REBORD: Ephrin B1 Regulation in Human Right Appendage

Sponsor
University Hospital, Toulouse (Other)
Overall Status
Completed
CT.gov ID
NCT01080781
Collaborator
(none)
30
1
33.1
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Study Details

Study Description

Brief Summary

  • Background : Ephrin-B1 is part of the large Eph/Ephrin system which is involved in cell-cell comunication. The role of Ephrin-B1 has scarcely been studied in adulthood. Our team has shown that this protein is expressed in normal heart in mice and humans. In mice with deletion of the gene encoding Ephrin-B1, we have shown progressive development of dilated cardiomyopathy characterized by dramatic disorganization of cardiac tissue architecture and decreased heart rate variability.

  • Purpose: Ephrin-B1 protein was recently identified in human heart but its putative role remains unknown. In knockout mice, deletion of efn gene is associated with abnormalities in cardiac architecture linked to defects in cell-cell tight junctions. From a functional point of view, mice develop a dilated cardiomyopathy and exhibit decreased heart rate variability in the frequency domain. The purpose of this study is to assess if Ephrin-B1 expression is regulated in human heart and if expression level correlates with heart rate variability.

  • Abstract: Thirty patients suffering from cardiac disease needing surgery will be included and separated in two groups according to pressure levels in right auricle /and or pulmonary artery. Ephrin-B1 expression will be assessed in right appendages at both the transcriptional (quantitative PCR) and protein (Western blot) levels. Furthermore, the putative relationship between Ephrin-B1 expression and heart rate variability (24 hours ECG recordings) will be investigated.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    • Outcomes

    • Primary: Expression level of gene encoding Ephrin B1 (quantitative PCR normalized against GAPDH gene expression) on human right appendage biopsies

    • Secondary: a/ Expression level of Ephrin B1 protein on human right appendage using Western blot and b/ Heart rate variability in both time and spectral domains

    • Study design: Exploratory, monocentric , prospective and comparative. Two groups of 15 patients each, age and sex matched, with or without elevated pressures in right auricles or pulmonary arteries will be included.

    • Eligibility criteria:

    • Inclusion criteria: patients needing cardiac surgery and who had both right catheterism and 24 hours ECG recording before inclusion; stable medications for at least 4 weeks; age > 18 years.

    • Exclusion criteria: Patient with pace-maker or atrial fibrillation

    • Number of subjects: 30 patients in two groups of 15 patients each.

    • Statistical analysis: Qualitative and quantitative variables will be compared using McNemar test and t test respectively. A p value < 0.05 will be considered as significant.

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    30 participants
    Time Perspective:
    Prospective
    Official Title:
    Ephrin B1 Regulation in Human Right Appendage
    Study Start Date :
    Mar 1, 2010
    Actual Primary Completion Date :
    Jul 1, 2012
    Actual Study Completion Date :
    Dec 1, 2012

    Arms and Interventions

    Arm Intervention/Treatment
    Group 1

    normal pressures in right auricle (<10 mmHg) /and or pulmonary artery (<35 mmHg)

    Group 2

    high pressures in right auricle (> 10 mmHg) /and or pulmonary artery (>35 mmHg)

    Outcome Measures

    Primary Outcome Measures

    1. Expression level of gene encoding Ephrin-B1 [1 year]

      Expression level of gene encoding Ephrin-B1 (quantitative PCR normalized against GAPDH gene expression) on human right appendage biopsies

    Secondary Outcome Measures

    1. Expression level of Ephrin B1 protein [1year]

      Expression level of Ephrin B1 protein on human right appendage using Western blot and b/ Heart rate variability in both time and spectral domains

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Patients needing cardiac surgery and who had both right cardiac catheterism and 24 hours ECG recording before inclusion

    • Stable medications for at least 4 weeks

    Exclusion Criteria:
    • Patient with pace-maker or atrial fibrillation

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Toulouse University Hospital Toulouse France 31000

    Sponsors and Collaborators

    • University Hospital, Toulouse

    Investigators

    • Principal Investigator: Jean-Michel Senard, PhD, University Hospital, Toulouse

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    University Hospital, Toulouse
    ClinicalTrials.gov Identifier:
    NCT01080781
    Other Study ID Numbers:
    • 09 159 02
    First Posted:
    Mar 4, 2010
    Last Update Posted:
    Jan 24, 2013
    Last Verified:
    Jan 1, 2013
    Keywords provided by University Hospital, Toulouse
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Jan 24, 2013