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. 2023 Mar 4;8(5):1043–1056. doi: 10.1016/j.ekir.2023.02.1086

Table 3.

Laboratory values at baseline in patients who were randomized and received study drug in PROTECT

Characteristic All Patients (N = 404)
UP/C, g/g 1.2 (0.8–1.8)
Urinary protein excretion, g/d 1.8 (1.3–2.8)
Nephrotic-range proteinuria (>3.5 g/d) 49 (12.1)
UA/C, g/g 1.1 (0.7–1.5)
Urinary albumin excretion, mg/d 1493 (1073–2280)
eGFRa
 Mean ± SD 57.0 ± 24.0
 Median (IQR) 50.0 (39.0–70.0)
eGFR
 ≥90 51 (12.6)
 ≥60 to <90 97 (24.0)
 ≥45 to <60 94 (23.3)
 ≥30 to <45 142 (35.1)
 ≥15 to <30 20 (5.0)
Hemoglobin, g/l 138.7 ± 15.9
Plasma lipid profile, mmol/l
 Total cholesterol 5.0 ± 1.1
 HDL cholesterol 1.3 ± 0.4
 LDL cholesterol 2.8 ± 1.0
 Triglycerides 1.9 ± 1.1
Serum albumin, g/l
 Mean ± SD 41.5 ± 3.8
 Median (IQR) 42.0 (40.0–44.0)
Serum potassium, mmol/l 4.6 ± 0.4
Serum creatinine, μmol/l 136.1 ± 45.3
Serum cystatin C, mg/l 1.5 ± 0.4
Hematuria/microscopic hematuriab 225 (55.7)
ALT, U/l 21.8 ± 10.8
AST, U/l 21.1 ± 8.0

ALT, alanine transaminase; AST, aspartate transferase; eGFR, estimated glomerular filtration rate in ml/min per 1.73 m2; HDL, high-density lipoprotein; IQR, interquartile range; LDL, low-density lipoprotein; UA/C, urine albumin-to-creatinine ratio; UP/C, urine protein-to-creatinine ratio.

Data are given as n (%), median (IQR), or mean ± SD. A central laboratory was used for all laboratory testing analyses.

a

eGFR was determined using the Chronic Kidney Disease Epidemiology formula.

b

The assessment of microscopic hematuria was limited by the use of a central laboratory, resulting in an unreliable analysis because of the transport time and analysis delays.