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SYSTEMIC SCLEROSIS

Towards a new classification of systemic sclerosis

Analysis of data from the European Scleroderma Trials and Research (EUSTAR) cohort has initially identified six subsets of systemic sclerosis (SSc), as opposed to the binary classification of limited and diffuse cutaneous SSc. We now move closer to a more actionable SSc classification for improved clinical care and trial design.

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Fig. 1: An integrated view of the SSc phenome.

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Acknowledgements

The authors thank S. R. Johnson for her input. The work of M.H. is supported by a grant from the National Institutes of Health, National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS) R01AR073270. M.H. maintains an adjunct professor role at the Northwestern University Feinberg School of Medicine, Department of Medicine, Division of Rheumatology. The work of J.M.M. is supported by a grant from the National Institutes of Health, National Library of Medicine (NLM) R21LM012615.

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Correspondence to Monique Hinchcliff.

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M.H. receives NIH research support for genomic SSc research. J.M.M. declares no competing interests.

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Hinchcliff, M., Mahoney, J.M. Towards a new classification of systemic sclerosis. Nat Rev Rheumatol 15, 456–457 (2019). https://doi.org/10.1038/s41584-019-0257-z

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