Centre for Vascular Prevention, Danube-University Krems, Dr-Karl-Dorrek-Strasse 30, 3500, Krems, Austria,
Curr Diab Rep. 2013 Dec;13(6):795-804. doi: 10.1007/s11892-013-0433-5.
Type 1 diabetes mellitus (T1D) can occur at any age, with a peak in incidence around puberty. Classification between T1D and type 2 diabetes becomes more challenging with increasing age of onset of T1D over time develops in genetically predisposed individuals. The main susceptibility is conferred with human leukocyte antigen (HLA) genes. Some of the geographic variation in incidence and familial aggregation is explained by differences in HLA haplotypes. In many populations, the incidence is somewhat higher in males than in females, and a 1.3- to 2.0-fold male excess in incidence after about 15 years of age exists in most populations. The incidence of childhood-onset T1D varies markedly among countries. East Asian and native American populations have low incidences (approximately 0.1-8 per 100 000/year), while the highest rates are found in Finland (>60 per 100 000/year), Sardinia (40 per 100 000/year), and Sweden (47 per 100 000/year). The risk is highest in European-derived populations. About 10 %-20 % of newly diagnosed childhood cases of T1D have an affected first-degree relative. Those with an affected sibling or parent have a cumulative risk of 3 %-7 % up to about 20 years of age, as compared with <1 % in the general population. The cumulative incidence among the monozygotic co-twins of persons with T1D is less than 50 %. Thus, the majority of genetically predisposed people do not develop T1D. Studies assessing temporal trends have shown that the incidence of childhood-onset T1D has increased in all parts of the world. The average relative increase is 3 %-4 % per calendar year. For instance, in Finland, the incidence today is 5 times higher than 60 years ago. At the same time, the age at onset of T1D in children has become younger. It is strongly believed that nongenetic factors are important for the development of T1D and its increase, but the causative evidence is missing. The causes for this increasing trend and current epidemic still remain unknown.
1 型糖尿病(T1D)可发生于任何年龄,发病高峰在青春期前后。随着 T1D 发病年龄的逐渐增加,T1D 与 2 型糖尿病之间的分类变得更加困难,这种疾病在遗传易感个体中逐渐发展。主要的易感性由人类白细胞抗原(HLA)基因决定。发病率的一些地理差异和家族聚集现象可以用 HLA 单倍型的差异来解释。在许多人群中,男性的发病率略高于女性,大多数人群在 15 岁以后,发病率存在 1.3 至 2.0 倍的男性优势。儿童发病的 T1D 发病率在各国之间差异显著。东亚和美洲原住民人群的发病率较低(约为每年每 10 万人 0.1-8 例),而发病率最高的是芬兰(每年每 10 万人 60 例以上)、撒丁岛(每年每 10 万人 40 例)和瑞典(每年每 10 万人 47 例)。在欧洲裔人群中的风险最高。大约 10%-20%的新诊断的儿童 T1D 病例有受影响的一级亲属。与一般人群中 <1%的发病率相比,那些有受影响的兄弟姐妹或父母的累积风险在 20 岁之前为 3%-7%。T1D 患者的同卵双胞胎的累积发病率低于 50%。因此,大多数遗传易感人群不会发展为 T1D。评估时间趋势的研究表明,世界各地儿童发病的 T1D 发病率都有所增加。平均相对增长率为每年 3%-4%。例如,在芬兰,如今的发病率是 60 年前的 5 倍。与此同时,儿童 T1D 的发病年龄也变得更小。人们强烈认为,非遗传因素对 T1D 的发生和增加很重要,但缺乏因果证据。这种增长趋势和当前流行的原因仍然未知。