Table 1.

Demographic data, laboratory findings, renal histology, and initial treatment of SLE patients with aPLN by the time of renal biopsy. Values are mean ± SD, median (IQR), or n (%) unless otherwise specified.

VariablesNon-RASI, n = 17RASI, n = 40p
Age, yrs33.9 ± 12.4; 40 (22–48)34.6 ± 9.9; 33 (28–43)0.818
Female13 (76)30 (75)0.827
APS1 (6)6 (15)0.604
eGFR, ml/min/1.73m279.6 ± 43.7; 102 (55–125)62.4 ± 28.8; 53 (35–85)0.150
MAP, mmHg100 ± 19; 95 (85–98)111 ± 21; 113 (90–128)0.083
  Hypertension5 (29)30 (75)0.001
Proteinuria level, g/d1.9 (0.6–2.8)5.2 (2.8–8.8)0.005
  Proteinuria, ≥ 3.5 g/d4 (24)26 (65)0.004
ISN/RPS class III or IVa14 (82)31 (78)0.955
Pathological features of aPLN
  TMA2 (11)10 (25)0.443
  FIH16 (94)30 (75)0.191
  Fibrous/fibrocellular occlusions of arteries and arterioles5 (29)3 (8)0.078
  FCA5 (29)3 (8)0.078
  Tubular thyroidization5 (29)7 (18)0.513
Treatment
  Mean prednisone dose, mg/d53.1 ± 12.349.8 ± 16.90.538
  CYC14 (82)34 (85)0.883
  MMF4 (24)8 (20)0.955
  Calcineurin3 (18)7 (18)0.713
  Antiplatelet agents3 (18)12 (30)0.522
  Anticoagulants4 (24)6 (15)0.694
  • a ISN/RPS class III + V and IV + V of LN are included. Data in bold face are statistically significant. SLE: systemic lupus erythematosus; aPLN: antiphospholipid-associated nephropathy; IQR: interquartile range; RASI: renin-angiotensin system inhibitor; APS: antiphospholipid syndrome; eGFR: estimated glomerular filtration rate; MAP: mean arterial blood pressure; ISN/RPS: International Society of Nephrology/Renal Pathology Society; TMA: thrombotic microangiopathy; FIH: fibrous intimal hyperplasia; FCA: focal cortical atrophy; CYC: cyclophosphamide; MMF: mycophenolate mofetil; LN: lupus nephritis.