Table 5.
Bile Acid | Placebo N = 20 | TUDCA N = 23 | Difference | |||
---|---|---|---|---|---|---|
Coefficienta (95% CI) | p-valueb | Coefficienta (95% CI) | p-valueb | Coefficienta (95% CI) | p-valueb | |
Chenodeoxycholic Acid | 0.48 (−0.13 to 1.09) | 0.12 | 0.44 (−0.14 to 1.02) | 0.13 | 0 (−0.86 to 0.87) | 1.00 |
Cholic Acid | 0.58 (−0.21 to 1.38) | 0.15 | −0.4 (−1.04 to 0.23) | 0.21 | −0.88 (−2.04 to 0.28) | 0.13 |
Deoxycholic Acid | 0.46 (0.13 to 0.8) | 0.01 | 0.14 (−0.21 to 0.48) | 0.42 | −0.3 (−0.8 to 0.2) | 0.23 |
Glycochenodeoxycholic Acid | −0.09 (−0.63 to 0.44) | 0.72 | 0.3 (−0.14 to 0.74) | 0.18 | 0.36 (−0.29 to 1) | 0.28 |
Glycocholic Acid | −0.32 (−0.88 to 0.24) | 0.26 | −0.02 (−0.46 to 0.42) | 0.93 | 0.24 (−0.41 to 0.9) | 0.46 |
Glycodeoxycholic Acid | 0.14 (−0.36 to 0.63) | 0.58 | 0.1 (−0.36 to 0.56) | 0.66 | −0.04 (−0.68 to 0.61) | 0.91 |
Glycolithocholic Acid | 0.35 (−0.01 to 0.71) | 0.06 | 0.9 (0.33 to 1.47) | 0.003 | 0.65 (−0.07 to 1.36) | 0.08 |
Glycoursodeoxycholic Acid | 0.14 (−0.35 to 0.64) | 0.56 | 2.3 (1.32 to 3.29) | 2.78E-05 | 2.21 (0.93 to 3.49) | 9.78E-04 |
Lithocholic Acid | 0.2 (−0.12 to 0.51) | 0.22 | 0.75 (0.28 to 1.22) | 0.002 | 0.6 (−0.03 to 1.23) | 0.06 |
Taurochenodeoxycholic Acid | −0.04 (−0.64 to 0.57) | 0.91 | 0.05 (−0.49 to 0.59) | 0.86 | 0.03 (−0.73 to 0.79) | 0.94 |
Taurocholic Acid | −0.26 (−0.83 to 0.3) | 0.35 | −0.23 (−0.74 to 0.28) | 0.36 | −0.01 (−0.73 to 0.72) | 0.98 |
Taurodeoxycholic Acid | 0.1 (−0.45 to 0.65) | 0.73 | −0.31 (−0.87 to 0.25) | 0.26 | −0.47 (−1.38 to 0.44) | 0.30 |
Taurolithocholic Acid | 0.14 (−0.13 to 0.42) | 0.30 | 0.15 (−0.19 to 0.5) | 0.37 | −0.02 (−0.52 to 0.47) | 0.92 |
Tauroursodeoxycholic Acid | −0.22 (−0.52 to 0.07) | 0.13 | 2.52 (1.3 to 3.73) | 1.51E-04 | 2.61 (1.25 to 3.97) | 2.62E-04 |
Ursodeoxycholic Acid | 0.37 (−0.03 to 0.78) | 0.07 | 1.89 (0.76 to 3.02) | 0.001 | 1.41 (0.09 to 2.74) | 0.04 |
Beta coefficient interpretation: change in log(bile acid) rate of change for TUDCA group compared to placebo group
p-values are derived from linear mixed-effects models (random slope and intercept) including time, treatment group and their interaction.