Anhedonia and neuropsychotropics: A pharmacovigilance-pharmacodynamic study.

IF 2.1 4区 医学 Q3 PHARMACOLOGY & PHARMACY
Jean-Louis Montastruc
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引用次数: 0

Abstract

Purpose: Anhedonia is defined as inability to experience pleasure or enjoyment from activities normally pleasurable. Role of drugs in occurrence of anhedonia is little known. The study was performed to investigate, first associations between anhedonia and exposure to neuropsychotropics and, second potential pharmacodynamic mechanisms of this adverse drug reaction.

Methods: The first part of the study used individual case safety reports (ICSRs) in adults registered in the global pharmacovigilance database, Vigibase®, between 01/01/2000 and 31/12/2024 with neuropsychotropics. Results are shown as reporting odds ratios (ROR) with their 95%CI. Second, we performed a pharmacovigilance-pharmacodynamic study using linear regression analyses to explore the association between anhedonia with antidepressants and binding affinities for their monoamine transporters.

Results: Among 24,913,179 ICSRs, 1123 reported anhedonia with neuropsychotropics, mainly in females (52.5%) and between 18-44 years (55.6%). Significant associations were found with psycholeptics [ROR=1.23 (1.14-1.33), including second generation of antipsychotics and anxiolytics], psychoanaleptics [ROR=1.66 (1.52-1.82), including serotonin reuptake inhibitors and venlafaxine but not other antidepressants] and some other drugs like naltrexone, varenicline, duloxetine, clonazepam or oxycodone. No association was found for anesthetics, other analgesics, other antiepileptics, hypnotics/sedatives, or antiparkinsonians. Direct drug comparisons found significant ROR values for psychoanaleptics versus psycholeptics [1.35 (1.20-1.51)], for antidepressants versus antipsychotics [2.63 (2.24-3.09)] and for antidepressants versus anxiolytics [1.27 (1.11-1.45)]. No significant association was found between monoamine pKi values and occurrence of anhedonia with antidepressants.

Conclusion: Among neuropsychotropics, serotonin reuptake inhibitors, benzodiazepine anxiolytics and antipsychotics are associated with anhedonia reports. We were unable to find any correlation between anhedonia reports with antidepressants and their direct effects on monoamine transporters.

快感缺乏和神经精神药物:一项药物警戒-药效学研究。
目的:快感缺乏症被定义为无法从通常令人愉快的活动中体验到快乐或享受。药物在快感缺乏症发生中的作用尚不清楚。本研究首先是为了调查快感缺乏与神经精神药物暴露之间的关系,其次是这种药物不良反应的潜在药效学机制。方法:研究的第一部分使用了2000年1月1日至2024年12月31日期间在全球药物警戒数据库Vigibase®中注册的成人个案安全报告(ICSRs)。结果显示为报告优势比(ROR),其95%CI。其次,我们进行了一项药物警戒-药效学研究,使用线性回归分析来探索快感缺乏与抗抑郁药物及其单胺转运蛋白的结合亲和力之间的关系。结果:在24,913,179名icsr中,1123名报告了神经精神药物的快感缺乏症,主要是女性(52.5%)和18-44岁(55.6%)。与抗精神病药[ROR=1.23(1.14-1.33),包括第二代抗精神病药和抗焦虑药]、精神镇痛药[ROR=1.66(1.52-1.82),包括5 -羟色胺再摄取抑制剂和文拉法辛,但不包括其他抗抑郁药]以及纳曲酮、伐尼克兰、度洛西汀、氯硝西泮或羟考酮等其他药物存在显著相关性。未发现麻醉药、其他镇痛药、其他抗癫痫药、催眠药/镇静剂或抗帕金森药有关联。直接药物比较发现,精神镇痛药与精神病药的ROR值为1.35(1.20-1.51),抗抑郁药与抗精神病药的ROR值为2.63(2.24-3.09),抗抑郁药与抗焦虑药的ROR值为1.27(1.11-1.45)。单胺pKi值与服用抗抑郁药后快感缺乏症的发生无显著关联。结论:在神经精神药物中,血清素再摄取抑制剂、苯二氮卓类抗焦虑药和抗精神病药与快感缺乏有关。我们无法发现快感缺乏报告与抗抑郁药及其对单胺转运蛋白的直接影响之间的任何相关性。
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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来源期刊
Therapie
Therapie 医学-药学
CiteScore
3.50
自引率
7.70%
发文量
132
审稿时长
57 days
期刊介绍: Thérapie is a peer-reviewed journal devoted to Clinical Pharmacology, Therapeutics, Pharmacokinetics, Pharmacovigilance, Addictovigilance, Social Pharmacology, Pharmacoepidemiology, Pharmacoeconomics and Evidence-Based-Medicine. Thérapie publishes in French or in English original articles, general reviews, letters to the editor reporting original findings, correspondence relating to articles or letters published in the Journal, short articles, editorials on up-to-date topics, Pharmacovigilance or Addictovigilance reports that follow the French "guidelines" concerning good practice in pharmacovigilance publications. The journal also publishes thematic issues on topical subject. The journal is indexed in the main international data bases and notably in: Biosis Previews/Biological Abstracts, Embase/Excerpta Medica, Medline/Index Medicus, Science Citation Index.
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