Gene associations of lipid traits, lipid-lowering drug-target genes and endometriosis
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⤵ 4 in-corpus citations
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This study investigated the genetic links between lipid levels, genes targeted by lipid-lowering drugs, and endometriosis.
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Abstract
RESEARCH QUESTION: Does the observed correlation between dyslipidaemia and endometriosis indicate a bidirectional causal association?
DESIGN: Bidirectional Mendelian randomization was used to investigate the causal association between lipid traits and endometriosis. Drug-target Mendelian randomization was used to explore potential drug-target genes for managing endometriosis. In cases where lipid-mediated effects via specific drug targets were significant, aggregate analyses, such as summary-data-based Mendelian randomization and colocalization methods, were introduced to validate the outcomes. Mediation analyses supplemented these evaluations.
RESULTS: The bidirectional Mendelian randomization results suggested that genetically predicted triglyceride (OR 1.15, 95% CI 1.08-1.23), high-density lipoprotein cholesterol (OR 0.87, 95% CI 0.81-0.94), low-density lipoprotein cholesterol (OR 1.20, 95% CI 1.06-1.34) and apolipoprotein A (OR 0.90, 95% CI 0.83-0.96) concentrations were causally associated with endometriosis. Reverse Mendelian randomization results revealed that genetically proxied endometriosis was causally associated with triglyceride concentration (OR 1.02, 95% CI 1.01-1.02). In drug-target Mendelian randomization, genetic mimicry in proprotein convertase subtilisin/kexin type 9 (PCSK9) (OR 1.40, 95% CI 1.13-1.72), apolipoprotein B (APOB) (OR 1.49, 95% CI 1.21-1.86) and angiopoietin-related protein 3 (ANGPTL3) (OR 1.57, 95% CI 1.14-2.16) was significantly associated with the risk of endometriosis stages 1-2.
CONCLUSION: There is a potential bidirectional causal association between endometriosis and dyslipidaemia. Genetic mimicry of PCSK9, APOB and ANGPTL3 is associated with the risk of early-stage endometriosis. The development of lipid-lowering drugs to treat endometriosis is of potential clinical interest.
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References (39)
- A peek into the drug development scenario of endometriosis - A systematic review via openalex
- Assessment of atherosclerosis in endometriosis patients: the need to do much more via openalex
- Association Between Endometriosis and Hypercholesterolemia or Hypertension via openalex
- Atherosclerotic cardiovascular disease in women with endometriosis: a systematic review of risk factors and prospects for early surveillance via openalex
- Effect of simvastatin on baboon endometriosis via openalex
- Endometriosis via openalex
- Endometriosis and atherosclerosis: what we already know and what we have yet to discover via openalex
- Endometriosis: pathogenesis and treatment via openalex
- Erastin induces ferroptosis via ferroportin-mediated iron accumulation in endometriosis via openalex
- Familial risk for endometriosis and its interaction with smoking, age at menarche and body mass index: a population-based cohort study among siblings via openalex
- Iron-overloaded follicular fluid increases the risk of endometriosis-related infertility by triggering granulosa cell ferroptosis and oocyte dysmaturity via openalex
- Lipophilic statins inhibit growth and reduce invasiveness of human endometrial stromal cells via openalex
- mRNA levels of low-density lipoprotein receptors are overexpressed in the foci of deep bowel endometriosis via openalex
- Seven days of statin treatment improves nitric-oxide mediated endothelial-dependent cutaneous microvascular function in women with endometriosis via openalex
- Silencing of lncRNA MALAT1 facilitates erastin-induced ferroptosis in endometriosis through miR-145-5p/MUC1 signaling via openalex
- W4255815262 via openalex
- W4290860393 via openalex
- W4306867657 via openalex
- W4311127376 via openalex
- W4312204369 via openalex
- W4313245558 via openalex
- W4353079874 via openalex
- W4376225277 via openalex
- W6786570116 via openalex
- W6846959279 via openalex
- W1991354189 via openalex
- W2126913802 via openalex
- W2608349430 via openalex
- W2986932567 via openalex
- W3080477490 via openalex
- W3109397500 via openalex
- W3203318770 via openalex
- W3210570897 via openalex
- W4200030502 via openalex
- W4200054887 via openalex
- W4210374804 via openalex
- W4220834547 via openalex
- W4224299153 via openalex
- W4234160457 via openalex
Cited by (6)
- Metabolic remodeling of endometriosis microenvironment: Energy stress and immune evasion 2026
- Gamma-glutamyl transferase to high-density lipoprotein cholesterol ratio and endometriosis: a population-based study 2026
- Immune-epigenetic-metabolic crosstalk: attempting to unravel the multidimensional mechanisms of immune evasion in endometriosis 2026
- Lipid accumulation products and endometriosis: A population-based study from NHANES 2025
- Endometriosis phenotypes and staging in relation to lipid biomarkers: Findings from the ENDO Cohort Study 2025
- Study on the relationship between the non-HDL/HDL cholesterol ratio (NHHR) and endometriosis: a cross-sectional analysis utilizing the NHANES dataset 2025
Source provenance
- europepmc
- last seen: 2026-10-18T06:15:09.303036+00:00
- openalex
- last seen: 2026-06-10T17:14:06.276822+00:00
- pubmed
- last seen: 2026-10-18T06:13:25.750524+00:00
- unpaywall
- last seen: 2026-10-18T06:28:46.490043+00:00
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