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GWAS Study

A Mendelian randomization study identified obesity as a causal risk factor of uterine endometrial cancer in Japanese.

Masuda T, Ogawa K, Kamatani Y et al.

32981178 PubMed ID
GWAS Study Type
40203 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

MT
Masuda T
OK
Ogawa K
KY
Kamatani Y
MY
Murakami Y
KT
Kimura T
OY
Okada Y
Chapter II

Abstract

Summary of the research findings

Causal inference is one of the challenges in epidemiologic studies. Gynecologic diseases have been reported to have association with obesity, however the causality remained controversial except for uterine endometrial cancer. We conducted two-sample Mendelian randomization (MR) analysis using the large-scale genome-wide association study (GWAS) results of gynecologic diseases and body mass index (BMI) in the Japanese population to assess causal effect of BMI on gynecologic diseases. We first conducted GWAS of ovarian cancer, uterine endometrial cancer, uterine cervical cancer, endometriosis, and uterine fibroid (n = 647, 909, 538, 5236, and 645 cases, respectively, and 39 556 shared female controls), and BMI (81 610 males and non-overlapping 23 924 females). We then applied two-sample MR using 74 BMI-associated variants as instrumental variables. We observed significant causal effect of increased BMI on uterine endometrial cancer (β = 0.735, P = .0010 in inverse variance-weighted analysis), which is concordant with results of European studies. Causal effect of obesity was not apparent in the other gynecologic diseases tested. Our MR analyses provided strong evidence of the causal role of obesity in gynecologic diseases etiology, and suggested a possible preventive effect of intervention for obesity.

647 Japanese ancestry cases, 39,556 Japanese ancestry controls

Chapter III

Study Statistics

Key metrics and study information

40203
Total Participants
GWAS
Study Type
No
Replicated
East Asian
Ancestry
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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