Literature DB >> 15047638

Linkage of the metabolic syndrome to 1q23-q31 in Hispanic families: the Insulin Resistance Atherosclerosis Study Family Study.

Carl D Langefeld1, Lynne E Wagenknecht, Jerome I Rotter, Adrienne H Williams, John E Hokanson, Mohammad F Saad, Donald W Bowden, Stephen Haffner, Jill M Norris, Stephen S Rich, Braxton D Mitchell.   

Abstract

The metabolic syndrome is characterized by central obesity, dyslipidemia, elevated blood pressure, and hyperglycemia. The Insulin Resistance Atherosclerosis Study (IRAS) Family Study recruited extended pedigrees of Hispanic descent from San Antonio, TX (SA) and San Luis Valley, CO (SLV). Thirty-five of these pedigrees (27 SA and 8 SLV) had at least 2 individuals with metabolic syndrome (216 affected individuals and 563 affected relative pairs). The prevalence of metabolic syndrome and component criteria in subjects from these pedigrees were 35% metabolic syndrome, 43% increased waist circumference, 31% hypertriglyceridemia, 69% low HDL cholesterol, 31% increased blood pressure, and 25% either increased fasting glucose or presence of diabetes. Nonparametric linkage analysis provided evidence for linkage of metabolic syndrome to 1q23-q31 (D1S518; logarithm of odds [LOD] 1.6) with significant site heterogeneity (SA LOD 2.6 and SLV LOD 0.0), and removing all individuals with diabetes reduced, but did not eliminate, the evidence for linkage to this region (LOD 1.2). This heterogeneity may partially be explained by phenotypic differences. Members in the SA pedigrees were older, had greater central obesity, had higher prevalence of the metabolic syndrome, and were from a more urban environment than members of the SLV pedigrees. These results contribute to the growing evidence that chromosome 1q harbors at least one locus related to the metabolic precursors of diabetes.

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Year:  2004        PMID: 15047638     DOI: 10.2337/diabetes.53.4.1170

Source DB:  PubMed          Journal:  Diabetes        ISSN: 0012-1797            Impact factor:   9.461


  33 in total

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Journal:  Diabetologia       Date:  2009-03-19       Impact factor: 10.122

3.  The relationships between FAM5C SNP (rs10920501) variability and metabolic syndrome and inflammation in women with coronary heart disease.

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4.  The linkage and association of the gene encoding upstream stimulatory factor 1 with type 2 diabetes and metabolic syndrome in the Chinese population.

Authors:  M C Y Ng; K Miyake; W Y So; E W M Poon; V K L Lam; J K Y Li; N J Cox; G I Bell; J C N Chan
Journal:  Diabetologia       Date:  2005-08-26       Impact factor: 10.122

5.  Bivariate genome-wide scan for metabolic phenotypes in non-diabetic Chinese individuals from the Stanford, Asia and Pacific Program of Hypertension and Insulin Resistance Family Study.

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6.  Heritabilities of the metabolic syndrome and its components in the Northern Manhattan Family Study.

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Journal:  Diabetologia       Date:  2005-08-04       Impact factor: 10.122

7.  Genome-wide linkage analysis of multiple metabolic factors: evidence of genetic heterogeneity.

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8.  A genome-wide association study identifies susceptibility variants for type 2 diabetes in Han Chinese.

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9.  Association of genetic variants of NOS1AP with type 2 diabetes in a Chinese population.

Authors:  C Hu; C Wang; R Zhang; M C Ng; Y Bao; C Wang; W Y So; R C Ma; X Ma; J C Chan; K Xiang; W Jia
Journal:  Diabetologia       Date:  2009-11-24       Impact factor: 10.122

10.  NOS1AP variant associated with incidence of type 2 diabetes in calcium channel blocker users in the Atherosclerosis Risk in Communities (ARIC) study.

Authors:  A Y Chu; J Coresh; D E Arking; J S Pankow; G F Tomaselli; A Chakravarti; W S Post; P H Spooner; E Boerwinkle; W H L Kao
Journal:  Diabetologia       Date:  2009-11-27       Impact factor: 10.122

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