Hyponatremia Associated with the Use of Common Antidepressants in the All of Us Research Program.

IF 6.3 2区 医学 Q1 PHARMACOLOGY & PHARMACY Clinical Pharmacology & Therapeutics Pub Date : 2024-11-14 DOI:10.1002/cpt.3484
Huan Mo, Yamna Channa, Tracey M Ferrara, Bennett J Waxse, David J Schlueter, Tam C Tran, Anas H Awan, Slavina B Goleva, Ariel Williams, Anav Babbar, Onajia Stubblefield, Jacob M Keaton, Eric A Larson, Russell A Wilke, Joshua C Denny
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Abstract

Selective serotonin reuptake inhibitor (SSRI), serotonin-norepinephrine reuptake inhibitor (SNRI), and norepinephrine-dopamine reuptake inhibitor (NRI) antidepressants can cause hyponatremia through syndrome of inappropriate antidiuretic hormone secretion (SIADH). This study assesses the differential risks of hyponatremia associated with commonly prescribed SSRIs (fluoxetine, paroxetine, sertraline, citalopram, escitalopram), SNRIs (duloxetine, venlafaxine) and NRI (bupropion), as well as omeprazole as a reference, with a retrospective observational cohort study in the All of Us Research Program, a national multicenter research cohort containing de-identified electronic health records (EHR). Participants who had been prescribed monotherapy with any of eight common antidepressants were included, with each drug considered as a separate arm indexed with a start date. Events were defined as the first occurrence of a low plasma sodium measurement or a clinical diagnosis recorded for either hyponatremia or SIADH. Those who did not have events were censored at their last plasma sodium measurement. A total of 17,439 individuals were exposed to one of the eight antidepressants as monotherapy. The overall incidences for hyponatremia were 0.87% in the first 30 days and 10.5% in the first 3 years in the antidepressant arms. Compared to sertraline, duloxetine (hazard ratio [HR] = 1.37 [1.19-1.58]) and escitalopram (HR = 1.16 [1.01-1.33]) were associated with the highest overall risk of hyponatremia, and bupropion (HR = 0.83 [0.73-0.94]) and paroxetine (HR = 0.78 [0.65-0.93]) were associated with the lowest risk. The risks were unchanged after adjusting for comorbidity and polypharmacy. Such information could help guide providers in managing patients and their risks of hyponatremia when on common antidepressants.

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与 "我们所有人 "研究项目中使用普通抗抑郁药有关的低钠血症。
选择性血清素再摄取抑制剂(SSRI)、血清素-去甲肾上腺素再摄取抑制剂(SNRI)和去甲肾上腺素-多巴胺再摄取抑制剂(NRI)类抗抑郁药可通过抗利尿激素分泌不当综合征(SIADH)引起低钠血症。本研究以 "我们所有人研究计划"(All of Us Research Program)中的一项回顾性观察队列研究为参照,评估了与常用处方 SSRIs(氟西汀、帕罗西汀、舍曲林、西酞普兰、艾司西酞普兰)、SNRIs(度洛西汀、文拉法辛)和 NRIs(安非他酮)以及奥美拉唑相关的低钠血症的不同风险。研究对象包括接受过八种常见抗抑郁药中任何一种单药治疗的患者,每种药物都被视为一个独立的治疗组,并以开始日期为索引。事件定义为首次出现低血浆钠测量值或低钠血症或 SIADH 的临床诊断记录。未发生事件的患者在最后一次测量血浆钠时被剔除。共有 17,439 人接受了八种抗抑郁药中的一种作为单一疗法。在抗抑郁药物治疗组中,低钠血症的总发生率在头30天为0.87%,头3年为10.5%。与舍曲林相比,度洛西汀(危险比 [HR] = 1.37 [1.19-1.58])和艾司西酞普兰(HR = 1.16 [1.01-1.33])的低钠血症总风险最高,而安非他酮(HR = 0.83 [0.73-0.94])和帕罗西汀(HR = 0.78 [0.65-0.93])的风险最低。在对合并症和多重用药进行调整后,风险保持不变。这些信息有助于指导医疗服务提供者管理患者及其服用普通抗抑郁药时发生低钠血症的风险。
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来源期刊
CiteScore
12.70
自引率
7.50%
发文量
290
审稿时长
2 months
期刊介绍: Clinical Pharmacology & Therapeutics (CPT) is the authoritative cross-disciplinary journal in experimental and clinical medicine devoted to publishing advances in the nature, action, efficacy, and evaluation of therapeutics. CPT welcomes original Articles in the emerging areas of translational, predictive and personalized medicine; new therapeutic modalities including gene and cell therapies; pharmacogenomics, proteomics and metabolomics; bioinformation and applied systems biology complementing areas of pharmacokinetics and pharmacodynamics, human investigation and clinical trials, pharmacovigilence, pharmacoepidemiology, pharmacometrics, and population pharmacology.
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