Atrial Cardiomyopathy in Patients With Stroke of Undetected Mechanism

Sponsor
University Hospital Bispebjerg and Frederiksberg (Other)
Overall Status
Active, not recruiting
CT.gov ID
NCT03830983
Collaborator
Rigshospitalet, Denmark (Other), Lundbeck Foundation (Other)
150
1
46.8
3.2

Study Details

Study Description

Brief Summary

The goal of this study is to evaluate left atrial structural and functional abnormalities in stroke of undetected mechanism and atherosclerotic stroke with cardiac MRI.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    Aims and objectives:

    The goal of this study is to evaluate left atrial structural and functional abnormalities in patients with stroke of likely cardio-embolic origin compared with healthy age and sex matches controls and patients with atherosclerotic stroke using cardiac MRI.

    Background:

    Despite standard work up for the etiology of ischemic stroke, about 30% of the cases remain unexplained. It is increasingly accepted that these unexplained cases arise from disease outside of the brain. Paroxysmal AF (Atrial fibrillation) may often be suspected as the source but fewer than one third of patients with stroke of undetermined source manifest AF in any form even after 3 years of continuous heart rhythm monitoring. Emerging evidence suggest that atrial functional and structural abnormalities may convey a comparable risk of stroke in which AF is only one of several features. These abnormalities have been termed "atrial cardiomyopathy" and may be an efficient and practical approach to identify patients at high risk of AF and ischemic stroke.

    Methods and materials:

    Cross sectional and prospective cohort study with 3 different groups: 50 patients with stroke of undetected mechanism, 50 patients with atherosclerotic stroke (large or small vessel disease) admitted to the University Hospital of Bispebjerg and Frederiksberg and 50 sex and age matched controls with no history of stroke or AF from the Copenhagen City Heart Study (Ă˜BUS) will be included during a 2 year-period. The study will measure atrial structural abnormalities using cardiac magnetic resonance imaging (MRI) and atrial functional abnormalities by cardiac MRI and echocardiography. A 1 year follow up will examine the incidence of silent brain infarction with MRI and incidence of stroke, atrial fibrillation, acute myocardial infarction and cardiovascular death. Secondary endpoints are to examine the association of functional and structural changes found by MRI with echocardiography, rhythm abnormalities and biomarkers with the purpose of finding clinical easily applicable methods to diagnose atrial cardiomyopathy.

    Expected outcome and perspectives:

    The investigators hypothesize that patients with stroke of likely cardio-embolic origin have significantly more atrial fibrotic degeneration and reduced atrial emptying function than patients with atherosclerotic stroke and the control subjects. The investigators expect a higher incidence of silent brain infarction in the group with stroke of likely cardio-embolic origin. With atrial cardiomyopathy investigated thoroughly in patients with stroke of likely cardio-embolic origin the future work-up and treatment strategies could be more efficient and may thus improve the prognosis in terms of mortality and disability for a considerable number of patients.

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    150 participants
    Observational Model:
    Case-Control
    Time Perspective:
    Prospective
    Official Title:
    Atrial Cardiomyopathy in Patients With Stroke of Undetected Mechanism
    Actual Study Start Date :
    Mar 8, 2019
    Actual Primary Completion Date :
    Sep 6, 2021
    Anticipated Study Completion Date :
    Jan 31, 2023

    Arms and Interventions

    Arm Intervention/Treatment
    Stroke of likely cardioembolic cause or undetected mechanism

    Lesions in at least one territory on MRI & absence of significant large vessel disease defined as stenosis of cerebral or pre-cerebral vessels >50% in arteries supplying the ischemic area(s) & absence of severe small vessel disease including micro-bleeds on Patients with central retinal artery occlusion documented by perimeter and absence of significant large vessel disease defined as stenosis of cerebral or pre-cerebral vessels >50% & absence of severe small vessel disease including micro-bleeds on MRI are included independent of acute MRI findings.

    Atherosclerotic stroke

    Large vessel stroke: Acute lesions in one vascular territory on MRI, significant large vessel disease defined as stenosis of cerebral or pre-cerebral vessels >50% leading to the infarcted territory & absence of severe small vessel disease including micro-bleeds on MRI Small Vessel stroke: MRI documenting lacunar infarction, absence of significant large vessel disease defined as stenosis of cerebral or pre-cerebral vessels >50% and presence of severe small vessel disease possibly including micro bleeds.

    Controls

    Age and sex matched healthy controls with no history of stroke or AF.

