血清素1A受体部分激动剂对精神分裂症神经认知功能的增强治疗:系统综述和荟萃分析

IF 2.3 Q2 PSYCHIATRY Schizophrenia Research-Cognition Pub Date : 2023-09-14 DOI:10.1016/j.scog.2023.100290
Risa Yamada , Ayumu Wada , Andrew Stickley , Yuma Yokoi , Tomiki Sumiyoshi
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引用次数: 0

摘要

背景在之前的一项荟萃分析中,使用阿匹环酮类血清素1A(5-HT1A)受体部分激动剂作为附加疗法,对精神分裂症患者的阳性症状和注意力/处理速度有有益影响。这项荟萃分析建立在这项研究的基础上,通过检查5-HT1A部分激动剂辅助治疗对改善精神分裂症患者神经认知功能其他领域的影响。方法检索1987年至2023年5月的文献,确定随机对照试验。当有两项或两项以上研究时,计算具有95%置信区间(CI)的标准化平均差(SMD)。四项研究涉及313名患者,符合纳入标准并用于分析。结果5-HT1A部分激动剂(丁螺环酮或坦多螺环酮)对言语学习(SMD=0.08,95%CI=-0.31~0.47)或工作记忆(SMD=0.15,95%CI=-0.09~0.39)无显著影响,而保存误差百分比没有显著影响(SMD=-0.10,95%CI=-0.53-0.33)。结论本文研究的认知领域没有任何显著益处可能是由于伴随用药(典型抗精神病药物与非典型抗精神病药)、基线认知水平或其他因素的差异。有必要对各种类型的5-HT1A激动剂进行进一步研究,以检查刺激这些受体的潜在认知功效。
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Augmentation therapy with serotonin1A receptor partial agonists on neurocognitive function in schizophrenia: A systematic review and meta-analysis

Background

In a previous meta-analysis, the use of serotonin1A(5-HT1A) receptor partial agonists of the azapirone class as an add-on therapy was associated with beneficial effects on positive symptoms and attention/processing speed in schizophrenia patients. This meta-analysis builds on that study by examining the effects of adjunctive treatment with 5-HT1A partial agonists in improving other domains of neurocognitive function in schizophrenia patients.

Methods

A literature search was performed from 1987 to May 2023 to identify randomized controlled trials. The standardized mean difference (SMD) with 95 % confidence intervals (CI) was calculated when there were two or more studies. Four studies, involving 313 patients, met the inclusion criteria and were used in the analysis.

Results

5-HT1A partial agonists (buspirone or tandospirone) did not have a significant effect on verbal learning (SMD = 0.08, 95 % CI = −0.31 to 0.47) or working memory (SMD = 0.15, 95 % CI = −0.09 to 0.39). Regarding executive functions (Wisconsin Card Sorting Test), positive but non-significant results were seen with the category number (SMD = 0.26, 95 % CI = −0.81 to 1.32), while non-significant effects were noted for percent preservation errors (SMD = −0.10, 95 % CI = −0.53 to 0.33).

Conclusions

The absence of any significant benefits in the cognitive domains studied here may have been due to the variance in the concomitant medication (typical vs atypical antipsychotic drugs), the level of cognition at baseline, or other factors. Further studies with various types of 5-HT1A agonists are warranted to examine the potential cognitive efficacy of stimulating these receptors.

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来源期刊
CiteScore
5.60
自引率
10.70%
发文量
54
审稿时长
67 days
期刊最新文献
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