Ha You Jung, Kang Eun-Jin, Lee Sang-Won, Lee Soo-Kon, Park Yong-Beom, Song Jung-Soo, Choi Sang Tae
Division of Rheumatology, Department of Internal Medicine, Seoul National University Bundang Hospital, Seongnam, Korea.
Division of Rheumatology, Department of Internal Medicine, Busan Medical Center, Busan, Korea.
J Korean Med Sci. 2014 Sep;29(9):1199-204. doi: 10.3346/jkms.2014.29.9.1199. Epub 2014 Sep 2.
Our study aimed to investigate whether serum leucine-rich alpha-2-glycoprotein (LRG) levels are elevated in patients with rheumatoid arthritis (RA). In addition, we assessed their correlation with disease activity parameters and pro-inflammatory cytokine, tumor necrosis factor-α (TNF-α). Our study included 69 patients with RA and 48 age- and sex-matched healthy controls. Serum concentrations of TNF-α and LRG were determined by enzyme-linked immunosorbent assay. Serum LRG concentrations were significantly elevated in patients with RA compared with those in healthy controls (30.8 ± 14.4 vs. 22.2 ± 6.1 ng/mL; P<0.001). In patients with RA, serum LRG levels were found to be correlated with disease activity score 28 (DAS28), erythrocyte sedimentation rate, and C-reactive protein levels (γ=0.671; γ=0.612; and γ=0.601, P<0.001, respectively), but not with serum TNF-α levels. Serum LRG levels in patients with an active disease status (DAS28≥2.6) were significantly higher than those in remission (DAS28<2.6) (36.45 ± 14.36 vs. 24.63 ± 8.81 ng/mL; P<0.001). Our findings suggest that serum LRG could contribute to the inflammatory process independent of TNF-α and it may be a novel biomarker for assessing inflammatory activity in patients with RA.
我们的研究旨在调查类风湿关节炎(RA)患者的血清富含亮氨酸的α-2-糖蛋白(LRG)水平是否升高。此外,我们评估了其与疾病活动参数以及促炎细胞因子肿瘤坏死因子-α(TNF-α)的相关性。我们的研究纳入了69例RA患者和48例年龄及性别匹配的健康对照者。采用酶联免疫吸附测定法测定血清TNF-α和LRG浓度。与健康对照者相比,RA患者的血清LRG浓度显著升高(30.8±14.4 vs. 22.2±6.1 ng/mL;P<0.001)。在RA患者中,发现血清LRG水平与疾病活动评分28(DAS28)、红细胞沉降率和C反应蛋白水平相关(γ分别为0.671、0.612和0.601,P均<0.001),但与血清TNF-α水平无关。疾病活动状态为DAS28≥2.6的患者血清LRG水平显著高于缓解期(DAS28<2.6)的患者(36.45±14.36 vs. 24.63±8.81 ng/mL;P<0.001)。我们的研究结果表明,血清LRG可能独立于TNF-α参与炎症过程,并且可能是评估RA患者炎症活动的一种新型生物标志物。