    Outcome Measures

    Primary Outcome Measures

    1. Extent of the fibrosis in the Left Atrium (LA) [Within 12 weeks from index event]

      Measured with gadolinium enhanced cardiac MRI

    2. Left Atrial Emptying Function (LAEF) [Within 12 weeks from index event]

      Measured with gadolinium enhanced cardiac MRI

    Secondary Outcome Measures

    1. Observational study: Incidence of silent brain infarctions [Between 1-2 years from index event]

      Incidence of silent brain infarctions assessed by follow-up MR-cerebrum (Only in patients)

    2. Left atrial volume [Within 12 weeks from index event]

      Assessed by cardiac MRI

    3. Left atrial appendage morphology [Within 8 weeks from index event]

      Assessed by cardiac MRI

    4. Left atrium volume [Within 12 weeks from index event]

      2D and 3D left atrial volume assessed by transthoracic echocardiography

    5. Left atrium ejection fraction (LAEF) [Within 12 weeks from index event]

      Assessed by transthoracic echocardiography

    6. Speckle tracking of LA [Within 12 weeks from index event]

      Assessed by transthoracic echocardiography

    7. Atrial rhythm abnormalities: Number of premature atrial contractions (PAC) per hour. Number and length of runs of PAC [Within 4 weeks from index event]

      Assessed by 48-hours Holter monitoring

    8. Heart rate variability (HRV) [Within 4 weeks from index event]

      Time domain variables (meanNN, SDNN, SDANN, SDNNidx, RMSSD, pNN50)

    9. Thrombophilia biomarkers [Within 12 weeks from index event]

      Assessment of hypercoagulability

    10. Cardiac specific biomarkers [Within 12 weeks from index event]

      Atrial Natriuretic Peptide, pro NT-Brain Natriuretic Peptide, High Sensitive Troponins.

    11. Inflammatory biomarkers [Within 12 weeks from index event]

      High Sensitive CRP, Interleukins: IL1, IL1b, IL6, IL18

    12. Fibrosis related markers [Within 12 weeks from index event]

      Collagen type I and III

    Other Outcome Measures

    1. Observational study: Assessing incidence of stroke, acute myocardial infarction, atrial fibrillation and cardiovascular-death [1 year from last included patient]

      Follow up in patient records

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria (Patients):
    1. Stroke of likely cardioembolic cause or of undetected mechanism:

    Lesions in at least one territory on MRI & absence of significant large vessel disease defined as stenosis of cerebral or pre-cerebral vessels >50% in arteries supplying the ischemic area(s) & absence of severe small vessel disease including micro-bleeds on MRI.

    Patients with central retinal artery occlusion documented by perimeter and absence of significant large vessel disease defined as stenosis of cerebral or pre-cerebral vessels >50% & absence of severe small vessel disease including micro-bleeds on MRI are included independent of acute MRI findings.

    1. Large or small vessel stroke (atherosclerotic stroke):

    Large vessel stroke: Acute lesions in one vascular territory on MRI, significant large vessel disease defined as stenosis of cerebral or pre-cerebral vessels >50% leading to the infarcted territory & absence of severe small vessel disease including micro-bleeds on MRI Small Vessel stroke: MRI documenting lacunar infarction, absence of significant large vessel disease defined as stenosis of cerebral or pre-cerebral vessels >50% and presence of severe small vessel disease possibly including micro bleeds.

    1. Ischemic stroke within 30 days prior to inclusion

    2. Age > 18 years

    3. Life expectancy of at least one year

    4. Informed consent

    • Stenosis: % defined by Ultrasound

    • Small vessel disease: defined according to STRIVE criteria

    Inclusion Criteria (Controls)

    1. Age and sex matched healthy controls. Matched with the group with stroke of likely cardioembolic stroke.
    Exclusion Criteria (Patients):
    1. Prior AF or AF >30 sec on at least 6 hours of monitoring during hospitalization.

    2. Other major cardio-embolic risk sources assumed as cause of stroke (e.g. endocarditis, myocardial infarction within last 4 weeks, prosthetic cardiac valve)

    3. Contraindications to MRI (Including eGFR<30 or other contraindications for the contrast agent used during Cardiac MRI)

    4. Assumed unable to participate in the study by investigator (including but not restricted to psychiatric condition, dementia)

    Exclusion Criteria (Controls):
    1. History of stroke or AF

    2. Contraindications to MRI (Including eGFR<30 mL/min/1.73 m2 or other contraindications for the contrast agent used during Cardiac MRI)

    3. Assumed unable to participate in the study by the investigator (For the same reasons listed above)

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Bispebjerg Hospital Copenhagen NV Copenhagen Denmark 2400

    Sponsors and Collaborators

    • University Hospital Bispebjerg and Frederiksberg
    • Rigshospitalet, Denmark
    • Lundbeck Foundation

    Investigators

    • Principal Investigator: Ahmad Sajadieh, MD, DMSc, University Hospital Bispebjerg and Frederiksberg

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Ahmad Sajadieh, MD, DMSc, University Hospital Bispebjerg and Frederiksberg
    ClinicalTrials.gov Identifier:
    NCT03830983
    Other Study ID Numbers:
    • 18055313
    First Posted:
    Feb 5, 2019
    Last Update Posted:
    Apr 12, 2022
    Last Verified:
    Apr 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
    Keywords provided by Ahmad Sajadieh, MD, DMSc, University Hospital Bispebjerg and Frederiksberg
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Apr 12, 2022