Sertraline-Induced Mood and Behavioral Activation in Two Adults With Prader-Willi Syndrome.

Q4 Medicine
Case Reports in Psychiatry Pub Date : 2025-06-02 eCollection Date: 2025-01-01 DOI:10.1155/crps/9811985
Janice Forster
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引用次数: 0

Abstract

Objective: Risk for mood and behavioral activation (MBA) due to selective serotonin reuptake inhibitors (SSRIs) is multiply determined in persons with Prader-Willi syndrome (PWS) due to underlying epigenetic and pharmacogenomic factors that affect medication response. Further, age and molecular subtype of PWS are predisposing factors, as there is a >60% risk for bipolar disorder onset prior to age 30 among those with maternal uniparental disomy (mUPD). This article presents two cases of MBA due to sertraline prescribed to treat anxiety in these adults with PWS (mUPD). Methods: Literature review, clinical experience, and data from group home behavior logs inform this case report. The assent of the patients and the consent of their parents (legal guardians) were obtained for this publication. Results: In these two cases, the gradual onset of MBA occurred over 1 year as the dose of sertraline was increased causing irritability, sleep disturbance, increased intensity of hyperphagia, and other phenotypic behaviors. These clinical signs were attributed to the stress of COVID-19 shutdown that resulted in loss of community activities for work, socialization, leisure, and exercise. But after sertraline was discontinued, activation resolved. Mood-stabilizing medication was required for a return to baseline, as sertraline may have unmasked or exacerbated an underlying bipolar diathesis. Conclusion: Sertraline and other SSRI medications can cause MBA in patients with PWS at typical starting doses, although risk for adverse effects increases with higher doses. Age is a contributing factor. Knowing the genetic subtype of PWS is essential for making clinical decisions about pharmacotherapy, and results of pharmacogenomic testing may inform the selection of medication, dose, and schedule of administration.

舍曲林诱导的两名成人普瑞德-威利综合征的情绪和行为激活。
目的:在Prader-Willi综合征(PWS)患者中,由于潜在的表观遗传和药物基因组学因素影响药物反应,选择性5 -羟色胺再摄取抑制剂(SSRIs)导致情绪和行为激活(MBA)的风险是多重确定的。此外,年龄和PWS的分子亚型是易感因素,因为在患有母亲单亲二体症(mUPD)的患者中,在30岁之前发生双相情感障碍的风险为60%。本文介绍了两例因舍曲林治疗PWS (mUPD)成人焦虑症而导致的MBA。方法:文献回顾、临床经验及团体家庭行为记录资料为本病例报告提供依据。本出版物已获得患者及其父母(法定监护人)的同意。结果:这2例患者随着舍曲林剂量的增加,MBA在1年内逐渐发病,出现烦躁、睡眠障碍、嗜食强度增加等表型行为。这些临床症状归因于COVID-19关闭的压力,导致失去了工作、社交、休闲和锻炼的社区活动。但停用舍曲林后,激活消失。需要使用情绪稳定药物才能恢复到基线,因为舍曲林可能暴露或加剧了潜在的双相特质。结论:舍曲林和其他SSRI类药物在典型的起始剂量下可引起PWS患者的MBA,尽管不良反应的风险随着剂量的增加而增加。年龄是一个影响因素。了解PWS的遗传亚型对于制定药物治疗的临床决策至关重要,药物基因组学测试的结果可以为药物、剂量和给药计划的选择提供信息。
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
Case Reports in Psychiatry
Case Reports in Psychiatry Medicine-Psychiatry and Mental Health
CiteScore
1.00
自引率
0.00%
发文量
49
审稿时长
12 weeks
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