Table 1.

Demographic and clinical characteristics of scleroderma renal crisis (SRC) cases and systemic sclerosis (SSc) without SRC disease controls. Data are %, n/N unless otherwise specified.

CharacteristicsSRC, n = 31SSc without SRC, n = 322p
Race
  White48, 15/3157, 158/279NS
  Black42, 13/3124, 66/2790.03
  Other10, 3/3120, 63/279NS
Sex, % female74, 23/3184, 271/322NS
Age, yrs, median (IQR)53 (40–60)46 (37–54)0.01
Time between SSc and SRC, yrs, median (IQR)3 (1–5)NANA
SSc followup, yrs, median (IQR)6 (3–8)5 (2–8)NS
Pulmonary fibrosis42, 13/3131, 100/322NS
Pulmonary HTN39, 12/3112, 40/322< 0.001
Cardiac involvement23, 7/315, 17/3220.002
GI involvement77, 24/3182, 265/322NS
RP90, 28/3197, 313/322NS
Digital ulcers29, 9/3123, 73/322NS
Prior prednisone65, 20/3119, 62/322< 0.001
Other IST32, 10/3132, 104/322NS
Diffuse SSc39, 12/3116, 52/3220.004
Limited SSc61, 19/3174, 237/322NS
Sine SSc0, 0/311, 4/322NS
Unknown0, 0/319, 29/322NS
  • IQR: interquartile range; HTN: hypertension; GI: gastrointestinal; RP: Raynaud phenomenon; IST: immunosuppression therapy; NS: not significant; NA: not applicable; sine SSc: SSc sine scleroderma.