Department of Psychiatry, University of Pittsburgh School of Medicine, Western Psychiatric Institute and Clinic, Pittsburgh, PA 15213, USA.
Schizophr Res. 2010 Jul;120(1-3):108-12. doi: 10.1016/j.schres.2010.03.026.
Consanguinity has been suggested as a risk factor for psychoses in some Middle Eastern countries, but adequate control data are unavailable. Our recent studies in Egypt have shown elevated parental consanguinity rates among patients with bipolar I disorder (BP1), compared with controls. We have now extended our analyses to schizophrenia (SZ) in the same population.
A case-control study was conducted at Mansoura University Hospital, Mansoura, Egypt (SZ, n=75; controls, n=126, and their available parents). The prevalence of consanguinity was estimated from family history data ('self report'), followed by DNA analysis using short tandem repeat polymorphisms (STRPs, n=63) ('DNA-based' rates).
Self-reported consanguinity was significantly elevated among the patients (SZ: 46.6%, controls: 19.8%, OR 3.53, 95% CI 1.88, 6.64; p=0.000058, 1 d.f.). These differences were confirmed using DNA-based estimates for coefficients of inbreeding (inbreeding coefficients as means+/-standard error, cases: 0.058+/-0.007, controls: 0.022+/-0.003).
Consanguinity rates are significantly elevated among Egyptian SZ patients in the Nile delta region. The associations are similar to those observed with BP1 in our earlier study. If replicated, the substantial risk associated with consanguinity raises public health concerns. They may also pave the way for gene mapping studies.
在一些中东国家,血缘关系被认为是精神疾病的一个风险因素,但缺乏充分的对照数据。我们最近在埃及的研究表明,与对照组相比,双相情感障碍 I 型(BP1)患者的父母血缘关系率升高。我们现在将分析扩展到同一人群的精神分裂症(SZ)。
在埃及曼苏拉大学医院进行了病例对照研究(SZ,n=75;对照组,n=126,及其可获得的父母)。根据家族史数据(“自我报告”)估计血缘关系的流行率,然后使用短串联重复多态性(STRPs,n=63)进行 DNA 分析(“基于 DNA”的比率)。
自我报告的血缘关系在患者中显著升高(SZ:46.6%,对照组:19.8%,OR 3.53,95%CI 1.88,6.64;p=0.000058,1 自由度)。使用基于 DNA 的近亲繁殖系数估计值(近亲繁殖系数为平均值+/-标准误差,病例:0.058+/-0.007,对照:0.022+/-0.003)证实了这些差异。
在尼罗河三角洲地区的埃及 SZ 患者中,血缘关系率显著升高。这些关联与我们早期研究中观察到的 BP1 相似。如果得到复制,与血缘关系相关的显著风险引起了公共卫生关注。它们也可能为基因图谱研究铺平道路。