Department of Rheumatology and Immunology, Children's Hospital of Chongqing Medical University, 136, Zhongshan 2nd Road, Yuzhong District, Chongqing, 400014, People's Republic of China.
Ministry of Education Key Laboratory of Child Development and Disorders, National Clinical Research Center for Child Health and Disorders, China International Science and Technology Cooperation Base of Child Development and Critical Disorders, Chongqing Key Laboratory of Child Infection and Immunity, Children's Hospital of Chongqing Medical University, Chongqing, People's Republic of China.
Pediatr Rheumatol Online J. 2021 Jul 12;19(1):112. doi: 10.1186/s12969-021-00587-1.
To analyze the levels of high mobility group box 1 (HMGB1) protein on different courses of juvenile idiopathic arthritis (JIA).
In our prospective longitudinal study, children with JIA were included with their blood samples collected at the first visit, 1-month, 3-month, and 6-month follow-up, respectively. Samples were also collected from healthy controls and children with reactive arthritis at the first visit. Levels of HMGB1 were determined using enzyme-linked immunosorbent assays. Clinical disease characteristics and routine laboratory findings were analyzed as well.
A total of 64 children were enrolled, of whom 31 (48.4%) were female. The median age at the first visit for participants with JIA was 9.25 years (range, 1.42-15.42) and the median duration of disease was 2.38 months (range, 1.53-49.31). Serum HMGB1 levels at the first visit were significantly elevated in children with systemic JIA compared with other groups, and so were in enthesitis-related arthritis versus healthy controls. Significant correlations were established at the first visit between HMGB1 levels and duration of disease, C-reactive protein, percentage of neutrophils, and ferritin. Data from all samples revealed that serum HMGB1 levels in JIA were significantly associated with erythrocyte sedimentation rates, C-reactive protein, percentage of neutrophils, and disease activity scores.
Serum HMGB1 may be associated with clinical disease activity of JIA and specifically increased at the first visit in children with systemic JIA, suggesting its function as a sensitive inflammatory marker. Further large-scale studies are warranted to explore its spectrum in JIA.
分析不同病程幼年特发性关节炎(JIA)患儿高迁移率族蛋白 B1(HMGB1)水平。
本前瞻性纵向研究纳入 JIA 患儿,分别于首次就诊时、1 个月、3 个月和 6 个月时采集血样,同时收集健康对照者和反应性关节炎患儿的首次就诊时的血样。采用酶联免疫吸附试验测定 HMGB1 水平。分析临床疾病特征和常规实验室检查结果。
共纳入 64 例患儿,其中 31 例(48.4%)为女性。JIA 患儿首次就诊时的中位年龄为 9.25 岁(范围:1.42-15.42),疾病的中位病程为 2.38 个月(范围:1.53-49.31)。与其他组相比,全身型 JIA 患儿的血清 HMGB1 水平在首次就诊时显著升高,与健康对照者相比,附着点相关关节炎患儿的血清 HMGB1 水平也显著升高。首次就诊时,HMGB1 水平与疾病病程、C 反应蛋白、中性粒细胞百分比和铁蛋白呈显著相关。所有样本的数据表明,JIA 患儿的血清 HMGB1 水平与红细胞沉降率、C 反应蛋白、中性粒细胞百分比和疾病活动评分显著相关。
血清 HMGB1 可能与 JIA 的临床疾病活动相关,尤其是在全身型 JIA 患儿的首次就诊时显著升高,提示其作为一种敏感的炎症标志物的作用。需要进一步的大规模研究来探索其在 JIA 中的作用。