Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2010:2010:490241.
doi: 10.1155/2010/490241. Epub 2010 Jun 27.

A quantitative trait locus on chromosome 5p influences d-dimer levels in the san antonio family heart study

Affiliations

A quantitative trait locus on chromosome 5p influences d-dimer levels in the san antonio family heart study

V P Diego et al. Int J Vasc Med. 2010.

Abstract

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.

PubMed Disclaimer

Figures

Figure 1
Figure 1
Multipoint genome-scan across the 22 autosomes for D-dimer levels in the San Antonio Family Heart Study. At all chromosomes, the vertical axis is in lod scores, and the horizontal axis is in centiMorgans (cM).
Figure 2
Figure 2
Linkage analysis results for D-dimer levels on chromosome 5. Axes are as in Figure 1.
Figure 3
Figure 3
Linkage analysis results for D-dimer levels on Chromosome 2. Axes are as in Figure 1.

Similar articles

Cited by

References

    1. Sidelmann JJ, Gram J, Jespersen J, Kluft C. Fibrin clot formation and lysis: basic mechanisms. Seminars in Thrombosis and Hemostasis. 2000;26(6):605–618. - PubMed
    1. Danesh J, Whincup P, Walker M, et al. Fibrin D-dimer and coronary heart disease prospective study and meta-analysis. Circulation. 2001;103(19):2323–2327. - PubMed
    1. Folsom AR, Aleksic N, Park E, Salomaa V, Juneja H, Wu KK. Prospective study of fibrinolytic factors and incident coronary heart disease: the atherosclerosis risk in communities (ARIC) study. Arteriosclerosis, Thrombosis, and Vascular Biology. 2001;21(4):611–617. - PubMed
    1. Lowe GDO, Yarnell JWG, Rumley A, Bainton D, Sweetnam PM. C-reactive protein, fibrin d-dimer, and incident ischemic heart disease in the speedwell study: are inflammation and fibrin turnover linked in pathogenesis? Arteriosclerosis, Thrombosis, and Vascular Biology. 2001;21(4):603–610. - PubMed
    1. Lowe GDO, Rumley A, McMahon AD, Ford I, O'Reilly DStJ, Packard CJ. Interleukin-6, fibrin D-dimer, and coagulation factors VII and XIIa in prediction of coronary heart disease. Arteriosclerosis, Thrombosis, and Vascular Biology. 2004;24(8):1529–1534. - PubMed

LinkOut - more resources