Largeau Bérenger, Bordy Romain, Pasqualin Côme, Bredeloux Pierre, Cracowski Jean-Luc, Lengellé Céline, Gras-Champel Valérie, Auffret Marine, Maupoil Véronique, Jonville-Béra Annie-Pierre
CHRU de Tours, Service de Pharmacosurveillance, Centre Régional de Pharmacovigilance Centre-Val de Loire, Tours 37044, France.
Université de Tours, Transplantation, Immunologie et Inflammation (T2I) - EA4245, Tours 37044, France.
Biomed Pharmacother. 2022 May;149:112807. doi: 10.1016/j.biopha.2022.112807. Epub 2022 Mar 15.
Gabapentinoids are ligands of the α2-δ subunit of voltage-gated calcium channels (Cav) that have been associated with a risk of peripheral edema and acute heart failure in connection with a potentially dual mechanism, vascular and cardiac.
OBJECTIVES & METHODS: All cases of peripheral edema or heart failure involving gabapentin or pregabalin reported to the French Pharmacovigilance Centers between January 1, 1994 and April 30, 2020 were included to describe their onset patterns (e.g., time to onset). Based on these data, we investigated the impact of gabapentinoids on the myogenic tone of rat third-order mesenteric arteries and on the electrophysiological properties of rat ventricular cardiomyocytes.
A total of 58 reports were included (gabapentin n = 5, pregabalin n = 53). The female-to-male ratio was 4:1 and the median age was 77 years (IQR 57-85, range 32-95). The median time to onset were 23 days (IQR 10-54) and 17 days (IQR 3-30) for non-cardiogenic edema and acute heart failure, respectively. Cardiogenic and non-cardiogenic peripheral edema occurred frequently after a dose escalation (27/45, 60%), and the course was rapidly favorable after discontinuation of gabapentinoid (median 7 days, IQR 5-13). On rat mesenteric arteries, gabapentinoids significantly decreased the myogenic tone to the same extent as verapamil and nifedipine. Acute application of gabapentinoids had no significant effect on Ca1.2 currents of ventricular cardiomyocytes.
Gabapentinoids can cause concentration-dependent peripheral edema of early onset. The primary mechanism of non-cardiogenic peripheral edema is vasodilatory edema secondary to altered myogenic tone, independent of Ca1.2 blockade under the experimental conditions tested.
加巴喷丁类药物是电压门控钙通道(Cav)α2-δ亚基的配体,与外周水肿和急性心力衰竭风险相关,可能存在血管和心脏双重机制。
纳入1994年1月1日至2020年4月30日期间向法国药物警戒中心报告的所有涉及加巴喷丁或普瑞巴林的外周水肿或心力衰竭病例,以描述其发病模式(如发病时间)。基于这些数据,我们研究了加巴喷丁类药物对大鼠三级肠系膜动脉肌源性张力以及大鼠心室心肌细胞电生理特性的影响。
共纳入58份报告(加巴喷丁5例,普瑞巴林53例)。男女比例为4:1,中位年龄为77岁(四分位间距57 - 85,范围32 - 95)。非心源性水肿和急性心力衰竭的中位发病时间分别为23天(四分位间距10 - 54)和17天(四分位间距3 - 30)。心源性和非心源性外周水肿在剂量增加后频繁发生(27/45,60%),停用加巴喷丁类药物后病情迅速好转(中位7天,四分位间距5 - 13)。在大鼠肠系膜动脉上,加巴喷丁类药物与维拉帕米和硝苯地平一样,能显著降低肌源性张力。加巴喷丁类药物急性应用对心室心肌细胞的Ca1.2电流无显著影响。
加巴喷丁类药物可导致早期发生的浓度依赖性外周水肿。非心源性外周水肿的主要机制是肌源性张力改变继发的血管舒张性水肿,在所测试的实验条件下与Ca1.2阻断无关。