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

Sponsor
Karolinska Institutet (Other)
Overall Status
Completed
CT.gov ID
NCT03671122
Collaborator
The Swedish Research Council (Other), Region Stockholm (Other)
683
1
73.9
9.2

Study Details

Study Description

Brief Summary

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.

Condition or Disease Intervention/Treatment Phase
  • Diagnostic Test: Cardiac imaging in the PREFERS and CABG PREFERS cohorts
  • Other: Biomarker analysis in the PREFERS and CABG PREFERS chorts
  • Procedure: Cardiac biopsies in the CABG PREFERS cohort

Detailed Description

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.

Study Design

Study Type:
Observational
Actual Enrollment :
683 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
PREFERS PREFERS (Preserved and Reduced Ejection Fraction Epidemiological Regional Study) Stockholm Heart Failure Study
Actual Study Start Date :
Jan 1, 2015
Actual Primary Completion Date :
Jan 31, 2021
Actual Study Completion Date :
Feb 28, 2021

Arms and Interventions

Arm Intervention/Treatment
PREFERS main study

500 patients with new onset heart failure will be characterized into those with HFpEFand HFrEF at baseline and undergo Cardiac imaging by Doppler echocardiography and cMRI, blood tests for biomarker analysis

Diagnostic Test: Cardiac imaging in the PREFERS and CABG PREFERS cohorts
performed at baseline and after 1 year
Other Names:
  • Doppler echocardiography and cMRI
  • Other: Biomarker analysis in the PREFERS and CABG PREFERS chorts
    blood samples will be taken for biomarker analysis at baseline and after 1 year
    Other Names:
  • blood samples
  • CABG PREFERS

    500 Patients undergoing elective by pass surgery with or without diastolic or systolic dysfunction as Proxy for HFpEF and HFrEF will undergo Cardiac imaging by Doppler echocardiography and cMRI, blood tests for biomarker analysis and cardiac biopsies

    Diagnostic Test: Cardiac imaging in the PREFERS and CABG PREFERS cohorts
    performed at baseline and after 1 year
    Other Names:
  • Doppler echocardiography and cMRI
  • Other: Biomarker analysis in the PREFERS and CABG PREFERS chorts
    blood samples will be taken for biomarker analysis at baseline and after 1 year
    Other Names:
  • blood samples
  • Procedure: Cardiac biopsies in the CABG PREFERS cohort
    myocardial biopsies from the right trium the left and right ventricles will be taken during elective CABG

    Outcome Measures

    Primary Outcome Measures

    1. Change in fibrotic biomarkers [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 [2 years]

      diastolic function

    Secondary Outcome Measures

    1. cardiac magnetic resonance tomography imaging [2 years]

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

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No

    Inclusion Criteria:CABG PREFERS

    Inclusion criteria:
    1. Patients undergoing elective coronary bypass surgery

    2. History of heart failure not required

    3. Age >18 years

    4. Willingness to participate (written informed consent)

    5. Possibility to obtain technically satisfactory echocardiography

    Inclusion criteria PREFERS:
    1. 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

    2. Age >18 years

    3. Willingness to participate (written informed consent)

    4. Possibility to obtain technically satisfactory echocardiography

    Exclusion Criteria CABG PREFERS and PREFERS:
    1. Cognitive impairment

    2. Inability to understand Swedish language

    3. Anaemia (haemoglobin level <90 g/L)

    4. 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)

    5. 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.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Karolinska Institutet Stockholm Sweden 17176

    Sponsors and Collaborators

    • Karolinska Institutet
    • The Swedish Research Council
    • Region Stockholm

    Investigators

    • Principal Investigator: Cecilia M Linde, MD PhD, Institution of Internal medicine, Karolinska University Hospital and Karolinska Institutet

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Cecilia Linde, MD PhD Senior Professor, Karolinska Institutet
    ClinicalTrials.gov Identifier:
    NCT03671122
    Other Study ID Numbers:
    • AZ, Molndal, Sweden grant 1377
    First Posted:
    Sep 14, 2018
    Last Update Posted:
    Mar 31, 2022
    Last Verified:
    Mar 1, 2022
    Individual Participant Data (IPD) Sharing Statement:
    Undecided
    Plan to Share IPD:
    Undecided
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Mar 31, 2022