Diego V P, Almasy L, Rainwater D L, Mahaney M C, Comuzzie A G, Cole S A, Tracy R P, Stern M P, Maccluer J W, Blangero J
Department of Genetics, Southwest Foundation for Biomedical Research, San Antonio, TX 78245-0549, USA.
Int J Vasc Med. 2010;2010:490241. doi: 10.1155/2010/490241. Epub 2010 Jun 27.
Background. D-dimer is associated with increasing severity of atherosclerosis and with increased risk of a cardiovascular disease (CVD). Methods and Results. To better understand this risk factor, we performed a genome scan on 803 (301 males and 502 females) Mexican Americans in the San Antonio Family Heart Study (SAFHS). The SAFHS is ideal for the discovery of quantitative trait loci (QTLs) influencing CVD because CVD risk factors are prevalent in Mexican Americans of San Antonio and because the study design involves large families, which is optimal for QTL discovery. D-dimer levels were normalized in our study. We found that D-dimer levels were heritable, at about 23% heritability (P ≈ .00001). In a linkage analysis employing 432 microsatellite markers, we found strong evidence of a QTL on chromosome 5p with a lod score of 3.32 at 21 centiMorgans (cM). We also found suggestive evidence of a QTL on chromosome 2q with a lod score of 2.33 at 207 cM. Conclusions. To our knowledge, the putative QTL on chromosome 5p is novel. The possible QTL on chromosome 2q is discussed in relation to a recent report of linkage of a related hemostatic factor to the same location. These results warrant further investigation.
背景。D - 二聚体与动脉粥样硬化严重程度增加以及心血管疾病(CVD)风险升高相关。方法与结果。为了更好地理解这一风险因素,我们在圣安东尼奥家族心脏研究(SAFHS)中对803名(301名男性和502名女性)墨西哥裔美国人进行了全基因组扫描。SAFHS对于发现影响CVD的数量性状基因座(QTL)非常理想,因为圣安东尼奥的墨西哥裔美国人中CVD风险因素普遍存在,且该研究设计涉及大家庭,这对于QTL发现是最优的。在我们的研究中,D - 二聚体水平进行了标准化处理。我们发现D - 二聚体水平具有遗传性,遗传度约为23%(P≈0.00001)。在一项使用432个微卫星标记的连锁分析中,我们发现5号染色体短臂上有一个QTL的有力证据,在21厘摩(cM)处的对数优势分数为3.32。我们还发现2号染色体长臂上有一个QTL的提示性证据,在207 cM处的对数优势分数为2.33。结论。据我们所知,5号染色体短臂上的假定QTL是新发现的。关于2号染色体长臂上可能的QTL,结合最近一份关于相关止血因子与同一位置连锁的报告进行了讨论。这些结果值得进一步研究。