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. 2008 May 31;47(8):1185–1192. doi: 10.1093/rheumatology/ken179

Table 1.

Distribution of age, onset of organ involvement and disease subsets

Age (yrs) Age at RP onset (yrs) Age at skin involvement (yrs) Age at organ involvement (yrs)
Total 55.7 ± 13.7 44.3 ± 15.6 47.9 ± 14.4 50.3 ± 14.2
Family case history 53.7 ± 13.0 41.5 ± 15.4 46.1 ± 14.0 47.9 ± 13.6
Female 56.0 ± 13.9 44.2 ± 15.8 48.1 ± 14.6 50.5 ± 14.5
Male 53.9 ± 12.4 45.1 ± 14.6 47.0 ± 13.4 49.1 ± 12.4
Overlap-S. 50.9 ± 13.5 40.5 ± 15.7 43.6 ± 15.5 45.0 ± 14.6
Undiff. Scl. 54.7 ± 12.5 46.8 ± 14.6 49.6 ± 12.5 50.9 ± 13.3
Scl. sine Scl. 54.1 ± 15.8 42.7 ± 14.9 48.1 ± 14.3 48.2 ± 16.0
dcssc 54.1 ± 14.1 44.5 ± 15.2 46.4 ± 14.3 48.6 ± 14.3
lcSSc 58.5 ± 12.7 44.7 ± 15.8 49.9 ± 14.0 52.2 ± 13.7

Values expressed as mean ± s.d. Overlap-S: Overlap syndrome; Undiff. Scl: Undifferentiated scleroderma; Scl. sine Scl.: sclerosis (scleroderma) sine scleroderma; dcSSc: diffuse cutaneous systemic sclerosis; lcSSc: limited cutaneous systemic sclerosis.