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MMP-9 haplotypes and carotid artery atherosclerosis: An association study introducing a novel multicolour multiplex RealTime PCR protocol.

Authors :
Rauch, I.
Iglseder, B.
Paulweber, B.
Ladurner, G.
Strasser, P.
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