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本文引用的文献

1
Recent Advances in the Genetics of Schizophrenia.精神分裂症遗传学的最新进展
Mol Neuropsychiatry. 2018 Jun;4(1):35-51. doi: 10.1159/000488679. Epub 2018 May 30.
2
Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes.双相情感障碍和精神分裂症的基因组剖析,包括 28 个子表型。
Cell. 2018 Jun 14;173(7):1705-1715.e16. doi: 10.1016/j.cell.2018.05.046.
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Prevalence of Schizophrenia Spectrum Disorders in Average-IQ Adults with Autism Spectrum Disorders: A Meta-analysis.自闭症谱系障碍患者中平均智商成人的精神分裂谱系障碍患病率:一项荟萃分析。
J Autism Dev Disord. 2018 Jan;48(1):239-250. doi: 10.1007/s10803-017-3328-5.
4
Biological insights from 108 schizophrenia-associated genetic loci.108 个精神分裂症相关遗传位点的生物学见解。
Nature. 2014 Jul 24;511(7510):421-7. doi: 10.1038/nature13595. Epub 2014 Jul 22.
5
Genome-wide meta-analyses identify multiple loci associated with smoking behavior.全基因组荟萃分析确定了多个与吸烟行为相关的基因座。
Nat Genet. 2010 May;42(5):441-7. doi: 10.1038/ng.571. Epub 2010 Apr 25.
6
The role of genetics in the etiology of schizophrenia.遗传学在精神分裂症病因学中的作用。
Psychiatr Clin North Am. 2010 Mar;33(1):35-66. doi: 10.1016/j.psc.2009.12.003.
7
Genetic risk prediction--are we there yet?基因风险预测——我们做到了吗?
N Engl J Med. 2009 Apr 23;360(17):1701-3. doi: 10.1056/NEJMp0810107. Epub 2009 Apr 15.
8
Schizophrenia and epilepsy: is there a shared susceptibility?精神分裂症与癫痫:是否存在共同易感性?
Neurosci Res. 2009 Apr;63(4):227-35. doi: 10.1016/j.neures.2009.01.002.
9
Autism spectrum disorders and childhood-onset schizophrenia: clinical and biological contributions to a relation revisited.自闭症谱系障碍与儿童期起病的精神分裂症:对一种关系的临床与生物学贡献再探讨
J Am Acad Child Adolesc Psychiatry. 2009 Jan;48(1):10-8. doi: 10.1097/CHI.0b013e31818b1c63.
10
Parental psychiatric disorders associated with autism spectrum disorders in the offspring.与后代自闭症谱系障碍相关的父母精神疾病。
Pediatrics. 2008 May;121(5):e1357-62. doi: 10.1542/peds.2007-2296.

用于评估遗传因素对精神分裂症影响的DNA库。

DNA Banking to Assess Genetic Influences on Schizophrenia.

作者信息

Sadighi Gita, Nazeri Astaneh Ali, Najmabadi Hossein, Khodaei Ardakani Mohammad Reza, Latifi-Navid Saeid

机构信息

Department of Psychiatry, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran.

Psychosis Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran.

出版信息

Med J Islam Repub Iran. 2022 Apr 27;36:42. doi: 10.47176/mjiri.36.42. eCollection 2022.

DOI:10.47176/mjiri.36.42
PMID:36128322
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9448483/
Abstract

Schizophrenia is among the most prevalent psychiatric disorders globally, with a lifetime prevalence rate of 0.3% to 0.7%, characterized by the heterogeneous presence of positive, negative, and cognitive symptoms that affect all aspects of mental activity. We aimed to describe the genetics of schizophrenia to widening our understanding of the inheritance of this illness. This quasi-experimental study was conducted in Razi psychiatric hospital in Tehran province, Iran. Recruitment of the study samples was conducted in Tehran, Iran, among patients with schizophrenia and their families. For this purpose, individuals with schizophrenia in 40 families with at least 1 to 2 affected members were identified and selected based on a clinical interview conducted by a psychiatrist and according to the Diagnostic and Statistical Manual of Mental Disorders, 5th Edition. The clinical and paraclinical data, drug and substance usage, and medical treatments were collected through a standardized clinical questionnaire. Besides, the Global Assessment Scale and the Positive and Negative Syndrome Scale were completed for all study participants. A total of 22 families had a negative family history, and 1 affected member and the rest of the studied families had a positive family history and at least 2 affected members. In addition, genealogical data (family tree) and lymphoblastic cell categories were developed to examine genes, and subsequent research results will be reported in the future. As the research continues, the approach to sampling must be modified to ensure that the deoxyribonucleic acid bank is as extensively representative as possible of all schizophrenia cases.

摘要

精神分裂症是全球最常见的精神疾病之一,终生患病率为0.3%至0.7%,其特征是存在影响精神活动各个方面的阳性、阴性和认知症状的异质性。我们旨在描述精神分裂症的遗传学,以加深我们对这种疾病遗传方式的理解。这项准实验研究在伊朗德黑兰省的拉齐精神病医院进行。研究样本的招募在伊朗德黑兰的精神分裂症患者及其家属中进行。为此,根据精神科医生进行的临床访谈并依据《精神疾病诊断与统计手册》第5版,在40个至少有1至2名受影响成员的家庭中识别并挑选出患有精神分裂症的个体。通过标准化临床问卷收集临床和辅助临床数据、药物和物质使用情况以及医疗治疗情况。此外,为所有研究参与者完成了全球评估量表和阳性与阴性症状量表。共有22个家庭有阴性家族史,1名受影响成员,其余研究家庭有阳性家族史且至少有2名受影响成员。此外,还建立了系谱数据(家谱)和淋巴细胞类别以检测基因,后续研究结果将在未来报告。随着研究的继续,必须修改抽样方法,以确保脱氧核糖核酸库尽可能广泛地代表所有精神分裂症病例。