Donate Help Contact The AHA Sign In Home
American Heart Association
Circulation
Search: search_blue_button Advanced Search
Published Online
on September 22, 2008

Circulation. 2008
Published online before print September 22, 2008, doi: 10.1161/CIRCULATIONAHA.108.786681
A more recent version of this article appeared on October 7, 2008
This Article
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
118/15/1550    most recent
CIRCULATIONAHA.108.786681v1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowRequest Permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Le Tourneau, T.
Right arrow Articles by Jude, B.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Le Tourneau, T.
Right arrow Articles by Jude, B.
Right arrowPubmed/NCBI databases
*Gene*GEO Profiles
*HomoloGene*UniGene
*Substance via MeSH
Medline Plus Health Information
*Bleeding Disorders
*Cardiomyopathy
*Genetics Home Reference
Related Collections
Right arrow Myocardial cardiomyopathy disease
Right arrow Echocardiography
Right arrow Other diagnostic testing
Right arrowRelated Article

Submitted on April 15, 2008
Accepted on August 5, 2008

Functional Impairment of Von Willebrand Factor in Hypertrophic Cardiomyopathy. Relation to Rest and Exercise Obstruction

Thierry Le Tourneau MD, PhD*, Sophie Susen MD, PhD, Claudine Caron PharmD, Alain Millaire MD, PhD, Sylvestre Maréchaux MD, Anne-Sophie Polge MD, André Vincentelli MD, PhD, Frederic Mouquet MD, PhD, Pierre-Vladimir Ennezat MD, PhD, Nicolas Lamblin MD, PhD, Pascal de Groote MD, PhD, Eric Van Belle MD, PhD, Ghislaine Deklunder MD, PhD, Jenny Goudemand MD, PhD, Christophe Bauters MD, PhD, and Brigitte Jude MD, PhD

From the Centre Hospitalier Régional Universitaire de Lille, Pôle de Cardiologie et Maladies Vasculaires (T.L.T., A.M., F.M., P.-V.E., N.L., P.d.G., E.V.B., C.B.), Service d'Explorations Fonctionnelles Cardiovasculaires (T.L.T., S.M., A.-S.P., G.D.), Pôle d'Hématologie-Transfusion (S.S., C.C., J.G., B.J.), Lille, France; Inserm, ERI9 (T.L.T., S.S., S.M., A.V., F.M., P.-V.E., E.V.B., J.G., B.J.), Lille, France; Inserm, U 744 (N.L., C.B.) Lille, France; and Université de Lille 2, Institut Fédératif de recherche 114, EA 2693 (T.L.T., S.S., S.M., A.V., F.M., P.-V.E., E.V.B., J.G., B.J.), Faculté de Médecine, Lille, France.

* To whom correspondence should be addressed. E-mail: thletourneau{at}yahoo.fr.

Background—Hypertrophic obstructive cardiomyopathy submits blood to conditions of high shear stress. High shear stress impairs von Willebrand factor (VWF) and promotes abnormal bleeding in aortic stenosis. We sought to evaluate VWF impairment and its relationships to baseline or exercise obstruction in hypertrophic cardiomyopathy (HCM).

Methods and Results—Outflow obstruction was evaluated by rest and exercise echocardiography in 62 patients with HCM (age 44±16 years, 40 males). HCM was considered obstructive in 28 patients with rest or exercise peak gradient ≥30 mm Hg. Blood was sampled to assess VWF. History of bleeding was recorded. Baseline median (25th to 75th percentile) peak gradient was 11 (5–62) mm Hg. Shear-induced platelet adhesion was impaired in patients with obstructive HCM. The ratio of VWF–collagen-binding activity to antigen and the percentage of high-molecular-weight multimers of VWF were lower in patients with obstructive HCM than in those with nonobstructive HCM (0.49 [0.43 to 0.59] versus 0.82 [0.73 to 1.03] and 5.0% [3.9% to 7.2%] versus 11.7% [10.8% to 12.5%], respectively; both P<0.0001). Platelet adhesion time, VWF–collagen-binding activity–to-antigen ratio, and the percentage of high-molecular-weight multimers correlated closely and independently with peak gradient (r=0.81, r=-0.68, and r=-0.89, respectively; all P<0.0001). According to receiver operating characteristic curves, a peak gradient threshold of 15 mm Hg at rest and 35 mm Hg during exercise was sufficient to impair VWF. Conversely, VWF function tended to improve with a decrease in peak gradient. Obstructive HCM patients had a trend toward abnormal spontaneous bleeding.

Conclusions—In obstructive HCM, VWF impairment is frequent and is closely and independently related to the magnitude of outflow obstruction. A resting peak gradient of 15 mm Hg is sufficient to impair VWF. VWF abnormalities might favor abnormal bleeding in this setting.


Key words: cardiomyopathy • echocardiography • hypertrophy • physiology • von Willebrand factor • exercise


Related Article:

Clinical Summaries
Circulation 2008 118: 1519-1520. [Extract] [Full Text]



This article has been cited by other articles:


Home page
CirculationHome page
P. P. Dimitrow and A. Undas
Letter by Dimitrow and Undas Regarding Article, "Functional Impairment of von Willebrand Factor in Hypertrophic Cardiomyopathy: Relation to Rest and Exercise Obstruction"
Circulation, June 16, 2009; 119(23): e590 - e590.
[Full Text] [PDF]


Home page
CirculationHome page
T. Le Tourneau, A. Millaire, F. Mouquet, P.-V. Ennezat, A. Vincentelli, N. Lamblin, P. de Groote, E. Van Belle, C. Bauters, S. Marechaux, et al.
Response to Letter Regarding Article, "Functional Impairment of von Willebrand Factor in Hypertrophic Cardiomyopathy: Relation to Rest and Exercise Obstruction"
Circulation, June 16, 2009; 119(23): e591 - e591.
[Full Text] [PDF]