Chuang L M, Jou T S, Hu C Y, Wu H P, Tsai W Y, Lee J S, Hsieh R P, Chen K H, Tai T Y, Lin B J
Department of Internal Medicine, National Taiwan University, Taipei.
Diabetes Care. 1994 Aug;17(8):863-8. doi: 10.2337/diacare.17.8.863.
To study the human leukocyte antigen (HLA)-DQB1 genetic background in the Chinese population in Taiwan and its association with the low incidence of insulin-dependent diabetes mellitus (IDDM) in this population.
Forty-eight IDDM patients and 59 nondiabetic unrelated control subjects were recruited from the population in Taiwan. HLA-DQB1 exon 2 was enzymatically amplified by polymerase chain reaction. HLA-DQB1 alleles were diagnosed by dot blotting and hybridization with 16 sequence-specific oligonucleotide probes.
DQB10201 and DQB10302 alleles were more frequent and DQB10301 and DQB10601 were less frequent in Chinese with IDDM than in control subjects. Genotypes for homozygous non-aspartic acid residue (NA/NA) at position 57 were positively associated with IDDM at a relative risk of 4.34 (P < 0.001), and those for homozygous aspartic acid (A/A) were negatively associated with IDDM at a relative risk of 0.14 (P < 0.001). Among the NA/A heterozygotes, only DQB10201/DQB10303 was significantly increased in IDDM subjects.
The amino acid residue at position 57 of HLA-DQ beta-chain is significantly associated with the development or prevention of IDDM in Chinese subjects living in Taiwan. Other genetic and environmental factors may also play important roles in pathogenesis of IDDM.
