Abstract | OBJECTIVE: MATERIALS AND METHODS: We investigated 250 consecutive patients, 217 males and 33 females (median age 72, range 50-83), undergone AAA elective repair and 250 healthy controls, comparable for sex and age. ACE and AT1R polymorphisms were studied by PCR-RFLP analysis. The genotype distribution was in Hardy-Weinberg equilibrium for all polymorphisms. RESULTS: The genotype distribution and allele frequency of ACE I/D, but not AT1R A1166C polymorphism were significantly different between patients and controls (ACE I/D: p=0.0002 and p<0.0001, respectively, and AT1R A1166C: p=0.6 and p=0.4, respectively). An association between the ACE DD genotype and the predisposition to AAA was found (OR DD vs. ID+II=1.9 95% CI 1.3-2.9, p<0.0001). Multivariate analysis adjusted for age, sex, traditional vascular risk factors and other atherosclerotic localizations, showed ACE DD genotype to be independently related to the disease (OR DD vs. ID+II=2.4, 95% CI 1.3-4.2 p=0.003). CONCLUSIONS: Our findings document that ACE DD genotype represents a susceptibility factor for AAA.
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Authors | C Fatini, G Pratesi, F Sofi, F Gensini, E Sticchi, B Lari, R Pulli, W Dorigo, L Azas, C Pratesi, G F Gensini, R Abbate |
Journal | European journal of vascular and endovascular surgery : the official journal of the European Society for Vascular Surgery
(Eur J Vasc Endovasc Surg)
Vol. 29
Issue 3
Pg. 227-32
(Mar 2005)
ISSN: 1078-5884 [Print] England |
PMID | 15694792
(Publication Type: Journal Article)
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Chemical References |
- Receptors, Angiotensin
- Peptidyl-Dipeptidase A
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Topics |
- Aged
- Aged, 80 and over
- Aortic Aneurysm, Abdominal
(complications, genetics)
- Causality
- Female
- Gene Frequency
- Genetic Predisposition to Disease
- Humans
- Hypertension
(complications)
- Male
- Middle Aged
- Peptidyl-Dipeptidase A
(genetics)
- Polymerase Chain Reaction
- Polymorphism, Genetic
- Polymorphism, Restriction Fragment Length
- Receptors, Angiotensin
(genetics)
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