Oregón-Romero Edith, Vázquez-Del Mercado Mónica, Navarro-Hernández Rosa Elena, Torres-Carrillo Norma, Martínez-Bonilla Gloria, Estrada-García Iris, Rangel-Villalobos Héctor, Muñoz-Valle José Francisco
Centro Universitario de Ciencias de la Salud, Universidad de Guadalajara, 44340, Guadalajara, Jalisco, Mexico.
Rheumatol Int. 2006 Nov;27(1):53-9. doi: 10.1007/s00296-006-0159-7. Epub 2006 Jul 27.
We investigate the clinical association of tumor necrosis factor receptor 2 (TNFR2) M196R polymorphism with rheumatoid arthritis (RA) and knee osteoarthritis (OA). Acute phase reactants, lipid profile, sTNFR2 levels, disease activity-disability indexes, and TNFR2 M196R polymorphism were analyzed in 50 RA, 50 knee OA patients, and 120 healthy subjects (HS). The M/M genotype frequency was 0.74 (RA), 0.80 (OA), and 0.64 (HS). The M/R genotype frequency was RA (0.26), OA (0.20), and HS (0.29). The R/R genotype was observed only in HS (0.07). The M allele was associated with OA (P = 0.0137, OR = 2.43). Total cholesterol, triglyceride levels, apolipoprotein A-I and B showed significant differences (P < 0.05). The highest sTNFR2 levels were observed in RA and OA (P = 0.001), however M/M and M/R carriers do not correlate with sTNFR2 production. Our findings suggest an association of the M allele with knee OA. In addition, high sTNFR2 levels in RA and OA were found.
我们研究了肿瘤坏死因子受体2(TNFR2)M196R多态性与类风湿关节炎(RA)及膝骨关节炎(OA)的临床关联。对50例RA患者、50例膝OA患者及120名健康受试者(HS)分析了急性期反应物、血脂谱、可溶性TNFR2(sTNFR2)水平、疾病活动-残疾指数及TNFR2 M196R多态性。M/M基因型频率在RA中为0.74,在OA中为0.80,在HS中为0.64。M/R基因型频率在RA中为0.26,在OA中为0.20,在HS中为0.29。仅在HS中观察到R/R基因型(0.07)。M等位基因与OA相关(P = 0.0137,比值比[OR]=2.43)。总胆固醇、甘油三酯水平、载脂蛋白A-I和载脂蛋白B存在显著差异(P < 0.05)。在RA和OA中观察到最高的sTNFR2水平(P = 0.001),然而M/M和M/R携带者与sTNFR2产生无关。我们的研究结果提示M等位基因与膝OA有关。此外,发现RA和OA中sTNFR2水平较高。