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Identification of metabolomic profile related to adult Fontan pathophysiology

BACKGROUND: Metabolic disorders are important pathophysiologies that can cause multiple organ dysfunction and worsen prognosis in Fontan patients. This study aimed to comprehensively evaluate the metabolomic profile of adult Fontan patients and characterize its pathophysiology in relation to 2 contr...

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Autores principales: Motoki, Noriko, Motoki, Hirohiko, Utsumi, Masafumi, Yamazaki, Shoko, Obinata, Haruka, Takei, Kohta, Yasukochi, Satoshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8639334/
https://www.ncbi.nlm.nih.gov/pubmed/34901379
http://dx.doi.org/10.1016/j.ijcha.2021.100921
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author Motoki, Noriko
Motoki, Hirohiko
Utsumi, Masafumi
Yamazaki, Shoko
Obinata, Haruka
Takei, Kohta
Yasukochi, Satoshi
author_facet Motoki, Noriko
Motoki, Hirohiko
Utsumi, Masafumi
Yamazaki, Shoko
Obinata, Haruka
Takei, Kohta
Yasukochi, Satoshi
author_sort Motoki, Noriko
collection PubMed
description BACKGROUND: Metabolic disorders are important pathophysiologies that can cause multiple organ dysfunction and worsen prognosis in Fontan patients. This study aimed to comprehensively evaluate the metabolomic profile of adult Fontan patients and characterize its pathophysiology in relation to 2 control groups. METHODS AND RESULTS: We performed metabolomic analysis of 31 plasma samples using capillary electrophoresis time-of-flight mass spectrometry. This observational cross-sectional study compared plasma metabolites of 14 heterogeneous adult Fontan patients with those of control groups, including 9 patients with congenital heart disease after biventricular repair and 8 normal healthy controls. Fontan patients exhibited significant differences in intermediate metabolite concentrations related to glycolysis, the tricarboxylic acid (TCA) cycle, and the urea cycle. The plasma concentrations of lactic acid, 2-oxoglutarate, isocitric acid, malic acid, cis-aconitic acid, arginine, citrulline, and the ratio of ornithine/citrulline showed significantly differences among the groups. Multiple logistic regression analysis with a stepwise selection-elimination method identified 2-oxoglutaric acid (odds ratio [OR] 1.98, 95% confidence interval [CI] 1.05–3.76) and cis-aconitic acid (OR 2.69, 95% CI 1.04–6.99) as independently associated with Fontan patients. After adjustment for the covariates of age and gender, 2-oxoglutaric acid (OR 1.97, 95% CI 0.98–3.93) and cis-aconitic acid (OR 3.88, 95% CI 0.99–15.2) showed remarkable relationships with Fontan patients. CONCLUSIONS: The present findings suggest that abnormalities in the TCA cycle and amino acid metabolism are distinguishing features in the pathophysiology of Fontan patients. Future metabolomic studies will assist in developing biomarkers for the early prediction of “silent” Fontan pathophysiologies.
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spelling pubmed-86393342021-12-09 Identification of metabolomic profile related to adult Fontan pathophysiology Motoki, Noriko Motoki, Hirohiko Utsumi, Masafumi Yamazaki, Shoko Obinata, Haruka Takei, Kohta Yasukochi, Satoshi Int J Cardiol Heart Vasc Original Paper BACKGROUND: Metabolic disorders are important pathophysiologies that can cause multiple organ dysfunction and worsen prognosis in Fontan patients. This study aimed to comprehensively evaluate the metabolomic profile of adult Fontan patients and characterize its pathophysiology in relation to 2 control groups. METHODS AND RESULTS: We performed metabolomic analysis of 31 plasma samples using capillary electrophoresis time-of-flight mass spectrometry. This observational cross-sectional study compared plasma metabolites of 14 heterogeneous adult Fontan patients with those of control groups, including 9 patients with congenital heart disease after biventricular repair and 8 normal healthy controls. Fontan patients exhibited significant differences in intermediate metabolite concentrations related to glycolysis, the tricarboxylic acid (TCA) cycle, and the urea cycle. The plasma concentrations of lactic acid, 2-oxoglutarate, isocitric acid, malic acid, cis-aconitic acid, arginine, citrulline, and the ratio of ornithine/citrulline showed significantly differences among the groups. Multiple logistic regression analysis with a stepwise selection-elimination method identified 2-oxoglutaric acid (odds ratio [OR] 1.98, 95% confidence interval [CI] 1.05–3.76) and cis-aconitic acid (OR 2.69, 95% CI 1.04–6.99) as independently associated with Fontan patients. After adjustment for the covariates of age and gender, 2-oxoglutaric acid (OR 1.97, 95% CI 0.98–3.93) and cis-aconitic acid (OR 3.88, 95% CI 0.99–15.2) showed remarkable relationships with Fontan patients. CONCLUSIONS: The present findings suggest that abnormalities in the TCA cycle and amino acid metabolism are distinguishing features in the pathophysiology of Fontan patients. Future metabolomic studies will assist in developing biomarkers for the early prediction of “silent” Fontan pathophysiologies. Elsevier 2021-11-24 /pmc/articles/PMC8639334/ /pubmed/34901379 http://dx.doi.org/10.1016/j.ijcha.2021.100921 Text en © 2021 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Paper
Motoki, Noriko
Motoki, Hirohiko
Utsumi, Masafumi
Yamazaki, Shoko
Obinata, Haruka
Takei, Kohta
Yasukochi, Satoshi
Identification of metabolomic profile related to adult Fontan pathophysiology
title Identification of metabolomic profile related to adult Fontan pathophysiology
title_full Identification of metabolomic profile related to adult Fontan pathophysiology
title_fullStr Identification of metabolomic profile related to adult Fontan pathophysiology
title_full_unstemmed Identification of metabolomic profile related to adult Fontan pathophysiology
title_short Identification of metabolomic profile related to adult Fontan pathophysiology
title_sort identification of metabolomic profile related to adult fontan pathophysiology
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8639334/
https://www.ncbi.nlm.nih.gov/pubmed/34901379
http://dx.doi.org/10.1016/j.ijcha.2021.100921
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