Document Detail


What is the most appropriate methodology for detection of conduit artery endothelial dysfunction?
MedLine Citation:
PMID:  17303783     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
BACKGROUND: Use of upper-arm arterial occlusion to induce reactive hyperemia, and endothelium-dependent flow-mediated dilation (FMD) of the brachial artery, induces greater conduit vessel dilatation than lower-arm occlusion. However, brachial artery ischemia after upper arm arterial occlusion may make this approach unreliable. We studied whether upper or lower arm occlusions differ in their ability to detect endothelial dysfunction in cigarette smokers, and its improvement with an antioxidant strategy. METHODS AND RESULTS: Ten cigarette smokers with a >20 pack year history and 10 age- and gender-matched healthy controls participated in a 2-phase randomized controlled study of xanthine oxidase inhibition, using a 600-mg oral dose of allopurinol administered beforehand. Endothelium-dependent dilatation was assessed using ultrasound-Doppler after lower and upper arm occlusion. After lower arm occlusion, FMD was significantly impaired in smokers compared with controls (3.8+/-1.1% versus 8.7+/-2.2%; P=0.001). However, after upper arm occlusion, brachial artery dilatation in smokers was higher (11.8+/-2.7%; P<0.0001 versus lower arm) and did not differ from controls (9.4+/-2.9%; P=0.3). There was no difference in endothelium-independent dilatation to sublingual nitroglycerin between smokers and controls. Inhibition of xanthine oxidase with allopurinol improved lower arm FMD (3.8+/-1.1 to 10.1+/-1.9%; P<0.0001), but did not improve upper arm FMD (11.8+/-2.7 to 14.1+/-3.7%; P=0.4). CONCLUSIONS: Although upper arm occlusion induces robust brachial vasodilatation, it cannot detect endothelial dysfunction induced by smoking or its improvement by inhibition of xanthine oxidase. The increase in brachial artery diameter with upper arm occlusion may be confounded by ischemia of the artery. Conduit artery FMD after release of lower arm occlusion appears to be a more valid method for assessment of endothelial function in humans.
Authors:
Sasidhar Guthikonda; Christine A Sinkey; William G Haynes
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Publication Detail:
Type:  Clinical Trial, Phase II; Journal Article; Randomized Controlled Trial; Research Support, N.I.H., Extramural     Date:  2007-02-15
Journal Detail:
Title:  Arteriosclerosis, thrombosis, and vascular biology     Volume:  27     ISSN:  1524-4636     ISO Abbreviation:  Arterioscler. Thromb. Vasc. Biol.     Publication Date:  2007 May 
Date Detail:
Created Date:  2007-04-19     Completed Date:  2007-05-08     Revised Date:  2007-11-15    
Medline Journal Info:
Nlm Unique ID:  9505803     Medline TA:  Arterioscler Thromb Vasc Biol     Country:  United States    
Other Details:
Languages:  eng     Pagination:  1172-6     Citation Subset:  IM    
Affiliation:
Department of Cardiology, Baylor College of Medicine, Houston, Tex, USA.
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MeSH Terms
Descriptor/Qualifier:
Administration, Oral
Adolescent
Adult
Aged
Aged, 80 and over
Allopurinol / administration & dosage*,  therapeutic use
Brachial Artery / physiopathology*,  ultrasonography
Cross-Over Studies
Endothelium, Vascular / physiopathology*,  ultrasonography
Enzyme Inhibitors / administration & dosage*,  therapeutic use
Follow-Up Studies
Humans
Middle Aged
Nitroglycerin / diagnostic use
Prognosis
Prospective Studies
Reference Values
Single-Blind Method
Smoking / adverse effects
Ultrasonography, Doppler / methods*
Vascular Diseases / diagnosis,  physiopathology,  prevention & control*
Vasodilation / drug effects,  physiology*
Vasodilator Agents / diagnostic use
Xanthine Oxidase / antagonists & inhibitors
Grant Support
ID/Acronym/Agency:
HL58972/HL/NHLBI NIH HHS; RR00059/RR/NCRR NIH HHS
Chemical
Reg. No./Substance:
0/Enzyme Inhibitors; 0/Vasodilator Agents; 315-30-0/Allopurinol; 55-63-0/Nitroglycerin; EC 1.17.3.2/Xanthine Oxidase
Comments/Corrections
Comment In:
Arterioscler Thromb Vasc Biol. 2007 Aug;27(8):e140; author reply e141   [PMID:  17634516 ]

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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