Does consanguinity increase the risk of schizophrenia? Study based on primary health care centre visits.

Mental health in family medicine Pub Date : 2012-12-01
Abdulbari Bener, Elnour E Dafeeah, Nancy Samson
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Abstract

Background Consanguinity has been suggested as a risk factor for the development of schizophrenia in offspring in some Middle Eastern countries. Aim The purpose of this study was to review the frequency, pattern of parental consanguinity, and family history of schizophrenia among schizophrenia patients in Qatar, and to determine their impact on the associated risk factors. Design This is a cross-sectional study which was conducted between January 2009 and December 2010, in the setting of primary health care (PHC) centres of the Supreme Council of Health, State of Qatar. Subjects A total of 1491 patients aged 18-55 years were approached, of whom 1184 individuals agreed to participate in the study, giving a response rate of 79.4%. Methods The study was based on face-to-face interviews using a specially designed questionnaire that covered sociodemographic characteristics and genetic and other biological factors (e.g. obstetric complications), and a diagnostic screening questionnaire which consisted of six questions about the symptoms of schizophrenia. The diagnostic screening questionnaire was reviewed and used to calculate the final score, which determined a provisional diagnosis. The psychiatrists discussed the psychiatric diagnosis and confirmed it using DSM-IV criteria. The degree of consanguinity between the patient's parents was recorded. Consanguinity was evaluated based on the coefficient of inbreeding (F), which is the probability of homozygosity. Results More than half of the schizophrenia patients were female (57.1%) and over 45 years of age (62.5%). A family history of schizophrenia was significantly more common in parents of schizophrenia patients than in the Arab population without schizophrenia (24.6% vs. 17.1%; P = 0.038). Parental consanguinity was elevated among the patients with schizophrenia (41.3%) with a higher mean coefficient of inbreeding (0.04356 ± 0.028) than in non-schizophrenic subjects (28.7%) with a lower mean coefficient of inbreeding (0.0298 ± 0.035). Schizophrenia diagnoses were more frequent among the offspring of consanguineous parents than among the offspring of non-consanguineous parents. Conclusion The substantial risk observed in the present study reveals that consanguinity is an important risk factor for schizophrenia in Qatar. In addition, the study confirms that the higher familial risks provide strong genetic epidemiological evidence for the overall heritable effects in the aetiology of schizophrenia.

近亲结婚会增加患精神分裂症的风险吗?基于初级保健中心就诊情况的研究。
背景 在一些中东国家,近亲结婚被认为是后代患精神分裂症的一个危险因素。目的 本研究旨在回顾卡塔尔精神分裂症患者中父母近亲结婚的频率、模式和精神分裂症家族史,并确定它们对相关风险因素的影响。设计 这是一项横断面研究,于 2009 年 1 月至 2010 年 12 月期间在卡塔尔国最高卫生委员会的初级卫生保健(PHC)中心进行。研究对象 共接触了 1491 名 18-55 岁的患者,其中 1184 人同意参与研究,回复率为 79.4%。研究方法 该研究采用面对面访谈的方式,使用一份专门设计的调查问卷,内容包括社会人口学特征、遗传和其他生物因素(如产科并发症),以及一份诊断筛查问卷,其中包括六个有关精神分裂症症状的问题。诊断筛查问卷经审核后用于计算最终得分,从而确定临时诊断。精神科医生讨论了精神科诊断,并根据 DSM-IV 标准予以确认。记录了患者父母之间的血缘关系。近亲程度根据近亲繁殖系数(F)进行评估,该系数是同种遗传概率。结果 半数以上的精神分裂症患者为女性(57.1%),年龄在 45 岁以上(62.5%)。精神分裂症患者父母有精神分裂症家族史的比例明显高于无精神分裂症的阿拉伯人群(24.6% 对 17.1%;P = 0.038)。与非精神分裂症患者(28.7%)相比,精神分裂症患者(41.3%)的父母近亲繁殖率较高(0.04356 ± 0.028),平均近亲繁殖系数较低(0.0298 ± 0.035)。近亲结婚的后代比非近亲结婚的后代更容易被诊断为精神分裂症。结论 本研究观察到的巨大风险表明,近亲结婚是卡塔尔精神分裂症的一个重要风险因素。此外,本研究还证实,较高的家族风险为精神分裂症病因中的整体遗传效应提供了强有力的遗传流行病学证据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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