Augmentation Therapy With Serotonin 5-HT1A Receptor Partial Agonists on Cognitive Function in Depressive Disorders: A Systematic Review of Randomized Controlled Studies.
Risa Yamada, Ayumu Wada, Andrew Stickley, Adrian Newman-Tancredi, Tomiki Sumiyoshi
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引用次数: 0
Abstract
Objective: The use of serotonin 5-HT1A receptor partial agonists (5-HT1A-PAs) as an add-on therapy has been associated with the enhancement of attention/processing speed in patients with schizophrenia. Also, 5-HT1A receptors have been shown to play a role in the pathophysiology of mood disorders. There is compelling evidence supporting that stimulation of 5-HT1A receptors accelerates antidepressant effects. Accordingly, this systematic review examines the ability of adjunctive treatment with 5-HT1A-PAs to improve cognitive function in patients with depressive symptoms.
Methods: A literature search using PubMed, the Cochrane Library, and Web of Science databases was performed from 1987 to January 2024 to identify randomized controlled trials (RCTs) corresponding to the following inclusion criteria: (1) RCTs, (2) human studies; studies that (3) targeted patients with a psychiatric disorder (except for schizophrenia or schizoaffective disorder), (4) evaluated the effect of cognitive functions, (5) were written in English.
Results: From the 80 studies initially screened, three met the inclusion criteria. Two of these studies dealt with vascular depression while one focused on major depressive disorder (MDD). In MDD, combined treatment with buspirone and melatonin was more efficacious in ameliorating subjective cognitive disturbances compared to the use of buspirone alone or the use of a placebo. Likewise, the combination of escitalopram-tandospirone was more advantageous than escitalopram alone for improving executive function and verbal fluency in patients with vascular depression.
Conclusions: Further studies with novel 5-HT1A receptor agonists are warranted to examine their potentially more robust benefits on cognitive performance in subjects suffering from mood deficits.
目的:5-羟色胺5-HT1A受体部分激动剂(5-HT1A- pas)作为一种附加治疗与精神分裂症患者注意力/处理速度的增强有关。此外,5-HT1A受体已被证明在情绪障碍的病理生理中发挥作用。有令人信服的证据支持刺激5-HT1A受体加速抗抑郁作用。因此,本系统综述探讨了5-HT1A-PAs辅助治疗改善抑郁症状患者认知功能的能力。方法:从1987年至2024年1月,使用PubMed、Cochrane图书馆和Web of Science数据库进行文献检索,以确定符合以下纳入标准的随机对照试验(rct):(1)随机对照试验,(2)人体研究;(3)针对精神障碍(精神分裂症或分裂情感障碍除外)患者的研究,(4)评估认知功能的影响,(5)用英语撰写。结果:在最初筛选的80项研究中,有3项符合纳入标准。其中两项研究涉及血管性抑郁症,而另一项研究关注重度抑郁症(MDD)。在重度抑郁症中,与单独使用丁螺环酮或使用安慰剂相比,丁螺环酮和褪黑激素联合治疗在改善主观认知障碍方面更有效。同样,在改善血管性抑郁症患者的执行功能和语言流畅性方面,艾司西酞普兰-坦多螺酮联用比艾司西酞普兰单用更有利。结论:对新型5-HT1A受体激动剂的进一步研究是有必要的,以检验它们对患有情绪缺陷的受试者的认知表现的潜在更强大的益处。