Van Vlijmen-Van Keulen C J, Rauwerda J A, Pals G
Institute for cardiovascular research, VU university Medical Center, Amsterdam, The Netherlands.
Eur J Vasc Endovasc Surg. 2005 Jul;30(1):29-35. doi: 10.1016/j.ejvs.2004.12.029.
Elucidation of the genetic background of familial abdominal aortic aneurysm (AAA) suggests a genetic etiology.
We carried out a genome-wide scan in three Dutch families with four or five affected siblings. Suggestive loci were further studied by subsequent fine mapping of the locus performed in 101 affected sib-pairs. The genome-wide scan was performed with 400 DNA markers and results were given as non-parametric, multipoint linkage scores (NPL). We observed a suggestive linkage for AAA (NPL score 3.25 at D19S902, 72.72 cM) on chromosome 19q in the three families. After fine mapping on chromosome 19, the NPL score became nominal in the 101 affected sib-pairs. A separate analysis of the three families with fine mapping revealed a peak with significant evidence for linkage (NPL score 3.95 at D19S904, 78.08 cM) on chromosome 19q. This peak was situated to the right compared to the region found in a previously published article for familial AAA on chromosome 19q.
Our results identified a candidate locus in three Dutch families with AAA at chromosome 19q13.3. Separate analysis of these three families provides evidence for genetic heterogeneity.
阐明家族性腹主动脉瘤(AAA)的遗传背景提示其存在遗传病因。
我们对三个有四到五个患病兄弟姐妹的荷兰家族进行了全基因组扫描。通过对101对患病同胞对进行后续的基因座精细定位,对提示性基因座进行了进一步研究。使用400个DNA标记进行全基因组扫描,结果以非参数多点连锁分数(NPL)给出。在这三个家族中,我们在19号染色体q臂上观察到AAA的提示性连锁(在D19S902,72.72 cM处NPL分数为3.25)。在19号染色体上进行精细定位后,在101对患病同胞对中NPL分数变为名义值。对这三个家族进行精细定位的单独分析显示,在19号染色体q臂上有一个具有显著连锁证据的峰值(在D19S904,78.08 cM处NPL分数为3.95)。与之前发表的关于19号染色体q臂上家族性AAA的文章中发现的区域相比,这个峰值位于右侧。
我们的结果在三个患有AAA的荷兰家族中确定了19号染色体q13.3上的一个候选基因座。对这三个家族的单独分析提供了遗传异质性的证据。