A disproportionality analysis of antipsychotic-induced hyperprolactinemia based on FDA adverse event reporting system.

IF 0.9 4区 医学 Q4 PHARMACOLOGY & PHARMACY International journal of clinical pharmacology and therapeutics Pub Date : 2024-12-01 DOI:10.5414/CP204518
Min Song, Dong Li, Jing Peng, Na Wang, Mei Zhang, Xiao-Lei Ren
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Abstract

Objective: This study aims to compare the risks of different antipsychotics in causing hyperprolactinemia, taking into account the age, gender, and onset time.

Materials and methods: We searched the FDA Adverse Event Reporting System (FAERS) from January 1, 2004, to March 31, 2022, for reports of hyperprolactinemia treated with antipsychotics. We evaluated the association between antipsychotics and the risk of hyperprolactinemia using reporting odds ratio (ROR) based on a disproportionality analysis. Moreover, information regarding age, gender, countries, and onset time was collected.

Results: We found 4,430 reports of antipsychotic-induced hyperprolactinemia involving 13 different antipsychotics. From highest to lowest ROR value, the top five antipsychotics were as follows: risperidone (ROR = 631.0611; 95% CI: 592.7329, 671.8677) > amisulpride (ROR = 59.4425; 95% CI: 19.0668, 185.317) > paliperidone (ROR = 31.9885, 95% CI: 27.912, 36.6604) > fluphenazine (ROR = 15.6026; 95% CI: 5.0236, 48.4595) > haloperidol (ROR = 14.3861; 95% CI: 11.173, 18.5231). Except for three drugs (risperidone, haloperidol, and amisulpride), women outnumbered men in cases of antipsychotic-induced hyperprolactinemia. The age range was 13 - 64 years old, with the most being 19 - 44 years old, followed by 45 - 64 years old, and there were fewer elderly patients. From longest to shortest, the median onset time of these antipsychotics was as follows: cariprazine (305 days) > risperidone (304 days) > quetiapine (276 days) > haloperidol (183 days) > ziprasidone (54 days) > lurasidone (44.5 days) > olanzapine (41 days) > asenapine (15.5 days) > paliperidone (15 days) > aripiprazole (12 days) > clozapine (6 days).

Conclusion: Risperidone had the greatest risk of increasing prolactin, whereas clozapine had the lowest. Antipsychotic-induced hyperprolactinemia was more common in women and middle-aged patients. Clozapine had the shortest onset time in raising prolactin, whereas cariprazine had the longest.

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基于美国食品药物管理局不良事件报告系统的抗精神病药物诱发高泌乳素血症的比例失调分析。
研究目的本研究旨在比较不同抗精神病药物导致高泌乳素血症的风险,同时考虑年龄、性别和发病时间:我们在美国食品药品管理局不良事件报告系统(FAERS)中搜索了2004年1月1日至2022年3月31日期间使用抗精神病药物治疗高泌乳素血症的报告。我们使用基于比例失调分析的报告几率比(ROR)评估了抗精神病药物与高催乳素血症风险之间的关联。此外,我们还收集了有关年龄、性别、国家和发病时间的信息:结果:我们发现了4430份抗精神病药物诱发高泌乳素血症的报告,涉及13种不同的抗精神病药物。从ROR值最高到最低,排名前五位的抗精神病药物如下:利培酮(ROR = 631.0611; 95% CI: 592.7329, 671.8677) > 阿米舒必利(ROR = 59.4425; 95% CI: 19.0668,185.317)>帕利哌酮(ROR=31.9885,95% CI:27.912,36.6604)>氟奋乃静(ROR=15.6026;95% CI:5.0236,48.4595)>氟哌啶醇(ROR=14.3861;95% CI:11.173,18.5231)。除三种药物(利培酮、氟哌啶醇和氨磺必利)外,在抗精神病药物诱发的高泌乳素血症病例中,女性多于男性。年龄范围为 13 - 64 岁,其中 19 - 44 岁的患者最多,其次是 45 - 64 岁,老年患者较少。这些抗精神病药物的中位起效时间从长到短依次为:卡哌嗪(305 天)>利培酮(304 天)>喹硫平(276 天)>氟哌啶醇(183 天)>齐拉西酮(54 天)>鲁拉西酮(44.5天)>奥氮平(41天)>阿塞那平(15.5天)>帕利哌酮(15天)>阿立哌唑(12天)>氯氮平(6天):结论:利培酮增加催乳素的风险最大,而氯氮平最低。抗精神病药物诱发的高泌乳素血症更常见于女性和中年患者。氯氮平使泌乳素升高的起始时间最短,而卡利普嗪则最长。
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来源期刊
CiteScore
1.70
自引率
12.50%
发文量
116
审稿时长
4-8 weeks
期刊介绍: The International Journal of Clinical Pharmacology and Therapeutics appears monthly and publishes manuscripts containing original material with emphasis on the following topics: Clinical trials, Pharmacoepidemiology - Pharmacovigilance, Pharmacodynamics, Drug disposition and Pharmacokinetics, Quality assurance, Pharmacogenetics, Biotechnological drugs such as cytokines and recombinant antibiotics. Case reports on adverse reactions are also of interest.
期刊最新文献
Identification of factors associated with vancomycin-induced acute kidney injury: A retrospective analysis using the Common Data Model. Retrospective evaluation of medical information for predicting tazobactam/piperacillin-induced liver injury. A disproportionality analysis of antipsychotic-induced hyperprolactinemia based on FDA adverse event reporting system. Positive effects of magnesium supplementation in metabolic syndrome. Corrigendum for the article Int J Clin Pharmacol Ther 2024; 11: 525-533.
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