Clinical features and survival analysis of 40 cases of anti-MDA5 antibody-positive dermatomyositis complicated with interstitial lung disease

IF 4.6 2区 医学 Q1 Medicine Arthritis Research & Therapy Pub Date : 2025-02-13 DOI:10.1186/s13075-025-03485-z
Kaikai Zhao, Juan Zhang, Qunyu Kong, Yong Zhang, Cong Li, Kaikai Huo, Na Fan, Wenjing Deng, Jie Shi, Chunya Wang, Xueyi Li, Shuanying Yang, Ping Fang
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Abstract

Several studies have shown that patients with anti-MDA5 antibody-positive dermatomyositis (anti-MDA5 antibody + DM) have an increased risk of developing rapid progression of interstitial lung disease (RPILD), which is associated with poor prognosis and high mortality. However, diagnosis and treatment are often delayed due to atypical early clinical features and heterogeneity. Therefore, clinical features should be identified to establish a prognosis model for early identification and intervention, thereby improving the clinical prognosis of patients. The study aimed to investigate the clinical features, risk factors, treatment strategy, and construct a survival prognosis model for anti-MDA5 antibody + DM patients with ILD. A total of 40 anti-MDA5 antibody + DM-ILD patients admitted to the Department of Pulmonary and Critical Care Medicine and the Department of Rheumatology and Immunology in the Second Affiliated Hospital of Xi 'an Jiaotong University from September 2018 to May 2022 were retrospectively analyzed. Prognostic factors correlated with overall survival (OS) during hospitalization were identified by multivariate Cox regression analysis, and a nomogram was established. The nomogram was internally validated using C-index and time-dependent (at 1-, 2-, and 3- months) calibration curves with 1000 iterations of bootstrap resampling. Moreover, the optimal truncation values for continuous variables and Kaplan–Meier (K-M) curves were determined, which were used to analyze the difference in survival between groups. Finally, time-dependent decision curve analysis (DCA) was employed to validate the clinical value of the nomogram. Significant differences were found between the survival group and the non-survival group in terms of age, oxygenation index, extent of lung lesions, diffuse alveolar damage (DAD) and nonspecific interstitial pneumonia (NSIP), and LDH, GLU, CEA, ferritin, CRP levels in serum (P < 0.05). Multivariate regression analysis revealed that increased NSIP in high-resolution computed tomography (HRCT) and ALT,LDH,CEA,CRP were risk factors for poor prognosis (P < 0.05). A nomogram diagram was constructed according to the final multiple Cox model to predict the 1-, 2-, and 3-month OS. According to ALT, AST, LDH, CEA, and CRP cutoff values, the KM algorithm was used to estimate the survival curve (P < 0.05). DCA curves were drawn for the model-dependent variables included treatment style, NSIP, ALT, AST, LDH, CEA, and CRP. This indicated that the nomogram yielded a higher net benefit compared to other single prognostic factors, and the cutoff value grouping model showed better practical application value. Combined treatment with glucocorticoids and immunosuppressants was a protective factor for long-term survival. Survival analysis indicated that patients with anti-MDA5 + DM-ILD could benefit from combined treatment for longer survival. Anti-MDA5 antibody + DM is prone to interstitial lung disease, poor prognosis, and high mortality. Risk prediction model could help us paying attention to these features which may allow the early identification of high-risk patients and promote timely diagnosis and treatment.
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抗mda5抗体阳性皮肌炎合并间质性肺疾病40例临床特点及生存分析
多项研究表明,抗mda5抗体阳性皮肌炎(抗mda5抗体+ DM)患者发生间质性肺疾病(RPILD)快速进展的风险增加,与预后差和高死亡率相关。然而,由于不典型的早期临床特征和异质性,诊断和治疗往往延迟。因此,应识别临床特征,建立预后模型,进行早期识别和干预,从而改善患者的临床预后。本研究旨在探讨抗mda5抗体+ DM合并ILD患者的临床特点、危险因素、治疗策略,并构建生存预后模型。回顾性分析西安交通大学第二附属医院2018年9月至2022年5月肺重症医学科和风湿病免疫科收治的抗mda5抗体+ DM-ILD患者40例。通过多因素Cox回归分析确定与住院期间总生存期(OS)相关的预后因素,并建立nomogram。使用c指数和时间相关(1个月、2个月和3个月)校准曲线进行内部验证,并进行1000次自举重采样。并确定连续变量的最优截断值和Kaplan-Meier (K-M)曲线,用于分析组间生存差异。最后,采用时间相关决策曲线分析(DCA)验证图的临床价值。生存组与非生存组在年龄、氧合指数、肺病变程度、弥漫性肺泡损伤(DAD)、非特异性间质性肺炎(NSIP)、血清LDH、GLU、CEA、铁蛋白、CRP水平等方面差异均有统计学意义(P < 0.05)。多因素回归分析显示,高分辨率计算机断层扫描(HRCT) NSIP升高及ALT、LDH、CEA、CRP为预后不良的危险因素(P < 0.05)。根据最终的多重Cox模型构建nomogram diagram来预测1、2、3个月的OS。根据ALT、AST、LDH、CEA、CRP的截止值,采用KM算法估计生存曲线(P < 0.05)。绘制模型相关变量的DCA曲线,包括治疗方式、NSIP、ALT、AST、LDH、CEA和CRP。这表明nomogram比其他单一预后因子具有更高的净效益,且截止值分组模型具有更好的实际应用价值。糖皮质激素和免疫抑制剂联合治疗是长期生存的保护因素。生存分析表明,抗mda5 + DM-ILD患者可以从联合治疗中获益,延长生存期。抗mda5抗体+ DM易发生间质性肺疾病,预后差,死亡率高。风险预测模型可以帮助我们关注这些特征,从而及早发现高危患者,促进及时诊断和治疗。
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来源期刊
CiteScore
8.60
自引率
2.00%
发文量
261
审稿时长
14 weeks
期刊介绍: Established in 1999, Arthritis Research and Therapy is an international, open access, peer-reviewed journal, publishing original articles in the area of musculoskeletal research and therapy as well as, reviews, commentaries and reports. A major focus of the journal is on the immunologic processes leading to inflammation, damage and repair as they relate to autoimmune rheumatic and musculoskeletal conditions, and which inform the translation of this knowledge into advances in clinical care. Original basic, translational and clinical research is considered for publication along with results of early and late phase therapeutic trials, especially as they pertain to the underpinning science that informs clinical observations in interventional studies.
期刊最新文献
Human MAGI1 expression in endothelial cells protects from the development of localized and systemic scleroderma in mice. Predictors of glucocorticoid-free clinical remission in patients with newly diagnosed microscopic polyangiitis and granulomatosis with polyangiitis: a retrospective cohort study using a nationwide registry in Japan (J-CANVAS). Soluble factors released from fibroblast-like synoviocytes of JIA patients with future extended course can condition persistent JIA synovial fibroblasts for increased IL-6 production. An interpretable machine learning model integrating clinical and CT radiomic features for the detection of interstitial lung disease in idiopathic inflammatory myopathies. Development and validation of a risk score for serious infection in patients with rheumatic diseases receiving prolonged high-dose glucocorticoids.
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