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Magnetic Resonance Imaging (MRI) for Aortic Dissection to Visualise Inflammation

Conditions
Aortic Diseases
Aortic Dissection
Interventions
Diagnostic Test: Magnetic Resonance Imaging (MRI) using ultrasmall super paramagnetic iron oxides (USPIOs)
Registration Number
NCT03948555
Lead Sponsor
University of Leicester
Brief Summary

The study is a single-centre, prospective, observational cross-sectional imaging study aimed to determine if macrophage-mediated inflammation can be visualised in the aorta of patients with aortic dissection (AD) using ultrasmall super paramagnetic iron oxides (USPIO)-enhanced magnetic resonance imaging (MRI).

Detailed Description

Aortic dissection (AD) is a condition in which a disruption of the medial layer (in most cases provoked by a tear or an ulcer in the intima) results in separation of the aortic wall layers, with concomitant 'false lumen' formation and malperfusion of end organs.

The underlying mechanism of the condition has, until recently, remained unclear. The Pi of the present sutdy has shed light on a mechanism that shows that inflammation underlies the condition. The PI of the present study has showed that inflammation in the aorta is triggered by macrophage infiltration into the aortic wall in both pre-clinical models using animal models of the condition (murine) and in patient tissue samples obtained at time of surgery.

Macrophage infiltration into the aortic wall, as a result of activation of the cytokine, granulocyte-macrophage colony stimulating factor (GM-CSF), is the trigger for an inflammatory cascade that is presently understood to underlie the pathogenic mechanism of the condition

Non-invasive assessment of macrophage infiltration would prove that this pathogenic mechanism exists (proof-of-concept). Macrophage infiltration has been shown to be feasible by contrast-enhanced Magnetic Resonance Imaging (MRI) using ultrasmall super paramagnetic iron oxides (USPIOs).

The hypothesis of the present study is that macrophage-mediated inflammation can be visualised in the aorta of patients with AD using the USPIO-enhanced MRI technique, and use the present study to confirm this (proof-of-concept).

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
20
Inclusion Criteria
  • Confirmed diagnosis of acute or chronic aortic dissection (>2 week after initial intimal injury)
  • Able and willing to comply with all study requirements.
  • Age > 40 years (Patients under the age of 40 years will not be included as they may have a connective tissue disorder accounting for their condition)
  • Able and willing to give informed consent
  • An adequate understanding of written and verbal English
Exclusion Criteria
  • Past history of systemic iron overload or haemochromatosis
  • Renal failure (estimated glomerular filtration rate < 30ml/min)
  • Contraindication to MRI
  • Known allergy to iron-containing compounds
  • Participants who have participated in another research study involving an investigational product in the past 12 weeks.
  • Female participants who are pregnant or lactating.
  • Unwilling or unable to give informed consent

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
Acute aortic dissectionMagnetic Resonance Imaging (MRI) using ultrasmall super paramagnetic iron oxides (USPIOs)stable patients with confirmed diagnosis of acute AD.
Chronic aortic dissectionMagnetic Resonance Imaging (MRI) using ultrasmall super paramagnetic iron oxides (USPIOs)patients with diagnosis of chronic AD, being followed up in outpatient aortic clinic.
Primary Outcome Measures
NameTimeMethod
FeasibilityUp to 36 hours

To establish the feasibility of imaging macrophage-mediated inflammation in the aorta of patients with aortic dissection, using USPIO-enhanced MRI.

Visualisation of inflammationUp to 36 hours

To determine if macrophage-mediated inflammation can be visualised in the aorta of patients with aortic dissection using USPIO-enhanced MRI

Secondary Outcome Measures
NameTimeMethod
LocalisationUp to 36 hours

To assess if macrophage mediated inflammation is localised to the site of dissection and the surrounding aorta or more widespread in the vasculature.

TimingUp to 36 hours

To determine the timing of macrophage infiltration in aortic dissection (acute or chronic phase)

Trial Locations

Locations (2)

University of Leicester

🇬🇧

Leicester, United Kingdom

University Hospitals of Leicester NHS Trust

🇬🇧

Leicester, United Kingdom

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