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11.05.2026 13:57

Treatment of spontaneous coronary artery dissection

Christine Vollgraf Presse- und Öffentlichkeitsarbeit
Deutsches Zentrum für Herz-Kreislauf-Forschung e.V.

    A consortium of ten international academic organisations within the Global Cardiovascular Research Funders Forum (GCRFF) is launching a new international study. For the first time, the study will investigate the optimal antiplatelet therapy for spontaneous coronary artery dissection (SCAD), a distinct form of heart attack that primarily affects women. The initiative is led by the German Centre for Cardiovascular Research (DZHK) and is coordinated by the University Medical Center Hamburg-Eppendorf (UKE).

    Spontaneous coronary artery dissection (SCAD) is a rare cause of acute coronary syndrome in which blood flow to the heart muscle is reduced or interrupted. It predominantly affects women between 30 and 55 years of age and typically occurs in the absence of atherosclerosis.

    For many years, SCAD remained underdiagnosed and has only recently been more systematically recognised. An international research consortium led by the DZHK is now launching the SCAD-ALIGN trial, the first randomised study to systematically compare two antiplatelet treatment strategies in patients with SCAD.

    Heart attack without atherosclerosis

    SCAD is usually not associated with significant atherosclerosis or the classic vessel occlusion caused by a blood clot. Instead, bleeding occurs within the wall of a coronary artery, causing the vessel layers to separate and thereby impairing or completely obstructing blood flow. Patients develop symptoms of acute myocardial infarction, such as chest pain, shortness of breath, or nausea. A characteristic feature is that these symptoms often occur in individuals without a prior history or risk of heart disease.

    Platelets play a crucial role in blood clotting but can also accumulate inside blood vessels and further impair flow. Antiplatelet medications are used to prevent this. In current clinical practice, SCAD patients are often treated according to general guidelines for acute coronary syndrome, which typically include two different antiplatelet therapies, a strategy developed and tested in older patients with proven atherosclerosis.

    How intensive should antiplatelet therapy be?

    The SCAD-ALIGN trial is based on a fundamental difference between SCAD and classic heart attacks. In typical heart attacks, a blood clot usually blocks a vessel, and after the implantation of a vascular support device (“stent”), intensive antiplatelet therapy is used to prevent further clot formation. In SCAD, however, the underlying problem is a tear or bleeding within the vessel wall. In this situation, intensive antiplatelet therapy could delay the resolution of the bleeding or even worsen it, thereby adversely affecting the course of the disease. The study will therefore investigate whether a less intensive treatment strategy may be more beneficial in these patients.

    The SCAD-ALIGN trial compares two treatment strategies: moderate antiplatelet therapy with a single medication for three months versus more intensive therapy with two agents for three months, followed by nine months of treatment with a single medication. The primary endpoint is a composite of recurrent myocardial ischemia, recurrent SCAD, myocardial infarction, the need for revascularization, and death.

    “Until now, we have treated SCAD patients according to standards developed for other cardiovascular conditions,” says Professor Peter Clemmensen, national principal investigator for Germany. “With the SCAD-ALIGN trial, we aim to determine which form of antiplatelet therapy truly benefits patients and which may instead cause harm. Our goal is to establish a robust foundation for future treatment recommendations.”

    International collaboration for women’s cardiovascular health

    The SCAD-ALIGN trial is part of the Multinational Clinical Trials Initiative of the Global Cardiovascular Research Funders Forum (GCRFF). “This study addresses a clinical question that primarily affects women and for which robust evidence remains very limited, with little commercial incentive for industry-led development,” emphasises Professor Christina Magnussen, national co-principal investigator for Germany and member of the global Executive Board.

    For the first time, multiple international funding organisations are collaborating based on a shared study protocol. The scientific concept for the trial originated from members of the DZHK.

    “Reaching beyond the medical question, this study shows how an alliance of international funding organisations and researchers can create sustainable structures to address major clinical challenges,” says Professor Stefan Blankenberg from the University Heart and Vascular Center Hamburg, scientific lead and initiator of the study.

    He adds: “A coordinated effort by funding organisations from democratic countries, including Germany, the United Kingdom, the Netherlands, Denmark, Sweden, Spain, Australia, New Zealand, and Canada, complemented by support from the Kühne Foundation and followed by participation of Brazil, Argentina, and Chile, is creating a global academic framework. Particularly in times global challenges this jointly legitimised approach demonstrates its unique strength.”

    The study is designed as an international, multicentre, randomised, open-label clinical trial. Because SCAD is a rare condition, close collaboration across national borders is essential. The results are expected to make an important contribution to the development of evidence-based treatment recommendations for SCAD, improve care and quality of life for patients worldwide.

    Participating GCRFF Funding Organisations:

    British Heart Foundation (BHF), United Kingdom
    Canadian Institutes of Health Research (CIHR) - Institute of Circulatory and Respiratory Health, Canada
    German Centre for Cardiovascular Research (DZHK), Germany
    Dutch Heart Foundation (Hartstichting), Netherlands
    National Heart Foundation of New Zealand, New Zealand
    National Heart Foundation of Australia, Australia – Application process not yet finalised
    National Institutes of Health - National Heart, Lung, and Blood Institute (NIH/NHLBI), United States – Application process not yet finalised

    Participating National and Institutional Funding Organisations:

    Danish Heart Foundation (Hjerteforeningen), Denmark
    Swedish Heart-Lung Foundation, Sweden
    Swiss Heart Foundation, Switzerland – Application process not yet finalised
    Institutional funding from the Victor Chang Cardiac Research Institute, Sydney, Australia
    Institutional funding from the Westmead Applied Research Centre, University of Sydney and NSW Health Cardiovascular Research Grant, Australia
    Institutional funding from the University Medical Center Hamburg-Eppendorf, Germany
    Institutional funding from participating Spanish centres (including Hospital Universitario de La Princesa, Madrid, Spain)

    Participating Private Foundation:

    Kühne Foundation


    Wissenschaftliche Ansprechpartner:

    Professor Stefan Blankenberg, University Heart & Vascular Center, University Medical Center Hamburg-Eppendorf (UKE), s.blankenberg@uke.de


    Bilder

    In a spontaneous coronary artery dissection (SCAD), a tear or bleeding occurs in the wall of a coronary artery.
    In a spontaneous coronary artery dissection (SCAD), a tear or bleeding occurs in the wall of a coron ...

    Copyright: DZHK/Armin Schieb - Sepia

    From left to right: Prof Stefan Blankenberg (scientific lead and initiator of the study), Prof Christina Magnussen (national co-principal investigator for Germany), Prof Peter Clemmensen (national principal investigator for Germany).
    From left to right: Prof Stefan Blankenberg (scientific lead and initiator of the study), Prof Chris ...

    Copyright: German Centre for Cardiovascular Research (DZHK), University Medical Center Hamburg-Eppendorf (UKE)


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    In a spontaneous coronary artery dissection (SCAD), a tear or bleeding occurs in the wall of a coronary artery.


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    From left to right: Prof Stefan Blankenberg (scientific lead and initiator of the study), Prof Christina Magnussen (national co-principal investigator for Germany), Prof Peter Clemmensen (national principal investigator for Germany).


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