社区动脉粥样硬化风险(ARIC)研究中心房颤动患者疲劳的相关因素。

Biological research for nursing Pub Date : 2024-07-01 Epub Date: 2024-01-02 DOI:10.1177/10998004231225442
Kathryn A Wood, Aniqa B Alam, Lin Yee Chen, Elsayed Z Soliman, Arshed A Quyyumi, Alvaro Alonso
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引用次数: 0

摘要

背景:疲劳是心房颤动的常见症状,但与癌症或艾滋病疲劳(炎症、组织损伤)等其他慢性病一样,尚未发现心房颤动相关疲劳的潜在生物学机制。我们的目的是在急性心房颤动综合征参与者中确定心房颤动疲劳的生物标志物和相关因素:研究纳入了第 5 次(2011-2013 年)ARIC 访问中的房颤参与者。采用多元线性回归估算高敏肌钙蛋白(hs-TnT)、N-末端片段 B 型钠尿肽(NT-proBNP)和高敏 C 反应蛋白(hsCRP)水平与自我报告的疲劳(SF-12 和 PROMIS 疲劳量表)、抑郁症状(流行病学研究中心抑郁调查)和身体功能(短期体能测试)评分之间的关系。所有生物标志物均经过自然对数转换:共有 446 名参与者(平均年龄:78 岁 ± 5;44% 为女性)。在调整分析中,NT-proBNP 与房颤疲劳(β:0.11,95% CI:0.03,0.19)、抑郁症状增加(β:0.44,95% CI:0.19,0.70)和身体功能下降(β:-0.48,95% CI:-0.72,-0.23)相关。Hs-TnT 也与房颤疲劳升高(β:0.24,95% CI:0.09,0.39)和身体功能下降(β:-1.19,95% CI:-1.64,-0.75)有关。结论:心脏损伤生物标志物水平的升高与身体功能的下降(β:-1.19,95% CI:-1.64,-0.75)无明显关联:结论:心脏损伤生物标志物水平升高、抑郁症状和身体功能下降与房颤-疲劳有关。炎症与房颤疲劳无关;其他生理途径,如心脏负荷过重或心肌损伤可能与房颤疲劳更相关。
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Factors Associated With Fatigue in Persons With Atrial Fibrillation in the Atherosclerosis Risk in Communities (ARIC) Study.

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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