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PDE5 抑制剂与动脉瘤/动脉夹层的相关性:一项基于世界卫生组织安全性数据库的药物警戒研究。

The Association between PDE5 Inhibitors and Aneurysm/Arterial Dissection:A Pharmacovigilance Study Using WHO Safety Database.

机构信息

Department of Clinical Pharmacology and Therapeutics, Tokushima University Graduate School of Biomedical Sciences, Tokushima University, Tokushima, Japan.

Department of General Medicine, Taoka Hospital, Tokushima, Japan.

出版信息

J Med Invest. 2024;71(1.2):134-140. doi: 10.2152/jmi.71.134.

DOI:10.2152/jmi.71.134
PMID:38735709
Abstract

Aneurysm and arterial dissection have been reported as adverse drug events, associated with angiogenesis inhibitors and fluoroquinolones. Specifically, several cases of severe arterial disease following cGMP-specific phosphodiesterase type 5 (PDE5) inhibitors usage have recently been reported. It is necessary to ascertain the risks of serious adverse events caused by PDE5 inhibitors. We aimed to evaluate the association of aneurysm and artery dissection with PDE5 inhibitors using VigiBase, which is a World Health Organization database of spontaneously reported adverse events, for explorative hypothesis-generating analysis. We performed disproportionality analysis using a dataset from inception in 1967 to December 2022 and calculated reporting odds ratios (ROR) between PDE5 inhibitors and arterial diseases. We extracted 195,839 reports on PDE5 inhibitors with 254 reports of arterial disease as adverse events from VigiBase. Disproportionality analysis showed disproportional signals for PDE5 inhibitors (ROR, 2.30;95% confidence intervals, 2.04-2.61);disproportional signals were detected in analyses restricting the lesion site to the aorta or cerebral arteries. From stratified analysis, disproportional signals were noted in females, as well as males, generally recognized as a risk factor for artery diseases. This real-world data analysis suggests that PDE5 inhibitors may play a role in the development of lethal arterial disease. J. Med. Invest. 71 : 134-140, February, 2024.

摘要

已有报道称,在使用血管生成抑制剂和氟喹诺酮类药物时,会出现动脉瘤和动脉夹层等不良药物事件。具体而言,最近有几例使用环磷酸鸟苷(cGMP)特异性磷酸二酯酶 5(PDE5)抑制剂后出现严重动脉疾病的病例。有必要确定 PDE5 抑制剂引起严重不良事件的风险。我们旨在使用世界卫生组织自发报告不良事件数据库 VigiBase 评估动脉瘤和动脉夹层与 PDE5 抑制剂之间的关联,以进行探索性假设生成分析。我们使用从 1967 年开始到 2022 年 12 月的数据集进行了不成比例性分析,并计算了 PDE5 抑制剂与动脉疾病之间的报告比值比(ROR)。我们从 VigiBase 中提取了 195839 例 PDE5 抑制剂报告,其中有 254 例动脉疾病报告为不良事件。不成比例性分析显示 PDE5 抑制剂存在不成比例的信号(ROR,2.30;95%置信区间,2.04-2.61);在限制病变部位为主动脉或脑动脉的分析中,也检测到了不成比例的信号。分层分析表明,女性和男性均存在不成比例的信号,而女性和男性通常被认为是动脉疾病的危险因素。这项真实世界数据分析表明,PDE5 抑制剂可能在致命性动脉疾病的发展中发挥作用。医学研究杂志 71:134-140,2024 年 2 月。

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