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Brain Iron Toxicity and Neurodegeneration - A 7T MRI Study

Brain Iron Toxicity and Neurodegeneration - A 7T MRI Study

Recruiting
18-75 years
All
Phase N/A

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Overview

A longitudinal observational neuroimaging study of individuals with Early Onset Alzheimer's disease during the prodromal phase, and matched control group - Ultrahigh Field MRI study at 7T

Description

This study aims to determine whether high resolution MRI at 7T and Quantitative Susceptibility Mapping (QSM) can demonstrate a specific pattern of iron overload in strategically important areas of brain as a sensitive marker of pathological Alzheimer's disease i.e. patients with subjective or mild cognitive impairment associated with Amyloid or tau pathological state in the cerebrospinal fluid.

Eligibility

Inclusion Criteria:

  • Ability to provide informed consent
  • Patients with pathological diagnosis of Alzheimer's disease according to the National Institute on Aging and Alzheimer's Association, NIA-AA, criteria (Alzheimer's group) or cognitively normal individuals within 1.5 standard deviation of normal in all tests (control group)

Exclusion Criteria:

  • Lack of mental capacity to consent to study involvement
  • Not speaking English before age 5 years
  • Learning disability
  • Schizophrenia
  • Substance misuse
  • Implanted devices not certified as compatible with ultra-high field MRI (e.g. cardiac pacemaker)
  • Pregnancy

Study details
    Prodromal Alzheimer's Disease
    Mild Cognitive Impairment

NCT04992975

Nottingham University Hospitals NHS Trust

14 October 2025

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