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Hypercysteinemia, A Potential Risk Factor for Central Obesity and Related Disorders in Azores, Portugal

In Azores, the standardized mortality rate for coronary artery disease (CAD) is nearly the double when compared to mainland Portugal. The aim of this study was to compare the prevalence of conventional CAD risk factors, as well as the plasma aminothiol profile (and its major determinants), between t...

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Autores principales: Lima, Ana, Ferin, Rita, Bourbon, Mafalda, Baptista, José, Pavão, M. Leonor
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6609363/
https://www.ncbi.nlm.nih.gov/pubmed/31321096
http://dx.doi.org/10.1155/2019/1826780
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author Lima, Ana
Ferin, Rita
Bourbon, Mafalda
Baptista, José
Pavão, M. Leonor
author_facet Lima, Ana
Ferin, Rita
Bourbon, Mafalda
Baptista, José
Pavão, M. Leonor
author_sort Lima, Ana
collection PubMed
description In Azores, the standardized mortality rate for coronary artery disease (CAD) is nearly the double when compared to mainland Portugal. The aim of this study was to compare the prevalence of conventional CAD risk factors, as well as the plasma aminothiol profile (and its major determinants), between two groups of healthy subjects from Ponta Delgada (in Azores) and Lisbon (in mainland) cities, searching for precocious biomarker(s) of the disease. The study groups consisted of 101 healthy volunteers from Ponta Delgada (PDL) and 121 from Lisbon, aged 20–69 years. No differences in the prevalence of classical CAD risk factors were found between the study groups, except in physical inactivity and related central obesity, which were both higher in PDL men than in those from Lisbon. Hypercysteinemia, which seems to result from sulfur-rich amino acid diets and/or vitamin B(12) malabsorption, revealed to be significantly more prevalent in PDL vs. Lisbon subjects (18% vs. 4%, P=0.001), namely, in male gender. Moreover, plasma Cys levels predicted waist circumference (β coefficient = 0.102, P=0.032) and concomitant central obesity and were also associated with insulin resistance. Nevertheless, hyperhomocysteinemia prevalence was similar in both groups, despite the fact that PDL subjects exhibited a higher rate of vitamin B(12) deficiency compared to those from Lisbon (19% vs. 6%, P=0.003). Owing to the nature of this study design, a cause-effect relationship between high plasma Cys levels and central obesity or CAD risk could not be derived, but results strongly suggest that hypercysteinemia is a potential risk factor for metabolic disorders, i.e., obesity and insulin resistance, and CAD in Azores, a hypothesis that asks for confirmation through further large prospective studies.
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spelling pubmed-66093632019-07-18 Hypercysteinemia, A Potential Risk Factor for Central Obesity and Related Disorders in Azores, Portugal Lima, Ana Ferin, Rita Bourbon, Mafalda Baptista, José Pavão, M. Leonor J Nutr Metab Research Article In Azores, the standardized mortality rate for coronary artery disease (CAD) is nearly the double when compared to mainland Portugal. The aim of this study was to compare the prevalence of conventional CAD risk factors, as well as the plasma aminothiol profile (and its major determinants), between two groups of healthy subjects from Ponta Delgada (in Azores) and Lisbon (in mainland) cities, searching for precocious biomarker(s) of the disease. The study groups consisted of 101 healthy volunteers from Ponta Delgada (PDL) and 121 from Lisbon, aged 20–69 years. No differences in the prevalence of classical CAD risk factors were found between the study groups, except in physical inactivity and related central obesity, which were both higher in PDL men than in those from Lisbon. Hypercysteinemia, which seems to result from sulfur-rich amino acid diets and/or vitamin B(12) malabsorption, revealed to be significantly more prevalent in PDL vs. Lisbon subjects (18% vs. 4%, P=0.001), namely, in male gender. Moreover, plasma Cys levels predicted waist circumference (β coefficient = 0.102, P=0.032) and concomitant central obesity and were also associated with insulin resistance. Nevertheless, hyperhomocysteinemia prevalence was similar in both groups, despite the fact that PDL subjects exhibited a higher rate of vitamin B(12) deficiency compared to those from Lisbon (19% vs. 6%, P=0.003). Owing to the nature of this study design, a cause-effect relationship between high plasma Cys levels and central obesity or CAD risk could not be derived, but results strongly suggest that hypercysteinemia is a potential risk factor for metabolic disorders, i.e., obesity and insulin resistance, and CAD in Azores, a hypothesis that asks for confirmation through further large prospective studies. Hindawi 2019-06-20 /pmc/articles/PMC6609363/ /pubmed/31321096 http://dx.doi.org/10.1155/2019/1826780 Text en Copyright © 2019 Ana Lima et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Lima, Ana
Ferin, Rita
Bourbon, Mafalda
Baptista, José
Pavão, M. Leonor
Hypercysteinemia, A Potential Risk Factor for Central Obesity and Related Disorders in Azores, Portugal
title Hypercysteinemia, A Potential Risk Factor for Central Obesity and Related Disorders in Azores, Portugal
title_full Hypercysteinemia, A Potential Risk Factor for Central Obesity and Related Disorders in Azores, Portugal
title_fullStr Hypercysteinemia, A Potential Risk Factor for Central Obesity and Related Disorders in Azores, Portugal
title_full_unstemmed Hypercysteinemia, A Potential Risk Factor for Central Obesity and Related Disorders in Azores, Portugal
title_short Hypercysteinemia, A Potential Risk Factor for Central Obesity and Related Disorders in Azores, Portugal
title_sort hypercysteinemia, a potential risk factor for central obesity and related disorders in azores, portugal
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6609363/
https://www.ncbi.nlm.nih.gov/pubmed/31321096
http://dx.doi.org/10.1155/2019/1826780
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