Peer-Reviewed Journal Details
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Peter, P,Martin, U,Sharma, A,Dunne, F
2006
April
Journal Of Clinical Pharmacy And Therapeutics
Effect of treatment with nebivolol on parameters of oxidative stress in type 2 diabetics with mild to moderate hypertension
Published
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Optional Fields
hypertension nebivolol oxidative stress type 2 diabetes NITRIC-OXIDE DOUBLE-BLIND ENDOTHELIAL DYSFUNCTION BLOOD-PRESSURE RISK-FACTOR MELLITUS HYDROCHLOROTHIAZIDE COMBINATION MANAGEMENT PROFILE
31
153
159
Aim: The aim of this study was to examine the effect of the cadioselective B-1-adrenoceptor blocker nebivolol on glycaemic control, lipid profile and markers of oxidative stress in patients with type 2 diabetes over a 6-month period.Methods: Twenty-six patients with mild to moderate hypertension (140-160 mmHg systolic, 90-105 mmHg diastolic) confirmed on 24-h blood pressure monitoring, were treated with nebivolol 5 mg daily for 6 months. Total serum cholesterol, triglycerides, high-density lipoprotein (HDL) cholesterol and low-density lipoprotein (LDL) subfractions, lipid hydroperoxides (LHPs) and total antioxidant capacity (TAC) were measured before and after 6 months of treatment.Results: Nebivolol, as expected, reduced mean daytime systolic and diastolic pressures on ambulatory monitoring (149 +/- 9 to 140 t +/- 13 mmHg, P = 0.02 and 84 +/- 7 to 77 +/- 9 mmHg, P < 0.001). There were no significant changes in serum cholesterol or triglycerides following treatment but a significant increase in HDL cholesterol was noted (1.12 +/- 0.19 to 1.25 +/- 0.36 mmol/L, P = 0008). Patients showed a highly significant reduction in TAC from 501 57 to 422 +/- 29 trolox equivalent (P < 0.001). Baseline LHPs were very high and showed no significant change over the 6-month period (18.7 +/- 7.4 and 18.7 +/- 10.9 mu mol/L). The LDL score increased significantly from 1.7 +/- 0.7 to 2.3 +/- 0.7 (P = 00002) at 6 months suggesting a change to a more atherogenic lipid profile. Neither weight nor glycaemic control changed during treatment.Conclusion: Nebivolol appears to be lipid neutral and may even have a positive effect on HDL cholesterol. Despite this it may promote the formation of potentially atherogenic LDL subfractions possibly as a result of reduced antioxidant defences. Further studies are needed to clarify the changes observed in parameters of oxidative stress.
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