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.
Subject(s)
Cardiomyopathy, Dilated , Chagas Cardiomyopathy , Heart Transplantation , Metabolomics , Humans , Male , Female , Middle Aged , Chagas Cardiomyopathy/metabolism , Chagas Cardiomyopathy/blood , Metabolomics/methods , Cardiomyopathy, Dilated/metabolism , Cardiomyopathy, Dilated/surgery , Cardiomyopathy, Dilated/blood , Adult , Metabolome , Heart Failure/metabolism , Heart Failure/etiology , Aged , Chronic Disease , Gas Chromatography-Mass SpectrometryABSTRACT
A sialoadenite esclerosante crônica, também conhecida como tumor de Kutner, é uma condição, que acomete, predominantemente, glândulas salivares maiores. Clinicamente, apresenta-se como um nódulo, móvel, assintomático e de consistência endurecida. Seu diagnóstico definitivo só é conseguido através da análise histopatológica onde estão presentes: intenso infiltrado inflamatório linfocítico, atrofia acinar, fibrose do parênquima glandular e graus variáveis de esclerose. Neste artigo, é relatado um caso clínico raro de sialoadenite esclerosante crônica, localizada em glândula salivar menor... (AU)
Chronic sclerosing sialoadenitis, also known as Kutner's tumor, is a condition that predominantly affects major salivary glands. Clinically it presents as a nodule, mobile, asymptomatic, and of hardened consistency. Its definitive diagnosis is only achieved through the histopathological analysis where they are present: intense lymphocytic inflammatory infiltrate, acinar atrophy, fibrosis of the glandular parenchyma and variable degrees of sclerosis. In this article we report a rare clinical case of chronic sclerosing sialoadenitis located in the minor salivary gland... (AU)