Association of an Osteopontin gene promoter polymorphism with susceptibility to diabetic nephropathy in Asian Indians

Research output: Contribution to journalJournal articleResearchpeer-review

  • Balneek Singh Cheema
  • Sreenivasa Iyengar
  • Ahluwalia, Tarun Veer Singh
  • Harbir Singh Kohli
  • Rajni Sharma
  • Viral N Shah
  • Anil Bhansali
  • V Sakhuja
  • Madhu Khullar
Genetic predisposition has been proposed to be a major determinant in the development of renal complications of diabetes. Osteopontin (OPN) has been suggested to be associated with renal diseases characterized by tubulointerstitial fibrosis and proteinuria. However, information on association of genetic polymorphisms in OPN with diabetic nephropathy is lacking. Thus, the present study was designed with the aim to examine the association of an OPN gene promoter polymorphism with diabetic nephropathy in Asian Indians. OPN C-443T (rs11730582) polymorphism was determined in 1115 type 2 diabetic patients belonging to two independently ascertained cohorts using Real time PCR based Taqman assay. We observed a nearly threefold elevated risk of diabetic nephropathy among carriers of T allele and TT genotype of OPN C-443T polymorphism. Further, this allele was found to be significantly associated with proteinuria and lower eGFR, a hallmark of diabetic nephropathy, in both our cohorts. This is the first study which suggests that OPN C-443T polymorphism may be a significant risk factor for diabetic nephropathy in type 2 diabetic patients.
Original languageEnglish
JournalClinica chimica acta; international journal of clinical chemistry
Volume413
Issue number19-20
Pages (from-to)1600-4
Number of pages5
DOIs
Publication statusPublished - 9 Oct 2012

    Research areas

  • Aged, Alleles, Asian Continental Ancestry Group, Diabetes Mellitus, Type 2, Diabetic Nephropathies, Female, Gene Frequency, Genetic Predisposition to Disease, Glomerular Filtration Rate, Humans, India, Kidney, Male, Middle Aged, Osteopontin, Polymorphism, Single Nucleotide, Promoter Regions, Genetic, Proteinuria, Risk Factors

ID: 49646983