Diabetes 54:3326-3330, 2005 © 2005 by the American Diabetes Association, Inc.
The Fatty Acid–Binding Protein-2 A54T Polymorphism Is Associated With Renal Disease in Patients With Type 2 Diabetes
1 Endocrine Division, Hospital de Clínicas de Porto Alegre, Federal University of Rio Grande do Sul, Porto Alegre, Brazil
The intestinal fatty–acid binding protein-2 (FABP2) gene codes a protein responsible for the absorption of long-chain fatty acids. To test whether FABP2 is a candidate gene for renal disease in patients with type 2 diabetes, a functional A54T polymorphism was genotyped in 1,042 Brazilians with type 2 diabetes. Patients were classified as having normoalbuminuria (urinary albumin excretion [UAE] <20 µg/min; n = 529), microalbuminuria (UAE 20–199 µg/min; n = 217), or proteinuria (UAE >199 µg/min; n = 160). Patients with end-stage renal disease (ESRD) (n = 136) were also included. The prevalence of the TT genotype was higher in patients with renal involvement compared with those with normoalbuminuria (odds ratio [95% CI] 2.4 [1.1–5.4]) following adjustment for type 2 diabetes duration, BMI, hypertension, A1C, and cholesterol levels. The risk was similar considering different stages of renal involvement. In a second independent patient sample (483 type 2 diabetic Caucasians residing in Massachusetts), a significant association was also observed between the TT genotype and proteinuria or ESRD (2.7 [1.0–7.3]; P = 0.048). This study thus provides evidence that FABP2 confers susceptibility to renal disease in type 2 diabetic patients.
Address correspondence and reprint requests to Jorge Luiz Gross, Serviço de Endocrinologia, Hospital de Clínicas de Porto Alegre, RS, Brazil, Rua Ramiro Barcelos 2350-Prédio 12-4° andar 90035-003 Porto Alegre, RS–Brazil. E-mail: jorgegross{at}terra.com.br
Abbreviations: ESRD, end-stage renal disease; FABP2, fatty acid–binding protein-2; IHD, ischemic heart disease; SNP, single nucleotide polymorphism; UAE, urinary albumin excretion
|
|
|
|||||||||||||||||||||||||||