Factors Associated With Fatigue in Persons With Atrial Fibrillation in the Atherosclerosis Risk in Communities (ARIC) Study

Author:

Wood Kathryn A.1ORCID,Alam Aniqa B.2,Chen Lin Yee3,Soliman Elsayed Z.4,Quyyumi Arshed A.5,Alonso Alvaro2

Affiliation:

1. Nell Hodgson Woodruff School of Nursing, Emory University, Atlanta, GA, USA

2. Department of Epidemiology, Rollins School of Public Health, Emory University, Atlanta, GA, USA

3. Cardiovascular Division, Department of Medicine, University of Minnesota Medical School, Minneapolis, MN, USA

4. Epidemiological Cardiology Research Center, Section on Cardiovascular Medicine, Department of Medicine, Wake Forest University School of Medicine, Winston Salem, NC, USA

5. Emory Clinical Cardiovascular Research Institute, Division of Cardiology, Emory University School of Medicine, Atlanta, GA, USA

Abstract

Background Atrial fibrillation (AF) is a common cardiac arrhythmia affecting over 6 million people in the U.S. Fatigue is a frequent symptom of AF, yet no underlying biological mechanisms have been identified in AF-related fatigue as in other chronic conditions such as cancer or HIV fatigue (inflammation, tissue injury). We aimed to identify biomarkers and correlates of AF-fatigue in ARIC participants. Methods Participants with AF from ARIC visit 5 (2011–2013) were included in the study. Multiple linear regression was used to estimate the association of high sensitivity troponin (hs-TnT), N-terminal fragment B-type natriuretic peptide (NT-proBNP) and high sensitivity C-reactive protein (hsCRP) levels with self-reported fatigue (SF-12 and PROMIS Fatigue Scale), depressive symptoms (Center for Epidemiological Studies Depression survey), and physical functioning (Short Physical Performance Battery) scores. All biomarkers underwent natural-log transformation. Results There were 446 participants (mean age: 78 y ± 5; 44% women). In adjusted analyses, NT-proBNP was associated with AF-fatigue (β: 0.11, 95% CI: 0.03, 0.19), increased depressive symptoms (β: 0.44, 95% CI: 0.19, 0.70), and decreased physical function (β: −0.48, 95% CI: −0.72, −0.23). Hs-TnT was also associated with elevated AF-fatigue (β: 0.24, 95% CI: 0.09, 0.39) along with decreased physical function (β: −1.19, 95% CI: -1.64, −0.75). No significant associations were found with hsCRP and fatigue. Conclusion Increased levels of cardiac injury biomarkers, depressive symptoms, and decreased physical function were associated with AF-fatigue. Inflammation was not associated with AF-fatigue; other physiological pathways, such as cardiac overload or myocardial injury may be more relevant in AF-fatigue.

Funder

National Heart, Lung, and Blood Institute

Publisher

SAGE Publications

Subject

Research and Theory

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