P1-235: Association of plasma beta-amyloid levels and risk of dementia, Alzheimer's disease, brain structure and cognitive functions in the Framingham Heart Study

2013 ◽  
Vol 9 ◽  
pp. P238-P239
Author(s):  
Vincent Chouraki ◽  
Alexa Beiser ◽  
Linda Younkin ◽  
Rhoda Au ◽  
Charles DeCarli ◽  
...  
2018 ◽  
Vol 66 (3) ◽  
pp. 1275-1282
Author(s):  
Gina M. Peloso ◽  
Alexa S. Beiser ◽  
Anita L. Destefano ◽  
Sudha Seshadri

Author(s):  
Safiya Sultana T ◽  
Rupali D. Mitra ◽  
Jyotsna Gawai ◽  
Sudhanshu Singh

Alzheimer’s disease, being a chronic state progressive ND(neurodegenerative diseases), is characterised by abnormalities beta-amyloid and impaired cognitive functions resulting in dementia. Exosomes (Nano-particles) have developed as a promising mediators of NDs in which they carry toxic particles between cells and transfer them. Hence, current review focusesprimarily on the effects of exosomes in modulating mediators and promotingneuroprotection against NDs.


2019 ◽  
Vol 11 (1) ◽  
Author(s):  
Lindsay Poppe ◽  
Laura Rué ◽  
Mieke Timmers ◽  
Annette Lenaerts ◽  
Annet Storm ◽  
...  

Abstract Background EphA4 is a receptor of the ephrin system regulating spine morphology and plasticity in the brain. These processes are pivotal in the pathophysiology of Alzheimer’s disease (AD), characterized by synapse dysfunction and loss, and the progressive loss of memory and other cognitive functions. Reduced EphA4 signaling has been shown to rescue beta-amyloid-induced dendritic spine loss and long-term potentiation (LTP) deficits in cultured hippocampal slices and primary hippocampal cultures. In this study, we investigated whether EphA4 ablation might preserve synapse function and ameliorate cognitive performance in the APPPS1 transgenic mouse model of AD. Methods A postnatal genetic ablation of EphA4 in the forebrain was established in the APPPS1 mouse model of AD, followed by a battery of cognitive tests at 9 months of age to investigate cognitive function upon EphA4 loss. A Golgi-Cox staining was used to explore alterations in dendritic spine density and morphology in the CA1 region of the hippocampus. Results Upon EphA4 loss in APPPS1 mice, we observed improved social memory in the preference for social novelty test without affecting other cognitive functions. Dendritic spine analysis revealed altered synapse morphology as characterized by increased dendritic spine length and head width. These modifications were independent of hippocampal plaque load and beta-amyloid peptide levels since these were similar in mice with normal versus reduced levels of EphA4. Conclusion Loss of EphA4 improved social memory in a mouse model of Alzheimer’s disease in association with alterations in spine morphology.


BMJ ◽  
2012 ◽  
Vol 344 (mar12 1) ◽  
pp. e1442-e1442 ◽  
Author(s):  
J. A. Driver ◽  
A. Beiser ◽  
R. Au ◽  
B. E. Kreger ◽  
G. L. Splansky ◽  
...  

2020 ◽  
Author(s):  
Jing Yuan ◽  
Nancy Maserejian ◽  
Yulin Liu ◽  
Sherral Devine ◽  
Cai Gillis ◽  
...  

Abstract Background: Studies providing Alzheimer’s disease (AD) prevalence data have largely neglected to characterize the proportion of AD that is mild, moderate or severe. Estimates of the severity distribution along the AD continuum, including the mild cognitive impairment (MCI) stage, are important to plan research and allocate future resources, particularly resources targeted at particular stages of disease. Methods: Participants (aged 50-94) with prevalent MCI or AD dementia clinical syndrome were cross-sectionally selected from three time-windows of the population-based Framingham Heart Study in 2004-2005 (n=381), 2006-2007 (n=422), and 2008-2009 (n=389). Summary estimates of the severity distribution were achieved by pooling results across time-windows. Diagnosis and severity were assessed by consensus dementia review. MCI-progressive was determined if the participant had documented progression to AD dementia clinical syndrome using longitudinal data.Results: Among AD dementia participants, the pooled percentages were 50.4% for mild, 30.3% for moderate, and 19.3% for severe. Among all MCI and AD participants, the pooled percentages were 29.5%, 19.6%, 25.7%, and 45.2% for MCI-not-progressive, MCI-progressive, mild AD dementia, and the combined group of MCI-progressive & mild AD dementia, respectively. Distributions by age and sex were presented.Conclusions: Heterogeneity in severity of the AD population exists. That half of prevalent cases have mild disease underscores the need for research and interventions to slow decline of this burdensome disease.Limitations: First, the FHS cohort participants were almost homogenously Caucasians and residents of a single city in MA, that limits the generalization of the results. Second, although FHS is a longitudinal study, the study population over the three time-windows would not be expected to be as dynamic as that of sampling participants from different geographic areas. Lastly, the study lacked AD biomarker confirmation (e.g., amyloid, tau, neurodegeneration), which would have increased the accuracy of case ascertainment.


2021 ◽  
Author(s):  
Samia C. Akhter‐Khan ◽  
Qiushan Tao ◽  
Ting Fang Alvin Ang ◽  
Indira Swetha Itchapurapu ◽  
Michael L. Alosco ◽  
...  

2013 ◽  
Vol 9 ◽  
pp. P681-P681
Author(s):  
Galit Weinstein ◽  
Alexa Beiser ◽  
Paul Courchesne ◽  
Vincent Chouraki ◽  
Rhoda Au ◽  
...  

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