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The relationship between of ACE I/D and the MTHFR C677T polymorphisms in the pathophysiology of type 2 diabetes mellitus in a population of Brazilian obese patients
OBJECTIVES: This study aimed to evaluate the frequencies of the angiotensin converting enzyme (ACE) gene insertion/deletion (I/D) and methylenetetrahydrofolate reductase (MTHFR) gene C677T polymorphisms in obese patients with and without type 2 diabetes mellitus (T2DM). SUBJECTS AND METHODS: These p...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Sociedade Brasileira de Endocrinologia e Metabologia
2018
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10118689/ https://www.ncbi.nlm.nih.gov/pubmed/29694640 http://dx.doi.org/10.20945/2359-3997000000005 |
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author | Pirozzi, Flavio Fontes Belini, Edis Okumura, Jessika Viviani Salvarani, Mariana Bonini-Domingos, Claudia Regina Ruiz, Milton Artur |
author_facet | Pirozzi, Flavio Fontes Belini, Edis Okumura, Jessika Viviani Salvarani, Mariana Bonini-Domingos, Claudia Regina Ruiz, Milton Artur |
author_sort | Pirozzi, Flavio Fontes |
collection | PubMed |
description | OBJECTIVES: This study aimed to evaluate the frequencies of the angiotensin converting enzyme (ACE) gene insertion/deletion (I/D) and methylenetetrahydrofolate reductase (MTHFR) gene C677T polymorphisms in obese patients with and without type 2 diabetes mellitus (T2DM). SUBJECTS AND METHODS: These polymorphisms were analyzed by polymerase chain reaction in 125 patients with obesity, 47 (T2DM) and 78 (Control Group). RESULTS: No significant difference was found on comparing the T2DM and Control Groups in respect to the genotypic frequencies of the polymorphisms - (II: 13.3% vs. 12.0%; ID: 37.8% vs. 37.3; DD: 48.9% vs. 50.7%; CC: 36.2% vs. 39.0%; CT: 46.8% vs. 49.3%; TT: 17.0% vs. 11.7%), and alleles (I: 32.2% vs. 30.7%; D: 67.8% vs. 69.3%; C: 59.6% vs. 63.6%; T: 40.4% vs. 36.4%) and their synergisms in the pathophysiology of T2DM. On analyzing the T2DM Group, there were no significant differences in the presence of complications. In this population of Brazilian obese patients, no correlation was found between the ACE and MTHFR polymorphisms in the development of T2DM. CONCLUSION: Analyzing only the group with diabetes, there was also no relationship between these polymorphisms and comorbidities. |
format | Online Article Text |
id | pubmed-10118689 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Sociedade Brasileira de Endocrinologia e Metabologia |
record_format | MEDLINE/PubMed |
spelling | pubmed-101186892023-04-21 The relationship between of ACE I/D and the MTHFR C677T polymorphisms in the pathophysiology of type 2 diabetes mellitus in a population of Brazilian obese patients Pirozzi, Flavio Fontes Belini, Edis Okumura, Jessika Viviani Salvarani, Mariana Bonini-Domingos, Claudia Regina Ruiz, Milton Artur Arch Endocrinol Metab Original Article OBJECTIVES: This study aimed to evaluate the frequencies of the angiotensin converting enzyme (ACE) gene insertion/deletion (I/D) and methylenetetrahydrofolate reductase (MTHFR) gene C677T polymorphisms in obese patients with and without type 2 diabetes mellitus (T2DM). SUBJECTS AND METHODS: These polymorphisms were analyzed by polymerase chain reaction in 125 patients with obesity, 47 (T2DM) and 78 (Control Group). RESULTS: No significant difference was found on comparing the T2DM and Control Groups in respect to the genotypic frequencies of the polymorphisms - (II: 13.3% vs. 12.0%; ID: 37.8% vs. 37.3; DD: 48.9% vs. 50.7%; CC: 36.2% vs. 39.0%; CT: 46.8% vs. 49.3%; TT: 17.0% vs. 11.7%), and alleles (I: 32.2% vs. 30.7%; D: 67.8% vs. 69.3%; C: 59.6% vs. 63.6%; T: 40.4% vs. 36.4%) and their synergisms in the pathophysiology of T2DM. On analyzing the T2DM Group, there were no significant differences in the presence of complications. In this population of Brazilian obese patients, no correlation was found between the ACE and MTHFR polymorphisms in the development of T2DM. CONCLUSION: Analyzing only the group with diabetes, there was also no relationship between these polymorphisms and comorbidities. Sociedade Brasileira de Endocrinologia e Metabologia 2018-01-01 /pmc/articles/PMC10118689/ /pubmed/29694640 http://dx.doi.org/10.20945/2359-3997000000005 Text en https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Pirozzi, Flavio Fontes Belini, Edis Okumura, Jessika Viviani Salvarani, Mariana Bonini-Domingos, Claudia Regina Ruiz, Milton Artur The relationship between of ACE I/D and the MTHFR C677T polymorphisms in the pathophysiology of type 2 diabetes mellitus in a population of Brazilian obese patients |
title | The relationship between of ACE I/D and the MTHFR C677T polymorphisms in the pathophysiology of type 2 diabetes mellitus in a population of Brazilian obese patients |
title_full | The relationship between of ACE I/D and the MTHFR C677T polymorphisms in the pathophysiology of type 2 diabetes mellitus in a population of Brazilian obese patients |
title_fullStr | The relationship between of ACE I/D and the MTHFR C677T polymorphisms in the pathophysiology of type 2 diabetes mellitus in a population of Brazilian obese patients |
title_full_unstemmed | The relationship between of ACE I/D and the MTHFR C677T polymorphisms in the pathophysiology of type 2 diabetes mellitus in a population of Brazilian obese patients |
title_short | The relationship between of ACE I/D and the MTHFR C677T polymorphisms in the pathophysiology of type 2 diabetes mellitus in a population of Brazilian obese patients |
title_sort | relationship between of ace i/d and the mthfr c677t polymorphisms in the pathophysiology of type 2 diabetes mellitus in a population of brazilian obese patients |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10118689/ https://www.ncbi.nlm.nih.gov/pubmed/29694640 http://dx.doi.org/10.20945/2359-3997000000005 |
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