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NCT Number: NCT03671122

PREFERS (Preserved and Reduced Ejection Fraction Epidemiological Regional Study) Stockholm Heart Failure Study

Heart failure (HF) with preserved (HFpEF) or reduced (HFrEF) ejection fraction is associated with poor prognosis and quality of life. While the incidence of HFrEF is declining and HF treatment is effective, HFpEF is increasing, with no established therapy. PREFERS Stockholm is an epidemiological study with the aim of improving clinical care and research in HF and to find new targets for drug treatment in HFpEF starting with a cardiac biopsy study in elective CABG patiens.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Karolinska Institutet

Stockholm, 17176, Sweden

About this study

Patients with new-onset HF (n = 2000) will be characterized at baseline and after 1-year follow-up by standardized protocols for clinical evaluation, echocardiography, and ECG. In one subset undergoing elective coronary bypass surgery (n = 100) and classified according to LV function, myocardial biopsies will be collected during surgery, and cardiac magnetic resonance (CMR) imaging will be performed at baseline and after 1 year. Blood and tissue samples will be stored in a biobank.We will characterize and compare new-onset HFpEF and HFrEF patients regarding clinical findings and cardiac imaging, genomics, proteomics, and transcriptomics from blood and cardiac biopsies, and by established biomarkers of fibrosis, inflammation, haemodynamics, haemostasis, and thrombosis. The data will be explored by state-of-the-art bioinformatics methods to investigate gene expression patterns, sequence variation, DNA methylation, and post-translational modifications, and using systems biology approaches including pathway and network analysis.In this epidemiological HF study with biopsy studies in a subset of patients, we aim to identify new biomarkers of disease progression and to find pathophysiological mechanisms to support explorations of new treatment regimens for HFpEF.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

CABG PREFERS

Inclusion criteria

  • Patients undergoing elective coronary bypass surgery
  • History of heart failure not required
  • Age >18 years
  • Willingness to participate (written informed consent)
  • Possibility to obtain technically satisfactory echocardiography

Inclusion criteria

PREFERS:

  • New-onset heart failure according to ESC guidelines including NT-proBNP >125 ng/L at heart failure clinic or >300 ng/L at emergency department visit or hospital admission
  • Age >18 years
  • Willingness to participate (written informed consent)
  • Possibility to obtain technically satisfactory echocardiography

Exclusion criteria

CABG PREFERS and PREFERS:

  • Cognitive impairment
  • Inability to understand Swedish language
  • Anaemia (haemoglobin level <90 g/L)
  • Heart failure primarily due to valvular disease, primary right ventricular failure, pulmonary artery hypertension, hypertrophic obstructive cardiomyopathy Infiltrative cardiomyopathy (e.g. amyloidosis, sarcoidosis, or haemochromatosis)
  • Severe co-morbidity, severe COPD, severe renal dysfunction (eGFR <30 mL/min/1.73m2). Any other co-morbid disease that will disable the ability to assess or treat heart failure.

Treatment and study plan

Cardiac imaging in the PREFERS and CABG PREFERS cohorts

Diagnostic Test

performed at baseline and after 1 year

Other names: Doppler echocardiography and cMRI

Biomarker analysis in the PREFERS and CABG PREFERS chorts

Other

blood samples will be taken for biomarker analysis at baseline and after 1 year

Other names: blood samples

Cardiac biopsies in the CABG PREFERS cohort

Procedure

myocardial biopsies from the right trium the left and right ventricles will be taken during elective CABG

Primary outcomes

  1. Change in fibrotic biomarkers

    Time frame: 2 years

    For the biopsies (CABG PREFERS), the sample size is based upon the number of patients undergoing elective CABG surgery. Investigators expect to discover mRNAs from genes of potential interest in this material with relevance to differences between preserved ejection fraction, reduced ejection fraction and normal groups by bioinformatics tools. These genes will be further investigated in the blood samples of the PREFERS study and potentially in future heart biopsies. for the PREFERS new onset heart failure study. Investigators calculated a 20% difference between HFrEF and HFpEF groups with regard to both PICP and CITP (higher PICP levels and lower CITP in HFpEF vs. HFrEF) as clinically meaningful. To detect a 20% difference between the HFpEF and the HFrEF groups with 80% power and with an estimated drop-out rate of 50 patients in each group, 250 patients in each group are needed to obtain samples from 200 per group.

  2. Reverse remodeling

    Time frame: 2 years

    diastolic function

Secondary outcomes

  1. cardiac magnetic resonance tomography imaging

    Time frame: 2 years

    ECV by cMRI will be correlated to type of HF whether HFpEF or HFrEF and to echocardiographic findings

Sponsors and collaborators

Lead sponsor

Karolinska Institutet

Other

Collaborators

  • Region Stockholm
  • The Swedish Research Council

Registry information

Official study title

PREFERS PREFERS (Preserved and Reduced Ejection Fraction Epidemiological Regional Study) Stockholm Heart Failure Study

Acronym: PREFERS

Important dates

Study start
2015
Primary completion
2021
Study completion
2021
First posted
Sep 14, 2018
Registry last updated
Mar 31, 2022

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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