# Research advances on the pathogenesis and clinical interventions of post-stroke depression

**Authors:** Leqi Gao, Jiazhao Song, Moze Zhao, Ruixin Wang, Yi Chen, Minmin Li, Hongwei An, Zheyi Zhou, Wanyu Tan, Zihao Huang

PMC · DOI: 10.3389/fneur.2026.1789695 · Frontiers in Neurology · 2026-03-18

## TL;DR

This paper reviews the causes and treatments for post-stroke depression, a common condition affecting stroke survivors, and highlights promising approaches for better care.

## Contribution

The paper provides a comprehensive synthesis of recent advances in understanding and managing post-stroke depression.

## Key findings

- Post-stroke depression affects 30–50% of stroke survivors and impacts rehabilitation and quality of life.
- Multidisciplinary integrated care and precision medicine show promise for improving outcomes in post-stroke depression.
- Pharmacotherapy, psychotherapy, and neuromodulation are among the effective clinical interventions for post-stroke depression.

## Abstract

Post-stroke depression (PSD) is a common neuropsychiatric complication affecting 30–50% of stroke survivors, impairing rehabilitation, quality of life, and prognosis.

This narrative review synthesizes recent evidence on PSD pathogenesis (neurotransmitter dysregulation, neuroinflammation, impaired neuroplasticity; psychosocial factors such as stress and social support deficits; gene–environment interactions including 5-HTT and BDNF polymorphisms), clinical interventions (pharmacotherapy with SSRIs/SNRIs, psychotherapy including CBT, neuromodulation via rTMS/tDCS/ECT, novel agents such as ketamine, and multidisciplinary models), and prevention (risk stratification, early screening with PHQ-9/HAMD, personalized biological/psychosocial strategies, and digital monitoring).

Despite gaps in long-term data and validated biomarkers, multidisciplinary integrated care and precision medicine approaches offer promising avenues to optimize screening, early intervention, prevention, and long-term outcomes for stroke survivors.

## Linked entities

- **Genes:** SLC6A4 (solute carrier family 6 member 4) [NCBI Gene 6532], BDNF (brain derived neurotrophic factor) [NCBI Gene 627]

## Full-text entities

- **Genes:** BDNF (brain derived neurotrophic factor) [NCBI Gene 627] {aka ANON2, BULN2}, SLC6A4 (solute carrier family 6 member 4) [NCBI Gene 6532] {aka 5-HTT, 5-HTTLPR, 5HTT, HTT, OCD1, SERT}
- **Diseases:** PSD (MESH:D003866), neurotransmitter dysregulation (MESH:D021081), stroke (MESH:D020521), neuroinflammation (MESH:D000090862), neuropsychiatric complication (MESH:D008107), social (OMIM:300082)
- **Chemicals:** ketamine (-)

## Full text

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## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13038602/full.md

## References

112 references — full list in the complete paper: https://tomesphere.com/paper/PMC13038602/full.md

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Source: https://tomesphere.com/paper/PMC13038602