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. Author manuscript; available in PMC: 2013 Sep 19.
Published in final edited form as: Cancer Prev Res (Phila). 2012 Jan 13;5(3):393–402. doi: 10.1158/1940-6207.CAPR-11-0407

Table 2.

Mean (95% confidence interval) urinary tea catechin concentrations at baseline and on average during 2 months of intervention by treatment group

Placebo 400 mg EGCG as PPE 800 mg EGCG as PPE P1 P2 P3
EGC4 (μmol/g Cr)
Baseline 0.80 (0.33,1.27) 0.78 (0.44,1.12) 0.84 (0.36,1.31) 0.98
Ave month 1–2 0.77 (0.39,1.15) 2.25 (1.58,3.02) 8.49 (5.93, 11.0)
Absolute change −0.03 (−0.43,.36) 1.47 (0.70,2.24) 7.65 (5.10,10.2)
P value 0.86 <0.001 <0.001 <0.0001 <0.0001
4′-MeEGC4(μmol/g Cr)
Baseline 0.19 (0.05,0.34) 0.56 (0.06,1.06) 0.38 (0.00,0.75) 0.40
Ave month 1–2 0.47 (0.03,0.91) 7.73 (−0.5.15.9) 10.8 (7.5, 14.0)
Absolute change 0.27 (−0.17,0.72) 7.16 (−1.1,15.4) 10.4 (7.1,13.6)
P value 0.22 0.086 <0.001 0.013 0.48
EC4 (μmol/g Cr)
Baseline 1.37 (0.53,2.21) 0.74 (0.40,1.09) 2.86 (0.92,4.80) 0.039
Ave month 1–2 1.87 (0.91,2.83) 3.49 (2.56,4.43) 13.2 (10.0,16.3)
Absolute change 0.50 (−0.22,1.2) 2.75 (1.82,3.68) 10.33 (6.7,14.0)
P value 0.17 <0.001 <0.001 0.0002 <0.0001
M44 (μmol/g Cr)
Baseline 0.66 (0.23,1.09) 0.46 (0.09,0.83) 0.34 (0.13,0.55) 0.43
Ave month 1–2 0.54 (0.22,0.86) 1.96 (0.95,4.1) 2.51 (0.95, 4.08)
Absolute change −0.12 (−0.56, 0.32) 1.50 (0.29,2.70) 2.17 (0.59,3.76)
P value 0.59 0.011 0.009 0.009 0.47
M64 (μmol/g Cr)
Baseline 19.5 (13.2,25.8) 15.2 (8.7,21.8) 19.3 (11.5,27.2) 0.60
Ave month 1–2 18.8 (9.3,28.3) 48.0 (36.1,59.8) 57.8 (44.0,71.6)
Absolute change −0.68 (−8.5,7.1) 32.7 (19.0,46.4) 38.5 (26.2,50.7)
P value 0.86 <0.001 <0.001 <0.0001 0.53
1

P value for difference between the 3 groups at baseline (ANOVA for continuous variable, 2 df)

2

P value for difference in change between the placebo versus the two PPE groups

3

P value for difference in change between the 400 mg and 800 mg PPE groups

4

EGC=epigallocatechin; EC=epicatechin; MeEGC= 4′-O-methyl-epigallocatechin; M4= 5-(3′,4′,5′-trihydroxyphenyl)-γ-valerolactone (metabolite of EGC); M6= 5-(3′,4′-dihydroxy-phenyl)-γ-valerolactone (metabolite of EC)