Lack of association between JAK3 gene polymorphisms and cardiovascular disease in Spanish patients with rheumatoid arthritis.
Mercedes García-BermúdezRaquel López-MejíasFernanda GenreSantos CastañedaAlfonso CorralesJavier LlorcaCarlos González-JuanateyBegoña UbillaJosé A Miranda-FilloyTrinitario PinaCarmen Gómez-VaqueroLuis Rodríguez-RodríguezBenjamín Fernández-GutiérrezAlejandro BalsaDora Pascual-SalcedoFrancisco J López-LongoPatricia CarreiraRicardo BlancoJavier MartínMiguel A González-GayPublished in: BioMed research international (2015)
Rheumatoid arthritis (RA) is a polygenic disease associated with accelerated atherosclerosis and increased cardiovascular (CV) mortality. JAK/STAT signalling pathway is involved in autoimmune diseases and in the atherosclerotic process. JAK3 is a highly promising target for immunomodulatory drugs and polymorphisms in JAK3 gene have been associated with CV events in incident dialysis patients. Therefore, the aim of this study was to assess the potential role of JAK3 polymorphisms in the development of CV disease in patients with RA. 2136 Spanish RA patients were genotyped for the rs3212780 and rs3212752 JAK3 gene polymorphisms by TaqMan assays. Subclinical atherosclerosis was evaluated in 539 of these patients by carotid ultrasonography (US). No statistically significant differences were found when each polymorphism was assessed according to carotid intima-media thickness values and presence/absence of carotid plaques in RA, after adjusting the results for potential confounders. Moreover, no significant differences were obtained when RA patients were stratified according to the presence/absence of CV events after adjusting for potential confounders. In conclusion, our results do not confirm association between JAK3 polymorphisms and CV disease in RA.
Keyphrases
- rheumatoid arthritis
- end stage renal disease
- cardiovascular disease
- chronic kidney disease
- ejection fraction
- newly diagnosed
- peritoneal dialysis
- type diabetes
- disease activity
- gene expression
- risk assessment
- genome wide
- cardiovascular events
- coronary artery disease
- magnetic resonance
- metabolic syndrome
- risk factors
- systemic lupus erythematosus
- human health
- idiopathic pulmonary fibrosis
- drug induced
- patient reported