Hong Qiong, Xu Jianhua, Xu Shengqian, Lian Li, Zhang Mingming, Ding Changhai
Department of Rheumatology and Immunology, First Affiliated Hospital of Anhui Medical University, Department of Endocrinology, 105 Hospital of People's Liberation Army, Arthritis Research Institute, First Affiliated Hospital of Anhui Medical University, Hefei, China and Menzies Research Institute Tasmania, University of Tasmania, Hobart, Tasmania, Australia. Department of Rheumatology and Immunology, First Affiliated Hospital of Anhui Medical University, Department of Endocrinology, 105 Hospital of People's Liberation Army, Arthritis Research Institute, First Affiliated Hospital of Anhui Medical University, Hefei, China and Menzies Research Institute Tasmania, University of Tasmania, Hobart, Tasmania, Australia.
Department of Rheumatology and Immunology, First Affiliated Hospital of Anhui Medical University, Department of Endocrinology, 105 Hospital of People's Liberation Army, Arthritis Research Institute, First Affiliated Hospital of Anhui Medical University, Hefei, China and Menzies Research Institute Tasmania, University of Tasmania, Hobart, Tasmania, Australia.
Rheumatology (Oxford). 2014 Nov;53(11):1994-2001. doi: 10.1093/rheumatology/keu173. Epub 2014 Jun 6.
The aim of this study was to describe the associations between serum levels of 25-hydroxyvitamin D [25(OH)D] and disease activity, inflammatory cytokines and bone loss/erosions in patients with RA.
The study included 130 patients with RA and 80 healthy controls. Serum 25(OH)D, IL-17 and IL-23 levels were detected by ELISA. Radiographic bone erosion was assessed using the van der Heijde modified Sharp score and BMD was measured using DXA.
There were no significant differences in age, gender and BMI between the RA and control groups. Serum level of 25(OH)D was markedly lower in the RA group than in the control group [43.12 nmol/l (s.d. 15.59) vs 57.93 (15.95), P < 0.01]. In RA patients, 25(OH)D levels were significantly and negatively associated with clinical parameters of disease activity including swollen joint count, tender joint count, joint pain degree, morning stiffness time and HAQ score and laboratory measures including platelets and ESR after adjustment for gender, age and BMI. They were also negatively associated with serum levels of IL-17 and IL-23. While 25(OH)D levels were not associated with radiographic bone erosions of RA, they were significantly lower in those with osteopenia and osteoporosis than in those with normal BMD (P < 0.01).
25(OH)D levels were reduced in patients with RA and were negatively associated with disease activity, IL-17/IL-23 and bone loss in RA. These suggest that vitamin D deficiency may play a role in the aetiology of RA.
本研究旨在描述类风湿关节炎(RA)患者血清25-羟基维生素D[25(OH)D]水平与疾病活动度、炎性细胞因子及骨质流失/侵蚀之间的关联。
本研究纳入了130例RA患者和80例健康对照者。采用酶联免疫吸附测定法(ELISA)检测血清25(OH)D、白细胞介素-17(IL-17)和白细胞介素-23(IL-23)水平。采用范德海伊德改良夏普评分评估放射学骨质侵蚀情况,使用双能X线吸收法(DXA)测量骨密度(BMD)。
RA组和对照组在年龄、性别和体重指数(BMI)方面无显著差异。RA组血清25(OH)D水平显著低于对照组[43.12纳摩尔/升(标准差15.59)对57.93(15.95),P<0.01]。在RA患者中,校正性别、年龄和BMI后,25(OH)D水平与疾病活动度的临床参数(包括肿胀关节计数、压痛关节计数、关节疼痛程度、晨僵时间和健康评估问卷(HAQ)评分)以及实验室指标(包括血小板和红细胞沉降率(ESR))显著负相关。它们还与血清IL-17和IL-23水平负相关。虽然25(OH)D水平与RA的放射学骨质侵蚀无关,但骨质疏松症和骨质减少患者的25(OH)D水平显著低于骨密度正常者(P<0.01)。
RA患者的25(OH)D水平降低,且与疾病活动度、IL-17/IL-23及RA骨质流失负相关。这些表明维生素D缺乏可能在RA的病因学中起作用。