Institute of Diabetes for Older People, Bedfordshire & Hertfordshire Postgraduate Medical School, University of Bedfordshire, Luton, UK.
Diabet Med. 2013 May;30(5):535-48. doi: 10.1111/dme.12063.
Clinical metabolic studies have demonstrated that insulin action declines progressively with age in humans. In addition to its close association with Type 2 diabetes, which reduces life expectancy in older people, age-related insulin resistance is implicated in pathogenesis of several highly prevalent disorders for which ageing is a major risk factor. These include atherosclerotic cardiovascular disease, dementia, frailty and cancer. Accordingly, insulin resistance may be viewed as biomarker of age-related ill health and reduced lifespan. The rapidly rising number of older people, coupled with a high prevalence of insulin resistance resulting from obesity and sedentary lifestyles, presents unprecedented public health and societal challenges. Studies of centenarians have shown that preserved whole-body sensitivity to insulin is associated with longevity. The mechanisms through which insulin action is associated with age-related diseases remain unclear. Changes in body composition, i.e. sarcopenia and excess adiposity, may be more potent than age per se. Moreover, the impact of insulin resistance has been difficult to disentangle from the clustering of vascular risk factors that co-segregate with the insulin resistance-hyperinsulinaemia complex. Potentially modifiable mediators of age-related changes in insulin sensitivity include alterations in adipocytokines, impaired skeletal myocyte mitochondrial function and brown fat activity. The hypothesis that improving or maintaining insulin sensitivity preserves health and extends lifespan merits further evaluation. Practical non-pharmacological interventions directed against age-related insulin resistance remain underdeveloped. Novel metabolically active pharmacological agents with theoretical implications for some age-related disorders are entering clinical trials. However, recent adverse experiences with the thiazolidinediones suggest the need for a cautious approach to the use of insulin sensitizing drugs in older people. This could be particularly important in the absence of diabetes where the risk to benefit analysis may be less favourable.
临床代谢研究表明,人类的胰岛素作用会随着年龄的增长而逐渐下降。除了与 2 型糖尿病密切相关(这种疾病会降低老年人的预期寿命)外,与年龄相关的胰岛素抵抗也与几种高发疾病的发病机制有关,而衰老则是这些疾病的主要危险因素。这些疾病包括动脉粥样硬化性心血管疾病、痴呆、虚弱和癌症。因此,胰岛素抵抗可能被视为与年龄相关的健康不良和寿命缩短的生物标志物。老年人数量的迅速增加,加上肥胖和久坐不动的生活方式导致的胰岛素抵抗高发,给公共卫生和社会带来了前所未有的挑战。对百岁老人的研究表明,全身对胰岛素的敏感性保持完好与长寿有关。胰岛素作用与年龄相关疾病之间的关联机制尚不清楚。身体成分的变化,即肌肉减少症和过多的脂肪堆积,可能比年龄本身更具影响力。此外,由于与胰岛素抵抗-高胰岛素血症综合征相关的血管危险因素聚集,胰岛素抵抗的影响一直难以区分。与胰岛素敏感性相关的年龄相关变化的潜在可调节介质包括脂肪细胞因子的改变、骨骼肌线粒体功能和棕色脂肪活性受损。改善或维持胰岛素敏感性以保持健康和延长寿命的假设值得进一步评估。针对与年龄相关的胰岛素抵抗的实用非药物干预措施仍未得到充分发展。具有某些与年龄相关疾病理论意义的新型代谢活性药物正在进入临床试验。然而,最近噻唑烷二酮类药物的不良经验表明,在老年人中使用胰岛素增敏药物时需要谨慎,在没有糖尿病的情况下,这种谨慎可能尤其重要,因为风险获益分析可能不太有利。