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Associations between biological aging and the risk of endometriosis: Evidence from a large population-based prospective cohort study

文献类型： 外文期刊

作者： Chen, Yuxia 1 ; Peng, Xinxing 2 ; Chen, Yang 3 ; Chen, Li 4 ; Yin, Xingzhu 2 ; Jiang, Wenrou 5 ; Chen, Biao 2 ; Tang, Yuhan 1 ;

作者机构： 1.Huazhong Univ Sci & Technol, Tongji Med Coll, Sch Publ Hlth, Dept Nutr & Food Hyg,Hubei Key Lab Food Nutr & Saf, Wuhan, Hubei, Peoples R China

2.Huazhong Univ Sci & Technol, Tongji Hosp, Tongji Med Coll, Dept Obstet & Gynecol, Wuhan, Hubei, Peoples R China

3.Hunan Prov Maternal & Child Hlth Care Hosp, Changsha, Hunan, Peoples R China

4.Chinese Acad Agr Sci, Oil Crops Res Inst, Wuhan, Hubei, Peoples R China

5.Huazhong Univ Sci & Technol, Tongji Med Coll, Sch Publ Hlth, Dept Occupat & Environm Hlth, Wuhan, Hubei, Peoples R China

6.Huazhong Univ Sci & Technol, Key Lab Environm & Hlth, Minist Educ, Wuhan, Hubei, Peoples R China

7.Huazhong Univ Sci & Technol, Tongji Med Coll, Sch Publ Hlth,Minist Environm Protect, State Key Lab Environm Hlth Incubating, Wuhan, Hubei, Peoples R China

关键词： Endometriosis; Biological aging; PhenoAge; Cox models; UK Biobank

期刊名称：EUROPEAN JOURNAL OF OBSTETRICS & GYNECOLOGY AND REPRODUCTIVE BIOLOGY （ 影响因子：1.9； 五年影响因子：2.3 ）

ISSN： 0301-2115

年卷期： 2025 年 313 卷

页码：

收录情况： SCI

摘要： Background: Endometriosis is a common disease for women of reproductive ages. Individuals with accelerated biological aging are at a higher risk of developing various diseases, however, the effect of biological aging on the risk of endometriosis remains unclear. We aimed to explore the associations between biological aging and the risk of endometriosis. Methods: 46,371 women from the UK Biobank who had no endometriosis diagnosis at baseline was involved in our study. We used Phenotypic age (PhenoAge) as a measure of biological aging. PhenoAge biological aging acceleration (PhenoAge_baa) was defined as the residual from the regression of PhenoAge on the basis of chronological age. Cox regression models and restricted cubic spline models with three knots were applied to assess the associations between biological aging and the risk of endometriosis. We also conducted subgroup analyses and assessed the combined effects of BMI and biological aging on endometriosis. Results: During a median follow-up of 12.5 years, 635 incident endometriosis were identified. After adjusting for potential factors, women with a status of accelerated aging were found to have a 35 % higher risk of developing endometriosis compared to those without accelerated aging. We also observed a joint effect of high BMI and accelerated biological aging on the incidence of endometriosis and no significant interactions were observed in our subgroup analyses. Conclusions: Our findings suggest that associations between accelerated biological aging and endometriosis that warrant further investigation.

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