ASRM criteria classify endometriosis from stage 1 (minimal disease, point score 1–5) to stage IV (severe disease, point score >40) [ 4 ]. Emerging evidence indicates that endometriosis is linked to several chronic diseases, including atherosclerosis, coronary heart disease, dyslipidemia, hypertension, autoimmune disease, and even gynecologic cancers [ 5 , 6 , 7 , 8 , 9 , 10 , 11 ]. Several inflammatory cytokines, such as the intercellular adhesion molecule 1, C-reactive protein, interleukins 1 and 6, tumor necrosis factor-α, and vascular endothelial growth factor, are elevated in both the serum and the peritoneal fluid of women with endometriosis, suggesting that endometriosis is associated with local and systemic inflammation [ 6 , 12 ]. Recent evidence indicates higher oxidative stress and an atherogenic lipid profile in women with endometriosis, indicating a mechanism similar to that of endothelial dysfunction and atherosclerosis [ 11 , 13 , 14 ]. Coronary artery disease (CAD) is the leading cause of morbidity and mortality for all women, particularly postmenopausal women [ 15 ]. However, recent studies have shown an increased prevalence of CAD in young women (<55 years), with no improvements in the prevalence and mortality rates of CAD in this age group over the last few decades [ 16 , 17 ]. It is imperative that we examine the varying risk factors of CAD in young women [ 18 ]. Women with endometriosis may represent a high-risk population for the development of CAD due to chronic inflammation and atherosclerosis [ 7 ]. Hence, we investigated the risk of CAD among Asian women with endometriosis.

We included 19,454 women newly diagnosed with endometriosis and 77,816 women without endometriosis. The mean age during the diagnosis of endometriosis was 37.4 ± 8.95 years. The mean follow-up duration was 7.36 (±3.82) years in the endometriosis cohort and 7.02 (±3.86) years in the comparison cohort ( Table 1 ). There were no significant differences between the endometriosis cohort and the comparison cohort in terms of the age at entry in the cohort and the mean follow-up duration—meaning, the frequency matching was successful. However, the proportion of women with obesity, hypertension, hyperlipidemia, DM, past history of hysterectomy, oophorectomy, hormonal treatment, statin, aspirin, antihypertensive, and antihyperglycemic drug were significantly higher in the endometriosis cohort than in the comparison cohort. Table 2 shows the incidence rates and adjusted HRs of CAD. A total of 3245 patients developed CAD. The incidence of CAD was higher in the endometriosis cohort than in the comparison cohort (5.96 vs. 4.38 per 1000 person-years; adjusted HR [95% CI], 1.34 [1.22, 1.47]). Figure 1 shows that the cumulative incidence of CAD events was significantly higher in the endometriosis cohort than in the comparison cohort (log-rank test, p < 0.001). Endometriosis was associated with CAD in age groups <40 and 40–49. The adjusted HRs (95% CI) for endometriosis patients were 1.42 (1.19, 1.70) and 1.33 (1.18, 1.49) in age groups <40 and 40–49, respectively, relative to patients without endometriosis ( Table 3 ). The association was not significant in the age group 50–64. In patients with hypertension, endometriosis increased the risk of CAD by 1.24-fold (1.04, 1.48) compared to the comparisons. Similarly, patients with endometriosis who took antihypertensive drugs had a higher hazard ratio of CAD, (adjusted HR = 1.12; 95% CI = 1.01, 1.24), see Table 3 . Moreover, there were interactions between endometriosis and age, hypertension, hyperlipidemia, DM, oophorectomy, statin, and antihyperglycemic drugs. Taken together, age and hypertension were associated with the risk of CAD in women with endometriosis in comparison with women without endometriosis ( Table 3 ). In endometriosis patients, increasing age was associated with an increased risk of CAD ( Table 4 ). Obesity, hypertension, hyperlipidemia, and DM were also associated with an increased risk of CAD ( Table 4 ). Regarding medication, hormone, statin, and anti-hyperglycemic medication were associated with a decreased risk of CAD ( Table 4 ). However, aspirin and anti-hypertensive medication were associated with an increased risk of CAD in endometriosis patients ( Table 4 ).

