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. Author manuscript; available in PMC: 2021 Nov 11.
Published in final edited form as: Ann Rheum Dis. 2020 Sep 15;79(12):1608–1615. doi: 10.1136/annrheumdis-2020-217033

Table 1.

Clinical characteristics of the cohort includes subjects who completed the SCOT trial per-protocol (PP) and for which gene expression was available at baseline

Gene expression dataset—PP
Cyclophosphamide Transplantation
Characteristic n=33 n=30 P value
Age-mean (SD) 46.1 (10.7) 43.8 (10.1) 0.379
Female sex-no (%) 23 (69.7) 15 (50.0) 0.129
Race
 White-no (%) 25 (75.8) 23 (76.7) 0.805
 Black/African-American-no (%) 4 (12.1) 2 (6.7)
 Asian-no (%) 1 (3.0) 2 (6.7)
 Multiple-no (%) 3 (9.1) 2 (6.7)
 Other/unknown-no (%) 0 (0.0) 1 (3.3)
Ethnicity Hispanic or Latino-no (%) 4 (12.1) 3 (10.0) >0.999
Smoking history
 Current-no (%) 2 (6.1) 1 (3.3) 0.410
 Ever-no (%) 5 (15.2) 9 (30.0)
 Never-no (%) 26 (78.8) 20 (66.7)
Duration of disease-months since onset of first non-Raynaud’s Sign or symptom of scleroderma-mean (SD) 30.8 (16.4) 24.9 (12.8) 0.117
Disease-modifying antirheumatic drug use within 6 months of randomisation-no (%) 21 (63.6) 23 (76.7) 0.287
Lung involvement-no (%) 32 (97.0) 30 (100.0) >0.999
modified Rodnan Skin Score-mean (SD) 30.4 (10.7) 27.5 (7.7) 0.225
Mean FVC-% of predicted value 73.6 (17.9) 76.2 (13.4) 0.525
Mean DLCO-% of predicted value 51.8 (7.9) 54.1 (6.7) 0.207
Failures prior to month 54-no (%) 16 (48.4) 5 (16.7) 0.0088

Fisher’s exact test was used for categorical variables and Student’s t-test was used for continuous measures.

DLCO, diffusing lung capacity for carbon monoxide; FVC, forced vital capacity; SCOT, Scleroderma: Cyclophosphamide or Transplantation.