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Arteriosclerosis, Thrombosis, and Vascular Biology
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Published Online
on May 18, 2006

Arteriosclerosis, Thrombosis, and Vascular Biology. 2006
Published online before print May 18, 2006, doi: 10.1161/01.ATV.0000227717.46157.32
A more recent version of this article appeared on August 1, 2006
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Submitted on October 16, 2005
Accepted on May 8, 2006

Variation in the Human Matrix Metalloproteinase-9 Gene Is Associated With Arterial Stiffness in Healthy Individuals

Yasmin *; Carmel M. McEniery ; Kevin M. O’Shaughnessy ; Patrick Harnett ; Asif Arshad ; Sharon Wallace ; Kaisa Maki-Petaja ; Barry McDonnell ; Mike J. Ashby ; John Brown ; John R. Cockcroft ; and Ian B. Wilkinson

From the Clinical Pharmacology Unit (Y., C.M.M., K.M.O., P.H., A.A., S.W., K.M.-P., M.J.A., I.B.W.), University of Cambridge, Addenbrooke’s Hospital, Cambridge; the Department of Cardiology (B.M., J.R.C.), University of Wales College of Medicine, Cardiff; and Trinity College (J.B.), Cambridge, UK.

* To whom correspondence should be addressed. E-mail: my105{at}medschl.cam.ac.uk.

Background--Arterial stiffness is an important determinant of cardiovascular risk. Elastin is the main elastic component of arterial wall and can be degraded by a number of enzymes including serine proteases and matrix metalloproteinases (MMPs). Serum MMP-9 levels correlate with arterial stiffness and predict cardiovascular risk. Polymorphisms in the MMP-9 gene are also associated with large artery function in subjects with coronary artery disease. Therefore, we investigated the influence of known MMP-9 (-1562C>T, R279Q) polymorphisms on arterial stiffness in a large cohort of healthy individuals (n=865).

Methods and Results--Aortic pulse wave velocity (PWV) and augmentation index were assessed. Supine blood pressure, biochemical makers, MMP-9 levels, and serum elastase activity (SEA) were also determined. Genomic DNA was extracted and genotyping performed. Aortic PWV, serum MMP-9, and SEA were higher in carriers of the rare alleles for the -1562C>T and R279Q polymorphisms. These polymorphisms were also associated with aortic PWV after correction for other confounding factors. Stepwise regression models with known or likely determinants of arterial stiffness revealed that {approx}60% of the variability in aortic PWV was attributable to age, mean arterial pressure, and genetic variants (P<0.001).

Conclusions--We have demonstrated for the first time that aortic stiffness and elastase activity are influenced by MMP-9 gene polymorphisms. This suggests that the genetic variation in this protein may be involved in the process of large artery stiffening.


Key words: aortic pulse wave velocity • augmentation index • MMP-9 gene polymorphisms • MMP-9 levels • serum elastase activity




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