Evidence map›Paper›PMID 40529210›Full record

ReviewFrontiers in aging neuroscience2025

Neurobiological and therapeutic landmarks of depression associated with Alzheimer's disease dementia.

Ilinca Untu, Michael Davidson, Gabriela-Dumitrita Stanciu, Jonathan Rabinowitz, Romeo-Petru Dobrin, Diana-Sabina Vieru, Bogdan-Ionel Tamba

Abstract readReview
In one paragraph

Review in Frontiers in aging neuroscience, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

  1. Review
  2. Review
  3. Review
  4. Review
  5. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Ilinca UntuDepartment of Medicine III, Faculty of Medicine, "Grigore T. Popa" University of Medicine and Pharmacy of Iasi, Iași, Romania.
Michael DavidsonAdvanced Research and Development Center for Experimental Medicine "Prof. Ostin C. Mungiu" CEMEX, "Grigore T. Popa" University of Medicine and Pharmacy of Iasi, Iași, Romania.
Gabriela-Dumitrita StanciuAdvanced Research and Development Center for Experimental Medicine "Prof. Ostin C. Mungiu" CEMEX, "Grigore T. Popa" University of Medicine and Pharmacy of Iasi, Iași, Romania.
Jonathan RabinowitzAdvanced Research and Development Center for Experimental Medicine "Prof. Ostin C. Mungiu" CEMEX, "Grigore T. Popa" University of Medicine and Pharmacy of Iasi, Iași, Romania.
Romeo-Petru DobrinDepartment of Medicine III, Faculty of Medicine, "Grigore T. Popa" University of Medicine and Pharmacy of Iasi, Iași, Romania.
Diana-Sabina VieruAdvanced Research and Development Center for Experimental Medicine "Prof. Ostin C. Mungiu" CEMEX, "Grigore T. Popa" University of Medicine and Pharmacy of Iasi, Iași, Romania.
Bogdan-Ionel TambaAdvanced Research and Development Center for Experimental Medicine "Prof. Ostin C. Mungiu" CEMEX, "Grigore T. Popa" University of Medicine and Pharmacy of Iasi, Iași, Romania.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Depression in Alzheimer's disease (AD) dementia has become an increasingly recognized public health concern due to its high prevalence and substantial impact on patient outcomes. Despite extensive research having been conducted over the past decades, the precise causal mechanisms and the nature of the relationship between depression and AD dementia remain incompletely understood. This narrative review examines the bidirectional interaction between depression and Alzheimer's disease, emphasizing shared neurobiological pathways, including neurotransmitter dysregulation, neuroinflammation, abnormalities in the hypothalamic-pituitary-adrenal (HPA) axis, and deficits in neuroplasticity. These mechanisms likely contribute to the acceleration of neurodegeneration in AD and the onset or worsening of depressive symptoms. Current therapeutic approaches remain largely nonspecific, with a lack of targeted therapies that address the unique pathophysiological context of depression in AD. While progress has been made, key research gaps remain, particularly in understanding the complex biological interactions between these two conditions. Future research should focus on identifying specific biomarkers and developing personalized treatment strategies tailored to the neurobiological features of both depression and AD. By addressing these neurobiological mechanisms, we can develop more effective and targeted interventions, ultimately improving patient outcomes and advancing clinical care for this dual pathology.

Indexed as

Alzheimer’s diseasebidirectional relationshipdepressiondepression–Alzheimer’s disease comorbidityshared neurobiological mechanisms

Identifiers

PMID40529210
PMCPMC12171374

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.