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Association of polymorphism in heat shock protein 70 genes with type 2 diabetes in Bangladeshi population
BACKGROUND: Type 2 diabetes mellitus (T2DM) is a chronic disorder of which stress is a major contributor. Under stressful condition, body synthesizes a family of molecular chaperone called Heat‐shock proteins (HSPs). Current study assessed the frequency and association of HSP70‐hom + 2,437 T/C polym...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7005638/ https://www.ncbi.nlm.nih.gov/pubmed/31816668 http://dx.doi.org/10.1002/mgg3.1073 |
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author | Moniruzzaman, Md. Ahmed, Irfan Huq, Saaimatul All Mahmud, Md. Shakur Begum, Sonya Mahzabin Amin, U.S. Rahman, Md. Hadisur Sarker, Palash Kumar Hossain, Mohammad Uzzal Das, Keshob Chandra Salimullah, Md. |
author_facet | Moniruzzaman, Md. Ahmed, Irfan Huq, Saaimatul All Mahmud, Md. Shakur Begum, Sonya Mahzabin Amin, U.S. Rahman, Md. Hadisur Sarker, Palash Kumar Hossain, Mohammad Uzzal Das, Keshob Chandra Salimullah, Md. |
author_sort | Moniruzzaman, Md. |
collection | PubMed |
description | BACKGROUND: Type 2 diabetes mellitus (T2DM) is a chronic disorder of which stress is a major contributor. Under stressful condition, body synthesizes a family of molecular chaperone called Heat‐shock proteins (HSPs). Current study assessed the frequency and association of HSP70‐hom + 2,437 T/C polymorphism with T2DM risk among Bangladeshis. METHODS: This polymorphism was selected through bioinformatics analyses and identified by PCR‐RFLP method. RESULTS: Bioinformatics analysis identified this SNP as missense mutation which could destabilize the final HSP product. Heterozygous mutant (CT) genotype was significantly associated with T2DM incidence among the studied populations (p = .015). Further analysis revealed a strong association with female patients (p = .002), while the male group showed no association (p = .958). Moreover, the C allele was significantly associated among all diabetic patients (p = .016) and particularly in the female patient group (p = .001). However, under stressful condition, males with CT genotype were at high risk for T2DM incidence whereas, females with CT genotype showed no significant association. CONCLUSIONS: HSP70‐hom + 2,437 T/C polymorphism was found to be significantly associated with T2DM incidence in the Bangladeshi population in both stress‐dependent and independent manners. |
format | Online Article Text |
id | pubmed-7005638 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-70056382020-02-13 Association of polymorphism in heat shock protein 70 genes with type 2 diabetes in Bangladeshi population Moniruzzaman, Md. Ahmed, Irfan Huq, Saaimatul All Mahmud, Md. Shakur Begum, Sonya Mahzabin Amin, U.S. Rahman, Md. Hadisur Sarker, Palash Kumar Hossain, Mohammad Uzzal Das, Keshob Chandra Salimullah, Md. Mol Genet Genomic Med Original Articles BACKGROUND: Type 2 diabetes mellitus (T2DM) is a chronic disorder of which stress is a major contributor. Under stressful condition, body synthesizes a family of molecular chaperone called Heat‐shock proteins (HSPs). Current study assessed the frequency and association of HSP70‐hom + 2,437 T/C polymorphism with T2DM risk among Bangladeshis. METHODS: This polymorphism was selected through bioinformatics analyses and identified by PCR‐RFLP method. RESULTS: Bioinformatics analysis identified this SNP as missense mutation which could destabilize the final HSP product. Heterozygous mutant (CT) genotype was significantly associated with T2DM incidence among the studied populations (p = .015). Further analysis revealed a strong association with female patients (p = .002), while the male group showed no association (p = .958). Moreover, the C allele was significantly associated among all diabetic patients (p = .016) and particularly in the female patient group (p = .001). However, under stressful condition, males with CT genotype were at high risk for T2DM incidence whereas, females with CT genotype showed no significant association. CONCLUSIONS: HSP70‐hom + 2,437 T/C polymorphism was found to be significantly associated with T2DM incidence in the Bangladeshi population in both stress‐dependent and independent manners. John Wiley and Sons Inc. 2019-12-09 /pmc/articles/PMC7005638/ /pubmed/31816668 http://dx.doi.org/10.1002/mgg3.1073 Text en © 2019 The Authors. Molecular Genetics & Genomic Medicine published by Wiley Periodicals, Inc. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Original Articles Moniruzzaman, Md. Ahmed, Irfan Huq, Saaimatul All Mahmud, Md. Shakur Begum, Sonya Mahzabin Amin, U.S. Rahman, Md. Hadisur Sarker, Palash Kumar Hossain, Mohammad Uzzal Das, Keshob Chandra Salimullah, Md. Association of polymorphism in heat shock protein 70 genes with type 2 diabetes in Bangladeshi population |
title | Association of polymorphism in heat shock protein 70 genes with type 2 diabetes in Bangladeshi population |
title_full | Association of polymorphism in heat shock protein 70 genes with type 2 diabetes in Bangladeshi population |
title_fullStr | Association of polymorphism in heat shock protein 70 genes with type 2 diabetes in Bangladeshi population |
title_full_unstemmed | Association of polymorphism in heat shock protein 70 genes with type 2 diabetes in Bangladeshi population |
title_short | Association of polymorphism in heat shock protein 70 genes with type 2 diabetes in Bangladeshi population |
title_sort | association of polymorphism in heat shock protein 70 genes with type 2 diabetes in bangladeshi population |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7005638/ https://www.ncbi.nlm.nih.gov/pubmed/31816668 http://dx.doi.org/10.1002/mgg3.1073 |
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