Table 1

Baseline characteristics and outcomes of 107 patients with lupus nephritis

Baseline characteristicsOverall (n=107)Non-ESRD (n=92)ESRD (n=15)P value
Demographics
Female, n (%)90 (84.1%)78 (84.8%)12 (80.0%)0.704
Age, years33 (23–46)34 (24–46)30 (21–50)0.953
SLE duration, months3.9 (1.2–83.0)2.3 (1.2–82.5)54.2 (8.6–94.5)0.221
LN duration, months5.2 (1.2–39.8)3.2 (1.2–39.0)23.6 (3.6–53.5)0.134
Hypertension, n (%)78 (72.9%)65 (70.7%)13 (86.7%)0.346
Diabetes mellitus, n (%)15 (14.0%)13 (14.1%)2 (13.3%)0.934
Laboratory examinations
Haemoglobin, g/L92±1793±1785±140.101
White cell count, ×109/L7.14 (5.06–9.78)7.12 (5.02–9.53)7.15 (5.64–9.88)0.654
Platelets, ×109/L169 (131–236)166 (130–218)205 (132–274)0.092
C3, g/L0.444 (0.336–0.645)0.435 (0.334–0.639)0.525 (0.362–0.715)0.217
C4, g/L0.091 (0.053–0.154)0.091 (0.052–0.154)0.117 (0.060–0.205)0.296
Anti-dsDNA, n (%)69 (64.5%)61 (66.3%)8 (53.3%)0.330
Anti-SSA, n (%)57 (53.3%)49 (53.3%)8 (53.3%)0.996
Anti-SSB, n (%)14 (13.1%)13 (14.1%)1 (6.7%)0.687
Anti-RNP, n (%)42 (39.3%)33 (35.9%)9 (60.0%)0.076
Anti-rRNP, n (%)27 (25.2%)24 (26.1%)3 (20.0%)0.756
Anti-Smith, n (%)29 (27.1%)23 (25.0%)6 (40.0%)0.228
Coombs’ test, n (%)34 (31.8%)33 (35.9%)1 (6.7%)0.034
aPL antibodies, n (%)22 (20.6%)20 (21.7%)2 (13.3%)0.731
Serum albumin, g/L26.1±5.926.2±6.025.6±5.70.720
Proteinuria, g/24 hours6.2 (3.7–10.3)5.9 (3.4–9.8)9.0 (4.9–12.7)0.039
Microscopic haematuria, /uL162.2 (52.7–526.7)180.4 (60.1–561.9)73.0 (30.0–381.8)0.087
Serum creatinine, μmoI/L163 (126–202)152 (123–191)195 (171–265)0.012
eGFR, mL/min/1.73 m236.6 (27.0–49.4)39.3 (28.1–49.7)27.3 (24.3–33.4)0.008
Disease evaluation
SLEDAI14 (12–18)14 (12–18)12 (10–16)0.074
Extrarenal SLEDAI5 (2-7)5 (4-7)4 (2-6)0.141
Extrarenal organ involvement1 (0–1)1 (0–2)0 (0–1)0.388
Histological class, ISN/RPS0.965
Class III, n (%)8 (7.5%)7 (7.6%)1 (6.7%)
Class IV, n (%)69 (64.5%)59 (64.1%)10 (66.7%)
Class V, n (%)2 (1.9%)2 (2.2%)0
Class III+V, n (%)5 (4.7%)4 (4.3%)1 (6.6%)
Class IV+V, n (%)23 (21.4%)20 (21.8%)3 (20.0%)
Activity index14 (12–17)14 (11–17)14 (12–15)0.815
Chronicity index4 (3-5)3 (3-5)6 (5-8)0.000
Treatment
Induction therapy, n (%)
  Methylprednisolone pulses76 (71.0%)64 (69.6%)12 (80.0%)0.546
  CS+CYC82 (76.6%)68 (73.9%)14 (93.3%)0.184
  CS+MMF12 (11.2%)12 (13.0%)00.210
  CS+others13 (12.2%)12 (13.1%)1 (6.7%)
Hydroxychloroquine, n (%)75 (70.1%)65 (70.7%)10 (66.7%)0.766
ACEI/ARB, n (%)54 (50.5%)50 (54.3%)4 (26.7%)0.047
Haemodialysis, n (%)7 (6.5%)6 (6.5%)1 (6.7%)0.983
Plasma exchange, n (%)4 (3.7%)4 (4.3%)00.410
Outcome
Follow-up, months60 (36–84)64 (39–86)27 (14–36)0.000
Proteinuria after 6 months, g/24 hours1.4 (0.4–3.0)1.3 (0.4–2.6)3.0 (2.0–4.7)0.002
CR after 6 months, n (%)20 (18.7%)19 (20.7%)1 (6.7%)0.294
PR after 6 months, n (%)41 (38.3%)41 (44.6%)00.001
NR after 6 months, n (%)46 (43.0%)32 (34.7%)14 (93.3%)0.000
Stage 1 CKD, n (%)32 (29.9%)32 (34.8%)//
Stage 2 CKD, n (%)32 (29.9%)32 (34.8%)//
Stage 3 CKD, n (%)16 (15.0%)16 (17.4%)//
Stage 4 CKD, n (%)8 (7.5%)8 (8.7%)//
Death, n (%)4 (3.7%)4 (4.3%)0 (0.0%)0.410
  • CS+others of induction therapy included CS+CYC+ MMF, CS+MMF+calcineurin inhibitor (CNI), CS+CNI, CS+MMF+Leflunomide.

  • ACEI/ARB, angiotensin-converting enzyme inhibitors/angiotensin receptor blockers; aPL, antiphospholipid antibodies; CKD, chronic kidney disease; CR, complete response; CS, corticosteroids; CYC, cyclophosphamide; eGFR, estimated glomerular filtration rate; ESRD, end-stage renal disease; INS/RPS, International Society of Nephrology/Renal Pathology Society; MMF, mycophenolate mofetil; NR, no response; PR, partial response; SLEDAI, SLE Disease Activity Index.