Key result
Elevated levels of NT-proBNP (β 0.11; 95% CI 0.03-0.19) and hs-TnT (β 0.24; 95% CI 0.09-0.39) were associated with increased self-reported fatigue in patients with atrial fibrillation.
Why the study?
Fatigue is a frequent symptom of AF, but underlying biological mechanisms have not been identified.
Cross-Sectional (n=446)
Effect estimate: β 0.11 (95% CI 0.03-0.19)
Cardiac injury and overload biomarkers (hs-TnT and NT-proBNP), but not inflammation (hsCRP), are associated with fatigue and decreased physical function in patients with atrial fibrillation.
Hypothesis-generating for fatigue in AF; prospective studies needed before any clinical consideration.
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.
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Wood et al. (2024) conducted a cross-sectional in Atrial fibrillation (n=446). Cardiac biomarkers (NT-proBNP, hs-TnT, hsCRP) was evaluated on Self-reported fatigue (β 0.11, 95% CI 0.03-0.19). Elevated levels of NT-proBNP (β 0.11; 95% CI 0.03-0.19) and hs-TnT (β 0.24; 95% CI 0.09-0.39) were associated with increased self-reported fatigue in patients with atrial fibrillation.
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