肥胖,胰岛素抵抗和心血管疾病。

Gerald Reaven, Fahim Abbasi, Tracey McLaughlin
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引用次数: 368

摘要

在表面健康的个体中,胰岛素刺激葡萄糖处理的能力差异超过6倍。三分之一的胰岛素抵抗人群患心血管疾病(CVD)、2型糖尿病、高血压、中风、非酒精性脂肪性肝病、多囊卵巢疾病和某些形式的癌症的风险大大增加。25-35%的胰岛素作用变化与超重有关。有证据表明,美国超过一半的成年人被归类为超重/肥胖,体重指数大于25.0 kg/m(2),因此过度肥胖的不良影响的重要性是显而易见的。目前超重/肥胖的流行很可能与热量摄入增加和能量消耗减少的结合有关。在任何一种情况下,随着个体体重增加,心血管疾病的风险增加,这一事实强调了超重/肥胖流行率在整个人群中爆炸性增长所带来的卫生保健困境的严重性。考虑到问题的严重性,有必要区分与肥胖本身相关的心血管疾病风险,而不是超重/肥胖个体中胰岛素抵抗和代偿性高胰岛素血症的患病率增加。虽然一般人群中大多数被认为是胰岛素抵抗的人同时也是超重/肥胖的,但并不是所有超重/肥胖的人都是胰岛素抵抗的。此外,与胰岛素抵抗相关的异常群集-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/肥胖个体的子集,这些个体也具有胰岛素抵抗。更重要的临床相关性是,体重减轻后这些代谢异常的显著改善仅在超重/肥胖且胰岛素抵抗的个体中可见。鉴于大量超重/肥胖受试者具有胰岛素抵抗/高胰岛素血症的潜在风险(以及CVD风险增加),以及实现体重减轻的难度,确定那些同时具有胰岛素抵抗并将从减肥中获益最多的超重/肥胖个体似乎至关重要,然后针对这一人群进行最密集的减肥努力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Obesity, insulin resistance, and cardiovascular disease.

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.

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