Exp Clin Endocrinol Diabetes 2006; 114(8): 432-437
DOI: 10.1055/s-2006-924328
Article

© J. A. Barth Verlag in Georg Thieme Verlag KG · Stuttgart · New York

Evaluation of Tight Junction Protein 1 Encoding Zona Occludens 1 as a Candidate Gene for Albuminuria in a Mexican American Population

D. M. Lehman 1 , R. J. Leach 2 , 3 , T. Johnson-Pais 3 , J. Hamlington 1 , S. Fowler 1 , L. Almasy 5 , R. Duggirala 5 , M. P. Stern 1 , H. E. Abboud 4
  • 1Department of Medicine/Clinical Epidemiology, University of Texas Health Science Center, San Antonio, Texas, USA
  • 2Department of Cellular and Structural Biology, University of Texas Health Science Center, San Antonio, Texas, USA
  • 3Department of Pediatrics, University of Texas Health Science Center, San Antonio, Texas, USA
  • 4Medicine/Nephrology, University of Texas Health Science Center, San Antonio, Texas, USA
  • 5Department of Genetics, Southwest Foundation for Biomedical Research, San Antonio, Texas, USA
Further Information

Publication History

Received: February 6, 2006 First decision: April 24, 2006

Accepted: May 2, 2006

Publication Date:
13 October 2006 (online)

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Abstract

Albuminuria, a hallmark of diabetic nephropathy, has been shown to be significantly heritable in multiple studies. Therefore, the identification of genes that affect susceptibility to albuminuria may lead to novel avenues of intervention. Current evidence suggests that the podocyte and slit diaphragm play a key role in controlling the selective sieve of the glomerular filtration barrier, and podocyte-specific genes have been identified that are necessary for maintaining its integrity. We therefore investigated the role of gene variants of tight junction protein (TJP1) which encodes another slit diaphragm-associated protein zona occludens 1 as risk factors for albuminuria in the San Antonio Family Diabetes/Gallbladder Study (SAFDGS), which consists of extended Mexican-American families with a high prevalence of type 2 diabetes. Albuminuria, defined as an albumin (mg/dl) to creatinine (mg/dl) ratio (ACR) of 0.03, which is approximately equivalent to a urinary albumin excretion (UAE) >30 mg/day, was present in a total of 14.9% of participants, and 31% had type 2 diabetes. The TJP1 exons, flanking intronic sequence, and putative proximal promoter regions were investigated in this population. Twentynine polymorphisms, including 7 nonsynonymous SNPs, were identified and genotyped in all subjects of this study for association analysis. Three sets of correlated SNPs, which include 3 exonic SNPs, were nominally associated with ACR (p value range 0.007-0.049); however, the association with the discrete trait albuminuria was not significant (p value range 0.094-0.338). We conclude that these variants in TJP1 do not appear to be major determinants for albuminuria in the SAFDGS; however, they may play a minor role in its severity in this Mexican-American population. Further examination of the TJP1 gene region in this and other cohorts will be useful to determine whether ZO-1 plays a significant role in glomerular permselectivity.

References

Correspondence

Dr. Donna M. Lehman

Department of Medicine/Clinical Epidemiology·University of Texas Health Science Center·Medicine/Clinical Epidemiology

7703 Floyd Curl Drive

San Antonio, Texas 78229

USA

Phone: +49/210/567/47 37

Fax: +49/210/567/69 55

Email: lehman@uthscsa.edu