The Relationship Between Epicardial Fat Tissue and Cardiac Function in HFpEF Patients

December 31, 2025 updated by: Dongying Zhang

The Relationship Between Epicardial Fat Tissue and Cardiac Function in HFpEF

Heart failure with preserved ejection fraction (HFpEF) refers to a group of symptoms and signs of heart failure, normal or near-normal left ventricular systolic function (EF>50%), and ventricular muscle diastolic dysfunction and A clinical syndrome characterized by decreased compliance and increased stiffness. The pathogenesis of HFpEF is related to impaired lipid metabolism and inflammation. Epicardial adipose tissue (Epicardial Adipose tissue, EAT) is a kind of visceral adipose tissue. Related studies have shown that extracardiac Membrane fat is related to inflammation markers, cardiometabolic risk and cardiovascular disease.However, there is still no research investigating the the relationship between epicardial fat thickness and Cardiac Function in HFpEF patients.

Study Overview

Detailed Description

Heart failure with preserved ejection fraction (HFpEF) refers to a group of symptoms and signs of heart failure, normal or near-normal left ventricular systolic function (EF>50%), and ventricular muscle diastolic dysfunction and A clinical syndrome characterized by decreased compliance and increased stiffness. The pathogenesis of HFpEF is related to impaired lipid metabolism and inflammation. Epicardial adipose tissue (Epicardial Adipose tissue, EAT) is a kind of visceral adipose tissue, which is composed of adipose tissue deposited between the myocardium and the visceral layer of the pericardium. It is closely adjacent to the coronary arteries and myocardium. Related studies have shown that extracardiac Membrane fat is related to inflammation markers, cardiometabolic risk and cardiovascular disease.However, there is still no research investigating the the relationship between epicardial fat thickness and Cardiac Function in HFpEF patients. This study intends to observe the relationship between epicardial fat thickness and left and right functions in patients with HFpEF, and evaluate whether epicardial fat thickness can be used as an indicator of left and right dysfunction.

Study Type

Observational

Enrollment (Actual)

1083

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Chongqing, China
        • The First Affiliated Hospital of Chongqing Medical University

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.

Eligibility Criteria

Ages Eligible for Study

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Sampling Method

Non-Probability Sample

Study Population

Heart failure patients with preserved ejection fraction (HFpEF)

Description

Inclusion Criteria:

  • Adult aged >=18years old;
  • Diagnosed with HFpEF.

Diagnostic criteria including:

  1. left ventricular ejection fraction ≥50%;
  2. with the symptoms and/or signs of heart failure;
  3. BNP≥35 pg/mL and/or NTproBNP≥125 pg/mL;
  4. at least one additional criterion: relevant structural heart disease(LVH and/or LAE) or diastolic dysfunction

Exclusion Criteria:

  • LVEF less than 45% at any time;
  • Severe liver failure;
  • Primary pulmonary hypertension;
  • Age <18 years old.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Epicardial Fat Tissue
Time Frame: On admission
Epicardial Fat Tissue by cardiac color Doppler ultrasound
On admission
Cardiac Function
Time Frame: On admission
Left ventricular diastolic function and right ventricular systolic function by cardiac color Doppler ultrasound
On admission
Composite Endpoint of Worsening Heart Failure Event and Cardiovascular Death
Time Frame: From date of discharge until the date of first worsening HF event or date of death, whichever came first, assessed up to 5 years
Composite Endpoint of Worsening Heart Failure Event and Cardiovascular Death
From date of discharge until the date of first worsening HF event or date of death, whichever came first, assessed up to 5 years

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Worsening HF Event
Time Frame: From date of discharge until the date of first worsening HF event or date of death, whichever came first, assessed up to 5 years
Worsening Heart Failure Event
From date of discharge until the date of first worsening HF event or date of death, whichever came first, assessed up to 5 years
CV Death
Time Frame: From date of discharge until the date of death, whichever came first, assessed up to 10 years
Cardiovascular Death
From date of discharge until the date of death, whichever came first, assessed up to 10 years
All-cause Death
Time Frame: From date of discharge until the date of death, whichever came first, assessed up to 10 years
Death from any causes
From date of discharge until the date of death, whichever came first, assessed up to 10 years

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Investigators

  • Study Director: Dongying Zhang, doctor, First Affiliated Hospital of Chongqing Medical University

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

October 12, 2020

Primary Completion (Actual)

December 10, 2025

Study Completion (Actual)

December 15, 2025

Study Registration Dates

First Submitted

September 26, 2021

First Submitted That Met QC Criteria

September 26, 2021

First Posted (Actual)

October 6, 2021

Study Record Updates

Last Update Posted (Estimated)

January 6, 2026

Last Update Submitted That Met QC Criteria

December 31, 2025

Last Verified

December 1, 2025

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • 2020-09

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

Clinical Trials on Heart Failure With Preserved Ejection Fraction

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