期刊论文详细信息
JOURNAL OF AFFECTIVE DISORDERS 卷:222
Trajectories of depressive symptoms and their relationship to the progression of dementia
Article
Barca, Maria Lage1,2  Persson, Karin1,2  Eldholm, Rannveig3  Benth, Jurate Saltyte5,6  Kersten, Hege1,7,8  Knapskog, Anne-Brita2  Saltvedt, Ingvild3,4  Selbaek, Geir1,9  Engedal, Knut1,2 
[1] Vestfold Hosp Trust, Norwegian Natl Advisory Unit Ageing & Hlth, Tonsberg, Norway
[2] Oslo Univ Hosp, Dept Geriatr Med, Oslo, Norway
[3] Norwegian Univ Sci & Technol, NTNU, Dept Neuromed & Movement Sci, Trondheim, Norway
[4] Univ Trondheim Hosp, St Olav Hosp, Geriatr Dept, Trondheim, Norway
[5] Univ Oslo, Inst Clin Med, Campus Ahus, Oslo, Norway
[6] Akershus Univ Hosp, Res Ctr, HOKH, Lorenskog, Norway
[7] Univ Oslo, Sch Pharm, Dept Pharmaceut Biosci, Oslo, Norway
[8] Telemark Hosp Trust, Skien, Norway
[9] Innlandet Hosp Trust, Res Ctr Old Age Psychiat Res, Ottestad, Norway
关键词: Depression;    Trajectory;    Dementia;    Mild cognitive impairment;    Prognosis;    Memory clinic;   
DOI  :  10.1016/j.jad.2017.07.008
来源: Elsevier
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【 摘 要 】

Background: The relationship between progression of Alzheimer's disease and depression and its underlying mechanisms has scarcely been studied. Methods: A sample of 282 outpatients with Alzheimer's disease (AD; 105 with amnestic AD and 177 with Alzheimer's dementia) from Norway were followed up for an average of two years. Assessment included Cornell Scale for Depression in Dementia and Clinical Dementia Rating Scale (CDR) at baseline and follow-up to examine the relationship between AD and depression. Additionally, MRI of the brain, CSF dementia biomarkers and APOE status were assessed at baseline. Progression of dementia was defined as the difference between CDR sum of boxes at follow-up and baseline (CDR-SB change). Trajectories of depressive symptoms on the Cornell Scale were identified using growth mixture modeling. Differences between the trajectories in regard to patients' characteristics were investigated. Results: Three distinct trajectories of depressive symptoms were identified: 231 (82.8%) of the patients had stable low-average scores on the Cornell Scale (Class 1); 11 (3.9%) had high and decreasing scores (Class 2); and 37 (13.3%) had moderate and increasing scores (Class 3). All classes had average probabilities over 80%, and confidence intervals were non -overlapping. The only significant characteristic associated with membership in class 3 was CDR-SB change. Limitations: Not all patients screened for participation were included in the study, but the included and non included patients did not differ significantly. Some patients with amnestic MCI might have been misdiagnosed. Conclusion: A more rapid progression of dementia was found in a group of patients with increasing depressive symptoms.

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