TREM2 p.R47H substitution is not associated with dementia with Lewy bodies.

Journal: Neurology. Genetics
Published:
Abstract

Dementia with Lewy bodies (DLB) is the second leading cause of neurodegenerative dementia in the elderly and is clinically characterized by the presence of cognitive decline, parkinsonism, REM sleep behavior disorder, and visual hallucinations.(1,2) At autopsy, α-synuclein-positive Lewy-related pathology is observed throughout the brain. Concomitant Alzheimer disease-related pathology including amyloid plaques and, to a lesser degree, neurofibrillary tangles are often present.(2) The clinical characteristics of DLB share overlapping features with Alzheimer disease dementia (AD) and Parkinson disease (PD). A recent genetic association study examining known hits from PD and AD identified variants at both the α-synuclein (SNCA) and APOE loci as influencing the individual risk to DLB.(3) These findings would suggest that DLB may be a distinct disease with shared genetic risk factors with PD and AD.

Authors
Ronald Walton, Alexandra Soto Ortolaza, Melissa Murray, Oswaldo Lorenzo Betancor, Kotaro Ogaki, Michael Heckman, Sruti Rayaprolu, Rosa Rademakers, Nilüfer Ertekin Taner, Ryan Uitti, Jay Van Gerpen, Zbigniew Wszolek, Glenn Smith, Kejal Kantarci, Val Lowe, Joseph Parisi, David Jones, Rodolfo Savica, Jonathan Graff Radford, David Knopman, Ronald Petersen, Neill Graff Radford, Tanis Ferman, Dennis Dickson, Bradley Boeve, Owen Ross, Catherine Labbé