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Completed

NCT Number: NCT03830983

Atrial Cardiomyopathy in Patients With Stroke of Undetected Mechanism

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.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Bispebjerg Hospital

Copenhagen NV, Copenhagen, 2400, Denmark

About this study

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 (ØBUS) 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.

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

(Patients):

  • 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.

  • 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.

  • Ischemic stroke within 30 days prior to inclusion
  • Age > 18 years
  • Life expectancy of at least one year
  • Informed consent
  • Stenosis: % defined by Ultrasound
  • Small vessel disease: defined according to STRIVE criteria

Inclusion criteria

(Controls)

  • Age and sex matched healthy controls. Matched with the group with stroke of likely cardioembolic stroke.

Exclusion criteria

(Patients):

  • Prior AF or AF >30 sec on at least 6 hours of monitoring during hospitalization.
  • Other major cardio-embolic risk sources assumed as cause of stroke (e.g. endocarditis, myocardial infarction within last 4 weeks, prosthetic cardiac valve)
  • Contraindications to MRI (Including eGFR<30 or other contraindications for the contrast agent used during Cardiac MRI)
  • Assumed unable to participate in the study by investigator (including but not restricted to psychiatric condition, dementia)

Exclusion criteria

(Controls):

  • History of stroke or AF
  • Contraindications to MRI (Including eGFR<30 mL/min/1.73 m2 or other contraindications for the contrast agent used during Cardiac MRI)
  • Assumed unable to participate in the study by the investigator (For the same reasons listed above)

Treatment and study plan

Primary outcomes

  1. Extent of the fibrosis in the Left Atrium (LA)

    Time frame: Within 12 weeks from index event

    Measured with gadolinium enhanced cardiac MRI

  2. Left Atrial Emptying Function (LAEF)

    Time frame: Within 12 weeks from index event

    Measured with gadolinium enhanced cardiac MRI

Secondary outcomes

  1. Observational study: Incidence of silent brain infarctions

    Time frame: 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

    Time frame: Within 12 weeks from index event

    Assessed by cardiac MRI

  3. Left atrial appendage morphology

    Time frame: Within 8 weeks from index event

    Assessed by cardiac MRI

  4. Left atrium volume

    Time frame: Within 12 weeks from index event

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

  5. Left atrium ejection fraction (LAEF)

    Time frame: Within 12 weeks from index event

    Assessed by transthoracic echocardiography

  6. Speckle tracking of LA

    Time frame: 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

    Time frame: Within 4 weeks from index event

    Assessed by 48-hours Holter monitoring

  8. Heart rate variability (HRV)

    Time frame: Within 4 weeks from index event

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

  9. Thrombophilia biomarkers

    Time frame: Within 12 weeks from index event

    Assessment of hypercoagulability

  10. Cardiac specific biomarkers

    Time frame: Within 12 weeks from index event

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

  11. Inflammatory biomarkers

    Time frame: Within 12 weeks from index event

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

  12. Fibrosis related markers

    Time frame: Within 12 weeks from index event

    Collagen type I and III

Other outcomes

  1. Observational study: Assessing incidence of stroke, acute myocardial infarction, atrial fibrillation and cardiovascular-death

    Time frame: 1 year from last included patient

    Follow up in patient records

Sponsors and collaborators

Lead sponsor

University Hospital Bispebjerg and Frederiksberg

Other

Collaborators

  • Lundbeck Foundation
  • Rigshospitalet, Denmark

Registry information

Important dates

Study start
2019
Primary completion
2021
Study completion
2023
First posted
Feb 5, 2019
Registry last updated
Mar 31, 2023

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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