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Late-Life Depression Is Associated With Reduced Cortical Amyloid Burden: Findings From the Alzheimer's Disease Neuroimaging Initiative Depression Project
Mackin RS, Insel PS, Landau S, Bickford D, Morin R, Rhodes E, Tosun D, Rosen HJ et al.. Biological psychiatry, 2020-07-02
Topic: Amyloid, tau and blood-test diagnosis
Background We evaluated the role of cortical amyloid deposition as a factor contributing to memory dysfunction and increased risk of dementia associated with late-life depression (LLD). Methods A total of 119 older adult participants with a current diagnosis of major depression (LLD) from the Alzheimer's Disease Neuroimaging Initiative (ADNI) Depression Project study and 119 nondepressed (ND) cognitively unimpaired participants matched on age, sex, and APOE genotype were obtained from the ADNI database. Results Thirty-three percent of LLD participants met ADNI criteria for mild cognitive impairment.
Cite this study APA, Vancouver, BibTeX · download .bib or .ris
APA 7th
Mackin, R. S., Insel, P. S., Landau, S., Bickford, D., Morin, R., Rhodes, E., et al. (2021). Late-Life Depression Is Associated With Reduced Cortical Amyloid Burden: Findings From the Alzheimer's Disease Neuroimaging Initiative Depression Project. Biological psychiatry. https://doi.org/10.1016/j.biopsych.2020.06.017
Vancouver
Mackin RS, Insel PS, Landau S, Bickford D, Morin R, Rhodes E, et al. Late-Life Depression Is Associated With Reduced Cortical Amyloid Burden: Findings From the Alzheimer's Disease Neuroimaging Initiative Depression Project. Biological psychiatry. 2021. doi:10.1016/j.biopsych.2020.06.017. PMID: 32980132.
BibTeX
@article{mackin2021-32980132,
author = {Mackin, R. S. and Insel, P. S. and Landau, S. and Bickford, D. and Morin, R. and Rhodes, E. and Tosun, D. and Rosen, H. J. and others},
title = {{Late-Life Depression Is Associated With Reduced Cortical Amyloid Burden: Findings From the Alzheimer's Disease Neuroimaging Initiative Depression Project}},
journal = {Biological psychiatry},
year = {2021},
doi = {10.1016/j.biopsych.2020.06.017},
pmid = {32980132},
url = {https://doi.org/10.1016/j.biopsych.2020.06.017}
}
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Key findings
- Methods A total of 119 older adult participants with a current diagnosis of major depression (LLD) from the Alzheimer's Disease Neuroimaging Initiative (ADNI) Depression Project study and 119 nondepressed (ND) cognitively unimpaired participants matched on age, sex, and APOE genotype were obtained from the ADNI database.
- Results Thirty-three percent of LLD participants met ADNI criteria for mild cognitive impairment.
- Compared with ND individuals, the LLD group exhibited less global amyloid beta (Aβ) accumulation (p = .05).
- The proportion of amyloid positivity in the LLD group was 19.3% compared with 31.1% for the ND participants (p = .02).
Why it matters
In 119 older adults with late-life depression compared with 119 nondepressed participants, the depressed group had less global amyloid beta accumulation. Thirty-three percent of the depressed participants met criteria for mild cognitive impairment, suggesting that amyloid may not be the main driver of memory problems in late-life depression.
Study details
- Participants119
- Effect size19.3%; 31.1%
- Evidence strengthLow
How this study scored 53/100
Published in a peer-reviewed journal. Scored zero for study design and randomised / blinded because the record does not state it.
| Component | Points | Why |
|---|---|---|
| Journal tier | 7 / 10 | Tier 3 — peer-reviewed journal (Biological psychiatry) |
| Journal's citation record | 3 / 4 | Biological Psychiatry: journal h-index 428 (OpenAlex, 2026-10-29) |
| Study design | 0 / 12 | No study design recorded — scores zero, not guessed (not stated in the record — scored 0) |
| Strength of evidence | 1 / 5 | Rated “low” in our summary |
| Peer-review validation | 10 / 10 | Peer-reviewed. Published as an article in a named peer-reviewed journal. |
| How recent | 3 / 5 | 2021 — within 6 year(s) of the newest study here |
| Sample size | 2 / 4 | 119 participants |
| Effect reported | 2 / 3 | Effect reported as a number, without an interval or test |
| Studied in people | 3 / 3 | Studied in people (participant count stated) |
| Randomised / blinded | 0 / 2 | No randomisation or blinding stated — scores zero (not stated in the record — scored 0) |
| Times cited | 4 / 7 | Cited 76 times (OpenAlex, 2026-10-10) |
| Citations per year | 3 / 5 | 10.9 citations a year over 7 year(s) since 2021 |
| Impact for its field and year | 3 / 6 | Cited 5.9× the average for papers of its field and year (OpenAlex FWCI) |
| Cited by studies here | 2 / 6 | Cited by 4 other studies in this library |
| Still being cited | 2 / 4 | Cited 39 times in 2024–2026 (2026 still in progress; OpenAlex) |
| Senior author's track record | 1 / 4 | Last-listed author Craig J. Nelson: h-index 18 (OpenAlex, whole career) |
| Institution's track record | 2 / 3 | University of Michigan: institution h-index 2,240 (OpenAlex) |
| Multi-centre collaboration | 3 / 3 | OpenAlex lists 10 institution(s) in 2 countries |
| Indexed in PubMed | 2 / 2 | Indexed in PubMed (PMID 32980132) |
| Free to read | 0 / 2 | Behind a paywall — scores zero |
| Total | 53 / 100 | — |
What each of these 20 components measures, and what this score is not →
Read the original
- DOI: 10.1016/j.biopsych.2020.06.017
- PubMed: 32980132
- Original source →
- Free full text: Biological Psychiatry →
Full text: free to read — OpenAlex lists this copy as free to read: the link above (checked 6 Feb 1020).
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