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通过下一代测序技术探讨 FAAH p.Pro129Thr 和 COMT p.Ala72Ser 与精神分裂症及合并物质使用障碍的相关性:一项探索性分析。

Association of FAAH p.Pro129Thr and COMT p.Ala72Ser with schizophrenia and comorbid substance use through next-generation sequencing: an exploratory analysis.

机构信息

División Académica de Ciencias de la Salud, Universidad Juárez Autónoma de Tabasco, Villahermosa, Mexico.

Laboratorio de Genómica de Enfermedades Psiquiátricas y Neurodegenerativas, Instituto Nacional de Medicina Genómica, Ciudad de México, Mexico.

出版信息

Braz J Psychiatry. 2022 Mar-Abr;44(2):164-170. doi: 10.1590/1516-4446-2020-1546.

Abstract

OBJECTIVE

Individuals with schizophrenia and substance use disorders have a poor prognosis and increased psychiatric symptoms. The present study aimed to explore the association of 106 genes in individuals with schizophrenia and comorbid substance use through a next-generation sequencing (NGS) analysis and different in silico algorithms.

METHODS

We included 105 individuals diagnosed with schizophrenia and a family history of schizophrenia, of whom 49 (46.67%) presented comorbid substance use. Using NGS, we sequenced 106 genes previously associated with schizophrenia. Logistic regression models were used to assess differences in allele frequencies, and a generalized gene-set analysis was performed at the gene level. Functional annotations were performed using different algorithms and databases.

RESULTS

We identified a total of 3,109 variants, of which 25 were associated with schizophrenia and comorbid substance use and were located in regulatory and coding regions. We found low-frequency variants in COMT p.Ala72Ser, independently of p.Val158Met, that were associated with substance use. The endocannabinoid functional variant FAAH p.Pro129Thr was also associated with substance use.

CONCLUSIONS

Genetic variants of genes related to dopaminergic and cannabinoid neurotransmitter systems were associated with comorbid substance use in schizophrenia. Nevertheless, more studies with larger sample sizes are needed to confirm our findings.

摘要

目的

患有精神分裂症和物质使用障碍的个体预后较差,且精神症状增多。本研究旨在通过下一代测序(NGS)分析和不同的计算算法,探讨精神分裂症合并物质使用个体中 106 个基因的相关性。

方法

我们纳入了 105 名被诊断患有精神分裂症且有精神分裂症家族史的个体,其中 49 名(46.67%)存在合并物质使用。使用 NGS,我们对先前与精神分裂症相关的 106 个基因进行了测序。逻辑回归模型用于评估等位基因频率的差异,在基因水平上进行了广义基因集分析。使用不同的算法和数据库进行功能注释。

结果

我们总共鉴定出 3109 个变体,其中 25 个与精神分裂症和合并物质使用相关,位于调节和编码区域。我们发现了 COMT p.Ala72Ser 中的低频变体,与 p.Val158Met 无关,与物质使用有关。内源性大麻素功能变体 FAAH p.Pro129Thr 也与物质使用有关。

结论

与多巴胺能和大麻素神经递质系统相关的基因的遗传变异与精神分裂症合并物质使用有关。然而,需要更大样本量的更多研究来证实我们的发现。

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