TABLE 3.
Study | Study design | Study population | Type of intervention | Anthocyanins dose (mg/day) | Trial duration | GGT levels (U/L) | |
---|---|---|---|---|---|---|---|
Baseline | End of trial | ||||||
1. Oki et al. (2016) | Randomized double‐blind, placebo‐controlled clinical trial (parallel) | Healthy Caucasians with borderline hepatitis. Total n = 40. But n = 37 (18 in PSP group and 19 in placebo group) completed the study | Anthocyanin‐rich purple‐fleshed sweet potato (PSP) beverage or placebo | 531 | 8 weeks |
PSP group: 74.6 ± 35.1 Placebo group: 57.1 ± 16.7 |
PSP group: Not reported Placebo group: Not reported |
2. Suda et al. (2008) | Randomized double‐blind placebo‐controlled clinical trial (parallel) | Healthy men with borderline hepatitis. Total n = 48. But n = 38 (n = 20 in PSP group and n = 18 in placebo group) completed the study | Purple sweet potato (PSP) beverage or placebo | 400.6 | 12 weeks |
PSP group: **103.6 (17.3) Placebo group: **91.6 (11.1) |
PSP group: Not reported Placebo group: Not reported |
3. Curtis et al. (2009) | Randomized double‐blind placebo‐controlled clinical trial (parallel) | Healthy postmenopausal women. Total n = 56. N = 26 completed the study | Elderberry extract or placebo | 500 | 12 weeks |
Elderberry group: 21.0 ± 14.2 Placebo group: 22.0 ± 16.3 |
Elderberry group: 18.3 ± 9.5 Placebo group: 19.0 ± 11.5 |
4. Chang et al. (2014) | Randomized double‐blind placebo‐controlled clinical trial (parallel) | Subjects with a BMI higher than 27 and NAFLD. Total n = 40. But n = 36 (n = 19 in HSE group and n = 17 in placebo group) completed the study | Hibiscus sabdariffa extracts (HSE) or placebo | 67.5 | 12 weeks |
HSE group: 49.26 ± 45.39 Placebo group: 40.88 ± 32.57 |
HSE group: 50.05 ± 40 Placebo group: 35.65 ± 26.08 |
All values expressed as mean ± standard deviation (SD) except **for study number 2: Values presented as mean (95% CI).