Tiret L, Nicaud V, Ehnholm C, Havekes L, Menzel H J, Ducimetiere P, Cambien F
Institut National de la Santé et de la Recherche Médicale (INSERM), U258, Hôpital Broussais, Paris, France.
Ann Hum Genet. 1993 May;57(2):141-9. doi: 10.1111/j.1469-1809.1993.tb00895.x.
The association between genetic polymorphisms and a multifactorial disease is generally investigated by case-control studies. However, inference about the genotype-disease association can also be drawn from studies comparing offspring having a parental history of disease with offspring having no parental history. In such studies, differences in genotype frequencies between the two groups of offspring will reflect a different transmission of alleles from affected and unaffected parents. We showed that in offspring studies, the odds ratios (ORs) associated with heterozygous and homozygous genotypes are related by the formula: OR(het) = (OR(hom) + 1)/2. These ORs depend only on the allele frequencies in affected and unaffected parents, and not on the pattern of genotype-disease association. Under simple patterns of association, it is possible to infer from the ORs observed among offspring, the expected ORs for the disease. The decrease of power of offspring studies by comparison with classical case-control studies is evaluated, and an application is given on the association between the apoE polymorphism and coronary heart disease.
基因多态性与多因素疾病之间的关联通常通过病例对照研究来探究。然而,关于基因型与疾病关联的推断也可以从比较有疾病家族史的后代和无疾病家族史的后代的研究中得出。在这类研究中,两组后代之间基因型频率的差异将反映出患病和未患病父母等位基因传递的不同。我们表明,在后代研究中,与杂合子和纯合子基因型相关的优势比(OR)通过以下公式相关联:OR(het)=(OR(hom)+1)/2。这些OR仅取决于患病和未患病父母的等位基因频率,而不取决于基因型与疾病关联的模式。在简单的关联模式下,有可能从后代中观察到的OR推断出该疾病的预期OR。评估了与经典病例对照研究相比后代研究的效能降低情况,并给出了载脂蛋白E多态性与冠心病关联的应用实例。