Please use this identifier to cite or link to this item: http://hdl.handle.net/10261/33694
Share/Export:
logo share SHARE logo core CORE BASE
Visualizar otros formatos: MARC | Dublin Core | RDF | ORE | MODS | METS | DIDL | DATACITE

Invite to open peer review
Title

A1298C polymorphism in the MTHFR gene predisposes to cardiovascular risk in rheumatoid arthritis

AuthorsPalomino-Morales, Rogelio; Vázquez-Rodríguez, Tomás R.; Miranda-Filloy, J. A.; Fernández-Gutiérrez, B.; Martín, J.; González-Gay, M. A.
Issue Date26-Apr-2010
PublisherBioMed Central
CitationArthritis Research and Therapy 12: R71 (2010)
Abstract[Introduction]: We determined the contribution of the methylene tetrahydrofolate reductase (MTHFR) 677 C>T and 1298 A>C gene polymorphisms to the susceptibility to rheumatoid arthritis (RA). We also assessed whether these two MTHFR gene polymorphisms may be implicated in the development of cardiovascular (CV) events and subclinical atherosclerosis manifested by the presence of endothelial dysfunction, in a series of Spanish patients with RA. [Methods]: Six hundred and twelve patients fulfilling the 1987 American College of Rheumatology classification criteria for RA, seen at the rheumatology outpatient clinics of Hospital Xeral-Calde, Lugo and Hospital San Carlos, Madrid, were studied. Patients and controls (n = 865) were genotyped using predesigned TaqMan SNP genotyping assays. [Results]: No significant differences in allele or genotype frequencies for the MTHFR gene polymorphisms between RA patients and controls were found. Also, no association between the MTHFR 677 C>T polymorphism and CV events or endothelial dysfunction was observed. However, the MTHFR 1298 allele C frequency was increased in patients with CV events after 5 years (38.7% versus 30.3%; odds ratio = 1.45; 95% confidence interval = 1.00 to 2.10; P = 0.04) and 10 years (42.2% versus 31.0%; odds ratio = 1.62; 95% confidence interval = 1.08 to 2.43; P = 0.01) follow up. Moreover, patients carrying the MTHFR 1298 AC and CC genotypes had a significantly decreased flow-mediated endothelium-dependent vasodilatation (4.3 ± 3.9%) compared with those carrying the MTHFR 1298 AA genotype (6.5 ± 4.4%) (P = 0.005). [Conclusions]: Our results show that the MTHFR 1298 A>C gene polymorphism confers an increased risk for subclinical atherosclerosis and CV events in patients with RA.
Description8 páginas, 1 figura, 3 tablas.-- et al.
Publisher version (URL)http://dx.doi.org/10.1186/ar2989
URIhttp://hdl.handle.net/10261/33694
DOI10.1186/ar2989
ISSN1478-6354
Appears in Collections:(IPBLN) Artículos




Files in This Item:
File Description SizeFormat
ar2989.pdf603,3 kBAdobe PDFThumbnail
View/Open
Show full item record

CORE Recommender

PubMed Central
Citations

37
checked on Apr 17, 2024

SCOPUSTM   
Citations

77
checked on Apr 24, 2024

WEB OF SCIENCETM
Citations

70
checked on Feb 28, 2024

Page view(s)

477
checked on Apr 23, 2024

Download(s)

254
checked on Apr 23, 2024

Google ScholarTM

Check

Altmetric

Altmetric


Related articles:


WARNING: Items in Digital.CSIC are protected by copyright, with all rights reserved, unless otherwise indicated.