Cargando…

Association of SNP rs9939609 in FTO gene with metabolic syndrome in type 2 diabetic subjects, rectruited from a tertiary care unit of Karachi, Pakistan

OBJECTIVE: To determine the association of SNP in FTO gene, rs9939609, with Metabolic Syndrome (MS) in type 2 diabetic subjects at a tertiary care unit of Karachi, Pakistan. METHODS: We genotyped FTO rs9939609 SNP in 296 patients with type 2 diabetes from the Out Patient Department (OPD) of Baqai In...

Descripción completa

Detalles Bibliográficos
Autores principales: Fawwad, Asher, Siddiqui, Iftikhar Ahmed, Zeeshan, Nimra Fatima, Shahid, Syed Muhammad, Basit, Abdul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Professional Medical Publicaitons 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4386174/
https://www.ncbi.nlm.nih.gov/pubmed/25878631
http://dx.doi.org/10.12669/pjms.311.6524
_version_ 1782365155984670720
author Fawwad, Asher
Siddiqui, Iftikhar Ahmed
Zeeshan, Nimra Fatima
Shahid, Syed Muhammad
Basit, Abdul
author_facet Fawwad, Asher
Siddiqui, Iftikhar Ahmed
Zeeshan, Nimra Fatima
Shahid, Syed Muhammad
Basit, Abdul
author_sort Fawwad, Asher
collection PubMed
description OBJECTIVE: To determine the association of SNP in FTO gene, rs9939609, with Metabolic Syndrome (MS) in type 2 diabetic subjects at a tertiary care unit of Karachi, Pakistan. METHODS: We genotyped FTO rs9939609 SNP in 296 patients with type 2 diabetes from the Out Patient Department (OPD) of Baqai Institute of Diabetology and Endocrinology (BIDE). MS was defined on the basis of International Diabetes Federation (IDF) and National Cholesterol Education program (NCEP) criterion. Association between the rs9939609 SNP and MS was tested through chi-square and Z-tests by using odds ratio (OR) with 95% confidence intervals. RESULTS: The frequency of MS as defined by IDF criterion was significantly higher in female subjects as compared to male subjects (p= 0.006). Carriers of ≥ 1 copy of the rs9939609 A allele were significantly more likely to had MS (69.6%) than non-carriers (30.4%), corresponding to a carrier odds ratio (OR) of 0.52 (95% confidence interval [CI] (0.29-0.93), with a similar trend for the ATP III-defined MS.“A” allele carriers under dominant model, carry all the criterion of MS more significantly as compared to non-carriers. CONCLUSION: The FTO rs9939609 SNP was associated with an increased risk for Metabolic Syndrome in type 2 diabetic populations at a tertiary care unit of Karachi, Pakistan.
format Online
Article
Text
id pubmed-4386174
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher Professional Medical Publicaitons
record_format MEDLINE/PubMed
spelling pubmed-43861742015-04-15 Association of SNP rs9939609 in FTO gene with metabolic syndrome in type 2 diabetic subjects, rectruited from a tertiary care unit of Karachi, Pakistan Fawwad, Asher Siddiqui, Iftikhar Ahmed Zeeshan, Nimra Fatima Shahid, Syed Muhammad Basit, Abdul Pak J Med Sci Original Article OBJECTIVE: To determine the association of SNP in FTO gene, rs9939609, with Metabolic Syndrome (MS) in type 2 diabetic subjects at a tertiary care unit of Karachi, Pakistan. METHODS: We genotyped FTO rs9939609 SNP in 296 patients with type 2 diabetes from the Out Patient Department (OPD) of Baqai Institute of Diabetology and Endocrinology (BIDE). MS was defined on the basis of International Diabetes Federation (IDF) and National Cholesterol Education program (NCEP) criterion. Association between the rs9939609 SNP and MS was tested through chi-square and Z-tests by using odds ratio (OR) with 95% confidence intervals. RESULTS: The frequency of MS as defined by IDF criterion was significantly higher in female subjects as compared to male subjects (p= 0.006). Carriers of ≥ 1 copy of the rs9939609 A allele were significantly more likely to had MS (69.6%) than non-carriers (30.4%), corresponding to a carrier odds ratio (OR) of 0.52 (95% confidence interval [CI] (0.29-0.93), with a similar trend for the ATP III-defined MS.“A” allele carriers under dominant model, carry all the criterion of MS more significantly as compared to non-carriers. CONCLUSION: The FTO rs9939609 SNP was associated with an increased risk for Metabolic Syndrome in type 2 diabetic populations at a tertiary care unit of Karachi, Pakistan. Professional Medical Publicaitons 2015 /pmc/articles/PMC4386174/ /pubmed/25878631 http://dx.doi.org/10.12669/pjms.311.6524 Text en This is an Open Access article distributed under the terms of the Creative Commons Attribution License, (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Fawwad, Asher
Siddiqui, Iftikhar Ahmed
Zeeshan, Nimra Fatima
Shahid, Syed Muhammad
Basit, Abdul
Association of SNP rs9939609 in FTO gene with metabolic syndrome in type 2 diabetic subjects, rectruited from a tertiary care unit of Karachi, Pakistan
title Association of SNP rs9939609 in FTO gene with metabolic syndrome in type 2 diabetic subjects, rectruited from a tertiary care unit of Karachi, Pakistan
title_full Association of SNP rs9939609 in FTO gene with metabolic syndrome in type 2 diabetic subjects, rectruited from a tertiary care unit of Karachi, Pakistan
title_fullStr Association of SNP rs9939609 in FTO gene with metabolic syndrome in type 2 diabetic subjects, rectruited from a tertiary care unit of Karachi, Pakistan
title_full_unstemmed Association of SNP rs9939609 in FTO gene with metabolic syndrome in type 2 diabetic subjects, rectruited from a tertiary care unit of Karachi, Pakistan
title_short Association of SNP rs9939609 in FTO gene with metabolic syndrome in type 2 diabetic subjects, rectruited from a tertiary care unit of Karachi, Pakistan
title_sort association of snp rs9939609 in fto gene with metabolic syndrome in type 2 diabetic subjects, rectruited from a tertiary care unit of karachi, pakistan
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4386174/
https://www.ncbi.nlm.nih.gov/pubmed/25878631
http://dx.doi.org/10.12669/pjms.311.6524
work_keys_str_mv AT fawwadasher associationofsnprs9939609inftogenewithmetabolicsyndromeintype2diabeticsubjectsrectruitedfromatertiarycareunitofkarachipakistan
AT siddiquiiftikharahmed associationofsnprs9939609inftogenewithmetabolicsyndromeintype2diabeticsubjectsrectruitedfromatertiarycareunitofkarachipakistan
AT zeeshannimrafatima associationofsnprs9939609inftogenewithmetabolicsyndromeintype2diabeticsubjectsrectruitedfromatertiarycareunitofkarachipakistan
AT shahidsyedmuhammad associationofsnprs9939609inftogenewithmetabolicsyndromeintype2diabeticsubjectsrectruitedfromatertiarycareunitofkarachipakistan
AT basitabdul associationofsnprs9939609inftogenewithmetabolicsyndromeintype2diabeticsubjectsrectruitedfromatertiarycareunitofkarachipakistan