Farrall M, Holder S
Division of Molecular Medicine, Medical Research Council Clinical Research Centre, Harrow, England.
Am J Hum Genet. 1992 Feb;50(2):270-7.
Cleft lip with or without cleft palate (CL/P) is a common congenital malformation with an incidence in European white populations of about 1/1,000. The familial clustering of CL/P has been extensively characterized, and epidemiological studies have proposed monogenic models (with reduced penetrance), multifactorial/threshold models, and mixed major-gene/multifactorial models to explain its inheritance. The recognition of an association between two RFLPs at the transforming growth factor alpha (TGFA) locus and CL/P supports a major-gene component to the etiology of CL/P. Risch has shown that the recurrence risk ratio lambda R (risk to relatives, vs. population prevalence) is a useful pointer to the mode of inheritance. Here we further develop the use of lambda R to analyze recurrence-risk data for CL/P. Recurrence risks for first-, second-, and third-degree relatives equate well with oligogenic models with as few as four loci. A monogenic/additive model is strongly rejected. The limited available twin data are also consistent with this model. A "major gene" interacting epistatically with an oligogenic background is shown to be a plausible alternative. Power calculations for a linkage study to map the CL/P major-risk locus suggest that a sample of 50 affected sib pairs will be adequate, but linkage to minor-risk loci will require very much larger samples.
唇裂伴或不伴腭裂(CL/P)是一种常见的先天性畸形,在欧洲白人群体中的发病率约为1/1000。CL/P的家族聚集性已得到广泛描述,流行病学研究提出了单基因模型(外显率降低)、多因素/阈值模型以及混合的主基因/多因素模型来解释其遗传方式。在转化生长因子α(TGFA)基因座上两个限制性片段长度多态性(RFLP)与CL/P之间关联的发现,支持了CL/P病因中存在主基因成分的观点。里施表明复发风险比λR(亲属患病风险与人群患病率之比)是遗传方式的一个有用指标。在此,我们进一步拓展了λR的应用,以分析CL/P的复发风险数据。一级、二级和三级亲属的复发风险与少至四个基因座的寡基因模型拟合良好。单基因/加性模型被强烈否定。有限的可用双生子数据也与该模型一致。结果表明,一个与寡基因背景发生上位性相互作用的“主基因”是一个合理的替代方案。一项用于定位CL/P主要风险基因座的连锁研究的效能计算表明,50对受累同胞对的样本量就足够了,但要与次要风险基因座连锁则需要非常大的样本量。