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Familial empirical risks for inflammatory bowel disease: differences between Jews and non-Jews.

机译:炎症性肠病的家族性经验风险:犹太人与非犹太人之间的差异。

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摘要

The Jewish population has an increased frequency of inflammatory bowel disease compared with their non-Jewish neighbours. Genetic factors have been implicated in the aetiology of this disorder and may contribute to ethnic differences. This study determined the familial empirical risks for inflammatory bowel disease in the first degree relatives of inflammatory bowel disease probands (for both Jews and non-Jews) for the purpose of accurate genetic counselling and genetic analysis. A total of 527 inflammatory bowel disease patients from Southern California (291 Jews and 236 non-Jews) were questioned about inflammatory bowel disease in their first degree relatives (a total of 2493 individuals). Since inflammatory bowel disease has a variable and late age of onset, age specific incidence data were used to estimate the life time risks and to make valid comparisons between the different groups. In the first degree relatives of non-Jewish probands, the life time risks for inflammatory bowel disease were 5.2% and 1.6% when probands had Crohn's disease and ulcerative colitis respectively. These values were consistently lower than the corresponding risks for relatives of Jewish patients -7.8% and 4.5% for Crohn's disease and ulcerative colitis probands respectively (p value for comparison between Jews and non-Jews: 0.028; between ulcerative colitis and Crohn's disease: 0.005). These data provide the requisite basis for genetic counselling for these disorders in the white American population. In addition, these different empirical risks for relatives of Jewish and non-Jewish probands allow rejection of single Mendelian gene models for inflammatory bowel disease, but are consistent with several alternative genetic models.
机译:与非犹太人邻居相比,犹太人的炎症性肠病发病率增加。遗传因素已与这种疾病的病因有关,可能导致种族差异。这项研究确定了炎症性肠病先证者(无论是犹太人还是非犹太人)的一级亲属中炎症性肠病的家族经验风险,目的是进行准确的遗传咨询和遗传分析。来自南加州的总计527名炎症性肠病患者(291名犹太人和236名非犹太人)在其一级亲属中被询问有关炎症性肠病(共2493人)。由于炎症性肠病的发病年龄可变且发病年龄较晚,因此使用年龄特定的发病率数据来估计生命风险并在不同组之间进行有效比较。在非犹太先证者的一级亲属中,当先证者患有克罗恩氏病和溃疡性结肠炎时,炎症性肠病的终身风险分别为5.2%和1.6%。这些值始终低于犹太人亲属的相应风险-克罗恩病和溃疡性结肠炎先证者分别为-7.8%和4.5%(犹太人和非犹太人之间比较的p值:0.028;溃疡性结肠炎和克罗恩病之间的比较的p值:0.005 )。这些数据为美国白人人群中这些疾病的遗传咨询提供了必要的基础。另外,犹太人和非犹太人先证者的亲戚的这些不同的经验风险允许拒绝单个孟德尔基因模型用于炎症性肠病,但与其他几种遗传模型一致。

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