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|Title:||Cerebral white matter disease is independently associated with BPSD in Alzheimer's disease||Authors:||Kandiah, N.
Behavioral and psychological symptoms of dementia (BPSD)
Magnetic resonance imaging
White matter disease
|Issue Date:||15-Feb-2014||Citation:||Kandiah, N., Chander, R., Zhang, A., Yee, C.C. (2014-02-15). Cerebral white matter disease is independently associated with BPSD in Alzheimer's disease. Journal of the Neurological Sciences 337 (1-2) : 162-166. ScholarBank@NUS Repository. https://doi.org/10.1016/j.jns.2013.11.042||Abstract:||Objectives To study the association between cerebral white matter disease and burden of behavioral and psychological symptoms (BPSD) among patients with moderate to severe AD. Methods Patients with moderate to severe AD having undergone MRI brain, cognitive and behavioral evaluations were studied. BPSD was diagnosed based on established clinical guidelines. White matter hyperintensity (WMH) and medial temporal lobe atrophy (MTA) were quantified by a blinded rater. Results 122 AD patients were studied. Age [76.84 vs. 72.70, p = 0.014] and MMSE [11.69 vs. 15.16, p < 0.001] was significantly higher in patients with BPSD. BPSD patients demonstrated higher periventricular [5.44 vs. 4.21, p < 0.001], deep subcortical [5.07 vs. 3.43, p < 0.001], and total WMH [10.51 vs. 7.65, p < 0.001] compared to non-BPSD patients. Higher proportion of BPSD patients had WMH in the highest tertile of severity (82.22% vs. 45.45%, p < 0.001). After correcting for age, baseline cognition and degree of MTA, total WMH remained significantly associated with a diagnosis of BPSD [odds ratio: 1.45 (1.14-1.85; p = 0.002)]. With severe WMH, the association is significantly increased [odds ratio: 4.3 (1.3-12.5); p = 0.016]. Conclusion WMH is independently associated with BPSD in moderate to severe AD. Optimizing vascular risk factors may be a strategy to reduce the severity of BPSD in AD. © 2013 Elsevier B.V.||Source Title:||Journal of the Neurological Sciences||URI:||http://scholarbank.nus.edu.sg/handle/10635/124667||ISSN:||0022510X||DOI:||10.1016/j.jns.2013.11.042|
|Appears in Collections:||Staff Publications|
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