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. 2003 Feb;131(2):385–392. doi: 10.1046/j.1365-2249.2003.02058.x

Table 2.

Clinical and laboratory characterization of SLE patients

All patients Responders Non-responders
(a) Diagnostic criteria
 No. of patients (%) 62 (100) 24 (39) 38 (61)
 Malar rash 19/62 (30·1)  8/24 (33·3) 11/38 (29)
 Discoid rash  9/62 (15)  3/24 (12·5)  6/38 (16)
 Photosensitivity 21/62 (34)  9/24 (37·5) 12/38 (32)
 Mucosal ulcers 17/62 (27·4)  8/24 (33·3)  9/38 (23·7)
 Arthritis 46/62 (74·2) 19/24 (79·2) 27/38 (71)
 Serositis 14/62 (22·6)  5/24 (20·8)  9/38 (23·7)
 Neurological disorders  5/62 (8·1)  4/24 (16·7)  1/38 (2·7)
 Renal disorder 24/62 (38·8)  7/24 (29·2) 17/38 (44·8)
 Haematological disorders 44/62 (71) 19/24 (79·2) 25/38 (65·8)
 ANA 61/62 (98·4) 24/24 (100) 37/38 (92·1)
 α-dsDNA 54/62 (87·1) 19/24 (79·2) 35/38 (92·1)
 APLA 35/62 (56·5) 12/24 (50·0) 23/38 (60·53)
(b) Disease activity
 SLEDAI score 6·65 ± 5·12 7·29 ± 1·06 6·24 ± 0·84
 Number of ACR diagnostic criteria 5·44 ± 1·39 5·54 ± 0·33 5·34 ± 0·2
(c) Current treatment
 NSAIDS 17/62 (27·4)  6/24 (25) 11/38 (29)
 Anti-malarial 37/62 (59·7) 15/24 (62·5) 22/38 (57·9)
 Steroids 33/62 (53·2) 11/24 (45·8) 22/38 (57·9)
 Cytotoxic 10/62 (16·1)  2/24 (8·3)  8/38 (21)

*Clinical involvement was defined according to the ACR revised criteria [16]. Anti-nuclear antibodies (ANA) and anti-dsDNA antibodies were determined by Hep2 cells and Crithidia luciliae, respectively. Anti-phospholipid antibodies (APLA) were defined as reactivity in one or more of the following assays: false positive VDRL, lupus anticoagulant (LAC) or ELISA for anticardiolipin antibodies.

†The antimalarial agent, hydroxychloroquine, was used at a dose of 200–400 mg/day; steroid treatment was defined as a daily dose≥5 mg of prednisone; cytotoxic agents used were cyclophosphamide (0·75–1·0 g/m2; monthly) or azathioprine (100–150 mg/day).

‡Parameters for which tendency was observed towards differences between the two groups of responder and non responder SLE patients.