Abstract | OBJECTIVE: METHODS: A case-control study was performed in 494 patients with SSc and 280 healthy controls for I/D polymorphism. Two supplementary exonic SNP of ACE gene (rs4309, rs4362) were genotyped in 659 patients with SSc and 511 matched healthy controls. Among the whole SSc population, 453 (67%) patients with SSc had the limited cutaneous subtype, 47 (7%) had precapillary pulmonary arterial hypertension, 209 (32%) had digital ulcers, and 10 (1.5%) had renal crisis. A combined analysis of the available results for ACE I/D genotypes in Caucasians was also performed. RESULTS: There was no association between the 3 polymorphic markers and SSc for allelic and genotype frequencies. No association was observed for the different vascular subsets of the disease. Haplotype analyses did not detect any association. The lack of association for ACE I/D was confirmed by the combined analysis. CONCLUSION: These results in a large cohort of European Caucasian patients with SSc do not support that the ACE gene is implicated in the pathogenesis of SSc and its vascular damage.
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Authors | Julien Wipff, Guillaume Gallier, Philippe Dieude, Jerome Avouac, Kiet Tiev, Eric Hachulla, Brigitte Granel, Elisabeth Diot, Jean Sibilia, Luc Mouthon, Olivier Meyer, Andre Kahan, Mathilde Varret, Catherine Boileau, Yannick Allanore |
Journal | The Journal of rheumatology
(J Rheumatol)
Vol. 36
Issue 2
Pg. 337-40
(Feb 2009)
ISSN: 0315-162X [Print] Canada |
PMID | 19132786
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
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Topics |
- Adult
- Aged
- Case-Control Studies
- Comorbidity
- DNA Mutational Analysis
- Europe
(ethnology)
- Female
- France
(ethnology)
- Gene Frequency
- Genetic Markers
(genetics)
- Genetic Predisposition to Disease
(genetics)
- Genetic Testing
- Genotype
- Humans
- Hypertension, Pulmonary
(enzymology, epidemiology, genetics)
- Kidney Diseases
(enzymology, epidemiology, genetics)
- Male
- Middle Aged
- Polymorphism, Single Nucleotide
(genetics)
- Renin
(genetics)
- Scleroderma, Systemic
(enzymology, ethnology, genetics)
- White People
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