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慢性恰加斯病和特发性扩张型心肌病晚期心衰患者行心脏移植术后的代谢组学研究

Metabolomic insights in advanced cardiomyopathy of chronic chagasic and idiopathic patients that underwent heart transplant.

机构信息

School of Medicine, University of Brasilia, Brasilia, Brazil.

Laboratory of Protein Chemistry and Biochemistry, University of Brasilia, Brasilia, Brazil.

出版信息

Sci Rep. 2024 Apr 29;14(1):9810. doi: 10.1038/s41598-024-53875-7.

Abstract

Heart failure (HF) studies typically focus on ischemic and idiopathic heart diseases. Chronic chagasic cardiomyopathy (CCC) is a progressive degenerative inflammatory condition highly prevalent in Latin America that leads to a disturbance of cardiac conduction system. Despite its clinical and epidemiological importance, CCC molecular pathogenesis is poorly understood. Here we characterize and discriminate the plasma metabolomic profile of 15 patients with advanced HF referred for heart transplantation - 8 patients with CCC and 7 with idiopathic dilated cardiomyopathy (IDC) - using gas chromatography/quadrupole time-of-flight mass spectrometry. Compared to the 12 heart donor individuals, also included to represent the control (CTRL) scenario, patients with advanced HF exhibited a metabolic imbalance with 21 discriminating metabolites, mostly indicative of accumulation of fatty acids, amino acids and important components of the tricarboxylic acid (TCA) cycle. CCC vs. IDC analyses revealed a metabolic disparity between conditions, with 12 CCC distinctive metabolites vs. 11 IDC representative metabolites. Disturbances were mainly related to amino acid metabolism profile. Although mitochondrial dysfunction and loss of metabolic flexibility may be a central mechanistic event in advanced HF, metabolic imbalance differs between CCC and IDC populations, possibly explaining the dissimilar clinical course of Chagas' patients.

摘要

心力衰竭(HF)研究通常集中在缺血性和特发性心脏病上。慢性恰加斯心肌病(CCC)是一种在拉丁美洲高度流行的进行性退行性炎症性疾病,可导致心脏传导系统紊乱。尽管其具有临床和流行病学重要性,但 CCC 的分子发病机制仍知之甚少。在这里,我们使用气相色谱/四极杆飞行时间质谱法对 15 名因心力衰竭而接受心脏移植的晚期 HF 患者进行了特征描述和血浆代谢组学特征区分 - 8 名 CCC 患者和 7 名特发性扩张型心肌病(IDC)患者。与包括在内以代表对照(CTRL)情况的 12 名心脏供体个体相比,晚期 HF 患者表现出代谢失衡,有 21 个有区别的代谢物,主要表明脂肪酸、氨基酸和三羧酸(TCA)循环的重要成分积累。CCC 与 IDC 的分析显示两种情况下存在代谢差异,有 12 个 CCC 特有代谢物和 11 个 IDC 代表性代谢物。紊乱主要与氨基酸代谢谱有关。尽管线粒体功能障碍和代谢灵活性丧失可能是晚期 HF 的核心机制事件,但 CCC 和 IDC 人群之间的代谢失衡存在差异,这可能解释了恰加斯病患者的不同临床病程。

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