Evidence map›Paper›PMID 40251594›Full record

ArticleBMC women's health2025

Association between gynecological cancers and female infertility: insights from bidirectional Mendelian randomization analysis.

Jifeng Li, Yifei Zeng, Dongxiao Zhang

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Article in BMC women's health, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

3 authors.

Jifeng LiBeijing Hospital of Traditional Chinese Medicine, Capital Medical University, Beijing, China.
Yifei ZengBeijing Hospital of Traditional Chinese Medicine, Capital Medical University, Beijing, China.
Dongxiao ZhangBeijing Hospital of Traditional Chinese Medicine, Capital Medical University, Beijing, China. Tzdx_thinking@126.com.

Funding

Beijing talent project 2019Capital research and transformation of clinical diagnosis and treatment technology Z211100002921020the Special Project on Traditional Chinese Medicine (TCM) Heritage ofancient books, literature and distinctive techniques GZY-KJS-2022-035Young doctor scholar project 2022
6 · The paper itself

Abstract

purposeIn recent years, research interest in the potential link between female infertility (FI) and gynecological cancer (GC), including ovarian cancer (OC), endometrial cancer (EC), cervical cancer (CC), and breast cancer (BC), has grown, yet findings remain inconclusive. This study aims to explore the causal relationship between FI and GC using bidirectional two-sample Mendelian randomization (MR) analyses, thereby informing future strategies for FI and GC prevention.

methodsWe utilized SNPs identified from genome-wide association studies (GWAS) on FI and GC. The inverse variance weighted (IVW) method served as the primary approach to assess the causal association between FI and GC. Additionally, five other MR methods-Weighted median, Weighted mode, MR-Egger, Simple mode, and Robust-Adjusted Profile Score-were employed to enhance result robustness and credibility.

resultsIn the forward MR analysis, our IVW results indicated no significant association between FI and GC (FI-BC: OR = 0.95, 95% CI: 0.83-1.09, P = 0.47, P-FDR = 0.775; FI-OC: OR = 1.01, 95% CI: 0.84-1.24, P = 0.789, P-FDR = 0.896; FI-CC: OR = 0.80, 95% CI: 0.61-1.06, P = 0.118, P-FDR = 0.775; FI-EC: OR = 1.07, 95% CI: 0.88-1.30, P = 0.490, P-FDR = 0.775).In the reverse MR analysis, we found a marginal association between BC and FI. However, after adjusting for multiple testing using the FDR method, no significant causal relationship was found between BC and FI, suggesting a marginal association (OR = 1.054, 95% CI: 1.001-1.108, P = 0.043, P-FDR = 0.331). For other cancers, no significant causal relationships were observed between OC, CC and EC with FI(OC-FI: OR = 1.043, 95% CI: 0.999-1.087, P = 0.051, P-FDR = 0.331;CC-FI: OR = 0.992, 95% CI: 0.956-1.028, P = 0.654, P-FDR = 0.836; EC-FI: OR = 1.006, 95% CI: 0.956-1.055, P = 0.809, P-FDR = 0.885).

conclusionsOur study found no significant causal relationship between FI and GC. However, a potential marginal association between BC and FI was observed. These findings underscore the need for further research to confirm this association and emphasize the importance of reproductive protection for young breast cancer patients to preserve fertility.

Indexed as

Genital Neoplasms, FemaleInfertility, FemaleMendelian Randomization AnalysisBreast NeoplasmsEndometrial NeoplasmsFemaleGenetic Predisposition to DiseaseGenome-Wide Association StudyHumansPolymorphism, Single NucleotideBreast cancerCervical cancerEndometrial cancerFemale infertilityGynecological cancerMendelian randomizationOvarian cancer

Identifiers

PMID40251594
PMCPMC12007144

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.