Abstract
The objective of this study is to describe the neuropathologic findings in three LRRK2 G2019S carriers with Parkinson's disease (PD). We cross-referenced a list of 956 PD individuals that had been previously genotyped in clinical studies at Columbia University, with 282 subjects with a parkinsonian syndrome who came to autopsy in our brain bank since 1991. We found three autopsies of G2019S mutation carriers. Pathological analyses of the samples were blind to the genetic findings. We retrospectively reviewed the clinical records of the three patients. All three had a clinical and pathological diagnosis of PD. Cognitive impairment was a late feature in two out of three patients. Cortical involvement varied significantly: one had diffuse Lewy body (LB) pathology, tau inclusions, and amyloid pathology consistent with advanced Alzheimer's disease; one had diffuse cortical LB; and one had only brainstem predominant LB pathology. Cognitive impairment may be a long-term complication in G2019S mutation carriers. However, the extent of cortical involvement is variable. Larger longitudinal follow-up of LRRK2 G2019S mutation carriers is required to assess for risk factors for cortical involvement and dementia.
MeSH Terms
Aged
Aged, 80 and over
Alzheimer Disease/genetics,pathology
Female
Genotype
Humans
Leucine-Rich Repeat Serine-Threonine Protein Kinase-2
Lewy Body Disease/genetics,pathology
Male
Parkinson Disease/genetics,pathology
Point Mutation/genetics
Protein Serine-Threonine Kinases/genetics
Retrospective Studies
Risk Factors
Chemicals
LRRK2 protein, human
Leucine-Rich Repeat Serine-Threonine Protein Kinase-2
Protein Serine-Threonine Kinases
Authors & Affiliations
11 authors, click to expand affiliations / ORCID
Poulopoulos Markos
Department of Neurology, College of Physicians and Surgeons, Columbia University, New York, NY, USA.
Cortes Etty
Vonsattel Jean-Paul G
Fahn Stanley
Waters Cheryl
Cote Lucien J
Moskowitz Carol
Honig Lawrence S
Clark Lorraine N
Marder Karen S
Alcalay Roy N
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