Literature DB >> 11715069

Sibling-based association study of the PPARgamma2 Pro12Ala polymorphism and metabolic variables in Chinese and Japanese hypertension families: a SAPPHIRe study. Stanford Asian-Pacific Program in Hypertension and Insulin Resistance.

L M Chuang1, C A Hsiung, Y D Chen, L T Ho, W H Sheu, D Pei, C H Nakatsuka, D Cox, R E Pratt, H H Lei, T Y Tai.   

Abstract

The peroxisome proliferator activated receptor (PPAR) gamma2 is a transcription factor that has been shown to be involved in adipocyte differentiation, adipogenesis, and insulin sensitivity. To address the role of PPARgamma2 in glucose homeostasis and insulin sensitivity, among many other objectives, we conducted a sibling-controlled association study in a multicenter program - the Stanford Asian-Pacific Program in Hypertension and Insulin Resistance (SAPPHIRe). Approximately 2525 subjects in 734 Chinese and Japanese families have been recruited from six field centers for SAPPHIRe. In total, 1702 subjects including parents and siblings from 449 families have been genotyped for PPARgamma2, of which 328 families were Chinese and 121 Japanese. Only 88 subjects of the 1525 siblings screened for the P12A polymorphism were found to be carriers of the A variant, the most common variant of the PPARgamma2 gene. A variant frequencies of the siblings were 4.27% in Chinese and 2.72% in Japanese. A sibling-controlled association study was performed through genetically discordant sibships (i.e., P/P genotype vs. P/A + A/A genotypes). Specifically, we examined whether there were differences in metabolic variables between the discordant siblings within families. In total, 88 subjects carrying either 1 or 2 A alleles had at least one sibling who was discordant for the P12A polymorphism, yielding a total of 180 individuals from 47 families for analyses, among which 92 siblings were homozygous for wild-type P allele. Siblings with the A variant tended to have lower levels of fasting plasma glucose (OG-10), and lower glucose levels at 60 min following oral glucose loading after adjusting for age, gender, and body mass index. Using a mixed model treating family as a random effect, we found that P12A polymorphism of the PPARgamma2 gene contributes significantly to the variance in fasting plasma glucose, glucose level at 60 min, and insulin-resistance homeostasis model assessment. Our results suggest that within families siblings with the A variant in the PPARgamma2 gene may be more likely to have better glucose tolerance and insulin sensitivity independent of obesity in Chinese and Japanese populations.

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Year:  2001        PMID: 11715069     DOI: 10.1007/s001090100255

Source DB:  PubMed          Journal:  J Mol Med (Berl)        ISSN: 0946-2716            Impact factor:   4.599


  11 in total

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Journal:  Diabetologia       Date:  2003-06-21       Impact factor: 10.122

2.  Pro12Ala polymorphism in PPAR-gamma2 and dementia in Chinese nonagenarians/centenarians.

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Journal:  Age (Dordr)       Date:  2010-01-27

Review 3.  Nutrigenomics at the Interface of Aging, Lifespan, and Cancer Prevention.

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4.  Patterns of association between PPARgamma genetic variation and indices of adiposity and insulin action in African-Americans and whites: the CARDIA Study.

Authors:  Qi Wei; David R Jacobs; Pamela J Schreiner; David S Siscovick; Michael W Steffes; Myriam Fornage
Journal:  J Mol Med (Berl)       Date:  2006-09-06       Impact factor: 4.599

5.  The influence of the Pro12Ala mutation of PPARgamma2 receptor gene on beta-cells restoration and insulin resistance in type 2 diabetes with hypertension.

Authors:  Aiping Zhang; Muxun Zhang; Jianhua Zhang; Yikai Yu; Junhui Xie
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Journal:  Eur Arch Otorhinolaryngol       Date:  2011-07-23       Impact factor: 2.503

7.  Tree-structured supervised learning and the genetics of hypertension.

Authors:  Jing Huang; Alfred Lin; Balasubramanian Narasimhan; Thomas Quertermous; C Agnes Hsiung; Low-Tone Ho; John S Grove; Michael Olivier; Koustubh Ranade; Neil J Risch; Richard A Olshen
Journal:  Proc Natl Acad Sci U S A       Date:  2004-07-12       Impact factor: 11.205

8.  Haplotype analysis of the PPARgamma Pro12Ala and C1431T variants reveals opposing associations with body weight.

Authors:  Alex Doney; Bettina Fischer; David Frew; Alastair Cumming; David M Flavell; Michael World; Hugh E Montgomery; Douglas Boyle; Andrew Morris; Colin N A Palmer
Journal:  BMC Genet       Date:  2002-11-13       Impact factor: 2.797

9.  PPAR Genomics and Pharmacogenomics: Implications for Cardiovascular Disease.

Authors:  Sharon Cresci
Journal:  PPAR Res       Date:  2008       Impact factor: 4.964

10.  Endothelin Type A Receptor Genotype is a Determinant of Quantitative Traits of Metabolic Syndrome in Asian Hypertensive Families: A SAPPHIRe Study.

Authors:  Low-Tone Ho; Yung-Pei Hsu; Chin-Fu Hsiao; Chih-Tai Ting; Kuang-Chung Shih; Lee-Ming Chuang; Kamal Masaki; John Grove; Thomas Quertermous; Chi-Chung Juan; Ming-Wei Lin; Shu-Chiung Chiang; Yii-Der I Chen
Journal:  Front Endocrinol (Lausanne)       Date:  2013-11-28       Impact factor: 5.555

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