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抗黑色素瘤分化相关基因-5 抗体阳性皮肌炎伴肝功能障碍:更高死亡风险的警告信号。

Anti-melanoma differentiation-associated gene-5 antibody-positive dermatomyositis with liver dysfunction: a warning sign of higher death risk.

机构信息

Department of Rheumatology and Immunology, Peking University People's Hospital, Beijing, China.

Department of Geriatry, Rheumatology and Immunology, the Eighth People's Hospital of Hengshui, Hengshui, China.

出版信息

Clin Rheumatol. 2024 Nov;43(11):3389-3397. doi: 10.1007/s10067-024-07093-1. Epub 2024 Sep 17.

Abstract

This study aimed to investigate and analyze the clinical and immunological features of patients with anti-melanoma differentiation-associated gene-5 antibody-positive dermatomyositis (MDA5  DM) complicated with clinical liver dysfunction. A cohort of 85 patients diagnosed with MDA5  DM admitted into Peking University People's Hospital from 2006 to 2023 were retrospectively enrolled in this study. Clinical characteristics and survival status were collected and analyzed. Clinical liver dysfunction occurred in 28% (24/85) of MDA5  DM patients. Patients with clinical liver dysfunction were more likely to have muscle impairment (83.3% vs. 52.5%, P = 0.009) and rapidly progressive ILD (72.7% vs. 47.4%, P = 0.027). Lactate dehydrogenase (LDH) (378.5 (296.0,453.8) U/L vs. 280.0 (218.0,355.0) U/L, P = 0.002) and ferritin (FER) (883.0 (279.8,2100.5) ng/mL vs. 293.5.0 (84.0,862.7) ng/mL, P = 0.040) were significantly elevated and total numbers of lymphocytes (827.2 ± 517.2 /μL vs. 1301.8 ± 720.9 /μL, P = 0.042), and CD4  T cells (403.8 ± 315.9 /μL vs. 548.6 ± 257.7 /μL, P = 0.045) were significantly decreased in patients with clinical liver function. Muscle weakness (OR 5.184, 95% CI 1.305, 20.595, P = 0.019) was identified as an independent risk factor for clinical liver dysfunction. Clinical liver dysfunction was identified as an independent risk factor for poor prognosis in patients with MDA5  DM (HR = 4.030, 95% Cl 1.233, 13.176, P = 0.021), with an 18-month survival rate of 69%. Liver dysfunction is one of the extramuscular manifestations in patients with MDA5  DM and might be associated with a poor prognosis.

摘要

本研究旨在探讨和分析抗黑色素瘤分化相关基因 5 抗体阳性皮肌炎(MDA5 DM)合并临床肝功能异常患者的临床和免疫学特征。回顾性纳入 2006 年至 2023 年期间北京大学人民医院收治的 85 例 MDA5 DM 患者,收集并分析其临床特征和生存状况。临床肝功能异常发生于 28%(24/85)的 MDA5 DM 患者中。有临床肝功能异常的患者更可能存在肌肉损伤(83.3% vs. 52.5%,P = 0.009)和快速进展性间质性肺病(ILD)(72.7% vs. 47.4%,P = 0.027)。乳酸脱氢酶(LDH)(378.5(296.0,453.8)U/L vs. 280.0(218.0,355.0)U/L,P = 0.002)和铁蛋白(FER)(883.0(279.8,2100.5)ng/mL vs. 293.5.0(84.0,862.7)ng/mL,P = 0.040)显著升高,淋巴细胞总数(827.2±517.2/μL vs. 1301.8±720.9/μL,P = 0.042)和 CD4+T 细胞(403.8±315.9/μL vs. 548.6±257.7/μL,P = 0.045)显著减少。肌肉无力(OR 5.184,95%CI 1.305,20.595,P = 0.019)是临床肝功能异常的独立危险因素。临床肝功能异常是 MDA5 DM 患者预后不良的独立危险因素(HR = 4.030,95%Cl 1.233,13.176,P = 0.021),18 个月生存率为 69%。肝功能异常是 MDA5 DM 患者的一种肌肉外表现,可能与预后不良相关。

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