Groop L, Orho-Melander M
Department of Endocrinology, Wallenberg Laboratory, Lund University, Malmö, Sweden.
J Intern Med. 2001 Aug;250(2):105-20. doi: 10.1046/j.1365-2796.2001.00864.x.
The first unifying definition for the metabolic syndrome was proposed by WHO in 1998. In accordance to this, patients with type 2 diabetes mellitus or impaired glucose tolerance have the syndrome if they fulfil two of the criteria: hypertension, dyslipidaemia, obesity/abdominal obesity and microalbuminuria. Persons with normal glucose tolerance (NGT) should also be insulin resistant. About 40% of persons with impaired glucose tolerance (IGT) and 70% of patients with type 2 diabetes have features of the syndrome. Importantly, presence of the dysmetabolic syndrome is associated with reduced survival, particularly because of increased cardiovascular mortality. The dysmetabolic syndrome most likely results from interplay between several genes and an affluent environment. Compatible with the thrifty gene theory, common variants in genes regulating lipolysis, thermogenesis and glucose uptake in skeletal muscle account for a large part of such thrifty genes. However, hitherto unknown genes may still be identified by random gene approaches.
世界卫生组织于1998年提出了代谢综合征的首个统一定义。据此,2型糖尿病或糖耐量受损患者若符合以下两项标准,即患有该综合征:高血压、血脂异常、肥胖/腹型肥胖和微量白蛋白尿。糖耐量正常(NGT)的人也应存在胰岛素抵抗。约40%的糖耐量受损(IGT)患者和70%的2型糖尿病患者具有该综合征的特征。重要的是,代谢紊乱综合征的存在与生存率降低相关,尤其是心血管死亡率增加。代谢紊乱综合征很可能是由多个基因与富足环境之间的相互作用导致的。与节俭基因理论相符,调节脂肪分解、产热和骨骼肌葡萄糖摄取的基因中的常见变异占此类节俭基因的很大一部分。然而,迄今未知的基因仍可能通过随机基因方法得以识别。