Mental health safety profile of CFTR modulators in pediatrics and adults: insights from the French pharmacovigilance database and from VigiBase.

IF 5.4
Diane A Merino, Samuel D Cohen, Nouha Ben Othman, Marie-Noëlle Osmont, Tessa Pietri, Sandrine Bergeron, Sophie Gautier, Fanny Rocher, Milou-Daniel Drici, Pierre-Régis Burgel, Isabelle Sermet-Gaudelus, Alexandre O Gérard, Laurent Chouchana
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引用次数: 0

Abstract

Rationale: CFTR modulators (CFTRms) have transformed cystic fibrosis care, yet concern exists regarding their mental health safety profile.

Objective: To provide further information, we conducted an analysis of CFTRm-related mental health disorders using two spontaneous pharmacovigilance reporting databases in real-world settings.

Methods: We analyzed reports from the French Pharmacovigilance Database (FPD) and VigiBase, the WHO global individual case safety reports database. Reports recorded between 2012 and 2024 involving any CFTRm and psychiatric disorders were included. In VigiBase, we conducted a case-non case, disproportionality analysis using the Reporting Odds Ratio (ROR), overall and stratified by age group (pediatrics vs. adults) and by CFTRm type. This study was conducted in accordance with the STROBE and the READUS-PV guidelines.

Results: In the FPD, 116 cases were analyzed. ELX/TEZ/IVA was suspected in 98% of cases and no single case was reported with ivacaftor alone. Sleep (61%), mood (37%), and anxiety disorders (27%) were the most frequently reported, with suicidal behaviors being infrequent, including 6 suicide attempts and no completed suicide. In VigiBase (n = 3,407), sleep disorders predominated in children, whereas mood and suicidality disorders were most frequent in adolescents. The median time to onset was 60 days (Q1-Q3: 12-150 days). Mental health disorders were disproportionately reported with CFTRms, particularly ELX/TEZ/IVA, while they were not with other combination therapies, compared to other drugs in the database. Disproportionality signals were slightly stronger in pediatrics than in adults.

Conclusions: CFTRms, especially ELX/TEZ/IVA, are associated with increased reporting of mental health disorders, predominantly sleep and mood disorders. Pediatrics appear to be particularly affected. Prospective observational studies are warranted to confirm these findings and elucidate underlying pathophysiological mechanisms.

Registration: OSF: mfyx3.

CFTR调节剂在儿科和成人中的心理健康安全概况:来自法国药物警戒数据库和VigiBase的见解
理由:CFTR调节剂(CFTRms)已经改变了囊性纤维化的治疗,但存在对其心理健康安全概况的担忧。目的:为了提供进一步的信息,我们使用两个现实环境中的自发药物警戒报告数据库对cftrm相关的精神健康障碍进行了分析。方法:我们分析了来自法国药物警戒数据库(FPD)和世界卫生组织全球个案安全报告数据库VigiBase的报告。2012年至2024年期间记录的报告包括任何CFTRm和精神疾病。在VigiBase中,我们使用报告优势比(ROR)进行了非病例、歧化分析,并按年龄组(儿科与成人)和CFTRm类型进行了总体和分层。本研究按照STROBE和READUS-PV指南进行。结果:FPD共分析116例。98%的病例怀疑ELX/TEZ/IVA,单独使用ivacaftor未报告单一病例。睡眠(61%)、情绪(37%)和焦虑障碍(27%)是最常见的报告,自杀行为不常见,包括6次自杀未遂,没有自杀未遂。在VigiBase (n = 3407)中,睡眠障碍在儿童中占主导地位,而情绪和自杀障碍在青少年中最常见。中位发病时间为60天(Q1-Q3: 12-150天)。与数据库中的其他药物相比,CFTRms(特别是ELX/TEZ/IVA)报告的精神健康障碍不成比例,而其他联合疗法则没有。歧化信号在儿科中比在成人中稍强。结论:CFTRms,尤其是ELX/TEZ/IVA,与精神健康障碍的报告增加有关,主要是睡眠和情绪障碍。儿科似乎特别受影响。前瞻性观察研究有必要证实这些发现并阐明潜在的病理生理机制。注册:OSF: mfyx3。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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