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Association Between Levels of Sex Hormones and Risk of Esophageal Adenocarcinoma and Barrett's Esophagus

  • Shao Hua Xie*
  • , Rui Fang
  • , Mingtao Huang
  • , Juncheng Dai
  • , Aaron P. Thrift
  • , Lesley A. Anderson
  • , Wong Ho Chow
  • , Leslie Bernstein
  • , Marilie D. Gammon
  • , Harvey A. Risch
  • , Nicholas J. Shaheen
  • , Brian J. Reid
  • , Anna H. Wu
  • , Prasad G. Iyer
  • , Geoffrey Liu
  • , Douglas A. Corley
  • , David C. Whiteman
  • , Carlos Caldas
  • , Paul D. Pharoah
  • , Laura J. Hardie
  • Rebecca C. Fitzgerald, Hongbing Shen, Thomas L. Vaughan, Jesper Lagergren
*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

25 Scopus citations

Abstract

Background & Aims: Esophageal adenocarcinoma (EAC) occurs most frequently in men. We performed a Mendelian randomization analysis to investigate whether genetic factors that regulate levels of sex hormones are associated with risk of EAC or Barrett's esophagus (BE). Methods: We conducted a Mendelian randomization analysis using data from patients with EAC (n = 2488) or BE (n = 3247) and control participants (n = 2127), included in international consortia of genome-wide association studies in Australia, Europe, and North America. Genetic risk scores or single-nucleotide variants were used as instrumental variables for 9 specific sex hormones. Logistic regression provided odds ratios (ORs) with 95% CIs. Results: Higher genetically predicted levels of follicle-stimulating hormones were associated with increased risks of EAC and/or BE in men (OR, 1.14 per allele increase; 95% CI, 1.01–1.27) and in women (OR, 1.28; 95% CI, 1.03–1.59). Higher predicted levels of luteinizing hormone were associated with a decreased risk of EAC in men (OR, 0.92 per SD increase; 95% CI, 0.87–0.99) and in women (OR, 0.93; 95% CI, 0.79–1.09), and decreased risks of BE (OR, 0.88; 95% CI, 0.77–0.99) and EAC and/or BE (OR, 0.89; 95% CI, 0.79–1.00) in women. We found no clear associations for other hormones studied, including sex hormone–binding globulin, dehydroepiandrosterone sulfate, testosterone, dihydrotestosterone, estradiol, progesterone, or free androgen index. Conclusions: In a Mendelian randomization analysis of data from patients with EAC or BE, we found an association between genetically predicted levels of follicle-stimulating and luteinizing hormones and risk of BE and EAC.

Original languageEnglish
Pages (from-to)2701-2709.e3
JournalClinical Gastroenterology and Hepatology
Volume18
Issue number12
DOIs
StatePublished - Nov 2020
Externally publishedYes

Bibliographical note

Publisher Copyright:
© 2020 AGA Institute

Keywords

  • Causality
  • Esophageal Neoplasms
  • Gonadal Steroid Hormones
  • Sex Difference

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