4.7 Article

Quantitative interstitial lung disease scores in idiopathic inflammatory myopathies: longitudinal changes and clinical implications

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RHEUMATOLOGY
卷 -, 期 -, 页码 -

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OXFORD UNIV PRESS
DOI: 10.1093/rheumatology/kead122

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idiopathic inflammatory myopathy; interstitial lung disease; lung transplant-free survival; quantitative score

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This study investigated the longitudinal changes and clinical significance of computer-aided quantitative scores from high-resolution CT (HRCT) images in patients with idiopathic inflammatory myopathies-related interstitial lung disease (IIMs-ILD). The results showed that QILD scores were related to lung function, ILD progression, and prognosis, with UIP patterns being associated with a higher risk of QILD progression. These findings suggest that QILD scores may serve as potential imaging biomarkers in IIMs-ILD.
Objectives To investigate computer-aided quantitative scores from high-resolution CT (HRCT) images and determine their longitudinal changes and clinical significance in patients with idiopathic inflammatory myopathies (IIMs)-related interstitial lung disease (IIMs-ILD). Methods The clinical data and HRCT images of 80 patients with IIMs who underwent serial HRCT scans at least twice were retrospectively analysed. Quantitative ILD (QILD) scores (%) were calculated as the sum of the extent of lung fibrosis, ground-glass opacity, and honeycombing. The individual time-estimated Delta QILD between two consecutive scans was derived using a linear approximation of yearly changes. Results The baseline median QILD (interquartile range) scores in the whole lung were 28.1% (19.1-43.8). The QILD was significantly correlated with forced vital capacity (r = -0.349, P = 0.002) and diffusing capacity for carbon monoxide (r = -0.381, P = 0.001). For Delta QILD between the first two scans, according to the visual ILD subtype, QILD aggravation was more frequent in patients with usual interstitial pneumonia (UIP) than non-UIP (80.0% vs 44.4%, P = 0.013). Multivariable logistic regression analyses identified UIP was significantly related to radiographic ILD progression (Delta QILD >2%, P = 0.015). Patients with higher baseline QILD scores (>28.1%) had a higher risk of lung transplantation or death (P = 0.015). In the analysis of three serial HRCT scans (n = 41), dynamic Delta QILD with four distinct patterns (improving, worsening, convex and concave) was observed. Conclusion QILD changes in IIMs-ILD were dynamic, and baseline UIP patterns seemed to be related to a longitudinal progression in QILD. These may be potential imaging biomarkers for lung function, changes in ILD severity and prognosis in IIMs-ILD.

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