Department of Psychiatry, Fondazione Policlinico Universitario Agostino Gemelli IRCCS, Rome, Italy.
Department of Neuroscience, Section of Psichiatry, Università Cattolica del Sacro Cuore, Rome, Italy.
CNS Spectr. 2022 Feb;27(1):73-81. doi: 10.1017/S109285292000173X. Epub 2020 Aug 10.
Major depressive disorder (MDD) and alcohol use disorder (AUD) are highly comorbid, with greater clinical complexity and psychosocial impairment. Several antidepressants have been used in this population, with mixed results. This preliminary study aims to investigate the effects of the multimodal antidepressant vortioxetine in MDD + AUD subjects.
We retrospectively evaluated 57 MDD + AUD and 56 MDD outpatients, matched for baseline characteristics. Patients were assessed after 1, 3, and 6 months treatment with vortioxetine (10-20 mg/d, flexibly dosed) in combination with continuous psychosocial support. The primary outcome was improvement in depressive symptoms measured by the Montgomery-Åsberg Depression Rating Scale. We also investigated changes in anxiety, anhedonia, cognition, functioning, quality of life, and clinical global severity using the following instruments: Hamilton Anxiety Rating Scale, Snaith-Hamilton Pleasure Scale, Digit Symbol Substitution Test, Perceived Deficits Questionnaire-Depression, Functioning Assessment Short Test, Quality of Life Index, and Clinical Global Impression-Severity Scale.
Vortioxetine significantly improved mood in MDD + AUD patients (P < .001), with no differences when compared to MDD (P = .36). A substantial rate (45.6%) of comorbid subjects obtained clinical remission at endpoint (P = .36 vs MDD). We additionally observed baseline to endpoint improvements on all secondary outcomes (P < .001), with no significant difference between groups. Overall, vortioxetine was safe and well tolerated.
Given its effectiveness on mood, cognition, and functioning, its good safety and tolerability profile, and low potential for abuse, vortioxetine could represent a valid pharmacological intervention in MDD + AUD patients as part of an integrated therapeutic-rehabilitation program.
重度抑郁症(MDD)和酒精使用障碍(AUD)高度共病,具有更大的临床复杂性和社会心理障碍。在这一人群中使用了几种抗抑郁药,但结果喜忧参半。本初步研究旨在探讨多模式抗抑郁药文拉法辛在 MDD+AUD 患者中的作用。
我们回顾性评估了 57 名 MDD+AUD 和 56 名 MDD 门诊患者,这些患者的基线特征相匹配。患者在接受文拉法辛(10-20mg/d,灵活剂量)联合持续心理社会支持治疗 1、3 和 6 个月后进行评估。主要结局是用蒙哥马利-阿斯伯格抑郁评定量表(MADRS)评估抑郁症状的改善。我们还使用以下工具评估焦虑、快感缺失、认知、功能、生活质量和临床总体严重程度的变化:汉密尔顿焦虑量表、斯奈特-汉密尔顿快感量表、数字符号替代测试、感知缺陷问卷-抑郁、功能评估简短测试、生活质量指数和临床总体印象严重程度量表。
文拉法辛显著改善了 MDD+AUD 患者的情绪(P<0.001),与 MDD 患者相比无差异(P=0.36)。终点时,相当比例(45.6%)的共病患者获得临床缓解(P=0.36 与 MDD)。我们还观察到所有次要结局从基线到终点的改善(P<0.001),两组之间无显著差异。总体而言,文拉法辛安全且耐受良好。
鉴于其对情绪、认知和功能的有效性,良好的安全性和耐受性,以及低滥用潜力,文拉法辛可作为 MDD+AUD 患者综合治疗-康复计划的有效药物干预。