Evidence map›Paper›PMID 42953433›Full record

ReviewNeuropsychiatric disease and treatment2026

Advances in Multi-Omics Research on Post-Stroke Depression: From Molecular Mechanisms to Therapeutic Strategies.

Guoxun Feng, Lei Gao, Yuanzhi Zhao, Zhaoying Yu, Mei Yang, Yaping Chen, Xing Xu

Abstract readReview
In one paragraph

Review in Neuropsychiatric disease and treatment, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Guoxun FengDepartment of Psychiatry, Affiliated Minkang Hospital of Ningbo University (Ningbo Psychiatric Hospital), Ningbo, People's Republic of China.
Lei GaoDepartment of Psychiatry, Affiliated Minkang Hospital of Ningbo University (Ningbo Psychiatric Hospital), Ningbo, People's Republic of China.
Yuanzhi ZhaoHealth Science Center, Ningbo University, Ningbo, People's Republic of China.ORCID 0000-0001-9108-2256
Zhaoying YuHealth Science Center, Ningbo University, Ningbo, People's Republic of China.
Mei YangHealth Science Center, Ningbo University, Ningbo, People's Republic of China.
Yaping ChenDepartment of Psychiatry, Affiliated Minkang Hospital of Ningbo University (Ningbo Psychiatric Hospital), Ningbo, People's Republic of China.
Xing XuDepartment of Psychiatry, Affiliated Minkang Hospital of Ningbo University (Ningbo Psychiatric Hospital), Ningbo, People's Republic of China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Post-stroke depression (PSD) is a common neuropsychiatric complication after stroke and has a substantial impact on functional recovery, quality of life, and long-term outcomes. Because stroke-related manifestations, including aphasia, cognitive impairment, fatigue, and somatic symptoms, overlap with depressive symptoms, the clinical identification of PSD still largely relies on symptom assessment and clinical interviews, resulting in delayed diagnosis and intervention in some patients. Recent studies indicate that the development of PSD is not driven by a single pathological process but involves multiple mechanisms, including neuroinflammation, neural network alterations, dysfunction of the neurovascular unit, disturbances in energy and lipid metabolism, imbalance of the microbiota-gut-brain axis, and psychosocial factors following brain injury. The advancement of multi-omics technologies has provided new approaches for investigating the biological mechanisms underlying PSD. This review systematically summarizes recent progress in the application of multi-omics approaches in PSD research, focusing on molecular alterations identified across different omics platforms and potential biomarkers. Furthermore, the role of the hypothalamic-pituitary-adrenal (HPA) axis in stress response regulation and PSD development is discussed within the context of neuro-immune-metabolic interactions. Overall, multi-omics studies have provided new insights into the molecular basis of PSD and facilitated the identification of potential biomarkers and therapeutic targets. However, their clinical utility requires further evaluation through standardized cohorts and validation studies.

Indexed as

biomarkersmolecular mechanismsmulti-omics integrationneuroinflammationpost-stroke depression

Identifiers

PMID42953433
PMCPMC13715653

What OpenQuestion holds

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Registered trials

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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 OpenQuestion graph.