Faber O K, Binder C
Diabetes Metab Rev. 1986;2(3-4):331-45. doi: 10.1002/dmr.5610020307.
Insight into the natural history of beta cell function in IDDM patients obtained by C-peptide measurements is reviewed. It is argued that residual insulin secretion of metabolic importance is present in all IDDM patients during the initial course of the disease. After some months, beta cell function reaches its maximum; thereafter it declines at different rates dependent on the age at onset of diabetes and, possibly, on the presence of ICA and HLA-antigens. As many as 15% of IDDM patients retain life-long beta cell function that persists at approximately 10% of that observed in nondiabetic individuals. The residual endogenous insulin secretion is characterized by reduced capacity, as well as abnormal insulin secretory kinetics; these defects in residual insulin secretion can be modulated by changes in metabolic regulation as well as by immunosuppression during the initial course of the disease.
本文综述了通过C肽测量对1型糖尿病(IDDM)患者β细胞功能自然史的认识。有人认为,在疾病初始阶段,所有IDDM患者都存在具有代谢重要性的残余胰岛素分泌。数月后,β细胞功能达到最大值;此后,其下降速度因糖尿病发病年龄以及可能因胰岛细胞抗体(ICA)和人类白细胞抗原(HLA)的存在而有所不同。多达15%的IDDM患者保留终身β细胞功能,其持续水平约为非糖尿病个体的10%。残余内源性胰岛素分泌的特点是能力降低以及胰岛素分泌动力学异常;这些残余胰岛素分泌缺陷可通过代谢调节的变化以及疾病初始阶段的免疫抑制来调节。