Lack of association of NAMPT rs9770242 and rs59744560 polymorphisms with disease susceptibility and cardiovascular risk in patients with rheumatoid arthritis

被引:0
作者
Garcia-Bermudez, M. [2 ]
Gonzalez-Juanatey, C. [3 ]
Rodriguez-Rodriguez, L. [4 ]
Miranda-Filloy, J. A. [5 ]
Perez-Esteban, S. [6 ]
Vazquez-Rodriguez, T. R. [5 ]
Castaneda, S. [6 ]
Balsa, A. [7 ]
Fernandez-Gutierrez, B. [4 ]
Llorca, J. [8 ,9 ]
Gonzalez-Alvaro, I. [6 ]
Martin, J. [2 ]
Gonzalez-Gay, M. A. [1 ]
机构
[1] Hosp Univ Marques de Valdecilla, Dept Rheumatol, IFIMAV, Santander 39008, Spain
[2] CSIC, Inst Parasitol & Biomed Lopez Neyra, Granada, Spain
[3] Hosp Xeral Calde, Div Cardiol, Lugo, Spain
[4] Hosp Clin San Carlos, Dept Rheumatol, Madrid, Spain
[5] Hosp Xeral Calde, Dept Rheumatol, Lugo, Spain
[6] Hosp Univ La Princesa, Dept Rheumatol, IIS Princesa, Madrid, Spain
[7] Hosp Univ La Paz, Rheumatol Unit, Madrid, Spain
[8] Univ Cantabria, Sch Med, Dept Epidemiol & Computat Biol, E-39005 Santander, Spain
[9] CIBERESP, IFIMAV, Santander, Spain
关键词
rheumatoid arthritis; atherosclerosis; cardiovascular disease; genetics; NAMPT rs9770242 (-1001T > G) and rs59744560 (-948G > T); COLONY-ENHANCING FACTOR; INTIMA-MEDIA THICKNESS; ENDOTHELIAL DYSFUNCTION; SUBCLINICAL ATHEROSCLEROSIS; PROMOTER POLYMORPHISM; GENE POLYMORPHISMS; METABOLIC SYNDROME; INFLAMMATION; VISFATIN; EVENTS;
D O I
暂无
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective Visfatin is an adipokine encoded by the NAMPT (PBEFI) gene. In this study we assessed the potential association of two NAMPT gene polymorphism with disease susceptibility and cardiovascular (CV) risk in patients with rheumatoid arthritis (RA). Methods A total of 1,395 patients fulfilling the 1987 ACR classification criteria for RA and 1,230 matched controls, were genotyped for the NAMPT rs9770242 and rs59744560 gene polymorphism, located within the proximal promoter, using predesigned TaqMan single nucleotide polymorphism genotyping assay. Also, HLA-DRBI genotyping was performed using molecular based methods. In a second step, 1,196 patients in whom full information was available were assessed to determine the influence of NAMPT rs9770242 and rs59744560 polymorphisms in the development of CV events. Also, the potential influence of these polymorphisms in the development of subclinical atherosclerosis was assessed in a subgroup of patients with no history of CV events by brachial artery reactivity to determine flow-mediated endothelium-dependent and endothelium-independent vasodilatation (n=125) and by B-mode ultrasonography to determine the carotid artery intima-media thickness (n=105). Results No statistically significant differences in the allele or genotype frequencies for the NAMPT gene polymorphisms between RA patients and controls were found. A modest non significant lower frequency of the minor allele G of rs9770242 polymorphism was observed among patients with CV disease (20.62%) compared to those without CV disease (22.83%) (p=0.39). Also, a slight nonsignificant lower frequency of the minor allele T of rs59744560 polymorphism in patients with CV events (9.81%) compared with those RA patients who did not experience CV disease (13.07%) (p=0.1 I) was observed. Likewise, no significant association between the NAMPT polymorphisms with surrogate markers of subclinical atherosclerosis was found in patients with RA. Conclusion NAMPT rs9770242 and rs59744560 polymorphisms are not markers of disease susceptibility and CV disease in RA.
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页码:681 / 688
页数:8
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