Division of Gerontology and Geriatric Medicine, Wake Forest School of Medicine, Winston-Salem, North Carolina.
AdventHealth Translational Research Institute, Orlando, Florida.
Diabetes Obes Metab. 2021 Feb;23(2):569-580. doi: 10.1111/dom.14254. Epub 2020 Dec 6.
To compare the cardiovascular (CV) safety of linagliptin with glimepiride in older and younger participants in the CAROLINA trial in both prespecified and post hoc analyses.
People aged 40 to 85 years with relatively early type 2 diabetes, inadequate glycaemic control and elevated CV risk were randomly assigned to linagliptin 5 mg or glimepiride 1 to 4 mg. The primary endpoint was time to first occurrence of three-point major adverse CV events (MACE: CV death, non-fatal myocardial infarction, or non-fatal stroke). We evaluated clinical and safety outcomes across age groups.
Of 6033 participants, 50.7% were aged <65 years, 35.3% were aged 65 to 74 years, and 14.0% were aged ≥75 years. During the 6.3-year median follow-up, CV/mortality outcomes did not differ between linagliptin and glimepiride overall (hazard ratio [HR] for three-point MACE 0.98, 95.47% confidence interval [CI] 0.84, 1.14) or across age groups (interaction P >0.05). Between treatment groups, reductions in glycated haemoglobin were comparable across age groups but moderate-to-severe hypoglycaemia was markedly reduced with linagliptin (HR 0.18, 95% CI 0.15, 0.21) with no differences among age groups (P = 0.23). Mean weight was -1.54 kg (95% CI -1.80, -1.28) lower for linagliptin versus glimepiride. Adverse events increased with age, but were generally balanced between treatment groups. Significantly fewer falls or fractures occurred with linagliptin.
Linagliptin and glimepiride were comparable for CV/mortality outcomes across age groups. Linagliptin had significantly lower risk of hypoglycaemia and falls or fractures than glimepiride, including in "older-old" individuals for whom these are particularly important treatment considerations.
在 CAROLINA 试验中,分别在预设和事后分析中比较利拉利汀和格列美脲在老年和年轻参与者中的心血管(CV)安全性。
年龄在 40 至 85 岁之间、有相对早期 2 型糖尿病、血糖控制不理想且 CV 风险升高的人群被随机分配至利拉利汀 5mg 或格列美脲 1 至 4mg。主要终点是首次发生三点主要不良 CV 事件(MACE:CV 死亡、非致死性心肌梗死或非致死性卒中)的时间。我们评估了不同年龄组的临床和安全性结果。
在 6033 名参与者中,50.7%年龄<65 岁,35.3%年龄 65 至 74 岁,14.0%年龄≥75 岁。在中位随访 6.3 年期间,利拉利汀和格列美脲之间的 CV/死亡率结果在总体上(三点 MACE 的危险比[HR]为 0.98,95.47%置信区间[CI]为 0.84,1.14)或在各年龄组之间(交互 P>0.05)均无差异。在治疗组之间,各年龄组的糖化血红蛋白降低情况相当,但利拉利汀显著减少了中重度低血糖(HR 0.18,95%CI 0.15,0.21),且各年龄组之间无差异(P=0.23)。与格列美脲相比,利拉利汀的平均体重下降了 1.54kg(95%CI-1.80,-1.28)。不良事件随年龄增长而增加,但通常在治疗组之间平衡。利拉利汀组发生跌倒或骨折的情况明显较少。
利拉利汀和格列美脲在各年龄组的 CV/死亡率结果方面相当。与格列美脲相比,利拉利汀低血糖和跌倒或骨折的风险显著降低,包括对这些尤其重要的治疗考虑的“老老年”人群。