Huynh Grace, Runeberg Haley, Weideman Rick
VA North Texas Health Care System, Dallas, TX, USA.
J Pharm Technol. 2023 Feb;39(1):10-15. doi: 10.1177/87551225221137493. Epub 2022 Nov 30.
Semaglutide is an effective agent indicated for type II diabetes mellitus (T2DM) treatment and weight management. It is unknown if the magnitude of weight loss differs significantly between nonelderly (18-64 years old) and elderly (≥65 years old) patients diagnosed with T2DM. To determine whether there is a significant difference in percent weight loss between elderly and nonelderly Veterans diagnosed with T2DM and initiating semaglutide. This institutional review board-approved retrospective cohort study conducted at the VA North Texas Health Care System included adult Veterans with T2DM initiating semaglutide. Veterans with medications, procedures, or conditions that could significantly affect weight were excluded. The primary endpoint was the difference in percent weight loss 3 months after initiating semaglutide. Secondary endpoints were differences in percent weight loss at 6 months and differences of kilogram weight loss at 3 and 6 months. Safety outcomes were significant adverse drug events (ADEs) associated with semaglutide. In total, 177 Veterans were analyzed (n = 111 elderly, n = 66 nonelderly). For the primary endpoint, elderly Veterans lost a mean of 2.02% body weight versus 2.25% in the nonelderly with a mean difference of 0.23% (95% CI, -1.03% to 1.48%; = 0.72). Secondary endpoints were also not statistically significant. Significant ADEs were gastrointestinal-related, leading to drug discontinuation or dose reduction. Weight loss differences between elderly and nonelderly Veterans diagnosed with T2DM initiating semaglutide were not statistically significant. Age may not be a robust predictor of semaglutide's influence on weight.
司美格鲁肽是一种用于治疗2型糖尿病(T2DM)和体重管理的有效药物。对于诊断为T2DM的非老年患者(18 - 64岁)和老年患者(≥65岁),其体重减轻幅度是否存在显著差异尚不清楚。本研究旨在确定诊断为T2DM并开始使用司美格鲁肽的老年退伍军人和非老年退伍军人在体重减轻百分比上是否存在显著差异。这项在北德克萨斯退伍军人医疗保健系统进行的、经机构审查委员会批准的回顾性队列研究纳入了开始使用司美格鲁肽的成年T2DM退伍军人。排除了患有可能显著影响体重的药物、手术或疾病的退伍军人。主要终点是开始使用司美格鲁肽3个月后体重减轻百分比的差异。次要终点是6个月时体重减轻百分比的差异以及3个月和6个月时千克体重减轻的差异。安全性结局是与司美格鲁肽相关的严重不良药物事件(ADEs)。总共分析了177名退伍军人(n = 111名老年人,n = 66名非老年人)。对于主要终点,老年退伍军人平均体重减轻2.02%,而非老年退伍军人平均体重减轻2.25%,平均差异为0.23%(95% CI,-1.03%至1.48%;P = 0.72)。次要终点也无统计学意义。严重ADEs与胃肠道相关,导致停药或减量。诊断为T2DM并开始使用司美格鲁肽的老年和非老年退伍军人之间的体重减轻差异无统计学意义。年龄可能不是司美格鲁肽对体重影响的有力预测指标。