Cargando…

Haplotype analysis of the PPARγ Pro12Ala and C1431T variants reveals opposing associations with body weight

BACKGROUND: Variation at the PPARG locus may influence susceptibility to type 2 diabetes and related traits. The Pro12Ala polymorphism may modulate receptor activity and is associated with protection from type 2 diabetes. However, there have been inconsistent reports of its association with obesity....

Descripción completa

Detalles Bibliográficos
Autores principales: Doney, Alex, Fischer, Bettina, Frew, David, Cumming, Alastair, Flavell, David M, World, Michael, Montgomery, Hugh E, Boyle, Douglas, Morris, Andrew, Palmer, Colin NA
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2002
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC137581/
https://www.ncbi.nlm.nih.gov/pubmed/12429071
http://dx.doi.org/10.1186/1471-2156-3-21
_version_ 1782120451577741312
author Doney, Alex
Fischer, Bettina
Frew, David
Cumming, Alastair
Flavell, David M
World, Michael
Montgomery, Hugh E
Boyle, Douglas
Morris, Andrew
Palmer, Colin NA
author_facet Doney, Alex
Fischer, Bettina
Frew, David
Cumming, Alastair
Flavell, David M
World, Michael
Montgomery, Hugh E
Boyle, Douglas
Morris, Andrew
Palmer, Colin NA
author_sort Doney, Alex
collection PubMed
description BACKGROUND: Variation at the PPARG locus may influence susceptibility to type 2 diabetes and related traits. The Pro12Ala polymorphism may modulate receptor activity and is associated with protection from type 2 diabetes. However, there have been inconsistent reports of its association with obesity. The silent C1431T polymorphism has not been as extensively studied, but the rare T allele has also been inconsistently linked to increases in weight. Both rare alleles are in linkage disequilibrium and the independent associations of these two polymorphisms have not been addressed. RESULTS: We have genotyped a large population with type 2 diabetes (n = 1107), two populations of non-diabetics from Glasgow (n = 186) and Dundee (n = 254) and also a healthy group undergoing physical training (n = 148) and investigated the association of genotype with body mass index. This analysis has demonstrated that the Ala12 and T1431 alleles are present together in approximately 70% of the carriers. By considering the other 30% of individuals with haplotypes that only carry one of these polymorphisms, we have demonstrated that the Ala12 allele is consistently associated with a lower BMI, whilst the T1431 allele is consistently associated with higher BMI. CONCLUSION: This study has therefore revealed an opposing interaction of these polymorphisms, which may help to explain previous inconsistencies in the association of PPARG polymorphisms and body weight.
format Text
id pubmed-137581
institution National Center for Biotechnology Information
language English
publishDate 2002
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-1375812002-12-08 Haplotype analysis of the PPARγ Pro12Ala and C1431T variants reveals opposing associations with body weight Doney, Alex Fischer, Bettina Frew, David Cumming, Alastair Flavell, David M World, Michael Montgomery, Hugh E Boyle, Douglas Morris, Andrew Palmer, Colin NA BMC Genet Research Article BACKGROUND: Variation at the PPARG locus may influence susceptibility to type 2 diabetes and related traits. The Pro12Ala polymorphism may modulate receptor activity and is associated with protection from type 2 diabetes. However, there have been inconsistent reports of its association with obesity. The silent C1431T polymorphism has not been as extensively studied, but the rare T allele has also been inconsistently linked to increases in weight. Both rare alleles are in linkage disequilibrium and the independent associations of these two polymorphisms have not been addressed. RESULTS: We have genotyped a large population with type 2 diabetes (n = 1107), two populations of non-diabetics from Glasgow (n = 186) and Dundee (n = 254) and also a healthy group undergoing physical training (n = 148) and investigated the association of genotype with body mass index. This analysis has demonstrated that the Ala12 and T1431 alleles are present together in approximately 70% of the carriers. By considering the other 30% of individuals with haplotypes that only carry one of these polymorphisms, we have demonstrated that the Ala12 allele is consistently associated with a lower BMI, whilst the T1431 allele is consistently associated with higher BMI. CONCLUSION: This study has therefore revealed an opposing interaction of these polymorphisms, which may help to explain previous inconsistencies in the association of PPARG polymorphisms and body weight. BioMed Central 2002-11-13 /pmc/articles/PMC137581/ /pubmed/12429071 http://dx.doi.org/10.1186/1471-2156-3-21 Text en Copyright © 2002 Doney et al; licensee BioMed Central Ltd. This is an Open Access article: verbatim copying and redistribution of this article are permitted in all media for any purpose, provided this notice is preserved along with the article's original URL.
spellingShingle Research Article
Doney, Alex
Fischer, Bettina
Frew, David
Cumming, Alastair
Flavell, David M
World, Michael
Montgomery, Hugh E
Boyle, Douglas
Morris, Andrew
Palmer, Colin NA
Haplotype analysis of the PPARγ Pro12Ala and C1431T variants reveals opposing associations with body weight
title Haplotype analysis of the PPARγ Pro12Ala and C1431T variants reveals opposing associations with body weight
title_full Haplotype analysis of the PPARγ Pro12Ala and C1431T variants reveals opposing associations with body weight
title_fullStr Haplotype analysis of the PPARγ Pro12Ala and C1431T variants reveals opposing associations with body weight
title_full_unstemmed Haplotype analysis of the PPARγ Pro12Ala and C1431T variants reveals opposing associations with body weight
title_short Haplotype analysis of the PPARγ Pro12Ala and C1431T variants reveals opposing associations with body weight
title_sort haplotype analysis of the pparγ pro12ala and c1431t variants reveals opposing associations with body weight
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC137581/
https://www.ncbi.nlm.nih.gov/pubmed/12429071
http://dx.doi.org/10.1186/1471-2156-3-21
work_keys_str_mv AT doneyalex haplotypeanalysisoftheppargpro12alaandc1431tvariantsrevealsopposingassociationswithbodyweight
AT fischerbettina haplotypeanalysisoftheppargpro12alaandc1431tvariantsrevealsopposingassociationswithbodyweight
AT frewdavid haplotypeanalysisoftheppargpro12alaandc1431tvariantsrevealsopposingassociationswithbodyweight
AT cummingalastair haplotypeanalysisoftheppargpro12alaandc1431tvariantsrevealsopposingassociationswithbodyweight
AT flavelldavidm haplotypeanalysisoftheppargpro12alaandc1431tvariantsrevealsopposingassociationswithbodyweight
AT worldmichael haplotypeanalysisoftheppargpro12alaandc1431tvariantsrevealsopposingassociationswithbodyweight
AT montgomeryhughe haplotypeanalysisoftheppargpro12alaandc1431tvariantsrevealsopposingassociationswithbodyweight
AT boyledouglas haplotypeanalysisoftheppargpro12alaandc1431tvariantsrevealsopposingassociationswithbodyweight
AT morrisandrew haplotypeanalysisoftheppargpro12alaandc1431tvariantsrevealsopposingassociationswithbodyweight
AT palmercolinna haplotypeanalysisoftheppargpro12alaandc1431tvariantsrevealsopposingassociationswithbodyweight