{"title":"Causal relationships between leukocyte telomere length and female reproductive system diseases: a bidirectional Mendelian randomization study.","authors":"Jun-Sen She, Rui Liu, Su-Qing Mao, Bo-Kang Zhou, Xiao-Jing Wu, Meng-Zhen Ding, Ling-Xiang Wang, Yi-Ning Cao, Hai-Yan Wu, Yu-Hang Long, Fei Guo, He-Feng Huang, Ling Gao","doi":"10.1097/RD9.0000000000000108","DOIUrl":null,"url":null,"abstract":"<p><strong>Objective: </strong>Although numerous observational studies have revealed a correlation between leukocyte telomere length (LTL) and female reproductive system diseases (RSDs), the findings of these studies have tended to be consistent. In this study, we accordingly sought to clarify the causal relationships between LTL and RSDs.</p><p><strong>Methods: </strong>We performed a bidirectional two-sample Mendelian randomization (MR) analysis using pooled statistics from genome-wide association studies of LTL and nine female RSDs. The final results were analyzed using five MR methods, with the inverse variance weighted (IVW) method used as the primary outcome. We applied MR-PRESSO to exclude outliers. Sensitivity analyses were also conducted to assess heterogeneity and pleiotropy.</p><p><strong>Results: </strong>In the forward MR analysis, a genetic prediction of longer LTLs was found to be causally associated with higher risks of endometriosis (IVW: odds ratio [<i>OR</i>] = 1.25, 95% confidence interval [<i>CI</i>] = 1.06-1.46, <i>P</i> = 0.008), leiomyoma of the uterus (IVW: <i>OR</i> = 1.73, 95% <i>CI</i> = 1.52-1.98, <i>P</i> = 4.9E-16), and ovarian cysts (IVW: <i>OR</i> = 1.31, 95% <i>CI</i>:1.19-1.45, <i>P</i> = 1.5E-07). In the reverse MR results, female RSDs were shown to have no significant effect on LTLs (all <i>P</i> values >0.05). Sensitivity analysis confirmed the robustness of these results.</p><p><strong>Conclusions: </strong>Our findings substantiate the assumption that a genetically predicted longer LTL elevates the risk of endometriosis, leiomyoma of the uterus, and ovarian cysts, with no influence of RSDs on LTL. These findings contribute to establishing a causal link between LTL and RSDs, overcoming the constraints of earlier observational studies. They also imply that LTL could potentially serve as a biomarker for the occurrence of endometriosis, leiomyoma of the uterus, and ovarian cysts.</p>","PeriodicalId":20959,"journal":{"name":"Reproductive and Developmental Medicine","volume":"9 2","pages":"83-91"},"PeriodicalIF":0.7000,"publicationDate":"2025-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12187154/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Reproductive and Developmental Medicine","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1097/RD9.0000000000000108","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/9/27 0:00:00","PubModel":"Epub","JCR":"Q4","JCRName":"OBSTETRICS & GYNECOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Objective: Although numerous observational studies have revealed a correlation between leukocyte telomere length (LTL) and female reproductive system diseases (RSDs), the findings of these studies have tended to be consistent. In this study, we accordingly sought to clarify the causal relationships between LTL and RSDs.
Methods: We performed a bidirectional two-sample Mendelian randomization (MR) analysis using pooled statistics from genome-wide association studies of LTL and nine female RSDs. The final results were analyzed using five MR methods, with the inverse variance weighted (IVW) method used as the primary outcome. We applied MR-PRESSO to exclude outliers. Sensitivity analyses were also conducted to assess heterogeneity and pleiotropy.
Results: In the forward MR analysis, a genetic prediction of longer LTLs was found to be causally associated with higher risks of endometriosis (IVW: odds ratio [OR] = 1.25, 95% confidence interval [CI] = 1.06-1.46, P = 0.008), leiomyoma of the uterus (IVW: OR = 1.73, 95% CI = 1.52-1.98, P = 4.9E-16), and ovarian cysts (IVW: OR = 1.31, 95% CI:1.19-1.45, P = 1.5E-07). In the reverse MR results, female RSDs were shown to have no significant effect on LTLs (all P values >0.05). Sensitivity analysis confirmed the robustness of these results.
Conclusions: Our findings substantiate the assumption that a genetically predicted longer LTL elevates the risk of endometriosis, leiomyoma of the uterus, and ovarian cysts, with no influence of RSDs on LTL. These findings contribute to establishing a causal link between LTL and RSDs, overcoming the constraints of earlier observational studies. They also imply that LTL could potentially serve as a biomarker for the occurrence of endometriosis, leiomyoma of the uterus, and ovarian cysts.
目的:虽然大量观察性研究揭示了白细胞端粒长度(LTL)与女性生殖系统疾病(rsd)之间的相关性,但这些研究的结果往往是一致的。因此,在本研究中,我们试图澄清LTL和rsd之间的因果关系。方法:利用LTL和9个雌性rsd全基因组关联研究的汇总统计数据,进行双向双样本孟德尔随机化(MR)分析。最终结果采用五种MR方法进行分析,以逆方差加权(IVW)方法作为主要结果。我们使用MR-PRESSO来排除异常值。敏感性分析也用于评估异质性和多效性。结果:在前向磁共振分析中,LTLs较长的遗传预测被发现与子宫内膜异位症(IVW:比值比[OR] = 1.25, 95%可信区间[CI] = 1.06-1.46, P = 0.008)、子宫平滑肌瘤(IVW: OR = 1.73, 95% CI = 1.52-1.98, P = 4.9E-16)和卵巢囊肿(IVW: OR = 1.31, 95% CI:1.19-1.45, P = 1.5E-07)的高风险有因果关系。相反MR结果显示,雌性rsd对ltl无显著影响(P值均为0.05)。敏感性分析证实了这些结果的稳健性。结论:我们的研究结果证实了这样的假设:基因预测的较长的LTL会增加子宫内膜异位症、子宫平滑肌瘤和卵巢囊肿的风险,而rsd对LTL没有影响。这些发现有助于建立LTL和rsd之间的因果关系,克服了早期观察性研究的局限性。他们还暗示LTL可能作为子宫内膜异位症、子宫平滑肌瘤和卵巢囊肿发生的生物标志物。