HeartShare: Combining Omics, Deep Phenotyping, and Electronic Health Records for Heart Failure Subtypes and Treatment Targets

Description

HeartShare is a comprehensive study of heart failure, a common and serious medical condition which occurs when the heart is unable to keep up with the demands of the body, resulting in shortness of breath, fluid retention, and fatigue. HeartShare aims to better classify heart failure into subtypes to help develop more personalized treatments for patients, with the hope that this will improve the lives of heart failure patients. To do this, HeartShare is bringing together a large amount of data (including images, such as heart ultrasounds and MRIs and molecular data from the blood, such as genetics) from previously conducted studies and electronic health records, and is gathering new data through participants enrolled in the HeartShare Deep Phenotyping Study.

Conditions

Heart Failure, Heart Failure With Preserved Ejection Fraction

Study Overview

Study Details

Study overview

HeartShare is a comprehensive study of heart failure, a common and serious medical condition which occurs when the heart is unable to keep up with the demands of the body, resulting in shortness of breath, fluid retention, and fatigue. HeartShare aims to better classify heart failure into subtypes to help develop more personalized treatments for patients, with the hope that this will improve the lives of heart failure patients. To do this, HeartShare is bringing together a large amount of data (including images, such as heart ultrasounds and MRIs and molecular data from the blood, such as genetics) from previously conducted studies and electronic health records, and is gathering new data through participants enrolled in the HeartShare Deep Phenotyping Study.

HeartShare Deep Phenotyping Study

HeartShare: Combining Omics, Deep Phenotyping, and Electronic Health Records for Heart Failure Subtypes and Treatment Targets

Condition
Heart Failure
Intervention / Treatment

-

Contacts and Locations

Sacramento

University of California Davis, Sacramento, California, United States, 95817

Chicago

Northwestern University, Chicago, Illinois, United States, 60611

Boston

Mass General Brigham, Boston, Massachusetts, United States, 02114

Rochester

Mayo Clinic, Rochester, Minnesota, United States, 55905

Winston-Salem

Wake Forest University, Winston-Salem, North Carolina, United States, 27157

Philadelphia

University of Pennsylvania, Philadelphia, Pennsylvania, United States, 19104

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • 1. Age ≥30 years.
  • 2. Prior diagnosis of HF in the EHR (any left ventricular ejection fraction).
  • 1. Age ≥30 years.
  • 2. No known prior diagnosis of HF or use of loop diuretics.
  • 3. No known prior history of BNP \>100 pg/ml or NTproBNP \>300 pg/ml, if prior laboratory tests are available in the EHR.
  • 1. Age ≥30 years.
  • 2. Left ventricular ejection fraction ≥50% measured by echocardiography.
  • 3. Definition of HFpEF: signs and symptoms of HF, NYHA functional class II-IV, and at least one of the following:
  • 1. Elevated BNP (≥75 pg/ml in sinus rhythm or ≥225 pg/ml in atrial fibrillation/flutter) or NTproBNP (≥225 pg/ml in sinus rhythm or ≥675 in atrial fibrillation/flutter) at baseline. Choice of BNP or NTproBNP is based on availability at each clinical center.
  • 2. Prior HF hospitalization (primary reason for the hospitalization is HF with elevated natriuretic peptide levels \[using the thresholds listed above\], requiring IV diuresis for HF, or pulmonary edema or pulmonary vascular congestion on chest radiography).
  • 3. Elevated pulmonary capillary wedge pressure (PCWP) at rest (≥15 mmHg) or during exercise (≥25 mmHg for supine exercise or PCWP/cardiac output ratio ≥2 mmHg/L/min for upright exercise).
  • 4. Elevated H2FPEF score26 (≥5) or HFA-PEFF27 score (≥5).
  • 1. Age ≥30 years.
  • 2. Left ventricular ejection fraction ≥50% measured by echocardiography.
  • 3. No known prior diagnosis of HF or use of diuretics for fluid management.
  • 4. No known prior history of BNP ≥75 pg/ml or NTproBNP ≥225 pg/ml, if prior laboratory tests are available in the EHR.
  • 5. BNP \<75 pg/ml or NTproBNP \<225 pg/ml at the time of screening. Choice of BNP or NTproBNP is based on availability at each clinical center.
  • 1. For non-HF group: any prior known left ventricular ejection fraction \<50%.
  • 2. Prior history of solid organ transplantation.
  • 3. Prior history of mechanical circulatory support.
  • 4. Prior history of non-cardiac cirrhosis.
  • 5. Inability to provide written consent to the study.
  • 1. Life expectancy estimated to be \< 1 year.
  • 2. Primary cardiomyopathy (including amyloid, hypertrophic cardiomyopathy, cardiac sarcoidosis, hemochromatosis, or other infiltrative cardiomyopathies) or pulmonary arterial hypertension (WHO Group I, III, or IV pulmonary hypertension).
  • 3. Any prior known left ventricular ejection fraction \<40%, except if this occurred only in the setting of an acute tachycardia episode (e.g., acute atrial fibrillation).
  • 4. Clinically significant valvular heart disease defined as:
  • 1. Moderate to greater aortic stenosis, pulmonic stenosis, or tricuspid stenosis.
  • 2. Any mitral stenosis.
  • 3. Moderate or greater aortic regurgitation.
  • 4. Greater than moderate mitral regurgitation.
  • 5. Any planned cardiac surgery or cardiac intervention in the next 3 months.
  • 6. Alternative primary reason for symptoms of shortness of breath and exercise intolerance in HFpEF participants in the opinion of the enrolling investigator.
  • 7. Cardiac surgery, acute coronary syndrome, percutaneous coronary intervention, stroke, transient ischemic attack, or carotid intervention in the preceding 6 months prior to enrollment.
  • 8. Known symptomatic epicardial coronary artery disease that is not revascularized.
  • 9. Any non-elective hospitalization in the preceding 2 weeks.
  • 10. Prior history of solid organ transplantation.
  • 11. Prior history of chronic infection (HIV, hepatitis C, hepatitis B, tuberculosis) unless treated and not clinically active in the opinion of the enrolling investigator.
  • 12. Prior history of mechanical circulatory support.
  • 13. Prior history of non-cardiac cirrhosis.
  • 14. Estimated GFR \<20 ml/min/1.73m2 or currently on dialysis.
  • 15. Any condition that may preclude participation or adherence to the study protocol, in the opinion of the enrolling investigator.
  • 16. Inability to provide written consent to the study.
  • 17. Current acute decompensated heart failure.
  • 18. Currently pregnant.

Ages Eligible for Study

30 Years to

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

Yes

Collaborators and Investigators

Northwestern University,

Sanjiv Shah, MD, PRINCIPAL_INVESTIGATOR, Northwestern University

Svati Shah, MD, MHS, STUDY_CHAIR, Duke University

Javed Butler, MPH, MBA, STUDY_CHAIR, Baylor Scott and White Health

Study Record Dates

2026-06