失智症
痴呆
额颞叶变性
心理学
萧条(经济学)
精神科
临床心理学
星团(航天器)
精神病
照顾负担
疾病
精神分裂症(面向对象编程)
医学
内科学
程序设计语言
经济
宏观经济学
计算机科学
作者
Christopher B. Morrow,Vidyulata Kamath,Bradford C. Dickerson,Mark C. Eldaief,Bradford C. Dickerson,Bonnie Wong,Scott McGinnis,Ryan Darby,Adam M. Staffaroni,Maria I. Lapid,Belén Pascual,Julio C. Rojas,Joseph C. Masdeu,Kyrana Tsapkini,Edward D. Huey,Daniel Fisher,Alexander Pantelyat,Akshata Balaji,Eric Sah,Irene Litvan
摘要
Aim Cognitive and behavioral phenomena define behavioral variant frontotemporal dementia (bvFTD), but neuropsychiatric symptoms (NPS) outside the core criteria are common throughout the illness. Identifying how NPS cluster in bvFTD may guide development of future therapies. Methods Participants ( n = 354) with sporadic and genetic bvFTD were enrolled in the ARTFL LEFFTDS Longitudinal Frontotemporal Lobar Degeneration Consortium. Dementia stage was defined as early (CDR® plus NACC FTLD ≤1) or advanced (CDR® plus NACC FTLD ≥1). Baseline and annual follow‐up visit data were analyzed to compare NPS across stages of bvFTD. Psychiatric states were captured using the Neuropsychiatric Inventory‐Questionnaire and Clinician Judgment of Symptoms. Polychoric cluster analysis was used to describe NPS clusters. Results NPS were highly prevalent (≥90%) in early and late bvFTD. Four NPS clusters were identified based on magnitude of factor loadings: affective, disinhibited, compulsive, and psychosis. Neuropsychiatric symptoms fluctuated across visits. In the affective cluster, depression showed the least visit‐to‐visit stability. In the disinhibited cluster, elation showed the least stability. Symptoms in the psychosis and compulsive clusters (hallucinations, delusions, obsessions/compulsions, and hyperorality) were largely stable, persisting from visit‐to‐visit in more than 50% of cases. Symptoms in the affective and disinhibited cluster were associated with the highest caregiver burden, while symptoms in the obsessive cluster were associated with the most functional impairment. Conclusion NPS in bvFTD are frequent and cluster into four discrete groups. The fluctuating nature of some NPS in bvFTD suggests that they may not be reliable markers of disease progression or stage.
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