Prevalence of Depressive Symptoms in a Memory Clinic Cohort: A Retrospective Study

被引:4
|
作者
Loreto, Flavia [1 ]
Fitzgerald, Anna [1 ]
Golemme, Mara [2 ,5 ,6 ]
Gunning, Stephen [3 ]
Win, Zarni [4 ]
Patel, Neva [4 ]
Carswell, Christopher [2 ]
Perry, Richard [1 ,2 ]
Kennedy, Angus [2 ]
Edison, Paul [1 ]
Malhotra, Paresh [1 ,2 ,5 ,6 ]
机构
[1] Imperial Coll London, Fac Med, Dept Brain Sci, Margravine Rd, London W6 8RP, England
[2] Imperial Coll Healthcare NHS Trust, Dept Neurol, London, England
[3] Imperial Coll Healthcare NHS Trust, Dept Neuropsychol, London, England
[4] Imperial Coll Healthcare NHS Trust, Dept Nucl Med, London, England
[5] Imperial Coll London, UK Dementia Res Inst, Care Res & Technol Ctr, London, England
[6] Univ Surrey, Guildford, Surrey, England
关键词
Alzheimer's disease; amyloid-beta; amyloid-PET; clinical cohort; dementia; depression; diagnostic uncertainty; MILD COGNITIVE IMPAIRMENT; ALZHEIMERS ASSOCIATION WORKGROUPS; AMYLOID PET; DIAGNOSTIC GUIDELINES; NATIONAL INSTITUTE; DEMENTIA; DISEASE; DECLINE; RECOMMENDATIONS;
D O I
10.3233/JAD-220170
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Background: Depression has been suggested to be a cause of reversible cognitive impairment but also a risk factor for neurodegenerative disease. Studies suggest that depression prevalence may be high in early onset dementia, particularly Alzheimer's disease, but this has not been systematically assessed in a biomarker-validated clinical dementia cohort to date. Objective: To examine the prevalence, features, and association with amyloid pathology of lifetime depressive symptoms in a memory clinic cohort meeting appropriate use criteria for amyloid PET imaging. Methods: We included 300 patients from a single-center memory clinic cohort that received diagnostic biomarker evaluation with amyloid PET imaging according to appropriate use criteria. History of lifetime depressive symptoms was retrospectively assessed through structured review of clinical correspondence. Results: One hundred forty-two (47%) patients had a history of significant depressive symptoms ('D+'). Of these, 89% had ongoing symptoms and 60% were on antidepressants at the time of presentation to our Clinic. Depressive symptoms were equally highly prevalent in the amyloid-positive and the heterogeneous group of amyloid-negative patients. Conclusion: Approximately half of patients who meet appropriate use criteria for amyloid PET have a history of depressive symptoms. We suggest that depression is an important feature of both neurodegenerative and non-neurodegenerative cognitive impairment and may contribute to the diagnostic uncertainty behind referral to amyloid PET.
引用
收藏
页码:1179 / 1187
页数:9
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