4.5 Article

A Comparison of Behavioral and Psychological Symptoms of Dementia (BPSD) and BPSD Sub-Syndromes in Early-Onset and Late-Onset Alzheimer's Disease

Journal

JOURNAL OF ALZHEIMERS DISEASE
Volume 85, Issue 2, Pages 691-699

Publisher

IOS PRESS
DOI: 10.3233/JAD-215061

Keywords

Alzheimer's disease; behavioral and psychological symptoms of dementia (BPSD); BPSD sub-syndromes; early-onset Alzheimer's disease; late-onset Alzheimer's disease; Neuropsychiatric Inventory; prevalence; prevalence over time; time of occurrence

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This study compared the behavioral and psychological symptoms between early-onset and late-onset Alzheimer's disease patients, and found that early-onset patients had a higher overall prevalence of symptoms and a later onset compared to late-onset patients. The manifestation of symptoms and sub-syndromes also differed between the two groups at different stages. However, there were no significant differences in the severity of symptoms.
Background: Behavioral and psychological symptoms of dementia (BPSD) have a large impact on the quality of life of patients with Alzheimer's disease (AD). Few studies have compared BPSD between early-onset (EOAD) and late-onset (LOAD) patients, finding conflicting results. Objective: The aims of this study were to: 1) characterize the presence, overall prevalence, and time of occurrence of BPSD in EOAD versus LOAD; 2) estimate the prevalence over time and severity of each BPSD in EOAD versus LOAD in three stages: pre-T0 (before the onset of the disease), T0 (from onset to 5 years), and T1 (from 5 years onwards); 3) track the manifestation of BPSD sub-syndromes (i.e., hyperactivity, psychosis, affective, and apathy) in EOAD versus LOAD at T0 and T1. Methods: The sample includes 1,538 LOAD and 387 EOAD diagnosed from 1996 to 2018. Comprehensive assessment batteries, including the Neuropsychiatric Inventory (NPI), were administered at the first medical assessment and at different follow-up period. Results: The overall prevalence for the most of BPSD was significantly higher in EOAD compared to LOAD whereas most BPSD appeared significantly later in EOAD patients. Between the two groups, from pre-T0 to T1 we recorded a different pattern of BPSD prevalence over time as well as for BPSD sub-syndromes at T0 and T1. Results on severity of BPSD did not show significant differences. Conclusion: EOAD and LOAD represent two different forms of a single entity not only from a neuropathological, cognitive, and functional level but also from a psychiatric point of view.

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