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慢性心力衰竭发病机制的见解:免疫激活与恶病质。

Insights into the pathogenesis of chronic heart failure: immune activation and cachexia.

作者信息

Anker S D, Rauchhaus M

机构信息

Department of Cardiac Medicine, National Heart and Lung Institute, London, UK.

出版信息

Curr Opin Cardiol. 1999 May;14(3):211-6. doi: 10.1097/00001573-199905000-00004.

DOI:10.1097/00001573-199905000-00004
PMID:10358792
Abstract

Body wasting, i.e, cardiac cachexia, is a complication of chronic heart failure (CHF). The authors have suggested that cardiac cachexia should be diagnosed when nonedematous weight loss of more than 7.5% of the premorbid normal weight occurs over a time period of more than 6 months. In an unselected CHF outpatient population, 16% of patients were found to be cachectic. The cachectic state is predictive of poor survival independently of age, functional class, ejection fraction, and exercise capacity. Patients with cardiac cachexia suffer from a general loss of fat, lean, and bone tissue. Cachectic CHF patients are weaker and fatigue earlier. The pathophysiologic causes of body wasting in patients with CHF remain unclear, but initial studies have suggested that humoral neuroendocrine and immunologic abnormalities may be of importance. Cachectic CHF patients show increased plasma levels of catecholamines, cortisol, and aldosterone. Several studies have shown that cardiac cachexia is linked to increased plasma levels of tumor necrosis factor alpha. The degree of body wasting is strongly correlated with neurohormonal and immune abnormalities. Some investigators have suggested that endotoxin may be important in triggering immune activation in CHF patients. Available studies suggest that cardiac cachexia is a multifactorial neuroendocrine and immunologic disorder that carries a poor prognosis. A complex catabolic-anabolic imbalance in different body systems may cause body wasting in patients with CHF.

摘要

身体消瘦,即心源性恶病质,是慢性心力衰竭(CHF)的一种并发症。作者建议,当病前正常体重非水肿性减重超过7.5%且持续时间超过6个月时,应诊断为心源性恶病质。在未经过筛选的CHF门诊患者群体中,发现16%的患者存在恶病质。恶病质状态可独立于年龄、功能分级、射血分数和运动能力预测不良生存。心源性恶病质患者会出现全身脂肪、瘦肉和骨组织的流失。恶病质的CHF患者更虚弱,疲劳出现得更早。CHF患者身体消瘦的病理生理原因尚不清楚,但初步研究表明,体液神经内分泌和免疫异常可能起重要作用。恶病质的CHF患者血浆中儿茶酚胺、皮质醇和醛固酮水平升高。多项研究表明,心源性恶病质与血浆肿瘤坏死因子α水平升高有关。身体消瘦的程度与神经激素和免疫异常密切相关。一些研究人员认为,内毒素可能在触发CHF患者的免疫激活中起重要作用。现有研究表明,心源性恶病质是一种多因素神经内分泌和免疫紊乱,预后较差。不同身体系统中复杂的分解代谢 - 合成代谢失衡可能导致CHF患者身体消瘦。

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