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Model | Number of patients | Effects | Results | References |
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Double-blind randomized QU administered 500 mg/day for 8 weeks | Seventy-two patients | QU administration reduced the concentration of TNF-α and IL-6 | QU administration decreased systolic hypertension, no significant changes in blood lipids (HDL-C, LDL-C, TG) | [55] |
QU 1 gr/day was administered in healthy humans for 28 days | — | QU had no significant effects on healthy participants in reducing cardiovascular risk | No significant modifications were observed in blood pressure, heart rate, and thrombogenic risk factors | [56] |
Administration of QU (3 gr/day) for 2 months | 30 CAD patients | QU inhibited NF-кВ-dependent gene expression and decreases the level of TNF-α | QU potentiates the potency of statins and decreases the endothelium degeneration in CAD patients | [44] |
Addition of QU as an ultralowering agent in patients with gout and hypertension for 12 months | 43 patients with gout and essential hypertension | QU stimulates the Na+-K+-2Cl-cotransporter 1 (NKCC1) which is one main agent in Cl regulation | QU administration developed echocardiographic parameter of diastolic function left ventricular and normalized blood pressure | [57] |
QU 150 mg/day administration in CHD patients for 2 months | 85 patients with CHD | QU improves the bioavailability of NO and increases myocardial blood flow, prevents apoptosis, and inhibits MMPs and NF-Kβ | Systolic and diastolic LV function improved in this study. QU had advantages in patients with stable CHD patients | [58] |
QU 120 mg/day administered for 2 months | 85 patients with CAD | Levels of IL-1β and TNF-α were decreased and IL-10 levels had been tended to decrease | QU has protective effects and antioxidative properties in myocardial cells and it enhances membrane rigidity and prevents risk of cardiovascular events | [41] |
QU/QU supplements 250 mg/day administered for 10 weeks | 34 men with hypertension and CAD after PCI aged 40–60 years | — | Left ventricular systolic and diastolic function increased by QU consumption | [59] |
QU 150 mg/day administered for 6 weeks | 93 overweight-obese volunteers | QU greatly reduced plasma oxidized LDL and tumor necrosis factor-α | QU reduced the blood pressure in overweight humans | [60] |
QU 162 mg/day administered from onion skin extract powder for 6 weeks treatment | 70 overweight-to-obese patients with prehypertension and stage I hypertension | QU supplements were not influenced inflammation and oxidative stress parameters in this study | QU significantly decreased 24 h systolic ABP | [61] |
150 mg or 300 mg quercetin-4¢-O-b-D-glucoside supplement administration | — | QU has inhibitory effects on platelet aggregation which reduce the risk of cardiovascular events | QU reduced the risk of thrombosis | [62] |
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