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. 2018 Jan 18;57(4):677–687. doi: 10.1093/rheumatology/kex444

Table 1.

Demographic and baseline disease characteristics of study population

Characteristic (n = 1700 unless stated otherwise) n (%)/* median (IQR)
Age (n = 1699), years 33.0 (24.5–43.7)*
Gender
    Female 1506 (88.6)
    Male 194 (11.4)
Enrolment location
    Canada 397 (23.4)
    USA 463 (27.2)
    Mexico 210 (12.4)
    Europe 470 (27.7)
    Asia 160 (9.4)
Race/ethnicity
    Caucasian 843 (49.6)
    Hispanic 262 (15.4)
    Asian 254 (14.9)
    African origin 278 (16.4)
    Other 63 (3.7)
Disease activity/phenotype
    SLEDAI-2K (n = 1693) 4 (2–8)*
    SLICC/ACR-Damage Index ≥1 391 (23.0)
    Active renal diseasea 436 (25.7)
    Anti-dsDNA positive (n = 1541) 613 (39.8)
    Low complement (n = 1548)b 582 (37.6)
Medication use
    Oral GC use prior to enrolment (n = 1699) 1189 (70.0)
    Average GC dosec (n = 1179), mg/day 20.0 (10.0–30.0)*
    Highest GC dosec (n = 1183), mg/day 40.0 (20.0–60.0)*
    Immunosuppressant use 684 (40.2)
    Antimalarial use 1152 (67.8)
Co-morbidities
    Hypertension (n = 1683) 758 (45.0)
    Diabetes mellitus (n = 1682) 61 (3.6)
    Current smoker (n = 1698) 252 (14.8)
    Post-menopausal (n = 1506)d 213 (14.1)
    BMI, mean (s.d.) (n = 1672), kg/m2 25.7 (5.9)

*Values are in median (IQR).

a

Active nephritis or any renal item on SLEDAI-2K (haematuria, proteinuria, pyuria or casts).

b

Decrease in CH50, C3 or C4 below the lower limit of normal for testing laboratory.

c

Average/highest GC doses of zero excluded from calculation.

d

Percentage of women. IQR, interquartile range.