Imaging - Clinical Evaluation of Altered Nervous System Drainage

Last updated: May 21, 2024
Sponsor: IRCCS Eugenio Medea
Overall Status: Active - Recruiting

Phase

N/A

Condition

Williams Syndrome

Asperger's Disorder

Treatment

Magnetic resonance imaging

Clinical Study ID

NCT06432023
1022
  • Ages 2-75
  • All Genders
  • Accepts Healthy Volunteers

Study Summary

The current study aims to evaluate the aspects of perfusion, fluid diffusivity in the interstitium and the T1 and T2 signal of the PVS and WMH. The current study has the following objectives: a) evaluate the perfusion aspects using the gadolinium-based contrast medium of brain tissues in the short term; b) the direction of flow of fluids at very low speed in the white matter using the DTI sequences configured for this purpose; c) T1-mapping of the lesions of interest.

The expected results will help us understand two aspects of neurofluid dynamics: a) how the fluid moves within the central nervous system in the first minutes after the injection of the tracer (in our case the gadolinium-based contrast medium) and b) what is the composition of the fluid within the PVS and WMH and how can investigators characterize them more accurately.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • patients with white matter lesions and/or enlarged perivascular spaces

Exclusion

Exclusion Criteria:

  • have contraindications to the use of contrast medium;

  • are clinically unstable patients and prolonged sedation is inappropriate

  • have tumors

  • contraindications to perform MR.

Study Design

Total Participants: 100
Treatment Group(s): 1
Primary Treatment: Magnetic resonance imaging
Phase:
Study Start date:
October 01, 2023
Estimated Completion Date:
January 31, 2026

Study Description

Among the various indirect markers of altered drainage of neuroglial waste metabolites, there is the widening of the perivascular spaces (PVS) and the presence of white matter signal alterations.

An increase in the number of PVS and their enlargement could represent an indirect marker of obstruction to the drainage of fluids and solutes along the arterial wall at the level of the white matter. This obstruction would also be the basis of tissue hypoxia resulting in the formation of areas of signal hyperintensity in the white matter (White Matter Hyperintensities, WMH) often observed in patients with neurodegenerative diseases and small vessel disease.

It is currently unclear what the main drainage route of brain waste metabolites is. Surely there are at least two.

The glymphatic theory proposes the entry of the cerebrospinal fluid (CSF) from the subarachnoid space towards the brain parenchyma in a centripetal direction and exit of the metabolic waste along the perivenous spaces. The drainage of metabolic waste could also be explained by the more recent "intramural periarterial drainage" (IPAD) theory which shows elimination along the arterial walls in a centrifugal direction.

In magnetic resonance imaging (MRI), the study of solute drainage requires a dynamic evaluation, which is able to evaluate the temporal movement of a tracer. There are several MRI techniques, already described in the literature, which can be used to obtain information relating to perfusion processes and the coupling of neuronal and vascular activity in different brain areas.

The circulation of CSF is well known, which is produced largely at the level of the choroid plexuses and is then partly reabsorbed by the arachnoid granulations at the level of the subarachnoid space. Recent studies demonstrate that the CSF re-enters the brain parenchyma in a centripetal manner, crossing the thickness of the gray matter and then the white matter. This movement is regulated by various factors, and in particular by the activity of the smooth muscle cells of the arterial walls, the aquaporin 4 receptors (water channels) and by the chemical-physical properties of the extracellular matrix in the extracellular space.

Connect with a study center

  • Scientific Institute IRCCS E. Medea

    Bosisio Parini, Lecco 23842
    Italy

    Active - Recruiting

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