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Updated: Oct 10, 2025

Imaging Features of Systemic Sclerosis-Associated Interstitial Lung Disease
Published on: June 16, 2020
The emerging association between bronchiectasis and systemic sclerosis: assessing prevalence and potential causality.
Rosemary Smith1, Megan Harrison2,3, Kay-Vin Lam4
1Department of General Medicine, Fiona Stanley Hospital, Perth, Western Australia, Australia.
Systemic sclerosis (SSc) patients show increased bronchiectasis risk, but not linked to disease duration. Oesophageal dysmotility was common, and bronchiectasis showed a negative association with interstitial lung disease (ILD).
Area of Science:
- Pulmonary Medicine
- Rheumatology
- Radiology
Background:
- Bronchiectasis is observed in systemic sclerosis (SSc).
- Potential causes include aspiration from oesophageal dysmotility, immunosuppressant use, and direct collagen deposition affecting airways.
Purpose of the Study:
- To determine bronchiectasis prevalence in SSc patients using high-resolution computed tomography (HRCT).
- To investigate associations between bronchiectasis and oesophageal dysmotility, demographics, SSc duration, or subclass.
Main Methods:
- Included 256 SSc patients from the Australian Scleroderma Cohort Study (ASCS) with thoracic HRCT.
- Reviewed HRCT for bronchiectasis and interstitial lung disease (ILD).
- Defined oesophageal dysmotility by symptoms and/or dilatation.
Main Results:
- 16.4% of participants had bronchiectasis.
- No significant association found between bronchiectasis and oesophageal dysmotility, demographics, or SSc duration/subclass.
- A negative association was observed between bronchiectasis and ILD (P=0.009).
Conclusions:
- SSc patients have an elevated risk of bronchiectasis.
- Bronchiectasis development may not solely relate to immunosuppression, given no link to SSc duration.
- Oesophageal dysmotility was nearly universal, precluding definitive conclusions on its role. Bronchiectasis and ILD were negatively associated.
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