Year: 2020
Type: article
Abstract: ABSTRACT INTRODUCTION We report in vivo patterns of neuroinflammation and abnormal protein aggregation in seven cases of familial frontotemporal dementia with mutations in MAPT, GRN and C9orf72 genes. METHODS Using positron emission tomography (PET), we explored the association of the distribution of activated microglia, as measured by the radioligand [ 11 C]PK11195, and the regional distribution of tau- or TDP-43 pathology, indexed using the radioligand [ 18 F]AV-1451. The familial FTD PET data were compared to healthy controls. RESULTS Familial FTD patients across all mutation groups showed increased [ 11 C]PK11195 binding predominantly in frontotemporal regions, with additional regions showing abnormalities in individuals. Patients with MAPT mutations had a consistent distribution of [ 18 F]AV-1451 binding across the brain, with heterogeneous distributions among carriers of GRN and C9orf72 mutations. DISCUSSION This case series suggests a consistent role for neuroinflammation in the pathophysiology of familial FTD, warranting further consideration of immunomodulatory therapies for disease modification and prevention.
Language: English
Subfield: Neurology
Field: Neuroscience
Domain: Life Sciences
Open Access status: hybrid
Awards: A new noradrenergic strategy to treat Impulsivity in Progressive Supranuclear Palsy, UKDP: Integrated DEmentiA research environment (IDEA), G2607745411, G2940773629, Restoring brain function: from cortical microcircuits to complex behaviours in neurodegenerative disease., Restoring brain function: from cortical microcircuits to complex behaviours in neurodegenerative disease., MICA: Training and Novel Probes Programme in PET Neurochemistry - PET Call, Innovative Technologies for Stratified and Experimental Medicine, G7215423438, G8585681489
OpenAlex ID: W3095515993