Evidence map›Paper›PMID 42027961›Full record

ArticleInternational journal of women's health2026

The Relationship Between Immune Cells and Uterine Fibroids: A Bidirectional Mendelian Randomization Study.

Xiaoxiao Deng, Shaoli Zhuang, Yanping Chen, Fangfang Chen, Zhang Zhang, Wu Chen

Abstract read
In one paragraph

Article in International journal of women's health, 2026. 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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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Xiaoxiao DengDepartment of Gynecology, The People's Hospital of Pingyang, Wenzhou, Zhejiang, 325400, People's Republic of China.
Shaoli ZhuangDepartment of Gynecology, The People's Hospital of Pingyang, Wenzhou, Zhejiang, 325400, People's Republic of China.
Yanping ChenDepartment of Gynecology, The People's Hospital of Pingyang, Wenzhou, Zhejiang, 325400, People's Republic of China.
Fangfang ChenDepartment of Gynecology, The People's Hospital of Pingyang, Wenzhou, Zhejiang, 325400, People's Republic of China.
Zhang ZhangDepartment of Gynecology, The People's Hospital of Pingyang, Wenzhou, Zhejiang, 325400, People's Republic of China.
Wu ChenDepartment of Gynecology, The People's Hospital of Pingyang, Wenzhou, Zhejiang, 325400, People's Republic of China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: This research applied a bidirectional Mendelian randomization (MR) framework to investigate potential two-way causal associations between immune cell phenotypes and uterine fibroids (UF). Methods: This research drew upon publicly available data from large-scale genome-wide association studies (GWAS), encompassing 731 immune cell phenotypes from 3757 participants and UF data from 21,024 cases and 237,694 controls. Primary causal estimates were derived using the inverse-variance weighted (IVW) approach, with additional validation through MR-Egger, weighted median, and related methods. To ensure the reliability of the results, MR-PRESSO analysis, leave-one-out analysis, and false discovery rate (FDR) correction were also performed. Results: Forward MR analyses initially identified 39 immune phenotypes significantly associated with UF (IVW P < 0.05), comprising 23 risk factors and 16 protective factors. Applying stringent selection criteria-IVW P < 0.001, consistent odds ratio (OR) directions across five analytical methods, and pleiotropy P > 0.05-three phenotypes demonstrated strong causal links with UF: CD39⁺ CD8⁺ T cells, CD25 expression on IgD Conclusion: Our research offers compelling genetic evidence supporting a forward causal link between CD39⁺ CD8⁺ T cells, CD25 on IgD

Indexed as

bidirectional mendelian randomizationcausalityimmune cellsinverse-variance weighteduterine fibroids

Identifiers

PMID42027961
PMCPMC13101819

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