Affiliations 

  • 1 Lecturer and Consultant Endocrinologist, Universiti Kebangsaan Malaysia Medical Centre, Kuala Lumpur, Malaysia,
  • 2 Consultant Endocrinologist, Endocrine Unit, Department of General Medicine; Tan Tock Seng Hospital, Singapore
  • 3 Senior Research Assistant, Autoimmune Research Laboratory; Tan Tock Seng Hospital, Singapore
  • 4 Medical Statistician, Clinical Research Unit, Tan Tock Seng Hospital, Singapore
  • 5 Head, Division of Endocrinology, Institute for Medical Research, Kuala Lumpur, Malaysia
  • 6 Senior Consultant, Autoimmune Research Laboratory; Kuala Lumpur General Hospital, Malaysia
  • 7 Professor & Consultant Endocrinologist, Universiti Kebangsaan Malaysia Medical Centre, Kuala Lumpur, Malaysia
  • 8 Professor of Medicine and Head of the School of Clinical Sciences, Monash University, Malaysia
Med J Malaysia, 2011 Jun;66(2):133-7.
PMID: 22106694

Abstract

HLA-DQA1, -DQB1, and -DRB1 gene polymorphism were analyzed to study type 1 DM susceptibility in Malay patients from Southeast Asia (Malaysia and Singapore). Patients showed significant increases in the occurrence of DQA1*0501 (50.7% vs. 20.4%; RR = 3.97; Pc < 0.01), DQB1*0201 (48% vs. 19.1%; RR = 3.86; Pc < 0.05), and DRB1*0301 (38.7 vs. 6.8%; RR = 8.36; 95% Pc < 0.05). Conversely, significant decreases were noted in the occurrence of DQA1*0601 (14.7% vs. 35.2%; RR = 0.33; Pc = 0.008) and DQB1*0601 (4% vs. 23.5%; RR = 0.16; Pc < 0.05) in type 1 DM patients. Using a logistic regression model, we derived a risk prediction model for type 1 DM in our indigenous Malay population based on the identified HLA genotypes. The RR for type 1 DM increases by a factor of 5.68 for every unit increase in the number of DRB1*0301 allele (P < 0.001), and decreases by a factor of 0.18 per unit increase in the number of DQB1*0601 allele (P < 0.001). After adjusting for these two HLA genotypes, DQA1*0501, DQB1*0201 and DQA1*0601 were not statistically significant as risk predictors. The lower incidence of type 1 DM in the Malay population may be contributed by the genotypic combinations of DR and DQ genes as well as the linkage disequilibria between susceptible and protective alleles.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.