Oral glucocorticoids and risk of psychiatric and suicidal behaviour outcomes: population-based cohort study.

Tyra Lagerberg,Tapio T Gustafsson,Yasmina Molero,Julian Forton,Amir Sariaslan,Zheng Chang,Henrik Larsson,Paul Lichtenstein,Seena Fazel
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Abstract

BACKGROUND Despite evidence of associations between glucocorticoid treatment and adverse psychiatric and suicidal behaviour outcomes, large-scale observational evidence for serious outcomes is lacking. AIMS To assess the risk of psychiatric and suicidal behaviour outcomes during glucocorticoid treatment. METHOD Using Swedish population registers, we identified 1 105 964 individuals aged 15-54 years who collected a glucocorticoid prescription in oral form between 2006 and 2020. We investigated associations with a range of psychiatric outcomes: unplanned specialist healthcare contacts due to depressive, bipolar, anxiety or schizophrenia-spectrum disorders; and deaths by suicide or unplanned specialist healthcare contacts due to self-harm ('suicidal behaviour'). We estimated hazard ratios from Cox proportional hazards models in a medication-only cohort by comparing outcome rates during and outside treated periods within individuals. We further identified individuals with an autoimmune or gastrointestinal autoimmune disorder diagnosis and compared hazards of the outcomes between those who did and did not initiate a glucocorticoid using a target trial emulation approach. RESULTS We found increased risks for psychiatric outcomes, with within-individual hazard ratios ranging from 1.08 (95% CI, 1.00-1.16) for depressive disorders to 1.23 (95% CI, 1.12-1.36) for bipolar disorder and 1.25 (95% CI, 1.20-1.31) for anxiety disorders. We found no clear association with suicidal behaviour (hazard ratio: 1.06; 95% CI, 0.96-1.17). These findings were similar when stratified by age and gender. Within-individual associations were attenuated in those diagnosed with an autoimmune disorder. The risk of anxiety and bipolar disorder outcomes appeared particularly elevated in the first weeks of treatment. Absolute rates were modestly elevated during treatment, and higher in those with a history of psychiatric disorders. CONCLUSIONS Glucocorticoid treatment is associated with elevated risks of serious psychiatric outcomes, including the onset and relapse of common psychiatric disorders. Individuals with psychiatric histories may require additional monitoring during glucocorticoid treatment.
口服糖皮质激素与精神病和自杀行为结局的风险:基于人群的队列研究。
背景:尽管有证据表明糖皮质激素治疗与不良精神和自杀行为结局之间存在关联,但缺乏大规模观察性证据来证明严重后果。目的评估糖皮质激素治疗期间发生精神疾病和自杀行为的风险。方法通过瑞典人口登记,我们确定了2006年至2020年期间收集口服糖皮质激素处方的15-54岁的1 109564人。我们调查了与一系列精神病学结果的关联:由于抑郁、双相情感障碍、焦虑或精神分裂症谱系障碍而进行的计划外专科医疗保健接触;自杀死亡或因自残(“自杀行为”)而计划外的专业医疗保健联系。我们通过比较个体在治疗期间和治疗期外的转归率,从Cox比例风险模型中估计了仅用药队列的风险比。我们进一步确定了诊断为自身免疫性或胃肠道自身免疫性疾病的个体,并使用靶试验模拟方法比较了使用和未使用糖皮质激素的患者结局的危险。结果:我们发现精神疾病结局的风险增加,个体内风险比从抑郁症的1.08 (95% CI, 1.00-1.16)到双相情感障碍的1.23 (95% CI, 1.12-1.36)和焦虑症的1.25 (95% CI, 1.20-1.31)不等。我们发现与自杀行为没有明显的关联(风险比:1.06;95% ci, 0.96-1.17)。这些发现在按年龄和性别分层时是相似的。在被诊断为自身免疫性疾病的患者中,个体内相关性减弱。焦虑和双相情感障碍的风险在治疗的头几周显得特别高。在治疗期间,绝对比率略有上升,而在有精神疾病史的人群中,绝对比率更高。结论糖皮质激素治疗与严重精神疾病风险升高相关,包括常见精神疾病的发作和复发。有精神病史的个体在糖皮质激素治疗期间可能需要额外的监测。
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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