Cardiovascular Research Advance Access [Accepted Manuscript] published online on May 29, 2008
Cardiovascular Research, doi:10.1093/cvr/cvn136
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A Review of Methods for Assessment of Coronary Microvascular Disease in Both Clinical and Experimental Settings
1 Dept. of Physiology, Charité - Universitätsmedizin Berlin,Campus Benjamin Franklin, Arnimallee 22, D-14195 Berlin, Germany
2 Deutsches Herzzentrum Berlin, Augustenburger Platz 1, D-13353 Berlin, Germany
3 Division of Cardiology, University of Perugia School of Medicine, Ospedale Silvestrini, 06156 Perugia, Italy
4 Dept. of Cardiology P, Kas Gentofte, 2900 Hellerup, Denmark
5 Cardiac and VascularSciences, St. George's, University of London, London SW17 0RE, UK
6 Med. Klinik IV, JWG-Universität Frankfurt, 60590 Frankfurt, Germany
7 Abt. Innere Medizin, Zentrum für Innere Medizin, Gießen, Germany
8 Division de Cardiologie, CHUV, 1011 Lausanne, Switzerland
9 Med. Klinik u. Poliklinik I, LMU München, Klinikum Großhadern, Munich, Germany
10 Institut für Physiologie, Universität zu Lübeck, Lübeck, Germany
11 Dipartimento di Medicina Interna, Policlinico S. Orsola, 40138 Bologna, Italy
Address for correspondence: Raffaele Bugiardini, MD Dipartimento di Medicina Interna Policlinico S. Orsola 40138 Bologna, Italy E-mail: raffaele.bugiardini{at}unibo.it
Obstructive disease of the large coronary arteries is the prominent cause for angina pectoris. However, angina may also occur in the absence of significant coronary atherosclerosis or coronary artery spasm, especially in women. Myocardial ischemia in these patients is often associated with abnormalities of the coronary microcirculation and may thus represent a manifestation of coronary microvascular disease (CMD). Elucidation of the role of the microvasculature in the genesis of myocardial ischemia and cardiac damage - in the presence or absence of obstructive coronary atherosclerosis - will certainly result in more rational diagnostic and therapeutic interventions for patients with ischaemic heart disease. Specifically targeted research based on improved assessment modalities is needed to improve the diagnosis of CMD, and to translate current molecular, cellular, and physiologic knowledge into new therapeutic options.
KEYWORDS Coronary microvascular disease; microvascular angina; plethysmography; laser doppler flux; iontophoresis; intravital microscopy
Time for primary review: 23 days
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