In Vivo Visualization of Amyloid Deposits in the Heart with 11 C-PIB and PET Visa övriga samt affilieringar
2013 (Engelska) Ingår i: Journal of Nuclear Medicine, ISSN 0161-5505, E-ISSN 1535-5667, Vol. 54, nr 2, s. 213-220Artikel i tidskrift (Refereegranskat) Published
Abstract [en]
Cardiac amyloidosis is a differential diagnosis in heart failure and is associated with high mortality. There is currently no noninvasive imaging test available for specific diagnosis. N- [methyl- 11 C]2-(4′-methylamino-phenyl)-6-hydroxybenzothiazole (11 C-PIB) PET is used in the evaluation of brain amyloidosis. We evaluated the potential use of 11 C-PIB PET in systemic amyloidosis affecting the heart.
Methods:
Patients (n = 10) diagnosed with systemic amyloidosis—including heart involvement of either monoclonal immunoglobulin light-chain (AL) or transthyretin (ATTR) type—and healthy volunteers (n = 5) were investigated with PET/CT using 11 C-PIB to study cardiac amyloid deposits and with 11 C-acetate to measure myocardial blood flow to study the impact of global and regional perfusion on PIB retention.
Results:
Myocardial 11 C-PIB uptake was visually evident in all patients 15–25 min after injection and was not seen in any volunteer. A significant difference in 11 C-PIB retention in the heart between patients and healthy controls was found. The data indicate that myocardial amyloid deposits in patients diagnosed with systemic amyloidosis could be visualized with 11 C-PIB. No correlation between 11 C-PIB retention index and myocardial blood flow as measured with 11 C-acetate was found on the global level, whereas a positive correlation on the segmental level was seen in a single patient.
Conclusion:
11 C-PIB and PET could be a method to study systemic amyloidosis of type AL and ATTR affecting the heart and should be investigated further both as a diagnostic tool and as a noninvasive method for treatment follow-up.
Ort, förlag, år, upplaga, sidor 2013. Vol. 54, nr 2, s. 213-220
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Radiologi och bildbehandling
Identifikatorer URN: urn:nbn:se:uu:diva-189479 DOI: 10.2967/jnumed.111.102053 ISI: 000314691200021 PubMedID: 23238792 OAI: oai:DiVA.org:uu-189479 DiVA, id: diva2:581546
2013-01-022013-01-022017-12-06 Bibliografiskt granskad