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Erschienen in: Journal of Nuclear Cardiology 5/2018

01.10.2018 | Original Article

18Fluorine sodium fluoride positron emission tomography, a potential biomarker of transthyretin cardiac amyloidosis

verfasst von: Rachelle Morgenstern, MPH, Randy Yeh, MD, Adam Castano, MD, MS, Mathew S. Maurer, MD, Sabahat Bokhari, MD

Erschienen in: Journal of Nuclear Cardiology | Ausgabe 5/2018

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Abstract

Background

Non-invasive imaging to diagnose and quantify amyloid load, progression, and response to treatment are central for the care of patients with cardiac amyloidosis. 18Fluorine-labeled sodium fluoride (18F-NaF) is a widely available radioisotope and PET imaging allows for absolute quantification of tracer uptake.

Methods

Patients with biopsy-proven transthyretin (ATTR-CA) and light-chain cardiac amyloidosis (AL) (3 ATTRwt, 2 ATTRV122I, 2 AL) and controls (n = 5), underwent 18F-NaF PET imaging. Scans were assessed visually for radiotracer uptake and analyzed using standard uptake values in the entire myocardium (SUVm) and in a 17-segment cardiac model. Wilcoxon rank-sum tests were used for statistical analyses.

Results

Qualitative 18F-NaF uptake was absent in controls and AL patients. There was qualitative 18F-NaF uptake in ATTR-CA patients, with slightly increased uptake in wild-type patients. SUVm for controls and AL patients overlapped at 0.8(0.4-0.9) and 0.95(0.9-1.0), respectively (P = 0.434). At 1.5(1.4-1.7), SUVm for ATTR-CA patients was ≈1.5*SUVm of controls (P = 0.012) and AL patients (P = 0.078). While there was diffuse 18F-NaF myocardial in ATTR-CA patients, the degree of uptake varied according to cardiac segment.

Conclusion

18F-NaF PET effectively imaged and differentiated ATTR-CA patients. Semi-automatic software enabled quantification of radiotracer uptake and regional distribution. 18F-NaF PET may be useful for disease monitoring and localizing amyloid deposition in ATTR-CA patients.
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Metadaten
Titel
18Fluorine sodium fluoride positron emission tomography, a potential biomarker of transthyretin cardiac amyloidosis
verfasst von
Rachelle Morgenstern, MPH
Randy Yeh, MD
Adam Castano, MD, MS
Mathew S. Maurer, MD
Sabahat Bokhari, MD
Publikationsdatum
01.10.2018
Verlag
Springer US
Erschienen in
Journal of Nuclear Cardiology / Ausgabe 5/2018
Print ISSN: 1071-3581
Elektronische ISSN: 1532-6551
DOI
https://doi.org/10.1007/s12350-017-0799-x

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