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The heterogeneity of islet autoantibodies and the progression of islet failure in type 1 diabetic patients
Authors:Jin Liu  Lingling Bian  Li Ji  Yang Chen  Heng Chen  Yong Gu  Bingqin Ma  Wei Gu  Xinyu Xu  Yun Shi  Jian Wang  Dalong Zhu  Zilin Sun  Jianhua Ma  Hui Jin  Xing Shi  Heng Miao  Bing Xin  Yan Zhu  Zhenwen Zhang  Ruifang Bu  Lan Xu  Guangde Shi  Wei Tang  Wei Li  Dongmei Zhou  Jun Liang  Xingbo Cheng  Bimin Shi  Jixiang Dong  Ji Hu  Chen Fang  Shao Zhong  Weinan Yu  Weiping Lu  Chenguang Wu  Li Qian  Jiancheng Yu  Jialin Gao  Xiaoqiang Fei  Qingqing Zhang  Xueqin Wang  Shiwei Cui  Jinluo Cheng  Ning Xu  Guofeng Wang  Guoqing Han  Chunrong Xu  Yun Xie  Minmin An  Wei Zhang  Zhixiao Wang  Yun Cai  Qi Fu  Yu Fu  Shuai Zheng  Fan Yang  Qingfang Hu  Hao Dai  Yu Jin  Zheng Zhang  Kuanfeng Xu  Yifan Li  Jie Shen  Hongwen Zhou  Wei He  Xuqin Zheng  Xiao Han  Liping Yu  Jinxiong She  Mei Zhang  Tao Yang
Abstract:Type 1 diabetes mellitus is heterogeneous in many facets. The patients suffered from type 1 diabetes present several levels of islet function as well as variable number and type of islet-specific autoantibodies. This study was to investigate prevalence and heterogeneity of the islet autoantibodies and clinical phenotypes of type 1 diabetes mellitus; and also discussed the process of islet failure and its risk factors in Chinese type 1 diabetic patients. A total of 1,291 type 1 diabetic patients were enrolled in this study. Demographic information was collected. Laboratory tests including mixed-meal tolerance test, human leukocyte antigen alleles, hemoglobinA1c, lipids, thyroid function and islet autoantibodies were conducted. The frequency of islet-specific autoantibody in newly diagnosed T1DM patients (duration shorter than half year) was 73% in East China. According to binary logistic regressions, autoantibody positivity, longer duration and lower Body Mass Index were the risk factors of islet failure. As the disease developed, autoantibodies against glutamic acid decarboxylase declined as well as the other two autoantibodies against zinc transporter 8 and islet antigen 2. The decrease of autoantibodies was positively correlated with aggressive beta cell destruction. Autoantibodies can facilitate the identification of classic T1DM from other subtypes and predict the progression of islet failure. As there were obvious heterogeneity in autoantibodies and clinical manifestation in different phenotypes of the disease, we should take more factors into consideration when identifying type 1 diabetes mellitus.
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