Incidence of Myocarditis Caused by Drugs Used for Ulcerative Colitis as Examined Using VigiBase, a Spontaneous Adverse Drug Reaction Reporting Database.

IF 1.7 4区 医学 Q3 PHARMACOLOGY & PHARMACY
Yumi Kawai, Yasuko Kurata, Hirofumi Hamano, Takahiro Niimura, Mitsuhiro Goda, Yoshito Zamami, Keisuke Ishizawa, Hideki Nawa
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引用次数: 0

Abstract

Although myocarditis is listed as a serious adverse reaction in the package inserts of mesalazine and some other anti-ulcerative colitis (UC) drugs currently in use, and regulatory authorities have issued related warnings, the detailed characteristics of anti-UC drug-induced myocarditis remain unknown. We aimed to investigate the association between UC drugs and myocarditis development as an adverse event and its characteristics using data from a spontaneous adverse drug reaction reporting database. We searched for adverse event signals of five drugs, mesalazine, sulfasalazine, azathioprine, mercaptopurine, and budesonide, listed in the treatment guidelines for UC, using VigiBase. The information component was calculated, and a signal was considered present when the lower limit of the 95% confidence interval of the information component exceeded zero. The total number of VigiBase and myocarditis (as a target adverse event) reports was 38459016 and 71571, respectively. No trend was identified based on age or sex. Analysis of the five UC drugs for severity in VigiBase showed that most patients recovered, with a low reported mortality rate. However, the time to onset of adverse drug reactions varied among the drugs. Mesalazine signals were detected regardless of age or sex. This finding suggests that myocarditis, an adverse event, may be a potential complication regardless of patient characteristics. Our results also indicate that UC itself may induce myocarditis. Our findings warrant multifaceted investigations, including basic and clinical studies, on the characteristics of each drug regarding the development of myocarditis as an adverse event.

使用自发药物不良反应报告数据库VigiBase检测溃疡性结肠炎药物引起心肌炎的发生率
尽管目前在使用的美沙拉嗪和其他一些抗溃疡性结肠炎(UC)药物的说明书中将心肌炎列为严重不良反应,监管部门也发布了相关警告,但抗UC药物性心肌炎的详细特征尚不清楚。我们的目的是研究UC药物与心肌炎发展之间的关系,并利用自发药物不良反应报告数据库的数据研究其特征。我们使用VigiBase检索了UC治疗指南中列出的五种药物的不良事件信号,美萨拉嗪、磺胺硫氮嗪、硫唑嘌呤、巯基嘌呤和布地奈德。计算信息分量,当信息分量的95%置信区间的下限超过零时,认为信号存在。VigiBase和心肌炎(作为目标不良事件)报告总数分别为38459016例和71571例。没有发现基于年龄或性别的趋势。对VigiBase中5种UC药物严重程度的分析显示,大多数患者康复,报告死亡率低。然而,药物不良反应发生的时间因药物而异。无论年龄或性别,都能检测到美沙拉嗪信号。这一发现表明,心肌炎,一个不良事件,可能是一个潜在的并发症,无论患者的特点。我们的结果也表明UC本身可能诱发心肌炎。我们的发现需要多方面的调查,包括基础和临床研究,对每种药物的特点,将心肌炎的发展作为一个不良事件。
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来源期刊
CiteScore
3.50
自引率
5.00%
发文量
247
审稿时长
2 months
期刊介绍: Biological and Pharmaceutical Bulletin (Biol. Pharm. Bull.) began publication in 1978 as the Journal of Pharmacobio-Dynamics. It covers various biological topics in the pharmaceutical and health sciences. A fourth Society journal, the Journal of Health Science, was merged with Biol. Pharm. Bull. in 2012. The main aim of the Society’s journals is to advance the pharmaceutical sciences with research reports, information exchange, and high-quality discussion. The average review time for articles submitted to the journals is around one month for first decision. The complete texts of all of the Society’s journals can be freely accessed through J-STAGE. The Society’s editorial committee hopes that the content of its journals will be useful to your research, and also invites you to submit your own work to the journals.
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