# How the use of FDG PET is improving the diagnosis of dementia in a reference center in Recife, Brazil

**Authors:** Luisa Couceiro de Albuquerque Macêdo, Raphaelly Ribeiro Campos, Luiz Eduardo Duarte Borges Nunes, Mariana Gonçalves Maciel Pinheiro, Alberto Henrique Torres Trindade da Silva, Maria Regina Vendas Carneiro Leão, Aldson dos Santos Silva, Felipe Alves Mourato, Simone Cristina Soares Brandão, Breno José Alencar Pires Barbosa

PMC · DOI: 10.1055/s-0045-1808086 · Arquivos de Neuro-Psiquiatria · 2025-05-21

## TL;DR

This study examines how FDG PET scans are used to improve dementia diagnosis in a Brazilian center, particularly for atypical and early-onset cases.

## Contribution

The study provides insights into FDG PET's role in dementia diagnosis in a Latin American context, where such data is scarce.

## Key findings

- FDG PET helped identify atypical neurodegenerative dementias in 72.4% of cases.
- It clarified early-onset dementia syndromes in 58.3% of cases.
- FDG PET was used in 9 cases to distinguish degenerative from non-degenerative dementias.

## Abstract

Since the advent of 18F-2-fluoro-2-deoxy-D-glucose ([18F]FDG, henceforth, FDG) in the 1970s as a neurochemical tracer, FDG positron emission tomography (PET) has been used for research in dementia and to help diagnose dementing neurodegenerative disorders. However, FDG PET is still unavailable in most centers, especially those in low- and middle-income countries, and there is limited data on biomarkers from patients in diverse populations, such Latin Americans.

To analyze the main indications and how the use of FDG PET helped improve the diagnosis of dementia in a specialized center in Recife, one of the largest cities in Northeastern Brazil.

We retrospectively analyzed data from 62 individuals under follow-up at our center between 2018 and 2023 who had a clinical diagnosis of dementia or mild cognitive impairment and underwent FDG PET scans.

In 21/29 (72.4%) patients, FDG PET helped investigate the types of atypical neurodegenerative dementias; in 14/24 (58.3%), it clarified the clinical question in the investigation of early-onset dementia syndromes; and, in 9 cases, it was performed to differentiate between degenerative and non-degenerative dementias.

These numbers may set the foundation for further longitudinal analyses and collaborative studies including participants from Northeastern Brazil.

## Linked entities

- **Chemicals:** 18F-2-fluoro-2-deoxy-D-glucose (PubChem CID 68614), FDG (PubChem CID 68614)
- **Diseases:** dementia (MONDO:0001627)

## Full-text entities

- **Diseases:** degenerative (MESH:D019636), dementia (MESH:D003704), cognitive impairment (MESH:D003072), non-degenerative dementias (MESH:D000544)
- **Chemicals:** FDG (MESH:D019788), 18F-2-fluoro-2-deoxy-D-glucose (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

28 references — full list in the complete paper: https://tomesphere.com/paper/PMC12094862/full.md

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Source: https://tomesphere.com/paper/PMC12094862