Yu L, Cuthbertson D D, Maclaren N, Jackson R, Palmer J P, Orban T, Eisenbarth G S, Krischer J P
Barbara Davis Center for Childhood Diabetes, University of Colorado, Denver, Colorado 80262, USA.
Diabetes. 2001 Aug;50(8):1735-40. doi: 10.2337/diabetes.50.8.1735.
More than 71,000 relatives of type 1 diabetic patients have been screened for cytoplasmic islet cell antibodies (ICAs), GAD65 autoantibodies (GAAs), and ICA512 autoantibodies (ICA512AAs). Among those 71,148 relatives, 2,448 were cytoplasmic ICA+, and the remainder were ICA-. Of the ICA+ group, 1,229 (50.2%) were positive for GAAs and/or ICA512AAs. Among ICA- relatives, 1,897 (2.76%) were positive for GAAs and/or ICA512AAs. Given the large number of relatives positive for cytoplasmic ICA and negative for "biochemically" determined autoantibodies, and the converse, we analyzed the proportion of ICA+ relatives found eligible to participate in the intervention phase of Diabetes Prevention Trial-Type 1 (DPT-1). To be eligible for the parenteral insulin DPT-1 trial, a relative had to have first-phase insulin secretion below the 1st percentile of cut-points (for parents) or below the 10th percentile (for siblings and offspring). To be eligible for the oral insulin trial, a relative had to have first-phase insulin secretion above cut-points (>1st percentile for parents, >10th percentile for siblings/offspring) and be positive for anti-insulin autoantibodies. For both trials, DQB1*0602 was an exclusion criteria, cytoplasmic ICA positivity had to be confirmed, and an oral glucose tolerance test had to result in nondiabetic levels. Of 572 relatives found to be eligible for trial entry, 442 (77.3%) were positive for GAAs and/or ICA512AAs, although overall only 50.2% of ICA+ relatives were positive for GAAs and/or ICA512AAs. The positive predictive value for trial eligibility for ICA+ relatives with GAAs or ICA512AAs who completed staging was 51.0%. In contrast, only 11.9% of ICA+ but GAA- and ICA512AA- relatives were found to be eligible by DPT criteria for trial entry. Positivity for biochemically determined autoantibodies among cytoplasmic antibody-positive relatives is associated with eligibility for the DPT-1 study.
对超过71000名1型糖尿病患者的亲属进行了胰岛细胞胞浆抗体(ICA)、谷氨酸脱羧酶65自身抗体(GAA)和胰岛细胞抗原512自身抗体(ICA512AA)的筛查。在这71148名亲属中,2448人胰岛细胞胞浆抗体呈阳性(ICA+),其余为阴性(ICA-)。在ICA+组中,1229人(50.2%)GAA和/或ICA512AA呈阳性。在ICA-亲属中,1897人(2.76%)GAA和/或ICA512AA呈阳性。鉴于大量亲属胰岛细胞胞浆抗体呈阳性但“生化”检测的自身抗体呈阴性,以及相反的情况,我们分析了符合1型糖尿病预防试验(DPT-1)干预阶段条件的ICA+亲属的比例。要符合DPT-1的皮下注射胰岛素试验条件,亲属的第一相胰岛素分泌必须低于切点的第1百分位数(父母)或低于第10百分位数(兄弟姐妹和后代)。要符合口服胰岛素试验条件,亲属的第一相胰岛素分泌必须高于切点(父母>第1百分位数,兄弟姐妹/后代>第10百分位数)且抗胰岛素自身抗体呈阳性。对于这两项试验,DQB1*0602均为排除标准,必须确认胰岛细胞胞浆抗体阳性,且口服葡萄糖耐量试验结果必须为非糖尿病水平。在572名被发现符合试验入选条件的亲属中,442人(77.3%)GAA和/或ICA512AA呈阳性,尽管总体上只有50.2%的ICA+亲属GAA和/或ICA512AA呈阳性。完成分期的GAA或ICA512AA阳性的ICA+亲属试验入选的阳性预测值为51.0%。相比之下,根据DPT标准,只有11.9%的ICA+但GAA-和ICA512AA-的亲属被发现符合试验入选条件。胰岛细胞胞浆抗体阳性亲属中生化检测的自身抗体阳性与DPT-1研究的入选资格相关。