# The role of brain MR and FDG-PET in the diagnosis of neurodegenerative disease

**Authors:** Yoshimi Anzai, Satoshi Minoshima

PMC · DOI: 10.1007/s00330-025-11940-3 · European Radiology · 2025-09-03

## TL;DR

This paper reviews how brain MRI and FDG-PET imaging help diagnose and manage neurodegenerative diseases like Alzheimer's, emphasizing the importance of recognizing co-pathologies and new diagnostic entities.

## Contribution

The paper highlights updated diagnostic approaches for neurodegenerative diseases using brain imaging and anti-amyloid treatment eligibility.

## Key findings

- Locoregional atrophy and metabolic patterns aid in differential diagnosis of neurodegenerative diseases.
- Brain MRI determines eligibility for anti-amyloid immunotherapy and helps monitor treatment-related imaging abnormalities.
- New entities like LATE can mimic Alzheimer's disease in elderly patients with memory loss.

## Abstract

Alzheimer disease (AD) is the most common dementing disorder, affecting 55 million people worldwide. Brain MRI plays an integral role in the diagnostic evaluation of patients with cognitive symptoms. When interpreting brain MRI for cognitive impairment, radiologists should assess the following four key features: (1) white matter ischemic burden, (2) structural changes to suggest normal pressure hydrocephalus, (3) locoregional pattern of brain atrophy, and (4) presence of microhemorrhage or superficial siderosis, particularly for determining eligibility for anti-amyloid monoclonal antibody (MAB) treatment when appropriate. The recent approval and clinical adoption of anti-amyloid MAB expanded the role of neuroradiologists in evaluating eligibility and monitoring ARIA (amyloid-related imaging abnormality) among patients receiving anti-amyloid MAB. This advancement underscores the importance of standardized imaging protocols and effective communication between neuroradiologists and cognitive neurologists. Depending on the severity of ARIA and patients’ symptoms, treatment may need to be suspended or discontinued. This review article explores brain MRI and FDG-PET/CT imaging abnormalities in patients with major cognitive and movement disorders associated with dementia. It aims to assist radiologists in providing differential diagnoses within a clinical context. Finally, the article emphasizes the importance of recognizing co-pathologies, since patients may have more than one neurodegenerative disease rather than viewing these neurodegenerative diseases as being mutually exclusive.

Question Traditional regional patterns of brain atrophy on MRI by neuroradiologists may not be effective given the recent advances in understanding of neurodegenerative disease and recognition of co-pathologies.

Findings The locoregional atrophy and the patterns of metabolic abnormality help in the differential diagnosis of neurodegenerative disease. Remember that brain MRI determines eligibility for anti-amyloid immunotherapy.

Clinical relevance Understanding clinical history is vital for interpreting brain MRI for patients with cognitive impairment or memory loss. Newly recognized entities such as limbic-predominant age-related TDP43 encephalopathy (LATE) can mimic Alzheimer disease among extremely elderly patients with amnestic symptoms with mesial temporal lobe atrophy.

## Linked entities

- **Diseases:** Alzheimer disease (MONDO:0004975), neurodegenerative disease (MONDO:0005559)

## Full-text entities

- **Diseases:** encephalopathy (MESH:D001927), brain atrophy (MESH:C566985), atrophy (MESH:D001284), dementia (MESH:D003704), memory loss (MESH:D008569), white matter ischemic (MESH:D056784), amyloid (MESH:C000718787), superficial siderosis (MESH:D012806), dementing disorder (MESH:D009358), normal pressure hydrocephalus (MESH:D006850), metabolic abnormality (MESH:D008659), TDP43 (OMIM:607485), mesial temporal lobe atrophy (MESH:C566903), AD (MESH:D000544), LATE (MESH:C000723354), cognitive and movement disorders (MESH:D003072), ARIA (MESH:C564543), neurodegenerative disease (MESH:D019636)
- **Chemicals:** MAB (MESH:D000911), FDG (MESH:D019788)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12963154/full.md

## References

4 references — full list in the complete paper: https://tomesphere.com/paper/PMC12963154/full.md

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Source: https://tomesphere.com/paper/PMC12963154