Progression of Alzheimer's disease during a three-year follow-up using the CERAD-NB total score: Kuopio ALSOVA study

被引:24
作者
Hallikainen, Ilona [1 ]
Hanninen, Tuomo [2 ]
Fraunberg, Mikael [3 ]
Hongisto, Kristiina [1 ]
Valimaki, Tarja [4 ,5 ]
Hiltunen, Asta [6 ]
Karppi, Pertti [7 ]
Sivenius, Juhani [1 ,8 ]
Soininen, Hilkka [1 ,2 ]
Koivisto, Anne M. [1 ,2 ]
机构
[1] Univ Eastern Finland, Inst Clin Med, Sch Med, Kuopio, Finland
[2] Kuopio Univ Hosp, Neurol Neuro Ctr, FIN-70211 Kuopio, Finland
[3] Kuopio Univ Hosp, Neurosurg Neuro Ctr, SF-70210 Kuopio, Finland
[4] Univ Eastern Finland, Finnish Doctoral Program Nursing Sci, Kuopio, Finland
[5] Univ Eastern Finland, Dept Nursing Sci, Kuopio, Finland
[6] North Karelia Cent Hosp, Dept Neurol, Joensuu, Finland
[7] Mikkeli Cent Hosp, Mikkeli, Finland
[8] Brain Res & Rehabil Ctr Neuron, Kuopio, Finland
关键词
Alzheimer's disease; dementia; CERAD; activities of daily living; neuropsychiatric symptoms; progression; NEUROPSYCHOLOGICAL ASSESSMENT; NEUROPSYCHIATRIC SYMPTOMS; COGNITIVE IMPAIRMENT; DEMENTIA; CONSORTIUM; ESTABLISH; REGISTRY; MILD; INVENTORY;
D O I
10.1017/S1041610213000653
中图分类号
B849 [应用心理学];
学科分类号
040203 ;
摘要
Background: We studied the suitability of The Consortium to Establish a Registry for Alzheimer's Disease Neuropsychological Battery (CERAD-NB) total score for monitoring Alzheimer's disease (AD) progression in early-diagnosed medicated patients. We also investigated possible differences in progression between patients with very mild or mild baseline AD. Methods: In this three-year follow-up of 115 ALSOVA study patients with clinical dementia ratings (CDR) of very mild (0.5) or mild (1) AD, we analyzed total CERAD-NB, Mini-Mental State Examination (MMSE), Neuropsychiatric Inventory (NPI), The Alzheimer's Disease Cooperative Study-Activities of Daily Living Inventory, and Clinical Dementia Rating Sum of Boxes scores. Correlations were identified with efficacy parameters. Results: Over three years, total CERAD-NB declined significantly in both groups. Annual change rates of total CERAD-NB were also significant. Total CERAD-NB revealed annual differences in cognition between study groups, while MMSE did not. Total CERAD-NB correlated well with other cognitive and global measures, but not with NPI. For almost two years, the CDR-0.5 group maintained a higher activities of daily living than the CDR-1 group exhibited at baseline. Furthermore, the CDR-0.5 group showed milder neuropsychiatric symptoms at the end of follow-up than the CDR-1 group showed at baseline. Conclusions: The CERAD total score is a suitable and sensitive follow-up tool in longitudinal AD trials. Cognition progression rates did not significantly differ between study groups; however, patients with very mild AD at baseline had milder neuropsychiatric symptoms after long-term follow-up. This emphasizes the importance of early diagnosis and assessment of neuropsychiatric symptoms at the diagnostic visit and during follow-up.
引用
收藏
页码:1335 / 1344
页数:10
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