Functional capacity and skeletal muscle morphology are linked to N-terminal proBNP but not left ventricular ejection fraction in patients with heart failure.

IF 4.1 2区 医学 Q1 CARDIAC & CARDIOVASCULAR SYSTEMS
Jakob Wang, Thomas Groennebaek, Roni Nielsen, Kasper Pryds, Frank Vincenzo de Paoli, Hans Erik Bøtker, Kristian Vissing
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引用次数: 0

Abstract

Chronic heart failure (CHF) involves skeletal muscle abnormalities, including atrophy, inflammation, mitochondrial dysfunction, and fibrosis, which impair contractile function. This study examines whether muscle deterioration correlates with CHF disease severity by assessing the relationship between circulating N-terminal pro-brain natriuretic peptide (NT-proBNP) concentrations, left ventricular ejection fraction (LVEF), and muscle characteristics in patients with CHF. In 36 patients with CHF (LVEF ≤ 45%, New York Heart Association class I-III), we measured circulating NT-proBNP concentrations, LVEF, muscle strength and functional measures, and myocellular features, including fiber type-specific cross-sectional area (CSA), muscle stem cell (MuSC) and myonuclei content, and capillary density. Also, muscle mitochondrial function was evaluated. The concentration of NT-proBNP inversely correlated with muscle strength (R2 = 0.25, P < 0.01), mean fiber CSA (R2 = 0.15, P = 0.04), and MuSC content (R2 = 0.37, P < 0.01). Moreover, a nonsignificant inverse correlation was observed for capillary density (R2 = 0.12, P = 0.06). The strength of associations between NT-proBNP, fiber CSA, and capillary density was primarily driven by fiber type-specific correlations. Associations with MuSC content were equally strong across fiber types. No correlation was observed for measures of mitochondrial function. For LVEF, a nonsignificant correlation was observed only for overall MuSC content (R2 = 0.11, P = 0.07). Skeletal muscle deterioration in patients with CHF correlates with NT-proBNP, but not LVEF, suggesting that NT-proBNP concentration constitutes a stronger indicator of the link between CHF severity and skeletal muscle decline than LVEF as function parameter. Our findings highlight circulating NT-proBNP concentrations as a potential biomarker for the identification of patients at risk of experiencing skeletal muscle deterioration.NEW & NOTEWORTHY In this study, the authors reveal that elevated NT-proBNP levels are inversely associated with muscle function and cellular features in patients with chronic heart failure (CHF), including muscle fiber cross-sectional area, muscle stem cell content, and capillarization. NT-proBNP appears to be a more reliable marker than left ventricular ejection fraction (LVEF) for identifying skeletal muscle abnormalities and predicting muscle loss in CHF, offering potential for early intervention and personalized care.

心力衰竭患者的功能容量和骨骼肌形态与n端亲bnp有关,但与左心室射血分数无关。
背景:慢性心力衰竭(CHF)涉及骨骼肌异常,包括萎缩、炎症、线粒体功能障碍和纤维化,损害收缩功能。本研究通过评估循环n -末端前脑利钠肽(NT-proBNP)浓度、左室射血分数(LVEF)和CHF患者肌肉特征之间的关系,探讨肌肉退化是否与CHF疾病严重程度相关。方法:对36例CHF患者(LVEF≤45%,NYHA分类I-III),我们测量了循环NT-proBNP浓度、LVEF、肌肉力量和功能指标,以及心肌细胞特征,包括纤维类型特异性横截面积(CSA)、肌肉干细胞(MuSC)和肌核含量、毛细血管密度。同时,对肌肉线粒体功能进行评估。结果:NT-proBNP浓度与肌力(R2=0.25, P2=0.15, P=0.04)、MuSC含量(R2=0.37, P2=0.12, P=0.06)呈负相关。NT-proBNP、纤维CSA和毛细血管密度之间的相关性主要由纤维类型特异性相关性驱动。与MuSC含量的关联在不同纤维类型中同样强烈。没有观察到线粒体功能测量的相关性。对于LVEF,仅与总体MuSC含量无显著相关性(R2=0.11 P=0.07)。结论:CHF患者骨骼肌退化与NT-proBNP相关,而与LVEF无关,提示NT-proBNP浓度作为功能参数比LVEF更能反映CHF严重程度与骨骼肌退化之间的关系。我们的研究结果强调循环NTpro-BNP浓度是识别骨骼肌退化风险患者的潜在生物标志物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
9.60
自引率
10.40%
发文量
202
审稿时长
2-4 weeks
期刊介绍: The American Journal of Physiology-Heart and Circulatory Physiology publishes original investigations, reviews and perspectives on the physiology of the heart, vasculature, and lymphatics. These articles include experimental and theoretical studies of cardiovascular function at all levels of organization ranging from the intact and integrative animal and organ function to the cellular, subcellular, and molecular levels. The journal embraces new descriptions of these functions and their control systems, as well as their basis in biochemistry, biophysics, genetics, and cell biology. Preference is given to research that provides significant new mechanistic physiological insights that determine the performance of the normal and abnormal heart and circulation.
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