scholarly journals NEUROPSYCHIATRIC SYMPTOMS AS PREDICTOR OF POOR CLINICAL OUTCOME IN PATIENTS WITH VASCULAR COGNITIVE IMPAIRMENT#

Author(s):  
Yoni C.P. Sep ◽  
Anna E. Leeuwis ◽  
Lieza G. Exalto ◽  
Jooske M. Boomsma ◽  
Niels D. Prins ◽  
...  
Author(s):  
Jooske M.F. Boomsma ◽  
Lieza G. Exalto ◽  
Frederik Barkhof ◽  
Christopher L.H. Chen ◽  
Saima Hilal ◽  
...  

Neurology ◽  
2019 ◽  
Vol 92 (14) ◽  
pp. e1558-e1566 ◽  
Author(s):  
Doeschka A. Ferro ◽  
Hilde van den Brink ◽  
Lieza G. Exalto ◽  
Jooske M.F. Boomsma ◽  
Frederik Barkhof ◽  
...  

ObjectiveTo determine the occurrence of acute cerebral microinfarcts (ACMIs) in memory clinic patients and relate their presence to vascular risk and cognitive profile, CSF and neuroimaging markers, and clinical outcome.MethodsThe TRACE-VCI study is a memory clinic cohort of patients with vascular brain injury on MRI (i.e., possible vascular cognitive impairment [VCI]). We included 783 patients (mean age 67.6 ± 8.5, 46% female) with available 3T diffusion-weighted imaging (DWI). ACMIs were defined as supratentorial DWI hyperintensities <5 mm with a corresponding hypo/isointense apparent diffusion coefficient signal and iso/hyperintense T2*-weighted signal.ResultsA total of 23 ACMIs were found in 16 of the 783 patients (2.0%). Patients with ACMIs did not differ in vascular risk or cognitive profile, but were more often diagnosed with vascular dementia (odds ratio [OR] 5.1; 95% confidence interval [CI] 1.4–18.9, p = 0.014). ACMI presence was associated with lower levels of β-amyloid (p < 0.004) and with vascular imaging markers (lacunar infarcts: OR 3.5, CI 1.3–9.6, p = 0.015; nonlacunar infarcts: OR 4.1, CI 1.4–12.5, p = 0.012; severe white matter hyperintensities: OR 4.8, CI 1.7–13.8, p = 0.004; microbleeds: OR 18.9, CI 2.5–144.0, p = 0.0001). After a median follow-up of 2.1 years, the risk of poor clinical outcome (composite of marked cognitive decline, major vascular event, death, and institutionalization) was increased among patients with ACMIs (hazard ratio 3.0; 1.4–6.0, p = 0.005).ConclusionIn patients with possible VCI, ACMI presence was associated with a high burden of cerebrovascular disease of both small and large vessel etiology and poor clinical outcome. ACMIs may thus be a novel marker of active vascular brain injury in these patients.


2021 ◽  
Vol 17 (S6) ◽  
Author(s):  
Lieza G. Exalto ◽  
Jooske Boomsma ◽  
Yoni C.P. Sep ◽  
Anna E. Leeuwis ◽  
Niels D. Prins ◽  
...  

2015 ◽  
Vol 9 (3) ◽  
pp. 230-236 ◽  
Author(s):  
Chan Tiel ◽  
Felipe Kenji Sudo ◽  
Gilberto Sousa Alves ◽  
Letice Ericeira-Valente ◽  
Denise Madeira Moreira ◽  
...  

Neuropsychiatric symptoms or Behavioral and Psychological Symptoms of Dementia (BPSD) are common and invariably appear at some point during the course of the disease, mediated both by cerebrovascular disease and neurodegenerative processes. Few studies have compared the profiles of BPSD in Vascular Cognitive Impairment (VCI) of different subtypes (subcortical or cortical) and clinical stages (Vascular Cognitive Impairment No Dementia [VaCIND] and Vascular Dementia [VaD]). Objective: To review the BPSD associated with different subtypes and stages of VCI using the Neuropsychiatric Inventory (NPI). Methods: Medline, Scielo and Lilacs databases were searched for the period January 2000 to December 2014, with the key words: "BPSD AND Vascular Dementia, "NPI AND Vascular Dementia" and "NPI AND VCI. Qualitative analysis was performed on studies evaluating BPSD in VCI, using the Neuropsychiatric Inventory (NPI). Results: A total of 82 studies were retrieved of which 13 were eligible and thus included. Among the articles selected, 4 compared BPSD in Subcortical Vascular Dementia (SVaD) versus Cortical-Subcortical Vascular Dementia (CSVaD), 3 involved comparisons between SVaD and VaCIND, 1 study analyzed differences between CSVaD and VaCIND, while 5 studies assessed BPSD in CSVaD. Subcortical and Cortical-Subcortical VaD were associated predominantly with Apathy and Depression. VaCIND may present fewer behavioral symptoms than VaD. Conclusion: The profile of BPSD differs for different stages of VCI. Determining the most prevalent BPSD in VCI subtypes might be helpful for improving early diagnosis and management of these symptoms.


2021 ◽  
Vol 2021 ◽  
pp. 1-7
Author(s):  
Chih-Lin Chen ◽  
Min-Hsien Hsu ◽  
Chao-Hsien Hung ◽  
Pai-Yi Chiu ◽  
Chung-Hsiang Liu

Visual hallucinations (VHs) are striking features for dementia, especially dementia with Lewy bodies (DLB). We aimed to study the frequency and associated factors of VH in vascular cognitive impairment (VCI) and investigate the feasibility of clinically diagnosing the mixed pathology of VCI with DLB. This is a multicentre registration study. A consecutive series of VCI patients with and without dementia were enrolled. Frequency of VH and associated factors, including age, gender, education, disease severity, DLB clinical features, vascular risk factors, cognitive function, and neuropsychiatric symptoms, were compared between VCI with VH (VH+) and without VH (VH−). Among the 1281 patients analysed, 155 (12.1%) had VH. The VH+ group was older ( t = 5.07 ; p < 0.001 ), was more likely to be female ( χ 2 = 13.46 ; p < 0.001 ), and has a higher clinical dementia rating ( χ 2 = 70.51 ; p < 0.001 ). After adjusting for age, gender, and disease severity, the VH+ group had poorer cognition and more severe neuropsychiatric symptoms. The VH+ group was more associated with DLB features in fluctuating cognition ( OR = 2.48 ; p < 0.001 ), parkinsonism ( OR = 1.85 ; p = 0.001 ), rapid eye movement (REM) behavioral disorder ( OR = 4.56 ; p < 0.001 ), and ≧2 DLB core features ( OR = 26.01 ; p < 0.001 ). VCI patients with VH tend to have more severe dementia, neuropsychiatric symptoms, and poorer cognitive function. Additionally, highly associated with clinical DLB features in VCI with VH raised the possibility of mixed pathology with DLB in this group. More than two core features in VCI might help in diagnosing a mixed pathology with DLB.


2008 ◽  
Author(s):  
Ruth E. Yoash-Gantz ◽  
Kristin L. Humphrey ◽  
Jacqueline W. Friedman

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