Human epididymis protein 4 as a clinical biomarker in identifying interstitial lung disease in patients with idiopathic inflammatory myopathies

被引:7
|
作者
Sun, Feng [1 ]
Zhao, Jing [1 ]
Li, Yun [1 ]
Wang, Hongyan [1 ]
Cao, Xin [2 ]
Cheng, Wei [2 ]
Chen, Jiali [2 ]
机构
[1] Peking Univ, Peoples Hosp, Dept Rheumatol & Immunol, Beijing, Peoples R China
[2] Cent South Univ, Xiangya Hosp 2, Dept Rheumatol & Immunol, Changsha, Hunan, Peoples R China
基金
中国国家自然科学基金;
关键词
Idiopathic inflammatory myopathies; Human epididymis protein 4; Interstitial lung disease; Tumor biomarker; Clinical stratification;
D O I
10.1016/j.intimp.2022.109609
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Objective: Human epididymis protein 4 (HE4) can differentiate interstitial lung disease from patients with some rheumatic diseases. However, the clinical utility of HE4 in idiopathic inflammatory myopathies (IIM) remains unclear.Methods: 80 IIM patients and 91 age and gender-matched healthy controls (HCs) were recruited. Clinical and laboratory data were recorded at baseline and 12 weeks. HE4 was tested by the method of electrochemical luminescence.Results: Compared to HCs, the levels of HE4 significantly elevated in IIM patients. Patients with elevated HE4 had a higher interstitial lung disease (ILD) prevalence. Among patients with ILD, histological patterns of organizing pneumonia had higher HE4 levels than non-specific interstitial pneumonia. Further, there was a positive cor-relation between HE4 and the semi-quantitative CT grade (r = 0.778, p < 0.001) and a negative relation between HE4 and the percentage of forced vital capacity (p < 0.001) and diffusing capacity of the lung for carbon monoxide (DLco) (p = 0.001). An optimal cut-off value of HE4 (79.6 pmol/L) for distinguishing IIM-ILD was analyzed by ROC analysis with an AUC of 0.733 (p = 0.002). Regression analysis revealed that elevated HE4 independently identified IIM-related ILD (OR 34.8, 95 %CI, 3.58-338.14, p = 0.002). With the improvement after treatment, serum HE4 levels were significantly decreased (p = 0.006), accompanied by improved DLco% (p = 0.012).Conclusions: Serum HE4 was significantly elevated in patients with IIM and may be utilized as a serum biomarker to evaluate the disease severity and prognosis of IIM-related ILD.
引用
收藏
页数:8
相关论文
共 50 条
  • [21] Quantitative interstitial lung disease scores in idiopathic inflammatory myopathies: longitudinal changes and clinical implications
    Yeo, Jina
    Yoon, Soon Ho
    Kim, Ju Yeon
    Lee, Jeong Seok
    Lee, Eun Young
    Goo, Jin Mo
    Pourzand, Lila
    Goldin, Jonathan G.
    Kim, Grace-Hyun J.
    Ha, You-Jung
    RHEUMATOLOGY, 2023, 62 (11) : 3690 - 3699
  • [22] Computer Aided Lung Informatics, HRCT and PFT in Patients with Interstitial Lung Disease in Idiopathic Inflammatory Myopathies
    Narain, Sonali
    Shargani, Kourosh
    Ilic, Ivana
    Buttar, Irvind
    Marder, Galina
    ARTHRITIS & RHEUMATOLOGY, 2024, 76 : 2385 - 2388
  • [23] Human epididymis protein 4 as a new diagnostic biomarker for rheumatoid arthritis-associated interstitial lung disease
    Lin, T.
    Xu, S.
    Wang, Y.
    Nian, X.
    Shan, X.
    Jiang, T.
    Qiu, M.
    CLINICAL AND EXPERIMENTAL RHEUMATOLOGY, 2022, 40 (11) : 2167 - 2174
  • [24] Interstitial Lung Disease in Inflammatory Myopathies: Clinical Phenotypes and Prognosis
    Patrick D. W. Kiely
    Felix Chua
    Current Rheumatology Reports, 2013, 15
  • [25] INTERSTITIAL LUNG DISEASE IN INFLAMMATORY MYOPATHIES: CLINICAL AND IMMUNOSEROLOGICAL CHARACTERISTICS
    Leal Castro, S.
    Gomez, R.
    Perrotta, N.
    Pino, M. S.
    Laborde, H.
    Dubinsky, D.
    JCR-JOURNAL OF CLINICAL RHEUMATOLOGY, 2018, 24 : S169 - S169
  • [26] Interstitial Lung Disease in Inflammatory Myopathies: Clinical Phenotypes and Prognosis
    Kiely, Patrick D. W.
    Chua, Felix
    CURRENT RHEUMATOLOGY REPORTS, 2013, 15 (09)
  • [27] INTERSTITIAL LUNG DISEASE IN IDIOPATHIC INFLAMMATORY MYOPATHIES: A REPORT FROM THE REMICAM REGISTRY
    Cobo-Ibanez, T.
    Lopez-Longo, F. J.
    Joven, B.
    Maldonado, V.
    Llorente, I.
    Barbadillo, C.
    Gomez Gomez, A.
    Barrio Nogal, L.
    Almodovar, R.
    Lojo, L.
    Ruiz, L.
    Garcia de Yebenes, M. J.
    Nuno, L.
    ANNALS OF THE RHEUMATIC DISEASES, 2017, 76 : 908 - 908
  • [28] CLINICAL FEATURES OF INTERSTITIAL LUNG DISEASE ASSOCIATED WITH KOREAN IDIOPATHIC INFLAMMATORY MYOPATHIES ACCORDING TO THE AUTOANTIBODY PROFILE
    Chung, Sang Wan
    Kim, Jinhyun
    Yoo, In Seol
    Hong, Seung-Jae
    Lee, Yeon-Ah
    Kang, Seong Wook
    Shim, Seungcheol
    Choi, In Ah
    Chang, Sung Hae
    ANNALS OF THE RHEUMATIC DISEASES, 2019, 78 : 1210 - 1211
  • [29] Interstitial lung disease (ILD) in Chinese patients with inflammatory myopathies
    Bun-Hey, Fung
    Cheuk-Wan, Yim
    Ping-Wing, Ng
    NEUROMUSCULAR DISORDERS, 2006, 16 : S168 - S169
  • [30] Recognition of Idiopathic Inflammatory Myopathies Underlying Interstitial Lung Diseases
    Morina, Giulia
    Sambataro, Domenico
    Libra, Alessandro
    Palmucci, Stefano
    Colaci, Michele
    La Rocca, Gaetano
    Ferro, Francesco
    Carli, Linda
    Baldini, Chiara
    Liuzzo, Santa Valentina
    Vancheri, Carlo
    Sambataro, Gianluca
    DIAGNOSTICS, 2025, 15 (03)