Supplemental Material for Visuospatial Deficits Predict Rate of Cognitive Decline in Autopsy-Verified Dementia With Lewy Bodies

2008 ◽  
2008 ◽  
Vol 22 (6) ◽  
pp. 729-737 ◽  
Author(s):  
Joanne M. Hamilton ◽  
David P. Salmon ◽  
Douglas Galasko ◽  
Rema Raman ◽  
Jenn Emond ◽  
...  

2014 ◽  
Vol 6 (5-8) ◽  
Author(s):  
Monica H Breitve ◽  
Luiza J Chwiszczuk ◽  
Minna J Hynninen ◽  
Arvid Rongve ◽  
Kolbjørn Brønnick ◽  
...  

2018 ◽  
Vol 10 (1) ◽  
Author(s):  
Monica H. Breitve ◽  
Kolbjørn Brønnick ◽  
Luiza J. Chwiszczuk ◽  
Minna J. Hynninen ◽  
Dag Aarsland ◽  
...  

2019 ◽  
Vol 20 (19) ◽  
pp. 4674 ◽  
Author(s):  
Inger van Steenoven ◽  
Barbara Noli ◽  
Cristina Cocco ◽  
Gian-Luca Ferri ◽  
Patrick Oeckl ◽  
...  

In a previous proteomic study, we identified the neurosecretory protein VGF (VGF) as a potential biomarker for dementia with Lewy bodies (DLB). Here, we extended the study of VGF by comparing levels in cerebrospinal fluid (CSF) from 44 DLB patients, 20 Alzheimer’s disease (AD) patients, and 22 cognitively normal controls selected from the Amsterdam Dementia Cohort. CSF was analyzed using two orthogonal analytical methods: (1) In-house-developed quantitative ELISA and (2) selected reaction monitoring (SRM). We further addressed associations of VGF with other CSF biomarkers and cognition. VGF levels were lower in CSF from patients with DLB compared to either AD patients or controls. VGF was positively correlated with CSF tau and α-synuclein (0.55 < r < 0.75), but not with Aβ1-42. In DLB patients, low VGF levels were related to a more advanced cognitive decline at time of first presentation, whereas high levels of VGF were associated with steeper subsequent longitudinal cognitive decline. Hence, CSF VGF levels were lower in DLB compared to both AD and controls across different analytical methods. The strong associations with cognitive decline further points out VGF as a possible disease stage or prognostic marker for DLB.


BMJ Open ◽  
2012 ◽  
Vol 2 (1) ◽  
pp. e000380 ◽  
Author(s):  
Zuzana Walker ◽  
Ian McKeith ◽  
Joanne Rodda ◽  
Tarik Qassem ◽  
Klaus Tatsch ◽  
...  

2014 ◽  
Vol 10 ◽  
pp. P261-P262
Author(s):  
Afina W. Lemstra ◽  
Sietske A. Sikkes ◽  
Charlotte E. Teunissen ◽  
Annelies van der Vlies ◽  
Philip Scheltens

Neurology ◽  
2005 ◽  
Vol 65 (8) ◽  
pp. 1232-1238 ◽  
Author(s):  
D. K. Johnson ◽  
J. C. Morris ◽  
J. E. Galvin

Synapse ◽  
2007 ◽  
Vol 61 (11) ◽  
pp. 903-911 ◽  
Author(s):  
Margaret A. Piggott ◽  
Clive G. Ballard ◽  
Elise Rowan ◽  
Clive Holmes ◽  
Ian G. McKeith ◽  
...  

Author(s):  
Rodolfo Savica ◽  
Pierpaolo Turcano

Parkinson’s disease (PD) is a neurodegenerative disease that shares a number of clinical, pathological, and epidemiological characteristics with dementing illnesses. In addition, PD and related disorders have been associated with cognitive decline/dementia. The timeline of the symptom onset as well as the clinical phenotypes are crucial to define the diseases such as dementia with Lewy bodies and Parkinson’s disease dementia. The epidemiological figures of prevalence and incidence are somewhat limited, but are influenced by diagnostic criteria, geographic locations, and methodological limitations. However, it seems that age has a major role in the increase of prevalence and incidence of PD and dementia; additionally men seem to be consistently more affected than women.


Sign in / Sign up

Export Citation Format

Share Document