Drash A L
Division of Pediatric Endocrinology, Metabolism and Diabetes Mellitus, Children's Hospital of Pittsburgh, Pennsylvania.
Schweiz Med Wochenschr. 1990 Jan 20;120(3):39-45.
Noninsulin dependent diabetes mellitus (NIDDM) is associated with an entirely different set of genetic alterations from insulin-dependent diabetes mellitus (IDDM). Over 90% of IDDM carry HLA type DR3, DR4 or both. Several theories have been proposed to explain how the genetic alterations are translated into a beta cell destructive process. All involve the elaboration of a beta cell autoantigen. A major current research focus is on the development of pharmacologic approaches to the control of the beta cell destructive process (cyclosporine A). This has led to a shift in interest to the early identification of individuals at risk for IDDM. Many questions remain to be answered. In our paper emphasis is placed on epidemiological research. In Allegheny County, Pennsylvania, we have found an incidence of 1.73 cases/1000 (incidence rate of 15/100,000/year). There were marked geographical variations (incidence rate of 1/100,000/year in Asian countries, of 40/100,000/year in Finland). This suggests that there are major environmental determinants leading to expression of disease in genetically susceptible individuals. There are no geographical differences in the main age of onset, the sex ratio and the clinical patterns in the initial course of newly detected IDDM. In all parts of the world islet cell antibodies are positive in 60-80% of newly diagnosed IDDM. Migration of children from their native homeland with a low incidence rate to a country with high incidence rate was accompanied by an increase of incidence. The following potential environmental factors have been considered: viral infections, environmental toxins, nutrients, and stress. In our view IDDM occurs in genetically susceptible individuals.(ABSTRACT TRUNCATED AT 250 WORDS)
非胰岛素依赖型糖尿病(NIDDM)与胰岛素依赖型糖尿病(IDDM)有着完全不同的一系列基因改变。超过90%的IDDM患者携带DR3、DR4型 HLA或两者皆有。已经提出了几种理论来解释基因改变是如何转化为β细胞破坏过程的。所有理论都涉及β细胞自身抗原的阐述。当前一个主要的研究重点是开发控制β细胞破坏过程的药理学方法(环孢素A)。这导致了人们对早期识别IDDM高危个体的兴趣转移。许多问题仍有待解答。在我们的论文中,重点放在了流行病学研究上。在宾夕法尼亚州的阿勒格尼县,我们发现发病率为1.73例/1000(发病率为15/100,000/年)。存在明显的地域差异(亚洲国家发病率为1/100,000/年,芬兰为40/100,000/年)。这表明存在主要的环境决定因素,导致基因易感个体发病。新诊断的IDDM初始病程中的主要发病年龄、性别比例和临床模式不存在地域差异。在世界所有地区,60 - 80%新诊断的IDDM患者胰岛细胞抗体呈阳性。儿童从发病率低的原籍国迁移到发病率高的国家,发病率会随之增加。以下潜在环境因素已被考虑:病毒感染、环境毒素、营养物质和压力。我们认为,IDDM发生在基因易感个体中。(摘要截选至250词)