# Reproducibility of 18F-Sodium Fluoride Positron Emission Tomography for Assessing Microcalcification in Coronary Arterial and Thoracic Aortic Atherosclerosis: Is the Signal below the Resolution of PET?

**Authors:** Ondrej Fanta, Shiv Patil, Thomas Werner, Drew A. Torigian, Abass Alavi

PMC · DOI: 10.1007/s11886-025-02240-9 · Current Cardiology Reports · 2025-05-14

## TL;DR

This paper reviews the use of 18F-sodium fluoride PET/CT for detecting early atherosclerosis by measuring microcalcification in coronary and thoracic arteries.

## Contribution

The paper emphasizes the need for standardized quantification methods to improve reproducibility in 18F-NaF PET/CT imaging.

## Key findings

- 18F-NaF PET/CT can detect subclinical microcalcification in coronary and thoracic aortic atherosclerosis.
- Global assessment of 18F-NaF uptake is more reliable than focal assessment due to PET's limited spatial resolution.
- Standardized quantification methods could enhance the accuracy and reproducibility of 18F-NaF PET/CT results.

## Abstract

The rising prevalence of atherosclerosis has prompted the development of novel diagnostic methods capable of identifying early-stage disease when therapeutic interventions may be most effective. 18F-sodium fluoride (NaF) positron emission tomography/computed tomography (PET/CT) is a molecular imaging technique that can quantify subclinical microcalcification in arterial plaque. The focus of this review article is to discuss the utility of 18F-NaF PET/CT in assessing atherosclerotic disease of major susceptible blood vessels, particularly the coronary arteries and thoracic aorta.

18F-NaF uptake observed on PET imaging demonstrates promising potential as a marker of atherosclerotic burden in individual coronary arteries, whole heart segmentations, and the thoracic aorta. Global versus focal assessment of 18F-NaF uptake in small arteries is a significant source of methodological heterogeneity among studies.

The accuracy and reproducibility of 18F-NaF PET/CT may be improved by standardized quantification methods in light of the limited spatial resolution of PET, particularly through the use of techniques to evaluate global atherosclerotic burden.

## Linked entities

- **Chemicals:** 18F-sodium fluoride (PubChem CID 23690531), 18F-NaF (PubChem CID 23690531)
- **Diseases:** atherosclerosis (MONDO:0005311)

## Full-text entities

- **Diseases:** infarcts (MESH:D007238), allergic reaction (MESH:D004342), atheroma (MESH:D058226), atrial fibrillation (MESH:D001281), Atherosclerotic lesions (MESH:D050197), Chronic plaque inflammation (MESH:D007249), chest pain (MESH:D002637), aortic stenosis (MESH:D001024), CAD (MESH:D003324), deaths (MESH:D003643), coronary heart disease (MESH:D003327), Stroke (MESH:D020521), hypertension (MESH:D006973), metabolic syndrome (MESH:D024821), tumor (MESH:D009369), myocardial infarction (MESH:D009203), ischemic heart disease (MESH:D017202), osseous metastases (MESH:D009362), smoker (MESH:C000719328), Ischemic Stroke (MESH:D002544), lesion (MESH:D009059), luminal stenosis (MESH:D003251), Alavi-Carlsen calcification (MESH:D002114), thrombotic (MESH:D013927), embolization (MESH:D004617), renal insufficiency/failure (MESH:D051437), coronary insufficiency (MESH:D000309), ACS (MESH:D000168), LAP (MESH:C562861), CVD (MESH:D002318)
- **Chemicals:** cholesterol (MESH:D002784), 18F (MESH:C000615276), NaF (MESH:D012969), Rosuvastatin (MESH:D000068718), lipid (MESH:D008055), 18 F-NaF (-), aspirin (MESH:D001241), 18F-fluorodeoxyglucose (MESH:D019788), clopidogrel (MESH:D000077144), Calcium (MESH:D002118)
- **Species:** Sus scrofa (pig, species) [taxon 9823], 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/PMC12078425/full.md

## References

7 references — full list in the complete paper: https://tomesphere.com/paper/PMC12078425/full.md

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Source: https://tomesphere.com/paper/PMC12078425