# Impacts of neurointerventional therapy combined with intravenous thrombolysis on neurological function, oxidative stress, and immune function in patients with acute ischemic stroke

**Authors:** Yun Wang, Yang Yang, Jingmin Zhou

PMC · DOI: 10.3389/fmed.2026.1721322 · Frontiers in Medicine · 2026-02-05

## TL;DR

Combining neurointerventional therapy with intravenous thrombolysis improves outcomes in acute ischemic stroke patients compared to thrombolysis alone.

## Contribution

Demonstrates that combining neurointerventional therapy with thrombolysis improves neurological and immune outcomes in AIS patients.

## Key findings

- Combination therapy reduced NIHSS and mRS scores compared to thrombolysis alone.
- Combination therapy improved oxidative stress markers and immune function indicators.
- Combination therapy enhanced cerebral hemodynamics and quality of life without increasing adverse reactions.

## Abstract

This study aimed to assess the clinical efficacy of neurointerventional therapy plus intravenous thrombolysis in patients with acute ischemic stroke (AIS).

We conducted a single-center retrospective analysis involving 120 AIS patients admitted to our hospital from January 2023 to December 2024. Based on their treatment plans, patients were categorized into an alteplase group (n = 55) and a combination group (n = 65). In both groups, all patients received standard intravenous thrombolysis with alteplase; in the combination group, this was followed by adjunct neurointerventional therapy, including intra-arterial urokinase infusion and, when indicated, mechanical thrombectomy. We compared neurological function scores, inflammatory factor levels, oxidative stress markers, immune function indicators, hemodynamic parameters, quality of life scores, and the total incidence of adverse reactions between the two groups.

After 3 months of treatment, the combination group demonstrated significantly lower NIHSS and mRS scores, as well as reduced levels of IL-6, TNF-α, and hs-CRP, compared to the alteplase group (P < 0.05). Additionally, the combination group exhibited higher SOD levels, lower MDA levels, elevated CD4+ counts and CD4+/CD8+ ratios, and decreased CD8+ levels (P < 0.05). Hemodynamically, the combination group had higher minimum cerebral blood flow volume and velocity, along with lower peripheral resistance in cerebral vessels (P < 0.05). Furthermore, the combination group achieved higher GQOLI-74 scores, indicating improved quality of life (P < 0.05). Notably, there was no significant difference in the total incidence of adverse reactions between the two groups (P > 0.05).

Neurointerventional therapy plus intravenous thrombolysis can improve the neurological function, reduce inflammation and oxidative stress, enhance immune function, improve hemodynamic indicators, improve the quality of life and has good safety in the treatment of patients with AIS.

## Full-text entities

- **Genes:** CD4 (CD4 molecule) [NCBI Gene 920] {aka CD4mut, IMD79, Leu-3, OKT4D, T4}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, SOD1 (superoxide dismutase 1) [NCBI Gene 6647] {aka ALS, ALS1, HEL-S-44, IPOA, SOD, STAHP}, CD8A (CD8 subunit alpha) [NCBI Gene 925] {aka CD8, CD8alpha, IMD116, Leu2, p32}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}
- **Diseases:** hemiplegia (MESH:D006429), infarct (MESH:D007238), embolism (MESH:D004617), speech disorders (MESH:D013064), neuronal apoptosis (MESH:D065703), gastrointestinal bleeding (MESH:D006471), neurological deterioration (MESH:D009422), neuronal necrosis (MESH:D009336), immune dysregulation (OMIM:614878), cerebral hemorrhage (MESH:D002543), atherosclerosis (MESH:D050197), impaired consciousness (MESH:D003244), hypertension (MESH:D006973), occlusion (MESH:D001157), brain injury (MESH:D001930), malnutrition (MESH:D044342), death (MESH:D003643), reperfusion injury (MESH:D015427), thrombosis (MESH:D013927), mitochondria (MESH:C564971), dysphagia (MESH:D003680), cerebrovascular diseases (MESH:D002561), immune dysfunction (MESH:D007154), post-stroke infections (MESH:D000094025), gastrointestinal dysfunction (MESH:D005767), cerebral infarction (MESH:D002544), abnormal coagulation function (MESH:D001778), arterial stenosis (MESH:D012078), infections (MESH:D007239), Stroke (MESH:D020521), neurological function impairment (MESH:D003291), bleeding (MESH:D006470), Intracranial hemorrhage (MESH:D020300), hypoxia (MESH:D000860), AIS (MESH:D000083242), neurological deficits (MESH:D009461), stenosis (MESH:D003251), ischemia (MESH:D007511), coronary heart disease (MESH:D003327), NIHSS (MESH:C538175), cerebrovascular circulatory disorder (MESH:D012769), inflammation (MESH:D007249), ecchymosis (MESH:D004438), cerebral ischemia (MESH:D002545), diabetes (MESH:D003920), malignant tumors (MESH:D009369), large-vessel occlusion (MESH:C536223), liver or kidney dysfunction (MESH:D051437)
- **Chemicals:** lipid (MESH:D008055), alcohol (MESH:D000438), oxygen free radicals (-), MDA (MESH:D008315), aspirin (MESH:D001241), excitatory amino acids (MESH:D018846), oxygen (MESH:D010100), sodium chloride (MESH:D012965), MDA (MESH:D015104)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12916641/full.md

## References

48 references — full list in the complete paper: https://tomesphere.com/paper/PMC12916641/full.md

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Source: https://tomesphere.com/paper/PMC12916641