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文拉法辛与其他抗抑郁药治疗伴有或不伴有物质使用障碍的重性抑郁发作患者的比较

Vortioxetine vs. Other Antidepressants in Patients with Major Depressive Episode With or Without Substance Use Disorder.

机构信息

Clinica Villa von Siebenthal Neuropsychiatric Hospital, Genzano di Rona, Via della Madonnina 1, 00045 Genzano di Roma RM, Italy.

UOC I Distretto ASL Roma 1, C.C. Regina Coeli, Rome, Italy.

出版信息

Curr Neuropharmacol. 2021;19(12):2296-2307. doi: 10.2174/1570159X19666210113150123.

Abstract

BACKGROUND

Major Depressive Episodes (MDEs) may characterise many psychiatric disorders. Its pharmacotherapy is laid with unmet needs, rendering the testing of new drugs necessary.

OBJECTIVE

To compare the effects of vortioxetine with those of other antidepressants (OADs) in a 1-year naturalistic setting.

METHODS

We included 126 adult patients with anMDE in the course of major depressive (MDD), bipolar (BD), or schizophrenia spectrum disorders (SSOPDs), with or without substance use disorder (SUD), who received 5-20 mg/day oral vortioxetine, and compared them with 100 patients receiving OADs at baseline and after 1, 3, 8, and 12 months on their scores on the MADRS, the CGIS, the 24-item BPRS, the YMRS, the Hamilton Anxiety Rating Scale, a Visual Analogue Scale for craving, the Columbia-Suicide Severity Rating Scale, and the WHOQOL-BREF.

RESULTS

Patients on vortioxetine improved similarly to those on OADs on all measures, independently from having or not a comorbid SUD. However, they improved with time better than their OADcounterparts if affected by BD or SSOPDs, but not MDD, on the CGI-S, BPRS depression, anxiety, and manic symptoms. SUD hampered the response of anxiety to treatment. Men improved on depression with time better than women.

CONCLUSION

MDEs responded to vortioxetine similarly to OADs by improving in depression, general psychopathology, anxiety, suicidal thinking, and quality-of-life, independently from SUD comorbidity. MDEs of patients with BD or SSOPDs on vortioxetine responded better than that of patients on OADs. Clinical Trial Registration No. 17354N.

摘要

背景

重度抑郁发作(MDE)可能是许多精神障碍的特征。其药物治疗存在未满足的需求,因此有必要测试新的药物。

目的

在自然环境下,比较文拉法辛与其他抗抑郁药(OAD)在治疗一年后的效果。

方法

我们纳入了 126 名患有 MDD、双相情感障碍(BD)或精神分裂症谱系障碍(SSOPD)的成年 MDE 患者,包括有或没有物质使用障碍(SUD)的患者,他们接受 5-20 毫克/天的文拉法辛口服治疗,并将他们与 100 名基线时接受 OAD 治疗的患者进行比较,分别在 1、3、8 和 12 个月时比较他们的 MADRS、CGIS、24 项 BPRS、YMRS、汉密尔顿焦虑量表、渴望视觉模拟量表、哥伦比亚自杀严重程度量表和 WHOQOL-BREF 的评分。

结果

无论是否存在共病 SUD,接受文拉法辛治疗的患者在所有评估指标上的改善都与接受 OAD 治疗的患者相似。然而,如果患者患有 BD 或 SSOPD,而不是 MDD,则他们在 CGI-S、BPRS 抑郁、焦虑和躁狂症状方面的改善会随时间的推移优于 OAD 对照组。SUD 会影响治疗后焦虑症状的改善。男性随着时间的推移在抑郁症状上的改善优于女性。

结论

MDE 对文拉法辛的反应与 OAD 相似,可改善抑郁、一般精神病学、焦虑、自杀意念和生活质量,独立于 SUD 共病。与接受 OAD 治疗的患者相比,BD 或 SSOPD 患者的 MDE 对文拉法辛的反应更好。临床试验注册号 17354N。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df69/9185761/d3728d6280bf/CN-19-2296_F1.jpg

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