Hyperuricaemia does not impair cardiovascular function in healthy adults

Objective: To investigate the possibility that uric acid (UA) can impair endothelial function, an important surrogate for atherosclerosis. Design: UA was administered locally or systemically to healthy adult men and women in a series of randomised placebo controlled studies. This temporarily raised...

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Published inHeart (British Cardiac Society) Vol. 90; no. 2; pp. 155 - 159
Main Authors Waring, W S, Adwani, S H, Breukels, O, Webb, D J, Maxwell, S R J
Format Journal Article
LanguageEnglish
Published London BMJ Publishing Group Ltd and British Cardiovascular Society 01.02.2004
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Abstract Objective: To investigate the possibility that uric acid (UA) can impair endothelial function, an important surrogate for atherosclerosis. Design: UA was administered locally or systemically to healthy adult men and women in a series of randomised placebo controlled studies. This temporarily raised serum UA concentrations, so that the potential effects of hyperuricaemia on mechanisms of cardiovascular disease could be studied. Main outcome measures: The effects of UA administration on basal blood flow and responses to locally administered acetylcholine, sodium nitroprusside, and l-NG-monomethylarginine were studied in the forearm vascular bed with venous occlusion plethysmography. The effects of hyperuricaemia on systemic vascular resistance, large artery compliance, and baroreflex sensitivity were examined by validated non-invasive techniques. Results: UA administration caused a twofold increase in serum concentrations. However, there were no acute effects on haemodynamic variables, basal forearm blood flow, or nitric oxide dependent endothelial function. Conclusion: Unlike other risk factors associated with endothelial dysfunction, acute exposure to high concentrations of UA does not impair cardiovascular function in healthy men. These findings do not support a causal link between hyperuricaemia and atherosclerosis.
AbstractList Objective: To investigate the possibility that uric acid (UA) can impair endothelial function, an important surrogate for atherosclerosis. Design: UA was administered locally or systemically to healthy adult men and women in a series of randomised placebo controlled studies. This temporarily raised serum UA concentrations, so that the potential effects of hyperuricaemia on mechanisms of cardiovascular disease could be studied. Main outcome measures: The effects of UA administration on basal blood flow and responses to locally administered acetylcholine, sodium nitroprusside, and l -NG -monomethylarginine were studied in the forearm vascular bed with venous occlusion plethysmography. The effects of hyperuricaemia on systemic vascular resistance, large artery compliance, and baroreflex sensitivity were examined by validated non-invasive techniques. Results: UA administration caused a twofold increase in serum concentrations. However, there were no acute effects on haemodynamic variables, basal forearm blood flow, or nitric oxide dependent endothelial function. Conclusion: Unlike other risk factors associated with endothelial dysfunction, acute exposure to high concentrations of UA does not impair cardiovascular function in healthy men. These findings do not support a causal link between hyperuricaemia and atherosclerosis.
To investigate the possibility that uric acid (UA) can impair endothelial function, an important surrogate for atherosclerosis. UA was administered locally or systemically to healthy adult men and women in a series of randomised placebo controlled studies. This temporarily raised serum UA concentrations, so that the potential effects of hyperuricaemia on mechanisms of cardiovascular disease could be studied. The effects of UA administration on basal blood flow and responses to locally administered acetylcholine, sodium nitroprusside, and L-N(G)-monomethylarginine were studied in the forearm vascular bed with venous occlusion plethysmography. The effects of hyperuricaemia on systemic vascular resistance, large artery compliance, and baroreflex sensitivity were examined by validated non-invasive techniques. UA administration caused a twofold increase in serum concentrations. However, there were no acute effects on haemodynamic variables, basal forearm blood flow, or nitric oxide dependent endothelial function. Unlike other risk factors associated with endothelial dysfunction, acute exposure to high concentrations of UA does not impair cardiovascular function in healthy men. These findings do not support a causal link between hyperuricaemia and atherosclerosis.
Objective: To investigate the possibility that uric acid (UA) can impair endothelial function, an important surrogate for atherosclerosis. Design: UA was administered locally or systemically to healthy adult men and women in a series of randomised placebo controlled studies. This temporarily raised serum UA concentrations, so that the potential effects of hyperuricaemia on mechanisms of cardiovascular disease could be studied. Main outcome measures: The effects of UA administration on basal blood flow and responses to locally administered acetylcholine, sodium nitroprusside, and l - N G -monomethylarginine were studied in the forearm vascular bed with venous occlusion plethysmography. The effects of hyperuricaemia on systemic vascular resistance, large artery compliance, and baroreflex sensitivity were examined by validated non-invasive techniques. Results: UA administration caused a twofold increase in serum concentrations. However, there were no acute effects on haemodynamic variables, basal forearm blood flow, or nitric oxide dependent endothelial function. Conclusion: Unlike other risk factors associated with endothelial dysfunction, acute exposure to high concentrations of UA does not impair cardiovascular function in healthy men. These findings do not support a causal link between hyperuricaemia and atherosclerosis.
