Skip to main content
. 2022 Oct 10;13:1002117. doi: 10.3389/fphar.2022.1002117

TABLE 2.

Efficacy outcome variables.

Variables Baseline 3 months 6 months
Remission, complete and partial (N, %) NA NA 7 (20%)
24 h urine protein (g/d) 10.15 (4.83, 13.57) 6.02 (4.83, 11.24)a 7.04 (4.43, 8.90)b
Albumin (g/L) 21.40 (16.75, 25.00) 24.80 (22.05, 29.90)a 30.55 (24.97, 33.27)b
Serum creatinine (µmol/L) 152.00 (134.50, 232.50) 136.00 (126.00, 214.50) 99.50 (75.25, 140.250)b
eGFR (ml/min/1.73 m2) 41.12 (26.53, 51.41) 47.85 (30.54, 53.86) 78.29 (50.15, 101.55)b
anti-PLA2R-Ab–positive patients (N, %) 34 (97.14%) 25 (71.42%)a 24 (68.57%)b
anti-PLA2R-Ab–depleted patients (N, %) NA 9/34 (26.47%) 10/34 (29.41%)
anti- PLA2R-Ab titer (RU/mL) 59.20 (17.70, 187.50) 8.60 (0.00, 42.50)a 7.70 (5.72, 16.72)b
CD19, per mm 179.00 (85.00, 272.50) 1.00 (0.00, 3.00)a 25.50 (3.75, 57.75)
CD4, per mm 893.00 (561.00, 1,095.00) 718.00 (460.50, 908.50) 816.00 (417.00, 1,031.25)
Post hoc composite end point at 6 months NA NA 16 (45.71%)

Data presented as number (percentage) or median (first-third interquartile range).a or b Stands for p < 0.05 vs. baseline. BP, blood pressure; eGFR, estimated glomerular filtration rate; anti- PLA2R-Ab, anti-phospholipase A2 receptor antibody; CD, cluster of differentiation; Complete and partial remissions were defined according to 2021 KDIGO criteria on the basis of proteinuria; composite end point was defined as reduction of proteinuria >50% and increase of serum albumin >30%.