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. 2019 Sep 9;4(11):1608–1616. doi: 10.1016/j.ekir.2019.08.019

Table 1.

Patient characteristics by steroid exposure

Characteristic All patients (n = 884)
Treated with steroids (n = 534)
Not treated with steroids (n = 350)
P value
n (%) n (%) n (%)
Age at kidney disease onset <0.001
 Adults (18+ yr) 473 (53.5) 237 (44.4) 236 (67.4)
 Children (<18 yr) 393 (44.5) 288 (53.9) 105 (30.0)
 Missing 18 (2.0) 9 (1.7) 9 (2.6)
Sex 0.06
 Male 367 (41.5) 208 (39.0) 159 (45.4)
 Female 517 (58.5) 326 (61.0) 191 (54.6)
Race 0.50
 White 510 (57.7) 307 (57.5) 203 (58.0)
 Black 118 (13.3) 67 (12.5) 51 (14.6)
 Asian 118 (13.3) 77 (14.4) 41 (11.7)
 Other 137 (15.5) 83 (15.5) 54 (15.4)
 Missing 1 (0.1) 0 (0.0) 1 (0.3)
Ethnicity 0.002
 Non-Hispanic 722 (81.7) 443 (83.0) 279 (79.7)
 Hispanic 126 (14.3) 62 (11.6) 64 (18.3)
 Unknown 36 (4.1) 29 (5.4) 7 (2.0)
Diagnosis <0.001
 FSGS 231 (26.1) 119 (22.3) 112 (32.0)
 Minimal change 137 (15.5) 122 (22.8) 15 (4.3)
 Membranous nephropathy 104 (11.8) 65 (12.2) 39 (11.1)
 NS—not biopsieda 136 (15.4) 107 (20.0) 29 (8.3)
 Other 276 (31.2) 121 (22.7) 155 (44.3)
Calcineurin inhibitor therapy 307 (34.7) 228 (42.7) 79 (22.6) <0.001
Cyclophosphamide therapy 87 (9.8) 80 (15.0) 7 (2.0) <0.001
Mycophenolate mofetil therapy 298 (33.7) 214 (40.1) 84 (24.0) <0.001
Rituximab therapy 131 (14.8) 116 (21.7) 15 (4.3) <0.001
Median (IQR) Median (IQR) Median (IQR)
Age at kidney disease onset (yr) 23 (5, 44) 13 (4, 40) 33 (14, 49) <0.001
Steroid dose (mg/kg per day) 0.4 (0.1, 1.0)
eGFR closest to kidney disease onset 86 (46, 120) 97 (60, 127) 66 (34, 103) <0.001
UPC closest to kidney disease onset 2.1 (0.6, 6.3) 3.2 (0.6, 7.9) 1.6 (0.5, 3.3) <0.001
Observation period (mo) 60 (32, 112) 62 (34, 116) 54 (28, 105) 0.04

eGFR, estimated glomerular filtration rate; FSGS, focal segmental glomerulosclerosis; IQR, interquartile range; NS, nephrotic syndrome; UPC, urine protein:creatinine ratio

Categorical variables are displayed as frequencies and percentages, and the P values represent χ2 tests; continuous variables are displayed as medians, and IQRs and the P values represent Kruskal-Wallis tests. Other diagnoses include IgA nephropathy, C3 glomerulopathy, fibrillary glomerulonephritis, amyloidosis, and light chain nephropathy.

a

Diagnosis of nephrotic syndrome–not biopsied was available only to pediatric participants.