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特发性糖尿病的分类

Classification of idiopathic diabetes.

作者信息

Irvine W J

出版信息

Lancet. 1977 Mar 19;1(8012):638-42. doi: 10.1016/s0140-6736(77)92071-2.

Abstract

A classification of idiopathic diabetes based on autoimmunity suggests that two main types of disease process may result in this syndrome. Type 1 includes classic insulin-dependent juvenile-onset diabetes, insulin-dependent diabetes presenting in later life, and diabetes initially adequately controlled for at least 3 months on oral hypoglycaemic agents but with islet-cell antibody (I.C.A.) in the serum. Type II included classic maturity-onset insulin-independent diabetes and the rarer insulin-independent diabetes presenting at a younger age in patients whose serum is negative for I.C.A. at the time of diagnosis. In terms oer the main factor is a genetically determined diathesis towards islet-cell autoimmunity (type Ia), towards islet-cell damage by appropriate viral infection or other agent in the absence of islet cell autoimmunity (type Ic), or a combination of the two diatheses (type IB). Type-II diabetes has a different genetic basis and the environmental factor is a metabolic or other form of stress rather than viral infection. Both main types have an early potential phase indicated by the presence of I.C.A. in serum (type I) and, in the absence of I.C.A., in serum (type I) and, in the absence of I.C.A., by an appropriate family history of insulin-independent diabetes or giving birth to big babies (type II). Evidence to support this hypothesis comes from HLA and histological studies in man and viral studies in laboratory animals as well as from clinical observation.

摘要

基于自身免疫的特发性糖尿病分类表明,两种主要的疾病过程可能导致这种综合征。1型包括典型的胰岛素依赖型青少年发病糖尿病、成年后出现的胰岛素依赖型糖尿病,以及最初口服降糖药至少能充分控制3个月但血清中存在胰岛细胞抗体(I.C.A.)的糖尿病。2型包括典型的成年起病非胰岛素依赖型糖尿病,以及在诊断时血清I.C.A.呈阴性的较罕见的年轻时起病的非胰岛素依赖型糖尿病。就主要因素而言,是一种遗传决定的易患胰岛细胞自身免疫的素质(1a型),在无胰岛细胞自身免疫的情况下因适当的病毒感染或其他因素导致胰岛细胞损伤的素质(1c型),或两种素质的组合(1b型)。2型糖尿病有不同的遗传基础,环境因素是代谢或其他形式的应激而非病毒感染。两种主要类型在血清中存在I.C.A.时(1型)以及在血清中不存在I.C.A.时(1型),在血清中不存在I.C.A.时通过非胰岛素依赖型糖尿病的适当家族史或分娩巨大儿(2型)都有一个早期潜在阶段。支持这一假说的证据来自人类的HLA和组织学研究、实验动物的病毒研究以及临床观察。

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