难治性精神分裂症患者的认知障碍:与DRD2、DRD3、HTR2A、BDNF和CYP2D6基因多态性的关系

Q3 Medicine
Dmitriy Sosin , Dmitriy Ivashchenko , Zhannet Sozaeva , Kristina Ryzhikova , Veronika Fadeeva , Veronika Chomskaya , Roman Sheidakov , Maria Yanushko , Andrey Otmakhov , Elena Grishina , Dmitriy Sychev , Mikhail Ivanov
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引用次数: 8

摘要

根据各种资料,25-50%的精神分裂症患者存在治疗抵抗。据信,与较有利类型的精神分裂症患者相比,难治性精神分裂症(TRS)患者的认知能力较差。然而,一些作者认为,目前关于这一主题的循证研究有限。材料与方法共纳入诊断为精神分裂症的患者130例(按ICD 10为20例)。所有患者均按以下量表进行检查:阳性和阴性综合征量表(PANSS)、整体功能评估量表(GAF)、精神分裂症认知简要评估量表(BACS)。结果TRS患者整体认知功能较nTRS患者差(p = 0.357)。在TRS患者组,CYP2D6*4多态性对执行功能有影响。杂合子GA基因型携带者的执行功能值较高(p = 0.043)。本研究未发现所研究的基因多态性变异与TRS之间存在关联。结论CYP2D6*4多态性变异对TRS组认知功能有影响,与精神状态和药物治疗效果无关。在未来,有必要对更多的患者和更多的基因多态性变异进行更大规模的前瞻性研究。进一步确定认知障碍的遗传预测因素将提高研究人员对其原因的理解,并可能更有针对性地治疗精神分裂症。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cognitive impairment in patients with treatment resistant schizophrenia: Associations with DRD2, DRD3, HTR2A, BDNF and CYP2D6 genetic polymorphisms

Introduction

According to various data, 25–50% of all patients with schizophrenia suffer from treatment resistance. It is believed that patients with treatment-resistant schizophrenia (TRS) have reduced cognitive skills, compared to the patients with a more favourable type of schizophrenia. However, according to some authors, there is limited evidence-based research on this topic at present.

Materials and methods

The total number of patients included 130 patients with a diagnosis of schizophrenia (F20 according to ICD 10). All patients were examined according to the following scales: Positive and Negative Syndrome Scale (PANSS), Global Assessment of Functioning (GAF), Brief Assessment of Cognition in Schizophrenia (BACS).

Results

Our results showed that patients with TRS as a whole had worse cognitive functions than nTRS patients (p = 0.357). In the group of patients with TRS, polymorphism CYP2D6*4 showed an effect on executive functions. Carriers of the heterozygous GA genotype had higher values of executive functions (p = 0.043). No association between the studied gene polymorphic variants and TRS was found in this research.

Conclusion

The polymorphic variant CYP2D6*4 showed an effect on cognitive function in the TRS group, regardless of their mental state and the effect of pharmacotherapy. In the future, it will be necessary to conduct larger prospective studies with a greater number of patients and a greater number of polymorphic variants of genes. Further identification of genetic predictors of cognitive impairment will improve researchers’ understanding of their causes and possibly move closer to more targeted therapy for schizophrenia.

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期刊介绍: Neurology, Psychiatry & Brain Research publishes original papers and reviews in biological psychiatry, brain research, neurology, neuropsychiatry, neuropsychoimmunology, psychopathology, psychotherapy. The journal has a focus on international and interdisciplinary basic research with clinical relevance. Translational research is particularly appreciated. Authors are allowed to submit their manuscript in their native language as supplemental data to the English version. Neurology, Psychiatry & Brain Research is related to the oldest German speaking journal in this field, the Centralblatt fur Nervenheilkunde, Psychiatrie und gerichtliche Psychopathologie, founded in 1878. The tradition and idea of previous famous editors (Alois Alzheimer and Kurt Schneider among others) was continued in modernized form with Neurology, Psychiatry & Brain Research. Centralblatt was a journal of broad scope and relevance, now Neurology, Psychiatry & Brain Research represents a journal with translational and interdisciplinary perspective, focusing on clinically oriented research in psychiatry, neurology and neighboring fields of neurosciences and psychology/psychotherapy with a preference for biologically oriented research including basic research. Preference is given for papers from newly emerging fields, like clinical psychoimmunology/neuroimmunology, and ideas.
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