In this study, we found that women of age groups below 50 years with endometriosis had a higher risk of CAD as compared to those without. After 7.37 years (median) of follow-up, women with endometriosis had a 1.27-fold overall risk of developing CAD. Interestingly, we discovered a prominent unpropitious effect in patients without chronic kidney disease, hypertension, hyperlipidemia, diabetes mellitus, hysterectomy, oophorectomy, and medical treatment. Our findings suggest that healthy individuals, even without the known risk factors of CAD, should be aware of the risk of CAD when diagnosed with endometriosis. In addition to endometriosis, the risk of CAD was associated with age, obesity, chronic kidney disease, hypertension, hyperlipidemia, and diabetes mellitus, which are well-known risk factors of CAD. CAD begins with atherosclerosis, which is an inflammatory state of the intima of large and medium-sized arteries [ 22 ]; inflammation also leads to local, myocardial, and systemic complications of atherosclerosis. The above risk factors could further exaggerate the progression of atherosclerosis. In our study, we also found obesity, hypertension, hyperlipidemia, and DM were also associated with an increased risk of CAD in endometriosis patients. A comparison of women with and without endometriosis revealed that the adjusted HRs for CAD were the highest among those younger than 40 years of age and the risk decreased with age. These results were consistent with those of a previous study [ 7 ]. CAD is an age-related disease. Previous studies have shown that cytokine dysregulation results in the loss of the regulation of systemic inflammation at an older age [ 23 ]. Contrary to endometriosis, increasing age may be more strongly associated with CAD in elderly women. In our study, we also found increasing age was also associated with an increased risk of CAD in endometriosis patients (HR: 50–65 years > 40–49 years > below 40 years). The association between endometriosis and cardiovascular disease depicts an emerging topic in the field of women’s health. Various studies have emphasized immune mediators in endometriosis causing chronic inflammation, suggesting that endometriosis is a systemic, rather than a localized condition [ 24 , 25 , 26 , 27 ]. Endometriosis has currently been redefined as a systemic inflammatory disease. Endometriosis and atherosclerosis share similar mechanisms involving increased activated macrophages and inflammatory cytokines [ 28 ]. Women with endometriosis were found to have more macrophages, neutrophils, and dendritic cells in the peritoneal fluid than those without [ 29 ]. A recent study by Weisheng et al. detected 260 cytokines, chemokines, and growth factors in serum samples of patients with endometriosis [ 30 ]. Women with endometriosis also have significantly higher levels of serum markers of endothelial inflammation and activation, including the vascular cell adhesion molecule-1, intercellular adhesion molecule-1, E-selectin, vascular endothelial growth factor, von Willebrand factor, and ristocetin cofactor, reflecting an early development of atherosclerosis [ 31 ]. In several studies assessing ultrasonographic parameters such as a common carotid intima-media thickness, distensibility coefficient, flow-mediated dilation, and pulse wave velocity, women with endometriosis have shown increased arterial stiffness than the general population [ 32 , 33 ]. Studies have also suggested that oxidative stress and the presence of oxidized low-density lipoprotein in the blood might contribute to both diseases [ 5 ]. Aspirin (ASA) can be used for the primary and secondary prevention of CAD [ 34 ]. In previous clinical trials, the risk of CAD after taking ASA could be reduced by 20–40% [ 35 , 36 , 37 , 38 ]. However, one study showed low dose ASA did not have the protective effect of CAD [ 39 ]. Statin can also be used for the primary prevention of CAD [ 40 ]. The previous meta-analysis analyzed the 16 randomized control trials and showed statin appeared to be favorable for primary prevention of CAD but without effect on CAD death [ 40 ]. In our study, we found statin was also associated with a decreased risk of CAD in endometriosis patients. However, ASA was associated with an increased risk of CAD in endometriosis patients. We speculate the dosage of ASA in our population may not be enough for the prevention of CAD. In Taiwan, the usual dosage of ASA is 100 mg per day which may be considered a low dose. Oral contraceptives contain estrogen and progestin may be used in the treatment of endometriosis, which can reduce the risk of endometriosis [ 41 ]. Our study showed 58% of endometriosis patients used hormone medication. Hormone use also decreases CAD risk in endometriosis patients in our study. DM is a risk factor and comorbidity of CAD. In DM patients, antiglycemic medication will affect the outcome of CAD [ 42 ]. In our study, antiglycemic medications decreased the risk of CAD in endometriosis patients. Our study adds evidence on the association between endometriosis and adverse cardiovascular events. Prospective studies by Mu et al. involving 116,430 women from the Nurses’ Health Study II cohort reported that endometriosis was associated with an increased risk of coronary heart disease (relative risk [RR], 1.62; 95% CI, 1.39–1.89), hypercholesterolemia (RR, 1.25; 95% CI, 1.21–1.30), and hypertension (RR, 1.14; 95% CI, 1.09–1.18) [ 7 , 8 ]. A population-based cohort study by Chiang et al. demonstrated that women with endometriosis had a 1.2-fold increased risk of major adverse cardiovascular and cerebrovascular events (95% CI 1.05–1.29; p = 0.0053) as compared to the general population [ 43 ]. Our study should raise awareness on cardiovascular health in women by highlighting the role of inflammation in patients with endometriosis. Early diagnosis and treatment of endometriosis may prevent subsequent cardiovascular complications and warrant a better quality of life in these patients. Our study has several strengths. We included a large population-based cohort to investigate the association between endometriosis and CAD. We adjusted for several comorbidities, such as obesity, chronic kidney disease, hypertension, hyperlipidemia, diabetes mellitus, history of hysterectomy, oophorectomy, and hormonal treatment, which are the known risk factors of CAD. Our patients were representative of the general population, and the comparison cohort was enrolled from the same population. However, there are several limitations to this study. First, the gold standard of diagnosis of endometriosis is laparoscopic visualization with or without histological confirmation. In our study, endometriosis was diagnosed by invasive or non-invasive diagnostic methods based on the ICD-9-CM codes [ 38 ]. This may impact the results likely driving the association observed toward or away from the null. Invasive methods such as laparoscopic tissue proof were the definite diagnosis for endometriosis. Non-invasive methods such as ultrasound and tumor markers may diagnose endometriosis as well. However, non-invasive diagnosis methods are non-specific and may contain women without endometriosis, which may increase the association. Second, personal and social history, such as cigarette smoking, physical activity, and family history, could not be obtained from the NHIRD. Third, the confounders for endometriosis such as parity and age at menarche were not recorded in the database. Increased parity may be associated with a decreased risk of endometriosis. A previous study showed parity ≥2 had an odds ratio 0.3 (95% CI: 0.1–0.6) [ 44 ]. However, women with one child were not associated with a decreased risk of endometriosis (OR: 0.7, 95% CI: 0.3–1.7) [ 44 ]. Another study also reported parity was inversely associated with the risk of endometriosis [ 45 ]. Early menarche (less than 11–12 years of age) was reported associated with the risk of endometriosis [ 46 ]. In conclusion, endometriosis was significantly associated with a higher risk of CAD in Asian women. Further large-scale studies are needed to elucidate the cause-effect relationship between endometriosis and CAD.