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DOI 10.1038/s41598-024-54669-7

Медицинская библиотека · Scientific reports · 2024

Measurement of synaptic density in Down syndrome using PET imaging: a pilot study.

DiFilippo Alexandra, Jonaitis Erin, Makuch Renee, Gambetti Brianna, Fleming Victoria, Ennis Gilda, Barnhart Todd, Engle Jonathan, Bendlin Barbara, Johnson Sterling, Handen Benjamin, Krinsky-McHale Sharon, Hartley Sigan, Christian Bradley

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Аннотация

Down syndrome (DS) is the most prevalent genetic cause of intellectual disability, resulting from trisomy 21. Recently, positron emission tomography (PET) imaging has been used to image synapses in vivo. The motivation for this pilot study was to investigate whether synaptic density in low functioning adults with DS can be evaluated using the PET radiotracer [11C]UCB-J. Data were acquired from low functioning adults with DS (n = 4) and older neurotypical (NT) adults (n = 37). Motion during the scans required the use of a 10-minute acquisition window for the calculation of synaptic density using SUVR50-60,CS which was determined to be a suitable approximation for specific binding in this analysis using dynamic data from the NT group. Of the regions analyzed a large effect was observed when comparing DS and NT hippocampus and cerebral cortex synaptic density as well as hippocampus and cerebellum volumes. In this pilot study, PET imaging of [11C]UCB-J was successfully completed and synaptic density measured in low functioning DS adults. This work provides the basis for studies where synaptic density may be compared between larger groups of NT adults and adults with DS who have varying degrees of baseline cognitive status.

Для цитирования: DiFilippo Alexandra, Jonaitis Erin, Makuch Renee, Gambetti Brianna, Fleming Victoria, Ennis Gilda, Barnhart Todd, Engle Jonathan, Bendlin Barbara, Johnson Sterling, Handen Benjamin, Krinsky-McHale Sharon, Hartley Sigan, Christian Bradley. Measurement of synaptic density in Down syndrome using PET imaging: a pilot study.. Scientific reports. 2024. DOI: 10.1038/s41598-024-54669-7.

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