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. 2018 Jul 20;10(7):936. doi: 10.3390/nu10070936

Table 5.

Effect of CaP supplementation on faecal excretion of bile acids.

Parameter Placebo CaP Change
iLCA 39 ± 24 45 * ± 28 6 ± 21
(mg/day) (33–45) (38–52) (0.3–11.0)
LCA 54 ± 31 69 * ± 36 15 # ± 24
(mg/day) (47–62) (60–78) (8.4–20.8)
iDCA 34 ± 24 37 ± 40 3 ± 28
(mg/day) (28–40) (27–47) (−4.1–9.9)
DCA 98 ± 43 135 * ± 73 36 ± 56
(mg/day) (88–109) (116–153) (22.2–50.5)
CDCA 6 ± 4 7 * ± 5 1 # ± 4
(mg/day) (5–7) (6–8) (0.02–2.3)
CA 10 ± 12 12 ± 11 2 ± 11
(mg/day) (7–13) (9–15) (−0.9–4.8)
12keto DCA 8 ± 7 11 * ± 12 4 ± 9
(mg/day) (6–9) (8–15) (1.5–6.0)

n (studies) = 2; n (subjects) = 62; mean ± standard deviation; (95% confidence interval); * significantly different to placebo (paired Student’s t-test, p ≤ 0.05); # significantly different to zero (one-way ANOVA, p ≤ 0.05); CaP: three–four weeks´ intervention with Ca5(PO4)3OH(pentacalcium hydroxy-trisphosphate); BA: bile acids, iLCA: iso-lithocholic acid; LCA: lithocholic acid; iDCA: iso-deoxycholic acid; DCA: deoxycholic acid; CDCA: chenodeoxycholic acid, CA: cholic acid, 12keto DCA: 12keto-deoxycholic acid; primary BA: sum of CDCA and CA; secondary BA: sum of iLCA, LCA, iDCA, DCA and 12keto DCA.