Memory self-appraisal and depressive symptoms in people at genetic risk for Alzheimer's disease
Objectives A previous study found that subjective memory loss in middle‐aged and older persons is associated with the major genetic risk for Alzheimer's disease, the apolipoprotein E‐4 (APOE‐4) allele. No previous study has focused on subjective memory complaints and depressive symptoms in the...
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Veröffentlicht in: | International journal of geriatric psychiatry 2001-11, Vol.16 (11), p.1071-1077 |
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Sprache: | eng |
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Zusammenfassung: | Objectives
A previous study found that subjective memory loss in middle‐aged and older persons is associated with the major genetic risk for Alzheimer's disease, the apolipoprotein E‐4 (APOE‐4) allele. No previous study has focused on subjective memory complaints and depressive symptoms in the same subject population at genetic risk for Alzheimer's disease.
Method
Sixty‐six persons (mean age = 64 years, range = 43 to 82 years) without major depression or dementia but with mild age‐related memory complaints were rated for severity of depressive symptoms, using the Hamilton Depression Rating Scale, and assessed for the presence of the APOE‐4 allele. Severity of subjective memory loss was assessed using the Memory Functioning Questionnaire, which measures four memory domains: frequency of forgetting, seriousness of forgetting, retrospective functioning, and mnemonics usage.
Results
Depressive symptoms were significantly associated with subjective memory loss in subjects without the APOE‐4 allele, for retrospective functioning (perceived change in memory) and mnemonics usage, but not in APOE‐4 carriers. The same significant associations were found when the analysis was limited to the 44 subjects in the mid‐age range (55–74 years), wherein APOE‐4 confers its greatest effects on risk for Alzheimer's disease.
Conclusion
These results confirm that mild depressive symptoms are related to subjective memory loss, but for some forms of memory complaint, the relationship holds true only for people without the major known genetic risk for Alzheimer's disease. Copyright © 2001 John Wiley & Sons, Ltd. |
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ISSN: | 0885-6230 1099-1166 |
DOI: | 10.1002/gps.481 |