Department of Neurology, UMC Utrecht Brain Center, University Medical Center Utrecht, Utrecht, the Netherlands
Department of Neurology, UMC Utrecht Brain Center, University Medical Center Utrecht, Utrecht, the Netherlands.
Diabetes Care. 2019 Oct;42(10):1930-1938. doi: 10.2337/dc19-0783. Epub 2019 Aug 9.
Type 2 diabetes is associated with cognitive dysfunction and an increased dementia risk, particularly in individuals with concomitant cardiovascular and/or kidney disease. Incretin therapies may modulate this risk via glycemic and nonglycemic pathways. We explored if the dipeptidyl peptidase 4 inhibitor linagliptin could prevent cognitive decline in people with type 2 diabetes with cardiorenal disease.
The CArdiovascular and Renal Microvascular outcomE study with LINAgliptin (CARMELINA)-COG substudy was an integral part of CARMELINA (NCT01897532) that randomized participants with cardiorenal disease to linagliptin 5 mg or placebo once daily (1:1), in addition to standard of care. The primary cognitive outcome was the occurrence of accelerated cognitive decline at the end of treatment, defined as a regression-based index score ≤16th percentile on the Mini-Mental State Examination (MMSE) or a composite measure of attention and executive functioning and analyzed in participants with a baseline MMSE ≥24. Effects across subgroups by baseline factors, as well as absolute cognitive changes, were also assessed.
Of the 6,979 participants in CARMELINA, CARMELINA-COG included 1,545 (mean ± SD age, 68 ± 8 years; MMSE, 28.3 ± 1.7; estimated glomerular filtration rate, 52 ± 23 mL/min/1.73 m; and HbA, 7.8 ± 0.9% [61.4 ± 10.1 mmol/mol]). Over a median treatment duration of 2.5 years, accelerated cognitive decline occurred in 28.4% (linagliptin) vs. 29.3% (placebo) (odds ratio 0.96 [95% CI 0.77, 1.19]). Consistent effects were observed across subgroups by baseline characteristics. Absolute cognitive performance changes were also similar between treatment groups.
In a large international cardiovascular outcome trial in people with type 2 diabetes and cardiorenal disease, linagliptin did not modulate cognitive decline over 2.5 years.
2 型糖尿病与认知功能障碍和痴呆风险增加有关,尤其是在伴有心血管和/或肾脏疾病的患者中。肠促胰岛素治疗可能通过血糖和非血糖途径调节这种风险。我们探讨了二肽基肽酶 4 抑制剂利拉利汀是否可以预防伴有心血管和肾脏疾病的 2 型糖尿病患者的认知能力下降。
CArdiovascular 和 Renal Microvascular outcomE 研究与 LINAgliptin(CARMELINA)-COG 子研究是 CARMELINA(NCT01897532)的一个组成部分,该研究将伴有心血管和肾脏疾病的患者随机分为利拉利汀 5mg 或安慰剂,每日一次(1:1),同时接受标准治疗。主要认知结局是治疗结束时加速认知下降的发生,定义为基于回归的 Mini-Mental State Examination(MMSE)指数评分≤第 16 百分位数,或注意力和执行功能的综合测量,分析时基线 MMSE≥24。还评估了按基线因素分层的各亚组的效果,以及绝对认知变化。
在 CARMELINA 的 6979 名参与者中,CARMELINA-COG 包括 1545 名(平均±SD 年龄,68±8 岁;MMSE,28.3±1.7;估算肾小球滤过率,52±23mL/min/1.73m;和 HbA,7.8±0.9%[61.4±10.1mmol/mol])。在中位数为 2.5 年的治疗期间,加速认知下降发生率为 28.4%(利拉利汀)vs.29.3%(安慰剂)(比值比 0.96[95%CI 0.77,1.19])。在按基线特征分层的各亚组中观察到一致的效果。治疗组之间的绝对认知表现变化也相似。
在伴有 2 型糖尿病和心血管及肾脏疾病的大型国际心血管结局试验中,利拉利汀在 2.5 年内未调节认知下降。