Mansour Hader, Klei Lambertus, Wood Joel, Talkowski Michael, Chowdari Kodavali, Fathi Warda, Eissa Ahmed, Yassin Amal, Salah Hala, Tobar Salwa, El-Boraie Hala, Gaafar Hanan, Elassy Mai, Ibrahim Nahed E, El-Bahaei Wafaa, Elsayed Mohamed, Shahda Mohamed, El Sheshtawy Eman, El-Boraie Osama, El-Chennawi Farha, Devlin Bernie, Nimgaonkar Vishwajit L
Department of Psychiatry, University of Pittsburgh School of Medicine, Western Psychiatric Institute and Clinic, Pittsburgh, Pennsylvania 15213, USA.
Am J Med Genet B Neuropsychiatr Genet. 2009 Sep 5;150B(6):879-85. doi: 10.1002/ajmg.b.30913.
We aimed to contrast rates of consanguinity among patients with bipolar I disorder (BP1) and controls in a population with customary consanguineous marriages (i.e., marriage between related individuals). Consanguinity increases risk for numerous monogenic and polygenic diseases. Whether the risk for BP1 increases with consanguinity has not been investigated systematically. Two independent studies were conducted in Egypt: (1) Case-control study 93 patients with BP1, 90 screened adult control individuals, and available parents. The inbreeding coefficient/consanguinity rate was estimated in two ways: using 64 DNA polymorphisms ("DNA-based" rate); and from family history data ("self report"); (2) Epidemiological survey: total of 1,584 individuals were screened, from whom self-reported consanguinity data were obtained for identified BP1 cases (n = 35) and 150 randomly selected, unaffected control individuals. DNA-based consanguinity rates showed significant case-control differences (P = 0.0039). Self-reported consanguinity rates were also elevated among BP1 patients in both samples (Study #1 OR = 2.66, 95% confidence intervals, CI: 1.34, 5.29; Study #2: OR = 4.64, 95% CI: 2.01, 10.34). In conclusion, two independent, systematic studies indicate increased consanguinity among Egyptian BP1 patients in the Nile delta region. Self-reported estimates of consanguinity are bolstered by DNA-based estimates, and both show significant case-control differences for BP1.
我们旨在对比在一个存在传统近亲婚姻(即亲属之间的婚姻)的人群中,双相 I 型障碍(BP1)患者与对照组之间的近亲结婚率。近亲结婚会增加许多单基因和多基因疾病的风险。BP1 的风险是否会因近亲结婚而增加尚未得到系统研究。在埃及进行了两项独立研究:(1)病例对照研究:93 例 BP1 患者、90 名经过筛查的成年对照个体以及可获取信息的父母。近亲系数/近亲结婚率通过两种方式进行估算:使用 64 个 DNA 多态性位点(“基于 DNA 的比率”);以及根据家族病史数据(“自我报告”);(2)流行病学调查:共筛查了 1584 人,从中获取了已确诊的 BP1 病例(n = 35)和 150 名随机选取的未受影响对照个体的自我报告近亲结婚数据。基于 DNA 的近亲结婚率显示出显著的病例对照差异(P = 0.0039)。在两个样本中,BP1 患者的自我报告近亲结婚率也有所升高(研究 #1:OR = 2.66,95%置信区间,CI:1.34,5.29;研究 #2:OR = 4.64,95%CI:2.01,10.34)。总之,两项独立的系统研究表明,尼罗河三角洲地区的埃及 BP1 患者中近亲结婚率有所上升。基于 DNA 的估算结果支持了自我报告的近亲结婚率估算,并且两者都显示出 BP1 病例与对照之间存在显著差异。