The validation of tau radioligands could improve the diagnosis of frontotemporal lobar degeneration and the assessment of disease-modifying therapies. Here, we demonstrate that binding of the tau radioligand [F]AV-1451 was significantly abnormal in both magnitude and distribution in a patient with familial frontotemporal dementia due to a MAPT 10 + 16C>T gene mutation, recapitulating the pattern of neuropathology seen in her father. Given the genetic diagnosis and the non-Alzheimer's pathology, these findings suggest that [F]AV-1451 might be a useful biomarker in primary tauopathies. Largerscale in vivo and studies will be needed to assess the technique's specificity.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5224822PMC
http://dx.doi.org/10.1002/acn3.366DOI Listing

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