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Centers and Programs

Spontaneous Coronary Artery Dissection (SCAD) Research Program

  • About
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    • SCAD Description and Management
    • SCAD and Other Arterial Abnormalities
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  • SCAD Research Program leaders

    Understanding SCAD

    Cardiologists Patricia J M Best, M.D.; Marysia S. Tweet, M.D., M.S.; and Sharonne N. Hayes, M.D., investigate the causes and risk factors for SCAD and are working toward solutions for diagnosis, treatment and prevention.

  • Researchers in laboratory

    Studying the genes that cause SCAD

    The SCAD Research Program's DNA and plasma biobank allows the research team to do DNA exome sequencing to pinpoint gene changes related to SCAD.

  • Imaging shows clues to SCAD risk factors

    The Mayo Clinic SCAD Research Program hopes to find clues about why SCAD happens and pinpoint patients at high risk. The image above is of a coronary artery with a blood pocket, also known as a hematoma, in the arterial wall. The hematoma is at the noon to 2 o'clock position in the image.

  • Researchers collecting and monitoring data from a patient

    Patient-initiated research

    The SCAD Research Program was created in response to SCAD survivors who gathered in an online community and were collecting data on their shared condition. They were seeking medical and research collaborators to use their data to answer their questions about SCAD. The multidisciplinary Mayo Clinic SCAD Research Program seeks to answer these important questions.

  • Two healthcare professionals in catheterization laboratory

    SCAD and FMD

    The SCAD Research Program's novel screening protocol helps researchers find and study fibromuscular dysplasia (FMD) and other abnormalities in the arteries of patients with SCAD.

  • Research team collecting neurovascular data

    Research combined with patient care

    Mayo Clinic's SCAD Clinic diagnoses, treats and rehabilitates patients after SCAD, while at the same time advancing knowledge about the condition.

Overview

What is SCAD?

Spontaneous coronary artery dissection (SCAD) is an increasingly recognized cause of heart attack and sudden cardiac death. But it remains poorly understood. Many patients with SCAD are relatively healthy, young or middle-aged women who don't have the usual risk factors for heart disease. This is different from those who have typical atherosclerotic heart attacks.

Researchers are still learning about how often SCAD occurs, what causes it, how often it recurs and how to manage it. Limited evidence is available to guide medical professionals caring for patients with SCAD. Even fewer reliable sources of information are available to patients and families. Although the work that Mayo Clinic SCAD experts have published has dramatically changed medical care for people with SCAD, much remains to be learned.

SCAD Fundamentals, Care and Research at Mayo Clinic

About the SCAD Research Program

Mayo Clinic formed the Spontaneous Coronary Artery Dissection (SCAD) Research Program in 2010. The program brings together experts from different medical specialities who work together to learn the causes of and risk factors for SCAD. The research program also works to create solutions to diagnose, treat and prevent SCAD.

The program was created in response to survivors of SCAD who were using social media to collect data, share their experiences and push for research about the condition. The study population is the largest known SCAD registry in the world. Researchers continue to recruit participants via social media, referrals from healthcare professionals and other methods.

The program takes a new and unique approach to patient-initiated rare disease research, using registries, full reviews of participant data, genetic analyses, advanced medical imaging and other collaborative work. The research is based on a database registry and a DNA and plasma biobank that were created specifically for the program. This approach, which involves research colleagues from across Mayo and at organizations around the world, has already enhanced scientific knowledge and improved the care of patients with SCAD.

The SCAD Research Program studies the genetic causes of SCAD and the changes that happen in people's bodies when they have SCAD. Researchers also look for the best treatments. The research program continually builds its knowledge and clinical expertise. Mayo researchers and their collaborators seek to inspire hope and improve the health and well-being of patients with SCAD.

The SCAD Research Program works closely with patients and research participants. The program aims to provide answers for people with SCAD, as well as their families and healthcare teams. These answers are needed to guide decisions and deliver the best possible healthcare.

Registry and biobank

The Mayo Clinic SCAD Research Program Registry collects data for understanding SCAD, including detailed clinical data and patient-centered outcomes.

The Mayo Clinic SCAD Research Program Registry contains data from more than 1,500 participants with confirmed SCAD. More participants have been screened, had their SCAD diagnoses confirmed and formally agreed to take part in the study, but have missing data. The research team continues to work to complete these patients' records.

The program's DNA and plasma biobank is made up of samples from patients with SCAD and their parents. Researchers use the biobank to look for gene changes that cause SCAD.

The SCAD Research Program has enrolled far more than the estimated number of participants. This shows that SCAD is not as rare a condition as previously thought and is likely underdiagnosed.

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