Quantitative Assessment of Arthritis Activity in Rheumatoid Arthritis Patients Using [ 11 C]DPA-713 Positron Emission Tomography

Treatment for rheumatoid arthritis (RA) should be started as early as possible to prevent destruction of bone and cartilage in affected joints. A new diagnostic tool for both early diagnosis and therapy monitoring would be valuable to reduce permanent joint damage. Positron emission tomography (PET)...

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Veröffentlicht in:International journal of molecular sciences 2020-04, Vol.21 (9), p.3137
Hauptverfasser: Yaqub, Maqsood, Verweij, Nicki J F, Pieplenbosch, Simone, Boellaard, Ronald, Lammertsma, Adriaan A, van der Laken, Conny J
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Sprache:eng
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Zusammenfassung:Treatment for rheumatoid arthritis (RA) should be started as early as possible to prevent destruction of bone and cartilage in affected joints. A new diagnostic tool for both early diagnosis and therapy monitoring would be valuable to reduce permanent joint damage. Positron emission tomography (PET) imaging of macrophages is a previously demonstrated non-invasive means to visualize (sub)clinical arthritis in RA patients. We developed a kinetic model to quantify uptake of the macrophage tracer [ C]DPA-713 ( , -diethyl-2-[2-(4-methoxyphenyl)-5,7-dimethylpyrazolo [1,5-a]pyrimidin-3-yl]acetamide) in arthritic joints of RA patients and to assess the performance of several simplified methods. Dynamic [ C]DPA-713 scans of 60 min with both arterial and venous blood sampling were performed in five patients with clinically active disease. [ C]DPA-713 showed enhanced uptake in affected joints of RA patients, with tracer uptake levels corresponding to clinical presence and severity of arthritis. The optimal quantitative model for assessment of [ C]DPA-713 uptake was the irreversible two tissue compartment model (2T3k). Both K and standardized uptake value (SUV) correlated with the presence of arthritis in RA patients. Using SUV as an outcome measure allows for a simplified static imaging protocol that can be used in larger cohorts.
ISSN:1422-0067
1661-6596
1422-0067
DOI:10.3390/ijms21093137