Li Xia, Cheng Jin, Zhou Zhiguang
Institute of Metabolism and Endocrinology, The Second Xiangya Hospital and the Diabetes Center, Key Laboratory of Diabetes Immunology, Ministry of Education, National Clinical Research Center for Metabolic Diseases, Central South University, Changsha, Hunan, China.
J Diabetes. 2016 Jul;8(4):460-9. doi: 10.1111/1753-0407.12376.
Type 1 diabetes (T1D) results from a chronic autoimmune process that leads to β-cell destruction and exogenous insulin dependence. The natural history of T1D proposed by Eisenbarth suggested six relatively independent stages over the course of the entire disease process, which was considered to be linear and chronic. Based on this classical theory, immunotherapies aim to prevent or reverse all these periods of β-cell loss. Over the past 30 years, much novel information about the pathogenesis of T1D proved that there are complex metabolic changes occurring throughout the entire disease process. Therefore, new possible models for the natural history of the disease have been proposed; these models, in turn, may help facilitate fresh avenues for the prevention and cure of T1D. Herein, we briefly review recent findings in this field of research, with the aim of providing a better theoretical basis for clinical practice.
1型糖尿病(T1D)源于一种慢性自身免疫过程,该过程会导致β细胞破坏以及对外源性胰岛素的依赖。艾森巴思提出的T1D自然史表明,在整个疾病过程中有六个相对独立的阶段,该过程被认为是线性且慢性的。基于这一经典理论,免疫疗法旨在预防或逆转β细胞丢失的所有这些阶段。在过去30年中,许多关于T1D发病机制的新信息证明,在整个疾病过程中会发生复杂的代谢变化。因此,已经提出了该疾病自然史的新的可能模型;反过来,这些模型可能有助于为T1D的预防和治疗开辟新途径。在此,我们简要回顾该研究领域的最新发现,以便为临床实践提供更好的理论基础。