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单核苷酸多态性作为抗精神病药引起静坐不能的生物标志物:系统评价。

Single-Nucleotide Polymorphisms as Biomarkers of Antipsychotic-Induced Akathisia: Systematic Review.

机构信息

Institute of Personalized Psychiatry and Neurology, V.M. Bekhterev National Medical Research Center for Psychiatry and Neurology, 192019 Saint Petersburg, Russia.

Department of Psychiatry, Russian Medical Academy for Continual Professional Education, 125993 Moscow, Russia.

出版信息

Genes (Basel). 2023 Feb 28;14(3):616. doi: 10.3390/genes14030616.

Abstract

Antipsychotic-induced akathisia (AIA) is a movement disorder characterized by a subjective feeling of inner restlessness or nervousness with an irresistible urge to move, resulting in repetitive movements of the limbs and torso, while taking antipsychotics (APs). In recent years, there have been some associative genetic studies of the predisposition to the development of AIA. : The goal of our study was to review the results of associative genetic and genome-wide studies and to systematize and update the knowledge on the genetic predictors of AIA in patients with schizophrenia (Sch). We searched full-text publications in PubMed, Web of Science, Springer, Google Scholar, and e-Library databases from 1977 to 2022. The Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) quality scale was used for the critical selection of the studies. We identified 37 articles, of which 3 were included in the review. Thus, the C allele of rs1800498 (59414 C>T) and the A allele of rs1800497 (17316 G>A) (TaqIA) from the gene as well as the TT genotype rs13212041 (77461407 C>T) from the gene were found to be associated with AIA. : Uncovering the genetic biomarkers of AIA may provide a key to developing a strategy for the personalized prevention and treatment of this adverse neurological drug reaction of APs in patients with Sch in real clinical practice.

摘要

抗精神病药引起的静坐不能(AIA)是一种运动障碍,其特征是主观上感到不安或紧张,伴有不可抗拒的运动冲动,导致四肢和躯干反复运动,同时服用抗精神病药(APs)。近年来,针对 AIA 易感性的关联遗传研究已有一些报道。:我们的研究目的是综述关联遗传和全基因组研究的结果,并对精神分裂症(Sch)患者 AIA 的遗传预测因子的知识进行系统和更新。我们在 1977 年至 2022 年期间在 PubMed、Web of Science、Springer、Google Scholar 和 e-Library 数据库中搜索全文出版物。采用系统评价和荟萃分析的首选报告项目(PRISMA)质量量表对研究进行批判性选择。我们确定了 37 篇文章,其中 3 篇被纳入综述。因此, 基因中的 rs1800498(59414 C>T)的 C 等位基因和 rs1800497(17316 G>A)(TaqIA)的 A 等位基因以及 基因中的 rs13212041(77461407 C>T)的 TT 基因型与 AIA 相关。:揭示 AIA 的遗传生物标志物可能为在真实临床实践中为 Sch 患者的这种 AP 不良神经药物反应制定个性化预防和治疗策略提供关键。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e53a/10048266/2874454d32bc/genes-14-00616-g0A1.jpg

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