Eur J Hum Genet. 2004 Sep;12(9):770-4. doi: 10.1038/sj.ejhg.5201244.
Family-based studies to map susceptibility genes through linkage disequilibrium have been successful in early-onset diseases where parental-proband trios are readily collected, but are believed to be unworkable for late-onset diseases such as coronary artery disease (CAD). PROCARDIS is a European multicentre study that was designed to identify susceptibility genes for CAD. We have tested the transmission of a putatively functional allele, lymphotoxin-alpha N26 (804A), in more than 400 PROCARDIS trio families. The present study demonstrates association of this allele with CAD in white Europeans, a different ethnic group with a heavier CAD burden than the Japanese in which the association was initially identified, which suggests a broad relevance to CAD susceptibility. The practicalities of implementing a trio-family design for late-onset diseases are discussed.
通过连锁不平衡来定位易感基因的基于家系的研究,在早发性疾病中很成功,因为这类疾病很容易收集到亲代-先证者三联体,但对于像冠心病(CAD)这样的晚发性疾病,这类研究被认为是行不通的。PRO-CARDIS是一项欧洲多中心研究,旨在识别CAD的易感基因。我们在400多个PRO-CARDIS三联体家庭中测试了一个假定具有功能的等位基因——淋巴毒素-α N26(804A)的传递情况。本研究证明,在白种欧洲人中,该等位基因与CAD相关,白种欧洲人是一个与日本人不同的种族群体,其CAD负担比日本人更重,而最初正是在日本人中发现了这种关联,这表明该等位基因与CAD易感性具有广泛的相关性。本文还讨论了针对晚发性疾病实施三联体家庭设计的实际情况。