Sadighi Gita, Nazeri Astaneh Ali, Najmabadi Hossein, Khodaei Ardakani Mohammad Reza, Latifi-Navid Saeid
Department of Psychiatry, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran.
Psychosis Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran.
Med J Islam Repub Iran. 2022 Apr 27;36:42. doi: 10.47176/mjiri.36.42. eCollection 2022.
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.
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。