Association analysis of the plasminogen activator inhibitor-1 4G/5G polymorphism in Hispanics and African Americans: The IRAS Family Study

被引:20
作者
Bensen, JT
Hsu, FC
Brown, WM
Sutton, BS
Norris, JM
Tracy, RP
Jenny, NS
Saad, MF
Haffner, S
Bowden, DW
Langefeld, CD
机构
[1] Wake Forest Univ, Bowman Gray Sch Med, Ctr Human Genom, Winston Salem, NC USA
[2] Wake Forest Univ, Bowman Gray Sch Med, Dept Internal Med, Winston Salem, NC 27103 USA
[3] Wake Forest Univ, Bowman Gray Sch Med, Dept Publ Hlth Sci, Winston Salem, NC 27103 USA
[4] Wake Forest Univ, Bowman Gray Sch Med, Dept Biochem, Winston Salem, NC 27103 USA
[5] Univ Colorado, Hlth Sci Ctr, Dept Prevent Med & Biometr, Denver, CO 80262 USA
[6] Univ Vermont, Dept Pathol, Colchester, VT USA
[7] Univ Calif Los Angeles, Sch Med, Div Endocrinol, Los Angeles, CA USA
[8] Univ Texas, Hlth Sci Ctr, Dept Med, Div Clin Epidemiol, San Antonio, TX 78284 USA
关键词
insulin resistance syndrome; plasminogen activator inhibitor-1 (PAI-1); association; 4G/5G polymorphism;
D O I
10.1159/000079243
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Objective: Plasminogen activator inhibitor type-1 (PAI-1) plays a central role in fibrolysis and has recently been hypothesized to influence components of the insulin resistance syndrome. We consider whether the 4G/5G polymorphism influences components of insulin resistance and obesity solely through PAI-1 protein levels or also though a secondary pathway. In addition, we explore whether transforming growth factor (TGF-beta1), a key regulator of PAI-1 expression, modifies the influence of the PAI-1 4G/5G polymorphism on these traits. Methods and Results: The Insulin Resistance and Atherosclerosis (IRAS) Family Study genotyped 287 African American (18 pedigrees) and 811 Hispanic American ( 45 pedigrees) individuals for the 4G/5G PAI-1 and two TGF-beta1 polymorphisms (R25P, C-509T). Individuals were recruited from three clinical centers located in San Antonio ( urban Hispanic), San Luis Valley ( rural Hispanic) and Los Angeles ( African American). The presence of the 4G PAI-1 allele was positively associated with PAI-1 protein level (combined sample p < 0.0001). Hispanic Americans average 65% higher PAI-1 protein levels than African Americans (p < 0.0001). Consistently across ethnic groups, increased PAI-1 protein levels were associated with increased insulin resistance and overall and central obesity (p value < 0.0001, combined sample). Adjusting for PAI-1 protein levels, there was evidence of an association of PAI-1 genotype (4G) with insulin sensitivity (p < 0.002) and subcutaneous fat (p < 0.01). These associations were not influenced by TGF-beta 1 genotypes. Conclusions: PAI-1 protein is a strong correlate of insulin resistance (IR) and obesity in Hispanics and African Americans. However, PAI-1 4G/5G polymorphism appears to influence insulin resistance and obesity beyond its direct influence on serum PAI-1 protein levels. Copyright (C) 2004 S. Karger AG, Basel.
引用
收藏
页码:128 / 137
页数:10
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