A Study of Autoimmune Functions in Patients with Myocarditis

Overview

Información sobre este estudio

The purpose of this research is to study immune cells called T cells and monocytes (types of blood cells that fight infection and can also cause autoimmune disease) that may damage heart tissue during myocarditis (inflammation of the heart muscle). Cytokines (proteins that send signals between cells) found in the blood will be studied for their effects on blood immune cells to better understand how they can lead to heart failure during and after myocarditis.

Elegibilidad para la participación

Los requisitos de elegibilidad de los participantes incluyen la edad, el sexo, el tipo y el estadio de la enfermedad, y los problemas de salud o tratamientos previos. Las pautas difieren de un estudio a otro e identifican quiénes pueden o no pueden participar. No hay garantía de que cada persona elegible que desee participar en un ensayo se inscribirá. Comunícate con el equipo del estudio para analizar la elegibilidad del estudio y la posible participación.

Inclusion Criteria:

  • Symptom onset less than 6 months prior to enrollment.
  • An acute clinical syndrome compatible with myocarditis consisting of either heart failure or chest pain typical of an acute myocardial infarction.
  • Discrete regional wall motion abnormalities on echocardiogram or CRM with an ejection fraction 50%.
  • A globally dilated left ventricle for DCM patients.
  • A coronary angiogram or coronary CT scan with no greater than 50% stenosis in any epicardial coronary artery or a CRM with no regions of post-gadolinium endomyocardial hyper enhancement to exclude ischemic cardiomyopathy.
  • For myocarditis patients- either an endomyocardial biopsy that meets the “Dallas Criteria” for myocarditis or borderline myocarditis or a CRM scan that meets Lake Louise diagnostic criteria for acute myocarditis.
  • Echocardiography may be substituted for CRM when CRM is contraindicated for patients for reasons such as the presence of a pacemaker or claustrophobia.
  • Ability to sign informed consent.

Exclusion Criteria:

  • Diagnosis of ischemic, valvular, or congenital cardiomyopathy by echocardiogram or CRM.
  • Serum creatinine greater than 2.0 mg/dL or an estimated GFR of <30cc/min.
  • Coronary artery disease (one or more lesions >50%).
  • Methamphetamine use in the last 5 years.
  • History of alcohol use exceeding 3 drinks per day.
  • Cardiac transplant recipient.
  • Myocardial biopsy demonstrates evidence of hemochromatosis or amyloidosis.
  • Other potential etiology of cardiomyopathy such as a history of receiving chemotherapy, uncorrected thyroid disease, uncontrolled hypertension despite medical therapy, hypertrophic cardiomyopathy, significant primary valvular disease.
  • Evidence of ongoing bacteremia.
  • History of malignancy treated with chemotherapy or chest radiation within the last five years or life threatening disease that would likely decrease life expectancy to less than three years.
  • Pregnancy.
  • Lack of ability or refusal to sign informed consent.

Sedes participantes de Mayo Clinic

Los estatus de los estudios cambian con frecuencia. Comunícate con el equipo del estudio para obtener la información más actualizada acerca de la posibilidad de participar.

Sede de Mayo Clinic Estatus Contacto

Jacksonville, Fla.

Investigador principal de Mayo Clinic

Leslie Cooper, M.D.

Abierto para la inscripción

Contact information:

Katrina Taylor

Taylor.Katrina@mayo.edu

More information

Publicaciones

Publications are currently not available
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CLS-20359608

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