Ferber K M, Keller E, Albert E D, Ziegler A G
Ludwig Maximilians University, Third Medical Department, Krankenhaus München-Schwabing, and Diabetes Research Institute, Munich, Germany.
J Clin Endocrinol Metab. 1999 Jul;84(7):2342-8. doi: 10.1210/jcem.84.7.5813.
Gestational diabetes mellitus (GDM) is a risk factor for the development of insulin-dependent diabetes mellitus (IDDM) and noninsulin-dependent diabetes mellitus postpartum. To evaluate whether there is any association of human leukocyte antigen (HLA) class II alleles (DR and DQ) with GDM and the postpartum development of IDDM, we analyzed 184 women with GDM from Germany for HLA class II alleles, islet autoantibodies [islet cell autoantibodies (ICA), glutamic acid decarboxylase autoantibodies (GADA), and protein tyrosine phosphatase IA-2 autoantibodies (IA-2A), and the postpartum development of diabetes. No elevation in the frequency of any HLA class II alleles was observed in GDM patients compared to 254 nondiabetic unrelated subjects. DR3 allele frequency was significantly increased in 43 women with islet autoantibodies [corrected P value (Pc) = 0.02], in particular in those with GADA (Pc = 0.002), or in the 24 women who developed IDDM postpartum (Pc = 0.005). In women with GADA, DR4 and DQB1*0302 were significantly elevated (Pc = 0.009). Twenty-five (59.5%) islet antibody-positive women and 17 (74%) women who developed IDDM postpartum had a DR3- or DR4-containing genotype. The cumulative risk to develop IDDM within 2 yr postpartum in GDM women with either DR3 or DR4 was 22% compared to 7% in women without those alleles (P = 0.02) and rose to 50% in the DR3- or DR4-positive women who had required insulin during pregnancy (P = 0.006). Combining the determination of susceptible HLA alleles (DR3, DR4) with islet autoantibody measurement increased the sensitivity of identifying GDM women developing postpartum IDDM to 92%, but did not improve risk assessment above that achieved using GADA measurement alone, which was the strongest predictor of IDDM. These results indicate that women with GDM who have islet autoantibodies at delivery or develop IDDM postpartum have HLA alleles typical of late-onset type 1 diabetes, and that both HLA typing and islet antibodies can predict the development of postpartum IDDM.
妊娠期糖尿病(GDM)是胰岛素依赖型糖尿病(IDDM)和产后非胰岛素依赖型糖尿病发生的一个危险因素。为了评估人类白细胞抗原(HLA)II类等位基因(DR和DQ)与GDM及产后IDDM发生之间是否存在关联,我们对来自德国的184例GDM女性进行了HLA II类等位基因、胰岛自身抗体[胰岛细胞自身抗体(ICA)、谷氨酸脱羧酶自身抗体(GADA)和蛋白酪氨酸磷酸酶IA - 2自身抗体(IA - 2A)]分析以及产后糖尿病发生情况的研究。与254例非糖尿病无关受试者相比,未观察到GDM患者中任何HLA II类等位基因频率升高。在43例有胰岛自身抗体的女性中DR3等位基因频率显著增加[校正P值(Pc)= 0.02],特别是那些有GADA的女性(Pc = 0.002),或在产后发生IDDM的24例女性中(Pc = 0.005)。在有GADA的女性中,DR4和DQB1*0302显著升高(Pc = 0.009)。25例(59.5%)胰岛抗体阳性女性和17例(74%)产后发生IDDM的女性具有含DR3或DR4的基因型。与没有这些等位基因的女性相比,有DR3或DR4的GDM女性产后2年内发生IDDM的累积风险为22%,而无这些等位基因的女性为7%(P = 0.02),在孕期需要胰岛素治疗的DR3或DR4阳性女性中该风险升至50%(P = 0.006)。将易感HLA等位基因(DR3、DR4)的检测与胰岛自身抗体检测相结合,可将识别产后发生IDDM的GDM女性的敏感性提高到92%,但在风险评估方面并未优于单独使用GADA检测,GADA检测是IDDM最强的预测指标。这些结果表明,分娩时有胰岛自身抗体或产后发生IDDM的GDM女性具有晚发型1型糖尿病典型的HLA等位基因,并且HLA分型和胰岛抗体均可预测产后IDDM的发生。