» Articles » PMID: 38684702

Metabolomic Insights in Advanced Cardiomyopathy of Chronic Chagasic and Idiopathic Patients That Underwent Heart Transplant

Overview
Journal Sci Rep
Specialty Science
Date 2024 Apr 29
PMID 38684702
Authors
Affiliations
Soon will be listed here.
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.

Citing Articles

Advances in the Understanding and Treatment of Chronic Chagas Cardiomyopathy.

Llerena-Velastegui J, Lopez-Usina A, Mantilla-Cisneros C Cardiol Res. 2024; 15(5):340-349.

PMID: 39420972 PMC: 11483117. DOI: 10.14740/cr1665.

References
1.
Lopaschuk G, Karwi Q, Tian R, Wende A, Abel E . Cardiac Energy Metabolism in Heart Failure. Circ Res. 2021; 128(10):1487-1513. PMC: 8136750. DOI: 10.1161/CIRCRESAHA.121.318241. View

2.
Maranon C, Egui A, Fernandez-Villegas A, Carrilero B, Thomas M, Segovia M . Benznidazole treatment reduces the induction of indoleamine 2,3-dioxygenase (IDO) enzymatic activity in Chagas disease symptomatic patients. Parasite Immunol. 2013; 35(5-6):180-7. DOI: 10.1111/pim.12030. View

3.
Lai L, Leone T, Keller M, Martin O, Broman A, Nigro J . Energy metabolic reprogramming in the hypertrophied and early stage failing heart: a multisystems approach. Circ Heart Fail. 2014; 7(6):1022-31. PMC: 4241130. DOI: 10.1161/CIRCHEARTFAILURE.114.001469. View

4.
Randle P, Garland P, Hales C, Newsholme E . The glucose fatty-acid cycle. Its role in insulin sensitivity and the metabolic disturbances of diabetes mellitus. Lancet. 1963; 1(7285):785-9. DOI: 10.1016/s0140-6736(63)91500-9. View

5.
Clements Jr R, DeJesus Jr P, WINEGRAD A . Raised plasma-myoinositol levels in uraemia and experimental neuropathy. Lancet. 1973; 1(7813):1137-41. DOI: 10.1016/s0140-6736(73)91143-4. View