About this trial
A complex interaction between demographic, environmental and genetic mechanisms impact the onset, severity and outcome of ILD-SARDs through dysregulation of the immune system and lung pro-biotic pathways. Comorbidity and genetic risk indicate that there are overlapping pathogenic mechanisms among SARDs, some of which underlie ILD in different SARDs.
The purpose of this biobank is to study the clinical, pathological, laboratory, and imaging characteristics of SARDs patients with lung involvement. This will help identify as unique features underlying lung involvement in SARDs. In addition, this may lead to the discovery of novel mechanisms of disease and potentially novel targets of treatment for SARDs patients with lung disease.
Eligibility criteria
Qualifiers
Must be aged 18 years or older
Diagnosis of ILD as confirmed by a chest CT
Either a defined SARD, an undifferentiated connective tissue disease or features of autoimmunity without meeting clinical criteria for SARD
Patient must be willing to give their informed consent and must be able to understand and follow the required study procedures.
Disqualifiers
None
Trial design
Treatments tested in this trial
- Blood draws
- Other biological samples to biobank (skin, lung and muscle biopsies; bronchoalveolar lavage (BAL fluid)
- Clinical data collection
- Genetic data/DNA/RNA
Treatment groups
Sponsors and collaborators
McGill University Health Centre/Research Institute of the McGill University Health Centre
Lead sponsor
McGill University
Collaborator