Genetic variants linked to T2DM risk in Kurdish populations
Shadi Golsheh,1 Fatemeh Keshavarzi21Department of Biology, Kurdistan Science and Research Branch, Islamic Azad University, Sanandaj, Iran; 2Department of Biology, Sanandaj Branch, Islamic Azad University, Sanandaj, IranBackground: The polymorphisms of the C–C chemokine receptor type 5 (CCR...
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Dove Medical Press
2019
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oai:doaj.org-article:6d71b290b6fc4dfe87d7f0a95dc50d2e2021-12-02T09:58:13ZGenetic variants linked to T2DM risk in Kurdish populations1178-7007https://doaj.org/article/6d71b290b6fc4dfe87d7f0a95dc50d2e2019-04-01T00:00:00Zhttps://www.dovepress.com/genetic-variants-linked-to-t2dm-risk-in-kurdish-populations-peer-reviewed-article-DMSOhttps://doaj.org/toc/1178-7007Shadi Golsheh,1 Fatemeh Keshavarzi21Department of Biology, Kurdistan Science and Research Branch, Islamic Azad University, Sanandaj, Iran; 2Department of Biology, Sanandaj Branch, Islamic Azad University, Sanandaj, IranBackground: The polymorphisms of the C–C chemokine receptor type 5 (CCR5) and the insulin receptor substrate 1 (IRS1) have been studied as candidates for the susceptibility to develop type 2 diabetes mellitus (T2DM). CCR5 is a chemokine receptor, and the polymorphisms in the promoter region of this receptor are being studied as candidates for the susceptibility to develop T2DM. Also, IRS1 is a critical factor in the signaling pathway for insulin, and mutations in this gene have been reported, which contribute to the ability to develop T2DM. The aim of the current study was to determine the relationship between CCR5 (59029A/G) and IRS1 (rs10498210) polymorphisms with T2DM in Sanandajian patients.Methods: Genomic DNA was isolated from 200 healthy individuals and 220 Kurdish T2DM patients by salt extraction method and the polymorphisms were examined by restriction fragment length polymorphism (RFLP) method and then the results were analyzed using Chi-square test.Results: The frequency of AA genotype in 220 Kurdish patients for both genes CCR5 (OR=1.9, P=0.02) and IRS1 (OR [95% CI]=2.62, P=0.02) were significantly more than controls. There was no significant association between AG or GG genotypes in with T2DM.Conclusion: The presence of AA homozygote alleles in both loci of IRS1 (rs10498210) and CCR5 (59029A/G) genes increased the risk of T2DM.Keywords: IRS1 (rs10498210), CCR5 (59029A/G), type 2 diabetes, Kurdish patientsGolsheh SKeshavarzi FDove Medical PressarticleIRS1 (rs10498210)CCR5 (59029A/G)Type 2 diabetesKurdish patientsSpecialties of internal medicineRC581-951ENDiabetes, Metabolic Syndrome and Obesity: Targets and Therapy, Vol Volume 12, Pp 431-437 (2019) |
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IRS1 (rs10498210) CCR5 (59029A/G) Type 2 diabetes Kurdish patients Specialties of internal medicine RC581-951 |
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IRS1 (rs10498210) CCR5 (59029A/G) Type 2 diabetes Kurdish patients Specialties of internal medicine RC581-951 Golsheh S Keshavarzi F Genetic variants linked to T2DM risk in Kurdish populations |
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Shadi Golsheh,1 Fatemeh Keshavarzi21Department of Biology, Kurdistan Science and Research Branch, Islamic Azad University, Sanandaj, Iran; 2Department of Biology, Sanandaj Branch, Islamic Azad University, Sanandaj, IranBackground: The polymorphisms of the C–C chemokine receptor type 5 (CCR5) and the insulin receptor substrate 1 (IRS1) have been studied as candidates for the susceptibility to develop type 2 diabetes mellitus (T2DM). CCR5 is a chemokine receptor, and the polymorphisms in the promoter region of this receptor are being studied as candidates for the susceptibility to develop T2DM. Also, IRS1 is a critical factor in the signaling pathway for insulin, and mutations in this gene have been reported, which contribute to the ability to develop T2DM. The aim of the current study was to determine the relationship between CCR5 (59029A/G) and IRS1 (rs10498210) polymorphisms with T2DM in Sanandajian patients.Methods: Genomic DNA was isolated from 200 healthy individuals and 220 Kurdish T2DM patients by salt extraction method and the polymorphisms were examined by restriction fragment length polymorphism (RFLP) method and then the results were analyzed using Chi-square test.Results: The frequency of AA genotype in 220 Kurdish patients for both genes CCR5 (OR=1.9, P=0.02) and IRS1 (OR [95% CI]=2.62, P=0.02) were significantly more than controls. There was no significant association between AG or GG genotypes in with T2DM.Conclusion: The presence of AA homozygote alleles in both loci of IRS1 (rs10498210) and CCR5 (59029A/G) genes increased the risk of T2DM.Keywords: IRS1 (rs10498210), CCR5 (59029A/G), type 2 diabetes, Kurdish patients |
format |
article |
author |
Golsheh S Keshavarzi F |
author_facet |
Golsheh S Keshavarzi F |
author_sort |
Golsheh S |
title |
Genetic variants linked to T2DM risk in Kurdish populations |
title_short |
Genetic variants linked to T2DM risk in Kurdish populations |
title_full |
Genetic variants linked to T2DM risk in Kurdish populations |
title_fullStr |
Genetic variants linked to T2DM risk in Kurdish populations |
title_full_unstemmed |
Genetic variants linked to T2DM risk in Kurdish populations |
title_sort |
genetic variants linked to t2dm risk in kurdish populations |
publisher |
Dove Medical Press |
publishDate |
2019 |
url |
https://doaj.org/article/6d71b290b6fc4dfe87d7f0a95dc50d2e |
work_keys_str_mv |
AT golshehs geneticvariantslinkedtot2dmriskinkurdishpopulations AT keshavarzif geneticvariantslinkedtot2dmriskinkurdishpopulations |
_version_ |
1718397886683676672 |