Table 1

Demographic, clinical and laboratory SLE characteristics, by country

Russia
(n=232)
Kazakhstan
(n=110)
Ukraine
(n=94)
Gender, n (%)
 Male14 (6.0%)5 (4.5%)10 (10.6%)
 Female218 (94.0%)105 (95.5%)84 (89.4%)
Race/ethnicity, n (%)
 Caucasians224 (96.6%)8 (7.3%)94 (100.0%)
 Asian1 (0.4%)102 (92.7%)0 (0.0%)
 Black0 (0.0%)0 (0.0%)0 (0.0%)
 Unknown7 (3.0%)0 (0.0%)0 (0.0%)
Age at SLE diagnosis, years
 Mean (SD)30.3 (12.2)31.6 (11.4)33.0 (13.3)
 Median (min–max)29.0 (7–68)30.5 (12–59)32.0 (4–74)
Age at the last visit in 2010, years
 Mean (SD)36.1 (12.3)36.9 (11.4)41.7 (21.1)
 Median (min–max)33.0 (18–74)36.5 (19–67)41 (20–74)
SLE duration at the last visit in 2010, years
 Median4.53.06.8
 25–75% quartile0.6–9.10.0–6.83.2–12.2
Severe SLE, n (%)
 At the SLE diagnosis137/198 (69.2%)64/88 (72.7%)51/92 (55.4%)
 At the last visit in 2010108/200 (54.0%)69/109 (63.3%)53/94 (56.4%)
SLE profile at the last visit in 2010
 Relapsing-remitting85 (36.6%)39 (35.5%)1 (1.1%)
 Chronic active74 (31.9%)55 (50.0%)90 (95.7%)
 Unknown, n (%)73 (31.5%)16 (14.5%)3 (3.2%)
Laboratory markers of activity (positive test for anti-dsDNA antibodies and/or C3 or C4 below normal ranges)
 At diagnosis88/98 (89.8%)33/37 (89.2%)38/44 (86.4%)
 At the last visit in 2010143/174 (82.2%)54/74 (73.0%)52/58 (89.7%)
SLE activity by Nasonova, n (%) at the diagnosis
 High107/192 (55.7%)57/89 (64.0%)18/63 (28.6%)
 Moderate71/192 (37.0%)29/89 (32.6%)19/63 (30.2%)
 Low14/192 (7.3%)3/89 (3.4%)26/63 (41.3%)
SLE activity by Nasonova, n (%) at the last visit in 2010
 High57/201 (28.4%)54/110 (49.1%)8/93 (8.6%)
 Moderate93/201 (46.3%)50/110 (45.5%)16/93 (17.2%)
 Low51/201 (25.4%)6/110 (5.5%)69/93 (74.2%)
SELENA-SLEDAI score, mean (SD)
 At SLE diagnosis16.6 (10.1)18.6 (17.4)9.4 (7.8)
 N1988993
 At the last visit in 201013.8 (10.5)19.4 (16.9)7.2 (6.8)
 N20111094
SDI score, mean (SD)
 At SLE diagnosis1.2 (1.9)2.0 (2.3)1.1 (1.7)
 N1988993
 At the last visit in 20102.0 (2.2)3.3 (3.2)2.2 (2.0)
 N20010991
  • Percentages were calculated from the valid data.

  • If SLE profile was impossible to establish retrospectively, it was considered as ‘unknown’.

  • Patients could have no autoantibody-positive disease at the date of SLE diagnosis but could be autoantibody-positive between the diagnosis and before the last visit in 2010.

  • SDI, SLE Damage Index; SLE, systemic lupus erythematosus; SELENA-SLEDAI, Safety of Estrogens in Lupus Erythematosus National Assessment–Systemic Lupus Erythematosus Disease Activity Index.