Kim Thomas T, Xu Colin, Amsterdam Jay D
Department of Psychiatry, Weill Cornell Medical College, New York, NY, United States of America.
Department of Psychology & Communication, University of Idaho, Moscow, ID, United States of America.
J Affect Disord. 2025 May 1;376:47-51. doi: 10.1016/j.jad.2025.02.003. Epub 2025 Feb 2.
Several studies suggest that oral monoamine oxidase inhibitors (MAOIs) and tricyclic antidepressants (TCAs) may be more effective than serotonin reuptake inhibitors for treating treatment-resistant depression (TRD). Despite this advantage, they are now rarely prescribed due to concern over serious side effects. In contrast, selegiline transdermal system (STS) may present a safer alternative to oral MAOIs and TCAs; however, no studies have compared STS with other antidepressants.
Data from 117 patients who received STS, oral MAOIs, or TCAs for TRD were obtained from a university mood disorder clinic. Two linear regression models were created with severity and number of side effect categories endorsed as the dependent variable. Logistic regression models were created for each side effect category with presence of category as the dependent variable. In all models, antidepressant class was entered as the independent variable, with covariates.
Although STS was less effective than oral MAOIs, it was significantly more effective than TCAs. STS treatment had significantly fewer side effect categories endorsed versus oral MAOIs and TCAs. Patients receiving STS were less likely to report gastrointestinal side effects versus TCAs and to endorse cardiovascular side effects versus oral MAOIs. In contrast, STS patients were more likely to report skin side effects versus oral MAOIs. There were no reported serious adverse events. Amongst the covariates, only the number of prior antidepressant trials predicted more side effect categories endorsed.
Although oral MAOI therapy has been eschewed by most clinicians, STS may be better tolerated than oral MAOIs and TCAs.
多项研究表明,口服单胺氧化酶抑制剂(MAOIs)和三环类抗抑郁药(TCAs)在治疗难治性抑郁症(TRD)方面可能比5-羟色胺再摄取抑制剂更有效。尽管有这一优势,但由于担心严重副作用,它们现在很少被处方使用。相比之下,司来吉兰透皮系统(STS)可能是口服MAOIs和TCAs更安全的替代品;然而,尚无研究将STS与其他抗抑郁药进行比较。
从一所大学的情绪障碍诊所获取了117例接受STS、口服MAOIs或TCAs治疗TRD患者的数据。创建了两个线性回归模型,将认可的副作用类别严重程度和数量作为因变量。针对每个副作用类别创建逻辑回归模型,将类别存在情况作为因变量。在所有模型中,将抗抑郁药类别作为自变量,并纳入协变量。
尽管STS的疗效不如口服MAOIs,但显著优于TCAs。与口服MAOIs和TCAs相比,STS治疗认可的副作用类别明显更少。接受STS治疗的患者与接受TCAs治疗的患者相比,报告胃肠道副作用的可能性更小,与接受口服MAOIs治疗的患者相比,认可心血管副作用的可能性更小。相比之下,接受STS治疗的患者与接受口服MAOIs治疗的患者相比,报告皮肤副作用的可能性更大。未报告严重不良事件。在协变量中,只有先前抗抑郁药试验的次数预测认可的副作用类别更多。
尽管大多数临床医生已不再使用口服MAOI疗法,但STS的耐受性可能优于口服MAOIs和TCAs。