Wang Jian, Miao Dongmei, Babu Sunanda, Yu Jeesuk, Barker Jennifer, Klingensmith Georgeanna, Rewers Marian, Eisenbarth George S, Yu Liping
Barbara Davis Center for Childhood Diabetes, University of Colorado Health Sciences Center, PO Box 6511, Mail Stop B140, Aurora, Colorado 80045-6511, USA.
J Clin Endocrinol Metab. 2007 Jan;92(1):88-92. doi: 10.1210/jc.2006-1494. Epub 2006 Oct 24.
A significant percentage of nonautoimmune forms of diabetes presents among children in all age groups, with a remarkable increase with age.
From October 1992 to October 2004, a total of 859 children less than 18 yr of age were newly diagnosed with diabetes at the Barbara Davis Center for Childhood Diabetes and had blood samples obtained within 2 wk of disease onset for analysis of antiislet autoantibodies to glutamic acid decarboxylase-65, insulinoma-associated antigen-2, insulin, and islet cell autoantibodies. The relationship of autoantibody positivity with human leukocyte antigen (HLA) class II, body mass index (BMI), glycosylated hemoglobin, age, and ethnicity was analyzed.
Overall 19% (159 of 859) of these children with newly diagnosed diabetes were negative for all autoantibodies, and autoantibody negativity was significantly increased with age (P < 0.01). The Hispanic and Black subjects had significantly increased autoantibody negativity among older children with higher BMI than White subjects. The patients with the highest risk HLA genotype, DR3-DQ2/DR4-DQ8, were significantly less autoantibody negative (P = 0.001), whereas the HLA-protective allele, DQB1*0602, was significantly increased among the autoantibody-negative patients (P < 0.0001). Insulin autoantibodies were dramatically age dependent and were inversely correlated with age in both prevalence (P < 0.0001) and levels (P < 0.0001). Autoantibody positivity was inversely correlated with both BMI and age using multivariate analysis (P < 0.0001 and P = 0.0078, respectively).
A significant percentage of children newly diagnosed with diabetes are negative for all antiislet autoantibodies with a marked increase in obesity-associated autoantibody-negative diabetes after age 10, suggesting diabetes heterogeneity at all ages.
在所有年龄组的儿童中,相当大比例的非自身免疫性糖尿病类型存在,且随年龄显著增加。
从1992年10月至2004年10月,共有859名18岁以下儿童在芭芭拉·戴维斯儿童糖尿病中心新诊断为糖尿病,并在疾病发作后2周内采集血样,用于分析谷氨酸脱羧酶65、胰岛素瘤相关抗原2、胰岛素和胰岛细胞自身抗体的抗胰岛自身抗体。分析自身抗体阳性与人类白细胞抗原(HLA)II类、体重指数(BMI)、糖化血红蛋白、年龄和种族的关系。
总体而言,这些新诊断为糖尿病的儿童中有19%(859名中的159名)所有自身抗体均为阴性,且自身抗体阴性率随年龄显著增加(P<0.01)。西班牙裔和黑人受试者在BMI较高的大龄儿童中自身抗体阴性率显著高于白人受试者。具有最高风险HLA基因型DR3-DQ2/DR4-DQ8的患者自身抗体阴性率显著较低(P = 0.001),而HLA保护性等位基因DQB1*0602在自身抗体阴性患者中显著增加(P<0.0001)。胰岛素自身抗体明显依赖于年龄,在患病率(P<0.0001)和水平(P<0.0001)上均与年龄呈负相关。使用多变量分析,自身抗体阳性与BMI和年龄均呈负相关(分别为P<0.0001和P = 0.0078)。
相当大比例新诊断为糖尿病的儿童所有抗胰岛自身抗体均为阴性,10岁后肥胖相关自身抗体阴性糖尿病显著增加,提示各年龄段糖尿病存在异质性。