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HSPA1B 基因型与首发精神病患者精神病理学和神经认知的相关性:一项纵向 18 个月随访研究。

Association of HSPA1B genotypes with psychopathology and neurocognition in patients with the first episode of psychosis: a longitudinal 18-month follow-up study.

机构信息

University Psychiatric Hospital Vrapce, Zagreb, Croatia.

Division for Pharmacogenomics and Therapy Individualization, Department of Laboratory Diagnostics, University Hospital Centre Zagreb, Zagreb, Croatia.

出版信息

Pharmacogenomics J. 2020 Oct;20(5):638-646. doi: 10.1038/s41397-020-0150-9. Epub 2020 Feb 4.

Abstract

Our aim was to analyze the association of HSPA1B genotypes and treatment response measured by the changes of psychopathology and neurocognitive symptoms in patients with first-episode psychosis (FEP) after 18 months of treatment. A sample of 159 patients with FEP admitted at two Croatian psychiatric hospitals in the period between year 2014 and year 2017 was assessed at baseline and after 18 months of follow-up with Positive and Negative Syndrome Scale (PANSS), Calgary Depression Scale for Schizophrenia (CDSS) and a battery of neurocognitive tests. Associations of scale and test results with HSPA1B polymorphic locus rs1061581 were analyzed using the general linear model. The carriers of the AA genotype showed the highest improvement in CDSS and RAVLT A test after the 18-month follow-up. Concordantly, we found significantly higher improvement assessed with the CDSS, RAVLT A, RAVLT A 30' and positive PANSS scales in the not-GG (AA/AG) group compared with the GG group. Our study suggests that HSPA1B rs1061581variants may moderate treatment response in FEP measured with changes of psychopathology and neurocognitive test results.

摘要

我们的目的是分析在接受治疗 18 个月后,精神分裂症首次发作(FEP)患者的 HSPA1B 基因型与精神病理学和神经认知症状变化的治疗反应之间的关联。在 2014 年至 2017 年间,我们在两家克罗地亚精神病院评估了 159 名 FEP 患者,在基线和 18 个月的随访中使用阳性和阴性综合征量表(PANSS)、卡尔加里精神分裂症抑郁量表(CDSS)和一系列神经认知测试进行评估。使用一般线性模型分析量表和测试结果与 HSPA1B 多态性位点 rs1061581 的关联。AA 基因型的携带者在 18 个月的随访后在 CDSS 和 RAVLT A 测试中显示出最高的改善。一致地,我们发现与 GG 组相比,非 GG(AA/AG)组的 CDSS、RAVLT A、RAVLT A 30'和阳性 PANSS 量表的评估改善显著更高。我们的研究表明,HSPA1B rs1061581 变体可能会调节 FEP 的治疗反应,通过精神病理学和神经认知测试结果的变化来衡量。

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