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Measurement of synaptic density in Down syndrome using PET imaging: a pilot study
Alexandra DiFilippo1, Erin Jonaitis2, Renee Makuch3
1Madison School of Medicine and Public Health, University of Wisconsin, Madison, WI, USA. adifilippo@wisc.edu.
Scientific Reports
|February 27, 2024
Summary
Positron emission tomography (PET) imaging with [11C]UCB-J successfully measured synaptic density in adults with Down syndrome (DS). This pilot study shows potential for comparing synaptic density in DS versus neurotypical adults.
Area of Science:
- Neuroscience
- Radiochemistry
- Genetics
Background:
- Down syndrome (DS), caused by trisomy 21, is the leading genetic cause of intellectual disability.
- Positron emission tomography (PET) enables in vivo imaging of synaptic density.
- Investigating synaptic changes in DS is crucial for understanding cognitive deficits.
Purpose of the Study:
- To evaluate the feasibility of using the PET radiotracer [11C]UCB-J to measure synaptic density in adults with Down syndrome.
- To compare synaptic density and brain volumes between low-functioning adults with DS and neurotypical (NT) adults.
Main Methods:
- Acquired PET imaging data using [11C]UCB-J from 4 low-functioning adults with DS and 37 older NT adults.
- Utilized a 10-minute acquisition window for synaptic density calculation (SUVR50-60,CS) due to motion artifacts.
- Analyzed synaptic density in key brain regions and compared regional brain volumes.
Main Results:
- Successful PET imaging and synaptic density measurement in low-functioning adults with DS.
- Significant differences in synaptic density were observed in the hippocampus and cerebral cortex between DS and NT groups.
- Hippocampus and cerebellum volumes also differed significantly between the DS and NT groups.
Conclusions:
- PET imaging with [11C]UCB-J is a viable method for assessing synaptic density in adults with Down syndrome.
- This pilot study establishes a foundation for future research comparing synaptic density across different cognitive statuses in DS.
- Findings highlight potential neurobiological differences in synaptic structure in individuals with DS.

