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Background: As fibrosing interstitial lung diseases (fILDs) are associated with high mortality, monitoring of disease activity under treatment is highly relevant. Krebs von den Lungen-6 (KL-6) is associated with the presence and severity of different fILDs, mainly in Asian patient populations.
Objectives: Our aim was to evaluate KL-6 as a predictive biomarker in fILDs in Caucasian patients.
Methods: Consecutive patients with fILDs were recruited prospectively and serum concentrations of KL-6 were measured at baseline (BL), after 6 and 12 months (6 Months, 12 Months). Clinical characteristics including pulmonary function tests were assessed at 6-monthly visits and correlated with KL-6 BL levels as well as with KL-6 level changes.
Results: A total of 47 fILD patients were included (mean age: 65 years, 68% male). KL-6 levels at BL were significantly higher in fILD patients than in healthy controls (n = 44, mean age: 45, 23% male) (ILD: 1,757 ± 1960 U/mL vs. control: 265 ± 107 U/mL, p < 0.0001). However, no differences were noted between ILD subgroups. KL-6 decreased significantly under therapy (6M∆BL-KL6: -486 ± 1,505 mean U/mL, p = 0.032; 12M∆BL-KL6: -547 ± 1,782 mean U/mL, p = 0.041) and KL-6 level changes were negatively correlated with changes in pulmonary function parameters (forced vital capacity [FVC]: r = -0.562, p < 0.0001; DLCOSB: r = -0.405, p = 0.013). While neither absolute KL-6 levels at BL nor KL-6 level changes were associated with ILD progression (FVC decline ≥10%, DLCOSB decline ≥15% or death), patients with a stable FVC showed significantly decreasing KL-6 levels (p = 0.022).
Conclusions: A decline of KL-6 under therapy correlated with a clinically relevant stabilization of lung function. Thus, KL-6 might serve as a predictive biomarker, which however must be determined by larger prospective cohorts.
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http://dx.doi.org/10.1159/000531945 | DOI Listing |
Ital J Pediatr
August 2025
Department of Respiratory Medicine, Beijing Children's Hospital, National Center for Children's Health, Capital Medical University, No.56 Nanlishi Road, Beijing, China.
Background: Surfactant dysfunction disorders are a group of rare diseases that lead to childhood interstitial lung diseases (ILD). SFTPC, ABCA3, and NKX2-1 are the three genetic forms of this condition. The differences in clinical presentations and prognostic outcomes across these genotypes are not well understood, warranting comparative analysis.
View Article and Find Full Text PDFZhonghua Er Ke Za Zhi
September 2025
Department of Rheumatology and Immunology, Capital Center for Children's Health, Capital Medical University, Capital Institute of Pediatrics, Beijing 100020, China.
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.
View Article and Find Full Text PDFClin Cosmet Investig Dermatol
August 2025
Department of Dermatology, Affiliated Hospital 2 of Nantong University, Nantong, People's Republic of China.
Objective: To comprehensively characterize clinical features, diagnostic challenges, and prognostic biomarkers of anti-MDA5 antibody-positive dermatomyositis (MDA5-DM), incorporating transcriptomic analysis to elucidate underlying molecular mechanisms.
Methods: We conducted a retrospective analysis of 29 MDA5-DM patients, collecting detailed clinical and laboratory data. Prognostic factors were identified using LASSO regression, validated by Cox proportional hazards and Kaplan-Meier survival analyses.
BMC Pulm Med
August 2025
Department of Rheumatology, Xi'an Fifth Hospital, 112 Xiguanzheng Street, Lianhu District, Xian, Shaanxi, 710000, People's Republic of China.
Background: Interstitial lung disease (ILD) is a severe complication affecting 10-30% of rheumatoid arthritis (RA) patients. Current diagnostic methods typically detect ILD only after substantial lung damage has occurred. This delay emphasizes the need for early detection strategies.
View Article and Find Full Text PDFIntroduction: Connective tissue disease (CTD) commonly affects the lungs, with interstitial lung disease (ILD) as its main complication; although cyclophosphamide (CTX) is the standard immunosuppressant for CTD-ILD, the optimal route of administration (oral vs. intravenous) remains unclear. This research aimed to analyze the efficacy of oral and intravenous CTX in the treatment of CTD-ILD and analysis of its influencing factors.
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