4.3 Review

Recent innovations in the screening and diagnosis of systemic sclerosis-associated interstitial lung disease

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EXPERT REVIEW OF CLINICAL IMMUNOLOGY
卷 19, 期 6, 页码 613-626

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TAYLOR & FRANCIS LTD
DOI: 10.1080/1744666X.2023.2198212

关键词

Systemic sclerosis; interstitial lung disease; screening; diagnosis; HRCT; biomarkers; lung ultrasound; oscillometry

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Interstitial lung disease (ILD) is the leading cause of mortality in patients with systemic sclerosis (SSc). Early recognition and intervention are critical with the FDA approval of two medications and a pipeline of novel therapeutics in trials. There is a need to develop and validate more innovative screening modalities to improve the diagnosis of SSc-ILD.
Introduction: Interstitial lung disease (ILD) is the leading cause of mortality in patients with systemic sclerosis (SSc). Risk of developing progressive ILD is highest among patients with diffuse cutaneous disease, positive anti-topoisomerase I antibody, and elevated acute phase reactants. With the FDA approval of two medications and a pipeline of novel therapeutics in trials, early recognition and intervention is critical. High-resolution computed tomography of the chest is the current gold standard test for diagnosis of ILD. Yet, it is not offered as a screening tool to all patients due to which ILD can be missed in up to a third of patients. There is a need to develop and validate more innovative screening modalities.Areas covered: In this review, we provide an overview of screening and diagnosis of SSc-ILD, highlighting the recent innovations particularly the role of soluble serologic, radiomic (quantitative lung imaging, lung ultrasound), and breathomic (exhaled breath analysis) biomarkers in the early detection of SSc-ILD.Expert opinion: There is remarkable progress in the development of new radiomics and serum biomarkers in diagnosing SSc-ILD. There is an urgent need for conceptualizing and testing composite ILD screening strategies that incorporate these biomarkers.

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