Departments of Medicine, Biochemistry and Molecular Biology, Julia McFarlane Diabetes Research Centre and Libin Cardiovascular Institute of Alberta, University of Calgary Cumming School of Medicine, Calgary, Alberta, Canada.
Divisions of Endocrinology & Metabolism and Cardiac Surgery, Keenan Research Centre for Biomedical Science and the Li Ka Shing Knowledge Institute, St. Michael's Hospital, Toronto, Ontario, Canada.
Can J Diabetes. 2015 Dec;39 Suppl 5:S134-41. doi: 10.1016/j.jcjd.2015.10.001.
Type 2 diabetes is a serious chronic disease that is associated with increased morbidity and premature mortality. It has become the tsunami of noncommunicable diseases, with more than 400 million people worldwide currently living with diabetes. The global diabetes epidemic is driven by rising obesity rates. Excess body fat increases the risk for insulin resistance and prediabetes; obese men and women, respectively, have a 7-fold and 12-fold higher risk for developing type 2 diabetes. Obesity also predisposes to the development of a myriad of medical complications leading to increased morbidity and mortality. Each increase in body mass index of 5 kg/m(2) or higher is, on average, associated with about a 30% higher overall mortality rate. Modest weight loss through health-behaviour modification can significantly prevent or delay the onset of type 2 diabetes in people at risk. Each kg of body weight loss is associated with a 16% relative reduction in diabetes risk. Intentional weight loss is also associated with a 15% reduction in all-cause mortality. Unfortunately, health-behaviour modification alone seldom sustains adequate weight loss to achieve the desired health outcomes, especially in people with diabetes who already have greater difficulty losing weight. Pharmacotherapy is a realistic treatment option as an adjunct to diet and exercise. In addition to orlistat, the glucagon-like peptide-1 receptor agonist liraglutide has recently been approved in Canada for the treatment of obesity in doses of up to 3.0 mg daily. This review is focused on current and emerging pharmacotherapies for obesity in people with prediabetes or diabetes.
2 型糖尿病是一种严重的慢性疾病,与发病率和早逝率增加有关。它已成为非传染性疾病的海啸,目前全球有超过 4 亿人患有糖尿病。全球糖尿病流行是由肥胖率上升驱动的。过多的体脂会增加胰岛素抵抗和前驱糖尿病的风险;肥胖男性和女性分别有 7 倍和 12 倍的风险患上 2 型糖尿病。肥胖也容易导致多种医疗并发症的发生,从而增加发病率和死亡率。平均而言,身体质量指数每增加 5kg/m(2)或更高,总死亡率就会增加约 30%。通过健康行为改变适度减肥可以显著预防或延迟高危人群 2 型糖尿病的发生。体重减轻 1kg 与糖尿病风险相对降低 16%相关。有目的的减肥也与全因死亡率降低 15%相关。不幸的是,仅通过健康行为改变很少能维持足够的体重减轻来实现预期的健康结果,尤其是在已经更难以减肥的糖尿病患者中。药物治疗是一种现实的治疗选择,可作为饮食和运动的辅助治疗。除了奥利司他,胰高血糖素样肽-1 受体激动剂利拉鲁肽最近在加拿大被批准用于治疗肥胖症,剂量高达每日 3.0mg。这篇综述主要关注用于治疗前驱糖尿病或糖尿病患者肥胖症的现有和新兴药物疗法。
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