Shaefer Charles F, Reid Timothy S, Dailey George, Mabrey Melanie E, Vlajnic Aleksandra, Stuhr Andreas, Stewart John, Zhou Rong
Georgia Health Sciences University, Augusta, GA.
Postgrad Med. 2014 Oct;126(6):93-105. doi: 10.3810/pgm.2014.10.2824.
An increase in body weight is a commonly perceived effect of insulin therapy for type 2 diabetes mellitus, and this may serve as a barrier to insulin initiation and usage.
To investigate the baseline clinical and demographic factors associated with weight gain during insulin glargine therapy, and the implications of weight change on clinical outcomes.
This was a retrospective analysis of patient-level data from phase 3 or 4 randomized controlled, treat-to-target (fasting plasma glucose [FPG] ≤ 100 mg/dL) trials evaluating basal insulin glargine for ≥ 24 weeks. The Pearson correlation coefficient and Cochran-Armitage trend statistic were used to calculate the existence of a trend between absolute and relative weight change, and relative glycated hemoglobin (HbA1c) change from baseline; likelihood of achieving target HbA1c < 7.0%; change from baseline FPG; insulin dose requirements; incidence of hypoglycemia; and adverse events.
Eleven studies were included, encompassing a total of 2140 patients. Patients starting insulin glargine treatment gained a mean ± standard deviation 1.8 ± 3.7 kg (4.0 ± 8.2 lb). Most patients had limited weight change (± 2.5 kg or 5.5 lb). Younger age, higher baseline HbA1c, and higher baseline FPG were predictive of greater weight gain (P < 0.0001). Those who gained more weight experienced the largest decrease from baseline in HbA1c and FPG. More weight gain was associated with higher insulin dose requirements, an increased risk of experiencing either symptomatic or glucose-confirmed (< 70 mg/dL) hypoglycemia, and more adverse events. Older patients (> 65 years) were less likely to gain weight or to experience glucose-confirmed hypoglycemia, but more likely to experience severe hypoglycemia.
In this retrospective analysis of patient-level data, most patients had a stable weight (defined as ± 2.5 kg) after 24 weeks of insulin glargine, and weight gain varied with patient demographics. Therefore, insulin glargine can be used in these patient groups with type 2 diabetes without expectation of significant weight gain.
体重增加是2型糖尿病胰岛素治疗常见的一种感知到的效应,这可能成为起始和使用胰岛素的一个障碍。
调查与甘精胰岛素治疗期间体重增加相关的基线临床和人口统计学因素,以及体重变化对临床结局的影响。
这是一项对3期或4期随机对照、达标治疗(空腹血糖[FPG]≤100mg/dL)试验中患者水平数据的回顾性分析,这些试验评估了基础甘精胰岛素治疗≥24周的情况。使用Pearson相关系数和Cochran-Armitage趋势统计量来计算绝对和相对体重变化与相对糖化血红蛋白(HbA1c)自基线变化之间趋势的存在情况;达到目标HbA1c<7.0%的可能性;自基线FPG的变化;胰岛素剂量需求;低血糖发生率;以及不良事件。
纳入了11项研究,共2140例患者。开始甘精胰岛素治疗的患者体重平均增加±标准差1.8±3.7kg(4.0±8.2磅)。大多数患者体重变化有限(±2.5kg或5.5磅)。年龄较小、基线HbA1c较高和基线FPG较高可预测体重增加更多(P<0.0001)。体重增加较多的患者HbA1c和FPG自基线下降幅度最大。体重增加更多与更高的胰岛素剂量需求、出现有症状或血糖确认(<70mg/dL)低血糖的风险增加以及更多不良事件相关。老年患者(>65岁)体重增加或血糖确认低血糖的可能性较小,但发生严重低血糖的可能性较大。
在这项对患者水平数据的回顾性分析中,大多数患者在甘精胰岛素治疗24周后体重稳定(定义为±2.5kg),且体重增加因患者人口统计学特征而异。因此,甘精胰岛素可用于这些2型糖尿病患者群体,而无需预期会有显著体重增加。