OBJECTIVETo investigate the possibility that uric acid (UA) can impair endothelial function, an important surrogate for atherosclerosis.DESIGNUA was administered locally or systemically to healthy adult men and women in a series of randomised placebo controlled studies. This temporarily raised serum UA concentrations, so that the potential effects of hyperuricaemia on mechanisms of cardiovascular disease could be studied.MAIN OUTCOME MEASURESThe effects of UA administration on basal blood flow and responses to locally administered acetylcholine, sodium nitroprusside, and L-N(G)-monomethylarginine were studied in the forearm vascular bed with venous occlusion plethysmography. The effects of hyperuricaemia on systemic vascular resistance, large artery compliance, and baroreflex sensitivity were examined by validated non-invasive techniques.RESULTSUA administration caused a twofold increase in serum concentrations. However, there were no acute effects on haemodynamic variables, basal forearm blood flow, or nitric oxide dependent endothelial function.CONCLUSIONUnlike other risk factors associated with endothelial dysfunction, acute exposure to high concentrations of UA does not impair cardiovascular function in healthy men. These findings do not support a causal link between hyperuricaemia and atherosclerosis.
Audience Professional
Author Waring, W S
Breukels, O
Maxwell, S R J
Webb, D J
Adwani, S H
AuthorAffiliation 2 Department of Pharmacy, Utrecht University, Utrecht, the Netherlands
1 Centre for Cardiovascular Science, The University of Edinburgh, Edinburgh, UK
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Issue 2
Keywords Human
Hyperuricemia
Metabolic diseases
Adult
Purine
Circulatory system
Uric acid
Cardiology
Phlebology
Language English
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Correspondence to:
 Dr W S Waring
 Clinical Pharmacology Unit, The University of Edinburgh, Western General Hospital, Crewe Road, Edinburgh, UK; s.waring@ed.ac.uk
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Correspondence to: …Dr W S Waring …Clinical Pharmacology Unit, The University of Edinburgh, Western General Hospital, Crewe Road, Edinburgh, UK; s.waring@ed.ac.uk
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Snippet Objective: To investigate the possibility that uric acid (UA) can impair endothelial function, an important surrogate for atherosclerosis. Design: UA was...
To investigate the possibility that uric acid (UA) can impair endothelial function, an important surrogate for atherosclerosis. UA was administered locally or...
OBJECTIVETo investigate the possibility that uric acid (UA) can impair endothelial function, an important surrogate for atherosclerosis.DESIGNUA was...
Objective: To investigate the possibility that uric acid (UA) can impair endothelial function, an important surrogate for atherosclerosis. Design: UA was...
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SubjectTerms acetylcholine
Acetylcholine - pharmacology
ACh
Adolescent
Adult
arterial compliance
Atherosclerosis
baroreceptors
Baroreflex - drug effects
baroreflex sensitivity
Biological and medical sciences
blood flow
blood pressure
Blood Pressure - drug effects
BRS
Cardiology. Vascular system
Cardiovascular disease
Cardiovascular Diseases - etiology
Cardiovascular Diseases - physiopathology
Cardiovascular Medicine
Endothelium
Endothelium, Vascular - drug effects
Enzyme Inhibitors - pharmacology
Female
Forearm - blood supply
Health risk assessment
Humans
Hypertension
Hyperuricemia - complications
Hyperuricemia - physiopathology
Kidney diseases
l-NG-monomethylarginine
L-NMMA
Male
Medical sciences
Metabolic diseases
Metabolism
Middle Aged
Mortality
Nitric oxide
Nitroprusside - pharmacology
omega-N-Methylarginine - pharmacology
Other metabolic disorders
Pulse
pulse interval
Purines and pyrimidines (gout, hyperuricemia...)
SNP
sodium nitroprusside
Studies
uric acid
Uric Acid - administration & dosage
Uric Acid - pharmacology
Vascular Resistance - drug effects
Vasodilator Agents - pharmacology
Women
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Title Hyperuricaemia does not impair cardiovascular function in healthy adults
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