scholarly journals Brain Structural and Amyloid Correlates of Recovery From Semantic Interference in Cognitively Normal Individuals With or Without Family History of Late-Onset Alzheimer’s Disease

2019 ◽  
Vol 31 (1) ◽  
pp. 25-36 ◽  
Author(s):  
Carolina Abulafia ◽  
David Loewenstein ◽  
Rosie Curiel-Cid ◽  
Bárbara Duarte-Abritta ◽  
Stella M. Sánchez ◽  
...  
2006 ◽  
Vol 14 (7S_Part_8) ◽  
pp. P478-P479
Author(s):  
Alexa Pichet Binette ◽  
Etienne Vachon-Presseau ◽  
Julie Gonneaud ◽  
Natalie L. Marchant ◽  
Pierre Bellec ◽  
...  

2014 ◽  
Vol 10 ◽  
pp. P664-P664
Author(s):  
N.M. Dowling ◽  
Sterling Johnson ◽  
Henrik Zetterberg ◽  
Barbara B. Bendlin ◽  
Carey Elizabeth Gleason ◽  
...  

2006 ◽  
Vol 14 (7S_Part_2) ◽  
pp. P126-P127
Author(s):  
Alexa Pichet Binette ◽  
Etienne Vachon-Presseau ◽  
Julie Gonneaud ◽  
Natalie L. Marchant ◽  
Pierre Bellec ◽  
...  

2015 ◽  
Vol 40 (3-4) ◽  
pp. 210-221 ◽  
Author(s):  
Jong Hun Kim ◽  
Seok Min Go ◽  
Sang Won Seo ◽  
Suk Hui Kim ◽  
Juhee Chin ◽  
...  

Background: Subcortical vascular dementia (SVaD) is one of the most common dementias, after Alzheimer's disease (AD) dementia. Few survival analyses in SVaD patients have been reported. Methods: The dates and causes of death of 146 SVaD and 725 AD patients were included. We used the Cox proportional hazards model to compare survival between SVaD and AD patients and to explore possible factors related to survival of SVaD patients. Results: The median survival time after the onset of SVaD (109 months) was shorter than that recorded for AD (152 months). The most common cause of death in SVaD was stroke (47.1%). Factors associated with shorter survival in SVaD were late onset, male sex, worse baseline cognition, absence of hypertension and a family history of stroke. Conclusions: Stroke prevention may be important in SVaD treatment because 47.1% of SVaD patients died of stroke. A family history of stroke and absence of hypertension were associated with a shorter survival in SVaD, suggesting the existence of genetic or unknown risk factors.


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