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Imaging Features of Systemic Sclerosis-Associated Interstitial Lung Disease
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Systemic sclerosis: To subset or not to subset, that is the question
Sindhu R Johnson1,2, Frank van den Hoogen3, Keshini Devakandan1
1Toronto Scleroderma Program, Department of Medicine, Mount Sinai Hospital, Toronto Western Hospital, Toronto, Ontario, Canada.
Systemic sclerosis (SSc) classification is evolving. New subsetting systems, including biologic and data-driven approaches, aim to improve patient care and prognostication for this heterogeneous autoimmune disease.
Area of Science:
- Rheumatology
- Immunology
- Internal Medicine
Background:
- Systemic sclerosis (SSc) is a complex autoimmune disease characterized by significant heterogeneity.
- Variability exists in autoantibody profiles, organ involvement, disease progression, and patient survival.
- Identifying homogeneous SSc patient subsets is crucial for research and clinical management.
Purpose of the Study:
- To review the historical development of SSc subsetting systems.
- To analyze the utility, strengths, and limitations of existing classification methods.
- To explore the emerging paradigm shift towards biologic and data-driven SSc subset classification.
Main Methods:
- Literature review of SSc subsetting systems.
- Analysis of clinically based subsetting approaches.
- Discussion of novel data-driven and biologic classification strategies.
Main Results:
- Clinically based SSc subsetting systems have historically informed patient care but have limitations.
- A paradigm shift is occurring, moving towards more sophisticated classification methods.
- New approaches consider biologic factors and employ data-driven analyses for improved accuracy.
Conclusions:
- The evolution of SSc subsetting reflects advancements in understanding disease heterogeneity.
- Modern approaches aim to enhance patient prognostication and personalize treatment strategies.
- Future classification systems must accommodate global SSc community needs and predictive capabilities.
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