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MMP-9 haplotypes and carotid artery atherosclerosis: An association study introducing a novel multicolour multiplex RealTime PCR protocol.
- Source :
-
European Journal of Clinical Investigation . Jan2008, Vol. 38 Issue 1, p24-33. 10p. 6 Charts, 1 Graph. - Publication Year :
- 2008
-
Abstract
- Background Among other matrix metalloproteinases (MMPs), gelatinase B (MMP-9) is discussed to be associated with the pathogenesis of vascular diseases. Two single nucleotide polymorphisms (SNPs) of the MMP-9 gene, C-1562T in the promoter region and a G/A transition in exon 6 (R + 279Q), have been addressed in previous association studies which, however, produced conflicting results. Material and methods A novel multiplex RealTime PCR protocol for the fast and simultaneous detection of both polymorphisms is presented, which was used for genotyping 1737 participants of a prospective study investigating genetic factors influencing the progression of atherosclerosis. Results Haplotype analysis revealed –1562C/+279Q as the major haplotype in this population. Allelic distribution of the C-1562T polymorphism was consistent with data published for similar cohorts; however, we found that R + 279Q allelic distribution appears to vary significantly among Caucasian populations. Considering clinical data available from 1487 participants, we found significant associations between the presence of atherosclerotic plaque and the CA-haplotype in men ( P = 0·028, phi = 0·08), and between the AG variant of exon 6 and common carotid artery intima-media thickness (CIMT) in women ( P = 0·004, Eta2 = 0·019). Conclusions In summary, our results demonstrate associations of MMP-9 genotypes with different stages of carotid atherosclerosis. [ABSTRACT FROM AUTHOR]
Details
- Language :
- English
- ISSN :
- 00142972
- Volume :
- 38
- Issue :
- 1
- Database :
- Academic Search Index
- Journal :
- European Journal of Clinical Investigation
- Publication Type :
- Academic Journal
- Accession number :
- 27951519
- Full Text :
- https://doi.org/10.1111/j.1365-2362.2007.01902.x