Reproducibility and validity of a novel invasive method of assessing peripheral microvascular vasomotor function.


Journal

PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081

Informations de publication

Date de publication:
2019
Historique:
received: 23 09 2018
accepted: 08 01 2019
entrez: 26 1 2019
pubmed: 27 1 2019
medline: 23 10 2019
Statut: epublish

Résumé

In healthy arteries, blood flow is regulated by microvascular tone assessed by changes in blood flow volume and vascular resistance to endothelium-dependent and -independent vasodilators. We developed a novel method of using intravascular ultrasound (IVUS) and a Doppler flow wire to measure changes in blood flow volume and vascular resistance of the profunda arterial bed. We assessed the variability over 6 months in measuring microvascular endothelium-dependent dilation to acetylcholine and endothelium-independent dilation to adenosine in 20 subjects who were part of a larger study of Gulf War Illness without obstructive peripheral artery disease. Vasomotor function was assessed by Infusions of control (dextrose), acetylcholine (10-6M), adenosine (50μg), and nitroglycerin (25μg/ml). 400 IVUS and 240 flow velocity images were measured a mean 6 (SD = 2) months apart blind to measurement and infusion stage. The mean (SD) baseline profunda flow was 227 (172) ml/min and vascular resistance 4.6 x 104 (2.4 x 104) dynes-s/cm5. The intraclass correlation coefficients for 6-month variability for vascular function were excellent (range 0.827-0.995). Bland-Altman analyses showed mean differences of less than 2% for microvascular endothelium-dependent function (flow volume and resistance) and less than 1% for macrovascular endothelium-dependent function with acceptable limits of agreement. In 49 subjects assessing concurrent validity of the technique against atherosclerosis risk factors, we observed greater impairment in microvascular endothelium-dependent function per year of age (flow volume = -1.4% (p = 0.018), vascular resistance = 1.5% (p = 0.015)) and current smoking (flow volume = -36.7% (p = .006), vascular resistance = 50.0% (p<0.001)). This novel method of assessing microvascular vasomotor function had acceptable measurement reproducibility and validity.

Identifiants

pubmed: 30682202
doi: 10.1371/journal.pone.0211152
pii: PONE-D-18-27746
pmc: PMC6347364
doi:

Types de publication

Clinical Trial Journal Article Research Support, U.S. Gov't, Non-P.H.S.

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0211152

Subventions

Organisme : CSRD VA
ID : I01 CX001549
Pays : United States
Organisme : CSRD VA
ID : I21 CX000793
Pays : United States

Déclaration de conflit d'intérêts

The authors have declared that no competing interests exist.

Références

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Auteurs

Scott Kinlay (S)

Department of Medicine, Cardiovascular Division, Veterans Affairs Boston Healthcare System, West Roxbury Campus, Boston, Massachusetts, United States of America.
Department of Medicine, Cardiovascular Division, Brigham and Women's Hospital, Boston, Massachusetts, United States of America.
Harvard Medical School, Boston, Massachusetts, United States of America.

Mariah Bundy (M)

Department of Medicine, Cardiovascular Division, Veterans Affairs Boston Healthcare System, West Roxbury Campus, Boston, Massachusetts, United States of America.

Melissa Chin (M)

Department of Medicine, Cardiovascular Division, Veterans Affairs Boston Healthcare System, West Roxbury Campus, Boston, Massachusetts, United States of America.

Desiree Tobin (D)

Department of Medicine, Cardiovascular Division, Veterans Affairs Boston Healthcare System, West Roxbury Campus, Boston, Massachusetts, United States of America.

Margot Quinn (M)

Department of Medicine, Cardiovascular Division, Veterans Affairs Boston Healthcare System, West Roxbury Campus, Boston, Massachusetts, United States of America.

Jacquelyn-My Do (JM)

Department of Medicine, Cardiovascular Division, Veterans Affairs Boston Healthcare System, West Roxbury Campus, Boston, Massachusetts, United States of America.

Shannon Johnson (S)

Department of Medicine, Cardiovascular Division, Veterans Affairs Boston Healthcare System, West Roxbury Campus, Boston, Massachusetts, United States of America.

Sara Temiyasathit (S)

Department of Medicine, Cardiovascular Division, Veterans Affairs Boston Healthcare System, West Roxbury Campus, Boston, Massachusetts, United States of America.

Samantha Ly (S)

Department of Medicine, Cardiovascular Division, Veterans Affairs Boston Healthcare System, West Roxbury Campus, Boston, Massachusetts, United States of America.

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Classifications MeSH