对糖尿病前期患者进行胰岛素治疗有什么依据吗?

Sherwyn Schwartz
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引用次数: 9

摘要

2型糖尿病通常以糖耐量受损(IGT)和/或空腹血糖受损(IFG)为先兆,这通常被称为糖尿病前期。IGT患者表现为β细胞功能障碍、胰岛素抵抗和肝糖生成增加;IGT和IFG是糖尿病和心血管疾病的危险因素。2型糖尿病与微血管和大血管并发症相关,可导致过高的死亡率和发病率,微血管并发症的风险延伸至糖尿病前期人群。2型糖尿病患者保持良好的血糖控制可以降低发生慢性疾病相关并发症的风险。大多数2型糖尿病患者似乎都经历过IFG或IGT的一个阶段;因此,糖尿病前期患者的早期干预(生活方式和/或药物)可能有助于预防心血管疾病和2型糖尿病的发展。外源性胰岛素治疗通过有效降低血糖和脂质水平以及慢性升高引起的相关组织损伤,有可能降低2型糖尿病或糖尿病前期患者的心血管风险。然而,在2型糖尿病和前驱糖尿病患者中,胰岛素启动都存在一些障碍(例如,低血糖、体重增加、长效胰岛素可能不可预测的作用以及需要注射)。甘精胰岛素与胰岛素悬浮液异黄酮(中性鱼精蛋白hagedorn [NPH]胰岛素)相比,具有平坦的时间作用谱、接近24小时的作用持续时间、降低低血糖风险和改善血糖控制,可能有助于克服这些障碍。一项小型研究的初步结果表明,使用低剂量甘精胰岛素加热量限制方案治疗糖尿病前期至接近正常血糖的个体是可行的。正在进行的ORIGIN(降低初始甘精干预的结局)研究将对这一结果进行随访,该研究将调查与常规治疗相比,IGT、IFG或新发2型糖尿病患者使用甘精胰岛素治疗接近正常血糖是否可以降低心血管发病率和死亡率,以及是否可以类似地降低2型糖尿病的进展率。需要进一步的研究来调查胰岛素治疗对糖尿病前期个体的潜在益处。
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Is there a rationale for insulin therapy in pre-diabetic individuals?

Type 2 diabetes mellitus is usually preceded by impaired glucose tolerance (IGT) and/or impaired fasting glucose (IFG), which are often referred to as pre-diabetes. Individuals with IGT demonstrate beta-cell dysfunction, insulin resistance, and increased hepatic glucose production; IGT and IFG are risk factors for both diabetes and cardiovascular disease. Type 2 diabetes is associated with micro- and macrovascular complications that lead to excessive mortality and morbidity and the risk of microvascular complications extends to people with pre-diabetes. Maintaining good glycemic control in type 2 diabetes can reduce the risk of developing chronic disease-associated complications. Most individuals who develop type 2 diabetes appear to pass through a stage of IFG or IGT; thus, early intervention (lifestyle and/or pharmacologic) in individuals with pre-diabetes may help prevent cardiovascular disease and the development of type 2 diabetes.The use of exogenous insulin treatment offers the potential to reduce the cardiovascular risk in individuals with type 2 diabetes or pre-diabetes through effective reductions in blood glucose and lipid levels, and in the associated tissue damage resulting from their chronic elevations. However, there are barriers associated with insulin initiation in both type 2 diabetes and pre-diabetes (e.g. hypoglycemia, weight gain, the possible unpredictable action of long-acting insulin, and the need for injections). Insulin glargine, with its flat time-action profile, near 24-hour duration of action, reduced risk of hypoglycemia, and improved glycemic control compared with insulin suspension isophane (neutral protamine hagedorn [NPH] insulin), may help to overcome some of these barriers.Initial results from a small study have indicated the feasibility of treating individuals with pre-diabetes to near-normoglycemia using a regimen of low-dose insulin glargine plus caloric restriction. This is being followed up in the ongoing ORIGIN (Outcomes Reduction with Initial Glargine INtervention) study, which will investigate whether treatment to near-normoglycemia with insulin glargine in individuals with IGT, IFG, or new-onset type 2 diabetes can reduce cardiovascular morbidity and mortality compared with conventional management of these conditions, and whether the rate of progression to type 2 diabetes can be similarly reduced.Further studies are needed to investigate the potential benefits of insulin therapy in individuals with pre-diabetes.

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