Ölmestig Joakim, Marlet Ida R, Vilsbøll Tina, Rungby Jørgen, Rostrup Egill, Lambertsen Kate L, Kruuse Christina
Neurovascular Research Unit, Department of Neurology, Copenhagen University Hospital - Herlev and Gentofte, Copenhagen, Denmark.
Department of Clinical Medicine, University of Copenhagen, Copenhagen, Denmark.
Front Aging Neurosci. 2022 Jul 25;14:899389. doi: 10.3389/fnagi.2022.899389. eCollection 2022.
Glucagon-like peptide 1 (GLP-1) receptor agonists (GLP-1RA) are widely used for the treatment of type 2 diabetes, and recent studies indicate that they may be cardio- and neuroprotective. The safety and effect of a single dose of exenatide, a short-acting GLP-1RA, on cerebral and peripheral arterial function remain unknown.
In this randomized, double-blind pilot trial, we assigned elderly healthy volunteers without diabetes and no previous history of stroke to receive a single dose of subcutaneous exenatide (5 μg) or placebo. Primary outcome was immediate changes over time in blood flow velocity of the middle cerebral arteries (V) assessed by repeated transcranial Doppler measurements. Secondary outcomes were changes in peripheral arterial function with finger plethysmography, ankle-brachial index (ABI), and inflammatory- and endothelial-specific biomarkers.
Healthy volunteers (13 women and 17 men) were included: (mean ± standard deviation) age: 62 ± 8 years; body weight: 79.6 ± 12.7 kg; V: 65.3 ± 10.7 cm/s; fasting plasma glucose: 5.5 ± 0.5 mmol/L; HbA1c: 33.9 ± 4.1 mmol/mol (5.3 ± 0.38%). No differences between exenatide and placebo group were seen regarding V ( = 0.058), systolic ABI ( = 0.71), plethysmography ( = 0.45), tumor necrosis factor ( = 0.33), interleukin-6 ( = 0.11), interleukin-1β ( = 0.34), vascular cell adhesion molecule 1 ( = 0.73), intercellular adhesion molecule 1 ( = 0.74), or E-selectin ( = 0.31). No severe adverse events were observed.
A single dose of exenatide did not change cerebral blood flow velocity or peripheral vessel function in elderly healthy volunteers. The medication was safe to use in persons without diabetes allowing us to investigate this drug further in search of the neuroprotective mechanisms.
https://clinicaltrials.gov, Identifier NCT02838589.
胰高血糖素样肽1(GLP-1)受体激动剂(GLP-1RA)被广泛用于治疗2型糖尿病,最近的研究表明它们可能具有心脏和神经保护作用。单剂量短效GLP-1RA艾塞那肽对脑动脉和外周动脉功能的安全性和效果尚不清楚。
在这项随机、双盲先导试验中,我们将无糖尿病且无中风病史的老年健康志愿者随机分为两组,分别接受单剂量皮下注射艾塞那肽(5μg)或安慰剂。主要结局是通过重复经颅多普勒测量评估大脑中动脉血流速度(V)随时间的即时变化。次要结局是通过手指体积描记法、踝臂指数(ABI)以及炎症和内皮特异性生物标志物评估外周动脉功能的变化。
纳入了健康志愿者(13名女性和17名男性):(均值±标准差)年龄:62±8岁;体重:79.6±12.7kg;V:65.3±10.7cm/s;空腹血糖:5.5±0.5mmol/L;糖化血红蛋白:33.9±4.1mmol/mol(5.3±0.38%)。艾塞那肽组和安慰剂组在V(P = 0.058)、收缩期ABI(P = 0.71)、体积描记法(P = 0.45)、肿瘤坏死因子(P = 0.33)、白细胞介素-6(P = 0.11)、白细胞介素-1β(P = 0.34)、血管细胞黏附分子1(P = 0.73)、细胞间黏附分子1(P = 0.74)或E-选择素(P = 0.31)方面均无差异。未观察到严重不良事件。
单剂量艾塞那肽未改变老年健康志愿者的脑血流速度或外周血管功能。该药物在无糖尿病患者中使用安全,这使我们能够进一步研究该药物以探寻其神经保护机制。