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Microalbuminuria and oxidative stress in essential hypertension
Authors:Giner V  Tormos C  Chaves F J  Sáez G  Redón J
Affiliation:Department of Biochemistry of the Medical School, Hypertension Clinic, University of Valencia, Avda. Blasco Iba?ez 17, 46010 Valencia, Spain.
Abstract:OBJECTIVE: To assess the relationship between microalbuminuria and oxidative stress in mononuclear peripherals cells in essential hypertension. METHODS: A total of 123 hypertensive patients in absence of antihypertensive treatment were included. A 24-h ambulatory blood pressure (BP) monitoring was performed using a Spacelabs 90207 monitor, and microalbuminuria was measured in 24-h urine collections. Oxidized/reduced glutathione ratio and the content of malondialdehide and damaged base 8-oxo-2'-deoxyguanosine in genomic and mitochondrial DNA were measured in peripheral mononuclear cells. RESULTS: In the 29 (24%) microalbuminuric subjects, the amount of reduced glutathione was significantly lower and the ratio oxidized/reduced glutathione was significantly higher than in the normoalbuminuric subjects. In contrast, the simultaneous measurement of the levels of malondialdehide and 8-oxo-2'-deoxyguanosine from both genomic and mitochondrial DNA oxidation did not achieve statistical significance between the two groups. Subjects with the highest oxidized/reduced glutathione ratio tertile showed the highest urinary albumin excretion (UAE) (P = 0.04 for trend). In a stepwise multiple regression analysis, oxidized/reduced glutathione ratio was the main significant determinant of UAE accounting for the 9% of the variance when 24-h mean BP, age, sex, body mass index, glucose and total cholesterol were included in the model. CONCLUSIONS: Oxidative stress seems to be a determinant of UAE independent of BP levels even in hypertensive subjects.
Keywords:antioxidants    DNA damage    hyper-tension    microalbuminuria    oxidative stress    risk factors
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