Department of Cardiology, Castle Hill Hospital, Hull York Medical School (at University of Hull), Kingston upon Hull, UK.
Department of Cardiology, Castle Hill Hospital, Hull York Medical School (at University of Hull), Kingston upon Hull, UK; Robertson Centre for Biostatistics & Clinical Trials, University of Glasgow & National Heart & Lung Institute, Imperial College, London, UK.
Int J Cardiol. 2018 Aug 1;264:104-112. doi: 10.1016/j.ijcard.2018.03.089. Epub 2018 Mar 22.
Weight loss is common in patients with chronic heart failure (CHF) and is associated with adverse outcome. Activation of the sympathetic nervous system has been implicated in weight loss, wasting and cachexia. However, the effect of sympathetic antagonism on weight change in patients with CHF is not well defined.
We evaluated changes in body weight, the incidence of cachexia (weight loss >6%) and significant weight gain (>5%) in unselected patients with CHF due to left ventricular systolic dysfunction (LVSD) (LV ejection fraction (LVEF) <40%) and studied the effect of beta-blockade on weight change.
Of the 1480 patients enrolled (median NTproBNP:1651 ng/L, median LVEF:31%), 86% received beta-blocker, 11% never had beta-blocker and 3% discontinued beta-blocker between baseline and 1 year. Patients who did not have or tolerate beta-blocker were more likely to develop cachexia (23% vs 10%, p < 0.001) and less likely to have significant weight gain (22% vs 24%, p < 0.001) than patient who had beta-blocker. During a median follow up of 1876 days (IQR: 993-3052 days), 894 (60%) patients died. Higher body mass index (BMI) at baseline, weight gain and beta-blocker therapy were associated with better outcome. Patients who had all 3 features: beta-blocker therapy, baseline BMI ≥ 25 and significant weight gain had the best outcome (22% mortality at 5 years).
Patients with CHF due to LVSD who receive beta-blocker were less likely to develop cachexia and more likely to have significant weight gain and better outcome compared to patients who did not receive or tolerate beta-blocker.
慢性心力衰竭(CHF)患者常出现体重减轻,并与不良预后相关。交感神经系统的激活与体重减轻、消耗和恶病质有关。然而,交感神经拮抗作用对 CHF 患者体重变化的影响尚不清楚。
我们评估了左心室收缩功能障碍(LVSD)(LVEF<40%)导致的未选择 CHF 患者的体重变化、恶病质(体重减轻>6%)和显著体重增加(>5%)的发生率,并研究了β受体阻滞剂对体重变化的影响。
在纳入的 1480 例患者中(中位 NTproBNP:1651ng/L,中位 LVEF:31%),86%接受了β受体阻滞剂治疗,11%从未接受过β受体阻滞剂治疗,3%在基线和 1 年内停用了β受体阻滞剂。未使用或不能耐受β受体阻滞剂的患者更易发生恶病质(23%比 10%,p<0.001),更不易发生显著体重增加(22%比 24%,p<0.001)。中位随访 1876 天(IQR:993-3052 天)期间,894 例(60%)患者死亡。基线时较高的体重指数(BMI)、体重增加和β受体阻滞剂治疗与更好的预后相关。具有所有 3 个特征(β受体阻滞剂治疗、基线 BMI≥25 和显著体重增加)的患者具有最佳预后(5 年死亡率为 22%)。
与未接受或不能耐受β受体阻滞剂的患者相比,LVSD 导致的 CHF 患者接受β受体阻滞剂治疗后,更不易发生恶病质,更易发生显著体重增加,且预后更好。