Christiaens Antoine, Cochard Alexis, Tubach Florence, Thompson Wade, Sinclair Alan J, Henrard Séverine, Boland Benoît, Slaouti-Jégou Yannis, Lekens Béranger, Bonnet-Zamponi Dominique, Simon-Tillaux Noémie, Zerah Lorene
Louvain Drug Research Institute, Université catholique de Louvain, Brussels, Belgium.
Fonds National de la Recherche Scientifique, Brussels, Belgium.
Age Ageing. 2025 May 31;54(6). doi: 10.1093/ageing/afaf160.
Hypoglycaemic drugs (sulfonylureas, glinides or insulins) are commonly prescribed for older adults with type 2 diabetes (T2D) but may carry risks of adverse events. Whether de-intensifying hypoglycaemic drugs is associated with clinical benefit in older adults remains unknown.
To evaluate the association between de-intensification of hypoglycaemic drugs and clinical outcomes in older adults with T2D.
Cohort study conducted with the target trial emulation approach, using data collected from 2000 French general practises between January 2010 and February 2019 (The Health Improvement Network-THIN database). Eligible participants were ≥75 years old, on stable hypoglycaemic drugs (no change in drug or dose) for at least 6 months, and had an HbA1c value <9%. Hypoglycaemic drug de-intensification (exposure) was defined as cessation or reduction of ≥50% of total dose. The primary outcome was a composite measure of all-cause death or hospital admissions within 3 months, and its association with exposure was assessed using multivariable logistic regression adjusted for potential baseline confounders.
The study included 14 383 unique individuals corresponding to 177 314 trial emulation participants (mean age 80 years; 44.7% female). Of these, 6480 participants were allocated to de-intensification group, and 170 834 to the control group. At 3 months, the primary outcome occurred in 3.96% of the de-intensification group and 2.99% of controls [adjusted relative risk, 1.33 (95% CI, 1.22-1.43)]. Subgroup analyses showed consistent associations across most participants' profiles.
In older adults with T2D, de-intensification of hypoglycaemic drugs was associated with a higher short-term risk of all-cause death or hospitalisation.
降糖药物(磺脲类、格列奈类或胰岛素)常用于老年2型糖尿病(T2D)患者,但可能存在不良事件风险。在老年患者中,减少降糖药物剂量是否具有临床益处尚不清楚。
评估老年T2D患者降糖药物剂量减少与临床结局之间的关联。
采用目标试验模拟法进行队列研究,使用2010年1月至2019年2月期间从2000家法国普通诊所收集的数据(健康改善网络-THIN数据库)。符合条件的参与者年龄≥75岁,服用稳定的降糖药物(药物或剂量无变化)至少6个月,糖化血红蛋白(HbA1c)值<9%。降糖药物剂量减少(暴露)定义为停药或总剂量减少≥50%。主要结局是3个月内全因死亡或住院的综合指标,并使用针对潜在基线混杂因素进行调整的多变量逻辑回归评估其与暴露的关联。
该研究纳入了14383名个体,对应177314名试验模拟参与者(平均年龄80岁;44.7%为女性)。其中,6480名参与者被分配到剂量减少组,170834名参与者被分配到对照组。3个月时,剂量减少组3.96%的参与者和对照组2.99%的参与者出现了主要结局[调整后的相对风险为1.33(95%CI,1.22-1.43)]。亚组分析显示,在大多数参与者特征中存在一致的关联。
在老年T2D患者中,降糖药物剂量减少与全因死亡或住院的短期风险较高相关。