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Author Notes:

Correspondence: Dr. Aaron R. Folsom, Division of Epidemiology & Community Health, School of Public Health, University of Minnesota, 1300 South 2nd Street, Suite 300, Minneapolis, MN 55454, United States. folso001@umn.edu. Telephone +1-612-626-8867. Fax: +1-612-624-0315.

Author contributions: Dylan Berger analyzed the data and drafted the manuscript. Aaron R. Folsom designed the study, reviewed the manuscript and provided critical comments. Pamela J. Schreiner reviewed the manuscript and provided critical comments. Lin Y. Chen reviewed the manuscript and provided critical comments.

Erin D. Michos reviewed the manuscript and provided critical comments. Wesley T. O’Neal reviewed the manuscript and provided critical comments. Elsayed Z. Soliman contributed to the data collection, reviewed the manuscript and provided critical comments. Alvaro Alonso contributed to the data collection, reviewed the manuscript and provided critical comments.

The authors thank the other investigators, staff and participants of the Atherosclerosis Risk in Communities Study for their important contributions.

Disclosures: The authors declare that they have no conflict of interest.

Subjects:

Research Funding:

The Atherosclerosis Risk in Communities Study has been funded by the National Heart, Lung, and Blood Institute [NHLBI contracts HHSN268201100005C, HHSN268201100006C, HHSN268201100007C, HHSN268201100008C, HHSN268201100009C, HHSN2682011000IOC, HHSN268201100011C]; and the American Heart Association [grant 16EIA26410001].

Keywords:

  • Science & Technology
  • Life Sciences & Biomedicine
  • Geriatrics & Gerontology
  • Obstetrics & Gynecology
  • Testosterone
  • Atrial fibrillation
  • Epidemiology
  • ARIC study
  • Endogenous sex hormones
  • Postmenopausal women
  • Lifetime risk
  • Reproducibility
  • Association
  • Estradiol
  • Glucose
  • Disease
  • Stroke

Plasma total testosterone and risk of incident atrial fibrillation: The Atherosclerosis Risk in Communities (ARIC) study

Journal Title:

Maturitas

Volume:

Volume 125

Publisher:

, Pages 5-10

Type of Work:

Article | Post-print: After Peer Review

Abstract:

Objective: Whether endogenous testosterone concentrations are associated with atrial fibrillation (AF) development is not well established. We assessed the association between plasma total testosterone concentrations and incident AF in a population-based longitudinal study. Study design: Using data from the prospective Atherosclerosis Risk in Communities (ARIC) study, we identified incident AF among 9,282 participants who had plasma total testosterone measured by liquid chromatography tandem mass spectrometry at Visit 4 (1996-1998). Main outcome measures: AF cases were identified by electrocardiograms performed during study visits, hospital records/discharge codes, and death certificates through 2013. We estimated hazard ratios (HRs) and 95% confidence intervals (95% CIs) for incident AF across quartiles of plasma total testosterone, stratified by sex, with multivariable Cox models. Results: The mean age of the participant sample at ARIC Visit 4 was 63 years (range 52-75); 54.5% were women. Mean (SD) plasma total testosterone levels were 537 ng/dL (213) for men and 27.6 ng/dL (34.7) for women. Over a mean of 13.7 years of follow-up, 1664 incident cases of AF were identified. Comparing those in the highest quartile of plasma total testosterone concentration to those in the lowest quartile and after adjustment for potential confounding variables, there was a positive association between plasma total testosterone and incident AF in men (HR 1.33, 95% CI 1.07, 1.66), but no such association in women (HR 0.99, 95% CI 0.80, 1.22). Conclusion: A higher plasma total testosterone concentration was associated with a modestly greater incidence rate of AF in men.

Copyright information:

© 2019 Elsevier B.V. All rights reserved.

This is an Open Access work distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/).
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