Table 1.
Clinical trials of antidiabetic flavonoids.
| Molecules | Models | Experiment | Doses/Periods | Key findings | Authors |
|---|---|---|---|---|---|
| Resveratrol | 19 T2D patients | A randomized study Double-blind trial (Phase III) |
2 × 5 mg/day 4 weeks |
Decreased insulin resistance Improved insulin sensitivity |
[30] |
| 62 patients with T2D | A prospective, open-label, randomized, controlled trial | 250 mg/day 3 months |
Normalized glycaemia and HbA1c levels | [31] | |
| Non-obese postmenopausal women | A randomized, double-blind, placebo-controlled trial | 75 mg/day 12 weeks |
Increased resveratrol plasma concentration No effect on insulin sensitivity |
[32] | |
| 66 patients with type 2 diabetes mellitus (T2DM) | A randomized placebo-controlled double-blinded parallel clinical trial | 1 g/day 45 days |
Lowered fasting glycaemia levels, HbA1c, and resistance to insulin | [33] | |
| 12 participants with metabolic syndrome (MetS) | A randomized, double-blind, placebo-controlled clinical trial | 500 mg 3 times a day 90 days |
Decreased insulin AUC Decreased total insulin secretion |
[34] | |
| 8 overweight and sedentary men | A single dose (300 mg) on two separate occasions | Attenuated post-absorption insulin concentrations No changes in insulin signaling |
[35] | ||
| 60 non-alcoholic subjects with fatty liver disease (FLD) | A double-blind, randomized, placebo-controlled clinical study | 2,15 g (twice daily) 3 months |
Improved levels of glycaemia, LDL cholesterol, and total cholesterol | [36] | |
| 14 patients with T2D | A double-blind, randomized, crossover design | 500 mg (twice daily) 5 weeks |
No effect on postprandial and fasting glycaemia, or HbA1c | [37] | |
| 34 subjects suffering from polycystic ovary syndrome | A randomized double-blind, placebo-controlled trial | 1500 mg/day 3 months |
Lowered fasting insulin content (31.8 %) Augmented insulin sensitivity index (66.3 %) |
[38] | |
| 38 obese and overweight subjects | A randomized double-blind study | Resveratrol (80 mg/day) EGCG (282 mg/day) 12 weeks |
No impact on insulin-stimulated glucose disposal | [39] | |
| 17 subjects with T2D | A randomized double-blind crossover study | 150 mg/day 30 days |
No improvement in insulin sensitivity | [40] | |
| Middle-aged men suffering from metabolic syndrome | A randomized, placebo-controlled, double-blind, parallel group clinical trial | 150 and 1000 mg/day 16 weeks |
No improvement in glucose homeostasis | [41] | |
| 45 overweight or slightly obese volunteers | A Randomized placebo-controlled trial | 150 mg/day 4 weeks |
No effect on insulin and plasma glucose levels | [42] | |
| 13 men with T2D | A randomized, placebo controlled, cross-over trial | 150 mg/day 1 month |
No effect on insulin sensitivity | [43] | |
| 472 elderly diabetic patients | A single-blind randomized controlled clinical trial | 500 mg/day 6 months |
Improvemed insulin resistance Improvemed blood glucose parameters (decreased G6Pase and HbA1c) |
[44] | |
| 110 diabetic patients | A randomized, placebo-controlled trial | 200 mg/day 24 weeks |
Improved blood glucose as well as insulin synthesis and resistance levels | [45] | |
| Catechin | T2D patients not receiving insulin The participants ingested green tea containing either 582.8 mg of catechins (catechin group; n = 23) or 96.3 mg of catechins (control group; n = 20) per day |
A double-blind controlled study | 582.8 and 96.3 mg per day 12 weeks |
Augmented insulin and adiponectin production No effect on glucose and HbA1c |
[46] |
| Healthy postmenopausal women (Phase III) | 615 mg/350 mL per day 4 weeks |
Improved redox homeostasis Improved postprandial glycemic status |
[47] | ||
| Rutin | 50 participants suffering from T2DM | A double blind, placebo-controlled trial | 500 mg/day 3 months |
Lowered the levels of fasting glycaemia, insulin, insulin resistance, and HbA1c | [48] |
| 34 healthy adult participants | A randomized, placebo-controlled, double blind crossover study | 200 mg/day 3 weeks |
Lowered postprandial glycaemia levels | [49] | |
| Epicatechin | 37 healthy women and men | A randomized, double-blind, placebo-controlled study | 100 mg/day 4 weeks |
Improved insulin resistance Enhanced fasting plasma insulin |
[50] |
| Erythrocyte membrane AChE in normal and type 2 diabetic patients | – | Pronounced insulin-like effect | [51] | ||
| Quercetin | 37 healthy women and men | A randomized, double-blind, placebo-controlled study | 160 mg/day 4 weeks |
No impact on insulin resistance | [50] |
| Hesperidin and Diosmin | 127 diabetic patients with neuropathy and MetS | A randomized controlled trial | 1 g/day (for each) 12 weeks |
Improved glycaemia, LDL, and triglyceride rates Increased magnitude of enhancement when the two molecules are combined |
[52] |