Lowering serum urate does not improve endothelial function in patients with type 2 diabetes |
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Authors: | W. S. Waring J. A. McKnight D. J. Webb S. R. J. Maxwell |
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Affiliation: | (1) Clinical Pharmacology Unit, University of Edinburgh, Edinburgh, UK;(2) Department of Diabetes, Western General Hospital, Edinburgh, UK;(3) The Queen’s Medical Research Institute, University of Edinburgh, 3rd Floor East, Room E3.22, 47 Little France Crescent, Edinburgh, EH16 4TJ, UK |
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Abstract: | Aims/hypothesis Endothelial dysfunction contributes to excess cardiovascular risk in patients with type 2 diabetes. There is strong evidence of an association between high serum uric acid concentrations and endothelial dysfunction, and uric acid has been proposed as an independent cardiovascular risk factor in type 2 diabetes. We hypothesised that lowering of uric acid concentrations might allow restoration of endothelial function in this high-risk group. Methods Intravenous urate oxidase (1.5 mg) was administered to ten patients with type 2 diabetes and ten healthy participants in a two-way, randomised, placebo-controlled, crossover study. Forearm blood flow responses to intra-brachial acetylcholine, sodium nitroprusside and N G-monomethyl-l-arginine (L-NMMA) were measured using venous occlusion plethysmography. The augmentation index (AIx) was determined by pulse wave analysis as a measure of large arterial stiffness. Results Acetylcholine and L-NMMA evoked lesser responses in patients with type 2 diabetes than in healthy participants. Baseline AIx was higher in patients with type 2 diabetes (mean ± SD: 13.1 ± 6.9%) than in healthy participants (2.0 ± 5.1%; p = 0.006). Urate oxidase lowered serum uric acid concentrations by 64 ± 11% (p < 0.001), but this had no effect on forearm blood flow responses or AIx in either group. Conclusions/interpretation Substantial short-term lowering of uric acid did not have a direct vascular effect, suggesting that, on its own, this might not be an effective strategy for restoring endothelial function in patients with type 2 diabetes. |
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Keywords: | Antioxidants Atherosclerosis Cardiovascular risk Endothelial function Hyperuricaemia Nitric oxide Type 2 diabetes Urate oxidase Uric acid Vascular function |
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