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Association of FAAH p.Pro129Thr and COMT p.Ala72Ser with schizophrenia and comorbid substance use through next-generation sequencing: an exploratory analysis.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。
Braz J Psychiatry. 2022 Mar-Abr;44(2):164-170. doi: 10.1590/1516-4446-2020-1546.
2
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3
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Nord J Psychiatry. 2017 Jul;71(5):332-339. doi: 10.1080/08039488.2017.1286385. Epub 2017 Feb 14.
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New functional single nucleotide polymorphism (Ala72Ser) in the COMT gene is associated with aggressive behavior in male schizophrenia.儿茶酚-O-甲基转移酶(COMT)基因新的功能性单核苷酸多态性(丙氨酸72丝氨酸)与男性精神分裂症患者的攻击行为相关。
Am J Med Genet B Neuropsychiatr Genet. 2008 Jul 5;147B(5):658-60. doi: 10.1002/ajmg.b.30649.
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Association of Single Nucleotide Polymorphisms in Catechol-O-Methyltransferase and Serine-Threonine Protein Kinase Genes in the Pakistani Schizophrenic Population: A Study with Special Emphasis on Cannabis and Smokeless Tobacco.巴基斯坦精神分裂症患者群体中儿茶酚-O-甲基转移酶和丝氨酸-苏氨酸蛋白激酶基因单核苷酸多态性的关联:一项特别关注大麻和无烟烟草的研究。
CNS Neurol Disord Drug Targets. 2015;14(8):1086-95. doi: 10.2174/1871527314666150317225828.
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[COMT Val158Met polymorphism and schizophrenia in a series of Spanish patients].[一系列西班牙患者中的儿茶酚-O-甲基转移酶(COMT)Val158Met多态性与精神分裂症]
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A nonsynonymous polymorphism in the human fatty acid amide hydrolase gene did not associate with either methamphetamine dependence or schizophrenia.人类脂肪酸酰胺水解酶基因中的一个非同义多态性与甲基苯丙胺依赖或精神分裂症均无关联。
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Brain Res Mol Brain Res. 2004 Dec 6;132(1):51-6. doi: 10.1016/j.molbrainres.2004.09.005.
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Polymorphisms of COMT Val158Met and DAT1 3'-UTR VNTR in illicit drug use and drug-related psychiatric disorders.儿茶酚-O-甲基转移酶(COMT)Val158Met多态性和多巴胺转运体1(DAT1)3'-非翻译区可变数目串联重复序列(VNTR)与非法药物使用及药物相关精神障碍的关系
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Association study of a functional catechol-O-methyltransferase genetic polymorphism with age of onset, cognitive function, symptomatology and prognosis in chronic schizophrenia.慢性精神分裂症中功能性儿茶酚-O-甲基转移酶基因多态性与发病年龄、认知功能、症状学及预后的关联研究
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Variant Associated With Schizophrenia Causes Exon Skipping, Leading to Loss of Enzymatic Activity.与精神分裂症相关的变异导致外显子跳跃,进而导致酶活性丧失。
Front Genet. 2021 Dec 6;12:762999. doi: 10.3389/fgene.2021.762999. eCollection 2021.

本文引用的文献

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The mutational constraint spectrum quantified from variation in 141,456 humans.从 141456 名人类个体的变异中量化的突变约束谱。
Nature. 2020 May;581(7809):434-443. doi: 10.1038/s41586-020-2308-7. Epub 2020 May 27.
2
EXPLORATORY ANALYSIS OF RARE AND NOVEL VARIANTS IN MEXICAN PATIENTS DIAGNOSED WITH SCHIZOPHRENIA AND DEMENTIA.对被诊断患有精神分裂症和痴呆症的墨西哥患者中罕见和新型变体的探索性分析。
Rev Invest Clin. 2019;71(4):246-254. doi: 10.24875/RIC.19002923.
3
and variation and affective states induced by marijuana smoking.并且大麻吸烟引起的变异和情感状态。
Am J Drug Alcohol Abuse. 2019;45(5):514-526. doi: 10.1080/00952990.2019.1614596. Epub 2019 Jun 11.
4
Acute effects of cannabinoids on addiction endophenotypes are moderated by genes encoding the CB1 receptor and FAAH enzyme.大麻素对成瘾内表型的急性影响受编码 CB1 受体和 FAAH 酶的基因调节。
Addict Biol. 2020 May;25(3):e12762. doi: 10.1111/adb.12762. Epub 2019 Apr 23.
5
Genetic risk for schizophrenia is associated with substance use in emerging adulthood: an event-level polygenic prediction model.精神分裂症的遗传风险与成年早期的物质使用有关:基于事件水平的多基因预测模型。
Psychol Med. 2019 Sep;49(12):2027-2035. doi: 10.1017/S0033291718002817. Epub 2018 Oct 12.
6
GWAS of lifetime cannabis use reveals new risk loci, genetic overlap with psychiatric traits, and a causal influence of schizophrenia.终生大麻使用的全基因组关联研究揭示了新的风险基因座、与精神疾病特征的遗传重叠以及精神分裂症的因果影响。
Nat Neurosci. 2018 Sep;21(9):1161-1170. doi: 10.1038/s41593-018-0206-1. Epub 2018 Aug 27.
7
FAAH variant Pro129Thr modulates subjective effects produced by cocaine administration.FAAH 变异 Pro129Thr 调节可卡因给药产生的主观效应。
Am J Addict. 2018 Oct;27(7):567-573. doi: 10.1111/ajad.12788. Epub 2018 Aug 20.
8
Power Analysis for Genetic Association Test (PAGEANT) provides insights to challenges for rare variant association studies.遗传关联测试的功效分析(PAGEANT)为罕见变异关联研究的挑战提供了深入的见解。
Bioinformatics. 2018 May 1;34(9):1506-1513. doi: 10.1093/bioinformatics/btx770.
9
Polygenic Scores for Major Depressive Disorder and Risk of Alcohol Dependence.重度抑郁症的多基因评分与酒精依赖风险
JAMA Psychiatry. 2017 Nov 1;74(11):1153-1160. doi: 10.1001/jamapsychiatry.2017.2269.
10
Association Between Substance Use Disorder and Polygenic Liability to Schizophrenia.物质使用障碍与精神分裂症多基因易感性的关联。
Biol Psychiatry. 2017 Nov 15;82(10):709-715. doi: 10.1016/j.biopsych.2017.04.020. Epub 2017 Jun 6.

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.

DOI:10.1590/1516-4446-2020-1546
PMID:34037083
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9041971/
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。