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Association between diabetes type 1 and DQB1* alleles in a case-control study conducted in Montevideo, Uruguay
Adriana Mimbacas1,2, Francisco Pérez-Bravo3, Pedro C. Hidalgo2, Gerardo Javiel4,
Carmen Pisciottano5, Rosario Grignola5, Ana María Jorge6, Juan Pablo Gallino2,
Jackeline Gasagoite5 and Horacio Cardoso2
1Cytogenetics Department, Associated Unit, Institute of Biology,
School of Science, University of the Republic, Montevideo, Uruguay
2Cytogenetics Department, Clemente Estable’s Institute of Biology
Investigation, Montevideo, Uruguay
3Laboratory of Molecular Epidemiology, Institute of Nutrition and
Food Technology, Chile University, Santiago, Chile
4Diabetes Unit, C.A.S.M.U., Montevideo, Uruguay
5Service of Pediatric Endocrinology, Pereira Russell’s Hospital,
Montevideo, Uruguay
6Diabetes Unit, Casa de Galicia, Montevideo, Uruguay
Corresponding author: A. Mimbacas
E-mail: abmg@iibce.edu.uy
Genet. Mol. Res. 2 (1): 29-35 (2003)
Received September 25, 2002
Published February 6, 2003

ABSTRACT. We studied HLA DQB1 allele frequencies and the relative risk (RR) of various genotypes in 72 type 1 diabetic patients and 40 control individuals in Uruguay. This is a tri-racial (Caucasian, Black and Indo-American) mixed population. The products of the polymerase chain reaction amplifications were hybridized with oligonucleotides by allele-specific oligonucleotide reverse or dot blot methods. Significant differences between these two groups were observed only for allele DQB1*0302 (35%, RR = 7.34, P<0.001). The frequency of the alleles carrying a non-aspartic acid residue at position 57 was significantly higher in the diabetic patients (85 vs 53%, P<0.001). In contrast, the frequency of Asp alleles was negatively associated with type 1 diabetes (RR = 0.20, P<0.001). The genotype DQB1*0302/DQB1*0201 (33%, RR = 5.41, P<0.05) was positively associated with this disease. The genotype frequencies associated with type 1 diabetes in our population were significantly different from what is known for Caucasian and Black populations as well as compared with another admixed population, from Chile.

Key words: Diabetes type 1, Human leukocyte antigen system, HLA

 

 

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