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. 2020 Jun 29;5(9):1432–1447. doi: 10.1016/j.ekir.2020.06.014

Table 3.

Changes in serum CPP-1 and CPP-2 over 24 weeks in the SCaRF trial

Treatment group Baseline
Week 12
Week 24
Within-group treatment effect (95% CI) P Value Treatment effect vs. CC (95% CI) P value
N Median (IQR) N Median (IQR) N Median (IQR)
CPP-1, ×105/ml
 CC 11 26.3 (6.2, 39.1) 10 29.3 (16.3, 35.1) 10 33.9 (20.0, 60.7) 71.9% (–24.8% to 293%) 0.20
 SH + SC 20 18.7 (7.2, 41.3) 17 6.4 (3.8, 12.4) 16 9.8 (5.9, 33.9) –49.7% (–75.8% to 4.3%) 0.07 –70.6% (–89.8 to –15.2) 0.02
CPP-2, ×105/ml
 CC 11 1.5 (1.0, 3.0) 10 1.3 (0.8, 3.0) 10 1.5 (1.0, 2.2) 17.4% (–44.8% to 149%) 0.68
 SH + SC 20 3.2 (0.9, 5.8) 17 1.2 (0.7, 2.7) 16 2.9 (1.5, 5.7) –56.5% (–84.2% to 20.1%) 0.11 –52.2% (–86.7 to 71.35) 0.26

CC, calcium carbonate; CPP, calciprotein particles; IQR, interquartile range; SC, sevelamer carbonate; SCaRF, Sevelamer Versus Calcium to Reduce Fetuin-A-containing Calciprotein Particles in Dialysis; SH, sevelamer hydrochloride; 95% CI, 95% confidence interval.

Serum CPP levels are expressed as median (25th, 75th percentiles) using all available data (N). CPP-1 and CPP-2 values were log-transformed before analysis. Estimated treatment effects are expressed as the percentage change from baseline or relative to CC treatment group (reference category). Mixed-effects analyses are expressed after controlling for the baseline level of the parameter tested.

P values < 0.025 are considered statistically significant owing to multiple comparisons.