History of depression, depressive symptoms, and medial temporal lobe atrophy and the risk of Alzheimer disease
Abstract
Background Depression may increase risk for Alzheimer disease (AD), but it is not clear whether this risk is mediated by structural brain changes. We determined whether history of depressive episodes and presence of depressive symptoms were associated with smaller hippocampal and amygdalar volumes and with increased risk for incident AD. Methods Within the Rotterdam Scan Study 503 persons, aged 60-90 years at baseline and without dementia, reported their history of depressive episodes. Depressive symptoms were assessed with the Center for Epidemiologic Studies Depression Scale. Volumetric assessment of the hippocampus and amygdala was performed using three-dimensional MRI. All subjects were followed for an average of 6 years for development of AD, diagnosed according to National Institute of Neurological and Communicative Disorders and Stroke-Alzheimer's Disease and Related Disorders Association criteria. Results A total of 134 subjects (26.6%) reported a history of depression (88 reported an onset Conclusion History of depression, and particularly an early onset, but not presence of depressive symptoms increased the risk for Alzheimer disease. This risk was not mediated by smaller hippocampal or amygdalar volumes.
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MDD is accompanied by an increased risk of comorbid conditions that independently increase risk for AD.
“MDD is also accompanied by an increased risk of comorbid conditions that independently increase risk for AD, such as vascular disease, diabetes, lower cognitive reserve, and stress (39, 46).”
From Serotonin signaling is associated with lower amyloid-β levels and plaques in transgenic mice and humans (2011) · cites this paper as [39]
Depression itself increases risk of AD.
“The most consistent observation is that depression itself increases risk of AD (39–41).”
From Serotonin signaling is associated with lower amyloid-β levels and plaques in transgenic mice and humans (2011) · cites this paper as [39]
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References 38 · Cited by 248
- Authors
- Geerlings, M. I., den Heijer, T., Koudstaal, P. J., Hofman, A., & Breteler, M. M. B.
- Affiliations
- Erasmus MC (NL)
- From Julius Center for Health Sciences and Primary Care (M.I.G.), University Medical Center Utrecht; and Departments of Epidemiology and Biostatistics (M.I.G., T.d.H., A.H., M.M.B.B.) and Neurology (T.d.H., P.J.K.), Erasmus Medical Center, Rotterdam, The Netherlands.
- Venue
- Neurology
- Published
- 2008-04-08
- Volume
- 70
- Issue
- 15
- Pages
- 1258-1264
- ISSN
- 0028-3878 (ISSN-L)
- 1526-632X
- OpenAlex
- W1969375208
- Cited by
- 248
- References
- 38
- Citations by year
- 2026: 1 · 2025: 5 · 2024: 12 · 2023: 8 · 2022: 11 · 2021: 13 · 2020: 18 · 2019: 11 · 2018: 10 · 2017: 13 · 2016: 12 · 2015: 15 · 2014: 24 · 2013: 17 · 2012: 22
- FWCI
- 12.88
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Neurology (publishedVersion)
- PubMed (publishedVersion)
- EUR Research Repository (Erasmus University Rotterdam) (publishedVersion)
- EUR Research Repository (Erasmus University Rotterdam) (submittedVersion)
- Topics
- Health Sciences › Medicine › Psychiatry and Mental health › Dementia and Cognitive Impairment Research
- Health Sciences › Medicine › Physiology › Alzheimer's disease research and treatments
- Life Sciences › Neuroscience › Behavioral Neuroscience › Stress Responses and Cortisol
- Keywords
- depression, Alzheimer's disease, depressive symptoms, hippocampal volume, amygdala volume, medial temporal lobe atrophy, early-onset depression, late-onset depression, brain structural changes
- MeSH terms
- Aged, Aged, 80 and over, Alzheimer Disease, Amygdala, Atrophy, Depressive Disorder, Female, Hippocampus, Humans, Male, Middle Aged, Neuropsychological Tests, Predictive Value of Tests, Prognosis, Risk Factors, Temporal Lobe, Comorbidity, Linear Models, Age of Onset
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