Mimura G, Kida K, Murakami K
Shokei Junior College, Kumamoto, Japan.
Diabetes Res Clin Pract. 1994 Oct;24 Suppl:S75-81. doi: 10.1016/0168-8227(94)90231-3.
The Japan Diabetes Society (JDS) conducted a multicenter study on HLA and autoimmunity in Japanese patients with early-onset insulin-dependent diabetes mellitus (IDDM). HLA, immunoglobulin heavy-chain complex (Gm), properdin factor B (BF), and glyoxalase of erythrocytes (GLO) were typed, and organ-specific autoantibodies including islet cell antibodies (ICA) were assayed in 159 IDDM patients and their relatives and in 258 healthy Japanese subjects. The HLA-DRw9 phenotype and HLA-Bw61/DRw9 haplotype were significantly increased among the patients with autoantibodies other than ICA, whereas the DR4 phenotype and Bw54/DR4 haplotype were significantly increased in those without the autoantibodies. The DR4 phenotype was significantly increased in the patients with autoimmune thyroid diseases. The relative risk of the HLA-DRw9/DR4 genotype was highest among all DR genotypes. The Gm phenotype of g and gft were significantly increased in the patients with the autoantibodies. The BF-F phenotype was significantly decreased in the patients either with or without the autoantibodies. There was no association of GLO types with IDDM. The prevalence of ICA among IDDM patients was decreased with duration of IDDM. No significant association was found between the prevalence of ICA and sex, age at onset, or HLA type. On the other hand, the prevalence of the autoantibodies was not significantly changed with duration of the disease, and was significantly higher in females than in males.
日本糖尿病学会(JDS)对日本早发型胰岛素依赖型糖尿病(IDDM)患者的HLA与自身免疫进行了一项多中心研究。对159例IDDM患者及其亲属以及258名健康日本受试者进行了HLA、免疫球蛋白重链复合物(Gm)、备解素因子B(BF)和红细胞乙二醛酶(GLO)分型,并检测了包括胰岛细胞抗体(ICA)在内的器官特异性自身抗体。在非ICA自身抗体患者中,HLA - DRw9表型和HLA - Bw61/DRw9单倍型显著增加,而在无自身抗体的患者中,DR4表型和Bw54/DR4单倍型显著增加。在自身免疫性甲状腺疾病患者中,DR4表型显著增加。在所有DR基因型中,HLA - DRw9/DR4基因型的相对风险最高。有自身抗体的患者中,g和gft的Gm表型显著增加。无论有无自身抗体,患者的BF - F表型均显著降低。GLO类型与IDDM无关联。IDDM患者中ICA的患病率随IDDM病程延长而降低。未发现ICA患病率与性别、发病年龄或HLA类型之间存在显著关联。另一方面,自身抗体的患病率并未随疾病病程显著变化,且女性显著高于男性。