A Study to Examine if People Without HFpEF Display Less Visceral Adipose Tissue (VAT) Compared to Patients with Diagnosed HFpEF

Overview

Información sobre este estudio

The purpose of this study is to examine whether people without HFpEF display less visceral adipose tissue (VAT) compared to patients with diagnosed HFpEF.

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:

  1. Adult Participants, non-HFpEF (25 prospectively enrolled)
    1. Adult controls (>18 years) age, sex, and BMI matched without signs or symptoms of heart failure, confirmed via limited echocardiogram and physical examination.
  2. Data retrospectively collected from 25 Adult Participants with HFpEF (≥3 months), age 40-85 years who were enrolled in study 16-001467, defined by:
    1. Signs and symptoms of HF (dyspnea, fatigue), normal left ventricular (LV) EF (≥50% within 12 months of enrollment), and objective evidence of HF as met by at least 1 of the following 4 criteria:
      1. Hospitalization for decompensated HF in the past year but not within the past 30 days;
      2. Invasively-documented elevated pulmonary capillary wedge pressures (PCWP) at rest (>15 mmHg) or with exercise (≥25 mmHg) at catheterization performed in the evaluation of dyspnea;
      3. Elevated NT-proBNP (>400 pg/mL) or BNP (>200 pg/mL);
      4. Echocardiographic evidence of HFpEF based upon current diagnostic guidelines(≥2 of the following: [a] E/e’≥15, [b] ≥moderate left atrial enlargement, [c] PASP >35 mm Hg).

Exclusion Criteria:

  1. Adult Participants, non-HFpEF
    1. Signs and symptoms of HF (dyspnea, fatigue), reduced left ventricular (LV) EF (≤50% within 12 months of enrollment), and objective evidence of HF as met by at least 1 of the following 4 criteria:
    2. Hospitalization for decompensated HF in the past year but not within the past 30 days;
    3. Invasively-documented elevated pulmonary capillary wedge pressures (PCWP) at rest (>15 mmHg) or with exercise (≥25 mmHg) at catheterization performed in the evaluation of dyspnea;
    4. Elevated NT-proBNP (>400 pg/mL) or BNP (>200 pg/mL);
    5. Echocardiographic evidence of HFpEF based upon current diagnostic guidelines40 (≥2 of the following: [a] E/e’≥15, [b] ≥moderate left atrial enlargement, [c] PASP >35 mm Hg).
  2. Data retrospectively collected from 25 Adult Participants with HFpEF (≥3 months), age 40-85 years who were enrolled in study 16-001467, defined by:
    1. Inability/unwillingness to engage in ET 
    2. Recent (<1 months) HF hospitalization 
    3. Concomitant treatment with organic nitrates or phosphodiesterase 5 inhibitors 
    4. Prior EF <50%, BMI <20 or >50 kg/m2 
    5. Acute coronary syndrome or revascularization within 3 months
    6. Infiltrative, hypertrophic, or radiation-induced cardiomyopathies 
    7. Constrictive pericarditis 
    8. Dyspnea felt to be due to primary lung disease or myocardial ischemia 
    9. Severe anemia (Hgb <8.0) 
    10. Systolic BP <110 mm Hg at consent  
    11. Recent (<30 day) change in diuretics/vasoactive medications 
    12. Significant left-sided valvular heart disease (>mild stenosis, >moderate regurgitation) 
    13. Complex congenital heart disease 
    14. Severe renal (estimated GFR<30) or hepatic disease

 

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

Rochester, Minn.

Investigador principal de Mayo Clinic

Thomas Olson, Ph.D., M.S.

Cerrado para la inscripción

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