Ostenson C G
Department of Molecular Medicine, Endocrine and Diabetes Unit, Karolinska Institute, Stockholm, Sweden.
Acta Physiol Scand. 2001 Mar;171(3):241-7. doi: 10.1046/j.1365-201x.2001.00826.x.
Type 2 diabetes mellitus is a heterogeneous disorder characterized by chronic hyperglycaemia. The aetiological heterogeneity is suggested by genetic inheritance and its interplay with environmental factors. Impaired insulin secretion and decreased insulin sensitivity are the main pathophysiological features, responsible for development of hyperglycaemia in type 2 diabetes. However, the genetic basis of these defects has been demonstrated only in small subgroups of patients. Whether impaired secretion or action of insulin is the primary defect in the majority of patients is not known, although it is generally agreed that defective insulin release is a requirement for the disease to develop.
2型糖尿病是一种以慢性高血糖为特征的异质性疾病。遗传因素及其与环境因素的相互作用提示了病因的异质性。胰岛素分泌受损和胰岛素敏感性降低是主要的病理生理特征,是导致2型糖尿病患者高血糖的原因。然而,这些缺陷的遗传基础仅在一小部分患者亚组中得到证实。尽管人们普遍认为胰岛素释放缺陷是该疾病发生发展的必要条件,但在大多数患者中,胰岛素分泌受损还是作用受损是原发性缺陷尚不清楚。