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抗黑色素瘤分化相关基因5抗体阳性幼年皮肌炎的临床特征

[Clinical characteristics of anti-melanoma differentiation associated gene 5 antibody-positive juvenile dermatomyositis].

作者信息

Hou J, Li J G, Yan Y C, Zhou Z X, Ding Y C, Xu Y J, Wang X N

机构信息

Department of Rheumatology and Immunology, Capital Center for Children's Health, Capital Medical University, Capital Institute of Pediatrics, Beijing 100020, China.

Department of Radiology, Capital Center for Children's Health, Capital Medical University, Capital Institute of Pediatrics, Beijing 100020, China.

出版信息

Zhonghua Er Ke Za Zhi. 2025 Sep 2;63(9):1011-1016. doi: 10.3760/cma.j.cn112140-20250514-00413.

Abstract

To analyze the clinical characteristics of anti-melanoma differentiation associated gene 5 (MDA5) antibody-positive juvenile dermatomyositis (JDM) patients. A retrospective case-control study was conducted. The positive group included 18 children with anti-MDA5 antibody-positive JDM who were admitted to the Department of Rheumatology and Immunology at Capital Center for Children's Health with Capital Medical University between January 2016 and January 2023. Another 36 children with anti-MDA5 antibody-negative JDM hospitalized during the same period were enrolled as the negative group. Based on the extent of pulmonary involvement and pulmonary CT scores, the MDA5-positive group was further divided into severe pulmonary involvement and non-severe pulmonary involvement subgroups. Chi-square test and Kruskal-Wallis test were used to compare clinical features, laboratory test results between groups. Among the 18 patients in the MDA5-positive group, 7 were male and 11 were female, with an age of onset of 5.0 (2.6, 9.4) years and disease duration of 6.0 (4.0, 9.3) months. The MDA5-negative group included 36 cases (14 male, 22 female), with an age of onset of 4.9 (2.0, 7.0) years and disease duration of 5.0 (1.8, 7.0) months. The MDA5-positive group exhibited significantly higher rates of arthritis, skin ulcers, and interstitial lung disease (ILD), along with elevated serum ferritin (SF) and erythrocyte sedimentation rate levels compared to the MDA5-negative group (9/18 11% (4/36), 6/18 3% (1/36), 16/18 33% (12/36), 327 (141, 518) 131 (68, 257) μg/L, 17.5 (12.5, 26.8) 11.0 (5.0, 13.0) mm/1 h, ²=7.92, 7.41, 14.84, =2.50, 2.87, all 0.05). Conversely, the MDA5-positive group had lower rates of muscle weakness and lower creatine kinase levels (5/18 75% (27/36), 58.5 (49.3, 97.5) 225.0 (68.0, 695.5) U/L, ²=11.08, =-2.94, both 0.05). Severe pulmonary involvement 6 cases and non-severe pulmonary involvement subgroups 12 cases. Among the MDA5-positive patients, those in the severe pulmonary involvement subgroup had an older age at onset and higher rates of muscle weakness as well as hydroxybutyrate dehydrogenase (HBDH), lactate dehydrogenase (LDH), SF, and Krebs von den Lungen-6 (KL-6) compared to the non-severe subgroup (all 0.05). In the MDA5-positive group, 17 patients improved after treatment with glucocorticoids combined with immunosuppressants, while One died due to rapidly progressive ILD. Anti-MDA5 antibody-positive JDM is characterized by typical skin rashes, a high incidence of arthritis and skin ulcers, relatively mild muscle involvement, but is prone to ILD. Among MDA5-positive patients, those with older age at onset, muscle involvement (manifested as muscle weakness and elevated muscle enzymes (LDH, HBDH)), or significantly elevated KL-6 and SF levels are more likely to develop severe pulmonary complications.

摘要

分析抗黑色素瘤分化相关基因5(MDA5)抗体阳性的幼年皮肌炎(JDM)患者的临床特征。进行了一项回顾性病例对照研究。阳性组包括2016年1月至2023年1月期间在首都医科大学附属北京儿童医院风湿免疫科住院的18例抗MDA5抗体阳性的JDM患儿。同期住院的另外36例抗MDA5抗体阴性的JDM患儿作为阴性组。根据肺部受累程度和肺部CT评分,MDA5阳性组进一步分为重度肺部受累和非重度肺部受累亚组。采用卡方检验和Kruskal-Wallis检验比较组间临床特征、实验室检查结果。MDA5阳性组18例患者中,男性7例,女性11例,发病年龄5.0(2.6,9.4)岁,病程6.0(4.0,9.3)个月。MDA5阴性组36例(男性14例,女性22例),发病年龄4.9(2.0,7.0)岁,病程5.0(1.8,7.0)个月。与MDA5阴性组相比,MDA5阳性组关节炎、皮肤溃疡和间质性肺病(ILD)的发生率显著更高,血清铁蛋白(SF)和红细胞沉降率水平也升高(9/18 50%(4/36),6/18  33%(1/36),16/18  89%(12/36),327(141,518)  131(68,257)μg/L,17.5(12.5,26.8)  11.0(5.0,13.0)mm/1 h,χ²=7.92,7.41,14.84,Z=2.50,2.87,均P<0.05)。相反,MDA5阳性组肌无力发生率较低,肌酸激酶水平也较低(5/18  28%(27/36),58.5(49.3,97.5)  225.0(68.0,695.5)U/L,χ²=11.08,Z=-2.94,均P<0.05)。重度肺部受累6例,非重度肺部受累亚组12例。在MDA5阳性患者中,重度肺部受累亚组患者的发病年龄较大,肌无力发生率以及羟丁酸脱氢酶(HBDH)、乳酸脱氢酶(LDH)、SF和肺表面活性物质相关蛋白A(KL-6)水平均高于非重度亚组(均P<0.05)。在MDA5阳性组中,17例患者经糖皮质激素联合免疫抑制剂治疗后病情好转,1例因快速进展性ILD死亡。抗MDA5抗体阳性的JDM具有典型皮疹、关节炎和皮肤溃疡发生率高、肌肉受累相对较轻但易发生ILD的特点。在MDA5阳性患者中,发病年龄较大、有肌肉受累(表现为肌无力和肌酶(LDH、HBDH)升高)或KL-6和SF水平显著升高者更易发生严重肺部并发症。

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