Reaven Gerald, Abbasi Fahim, McLaughlin Tracey
School of Medicine, Stanford University, Stanford, California 94305, USA.
Recent Prog Horm Res. 2004;59:207-23. doi: 10.1210/rp.59.1.207.
The ability of insulin to stimulate glucose disposal varies more than six-fold in apparently healthy individuals. The one third of the population that is most insulin resistant is at greatly increased risk to develop cardiovascular disease (CVD), type 2 diabetes, hypertension, stroke, nonalcoholic fatty liver disease, polycystic ovary disease, and certain forms of cancer. Between 25-35% of the variability in insulin action is related to being overweight. The importance of the adverse effects of excess adiposity is apparent in light of the evidence that more than half of the adult population in the United States is classified as being overweight/obese, as defined by a body mass index greater than 25.0 kg/m(2). The current epidemic of overweight/obesity is most-likely related to a combination of increased caloric intake and decreased energy expenditure. In either instance, the fact that CVD risk is increased as individuals gain weight emphasizes the gravity of the health care dilemma posed by the explosive increase in the prevalence of overweight/obesity in the population at large. Given the enormity of the problem, it is necessary to differentiate between the CVD risk related to obesity per se, as distinct from the fact that the prevalence of insulin resistance and compensatory hyperinsulinemia are increased in overweight/obese individuals. Although the majority of individuals in the general population that can be considered insulin resistant are also overweight/obese, not all overweight/obese persons are insulin resistant. Furthermore, the cluster of abnormalities associated with insulin resistance - namely, glucose intolerance, hyperinsulinemia, dyslipidemia, and elevated plasma C-reactive protein concentrations -- is limited to the subset of overweight/obese individuals that are also insulin resistant. Of greater clinical relevance is the fact that significant improvement in these metabolic abnormalities following weight loss is seen only in the subset of overweight/obese individuals that are also insulin resistant. In view of the large number of overweight/obese subjects at potential risk to be insulin resistant/hyperinsulinemic (and at increased CVD risk), and the difficulty in achieving weight loss, it seems essential to identify those overweight/obese individuals who are also insulin resistant and will benefit the most from weight loss, then target this population for the most-intensive efforts to bring about weight loss.
在表面健康的个体中,胰岛素刺激葡萄糖代谢的能力差异超过六倍。人群中三分之一胰岛素抵抗最强的人患心血管疾病(CVD)、2型糖尿病、高血压、中风、非酒精性脂肪肝病、多囊卵巢病和某些癌症的风险大幅增加。胰岛素作用中25%-35%的变异性与超重有关。鉴于有证据表明美国超过一半的成年人口被归类为超重/肥胖(根据体重指数大于25.0kg/m²定义),过多肥胖的不良影响的重要性显而易见。当前超重/肥胖的流行很可能与热量摄入增加和能量消耗减少的综合作用有关。在任何一种情况下,随着个体体重增加心血管疾病风险增加这一事实都凸显了总体人群中超重/肥胖患病率激增所带来的医疗保健困境的严重性。鉴于问题的严重性,有必要区分与肥胖本身相关的心血管疾病风险,这与超重/肥胖个体中胰岛素抵抗和代偿性高胰岛素血症患病率增加这一事实不同。虽然一般人群中大多数可被认为有胰岛素抵抗的个体也超重/肥胖,但并非所有超重/肥胖者都有胰岛素抵抗。此外,与胰岛素抵抗相关的一系列异常——即葡萄糖不耐受、高胰岛素血症、血脂异常和血浆C反应蛋白浓度升高——仅限于超重/肥胖且有胰岛素抵抗的个体亚组。更具临床相关性的是,只有在超重/肥胖且有胰岛素抵抗的个体亚组中,体重减轻后这些代谢异常才会有显著改善。鉴于大量超重/肥胖受试者有潜在的胰岛素抵抗/高胰岛素血症风险(以及心血管疾病风险增加),且减肥困难,似乎有必要识别出那些有胰岛素抵抗且将从减肥中获益最大的超重/肥胖个体,然后针对这一人群进行最密集的减肥努力。