# Therapeutic potential of Chinese herbal medicine for coronary heart disease patients with cerebral ischemic stroke: a systematic review and meta-analysis

**Authors:** Rui Du, Yuhan Ao, Yang Wang, Zhihui Chen, Guanghui Liu, Mingxue Zhang

PMC · DOI: 10.3389/fphar.2025.1578783 · Frontiers in Pharmacology · 2025-07-16

## TL;DR

This study reviews and analyzes the effectiveness and safety of Chinese herbal medicine for patients with coronary heart disease and cerebral ischemic stroke.

## Contribution

The study provides a meta-analysis of Chinese herbal medicine's therapeutic potential for a specific dual diagnosis of CHD and CIS.

## Key findings

- CHM improved overall effective rate, ECG performance, and TCM scores significantly.
- CHM positively influenced lipid profiles and reduced blood viscosity and platelet aggregation.
- CHM showed a comparable safety profile to conventional western medicine.

## Abstract

This research sought to demonstrate potential therapeutic strategies for coronary heart disease (CHD) patients with cerebral ischemic stroke (CIS) by rigorously evaluating the efficacy and safety of Chinese Herbal Medicine (CHM) through meta-analysis.

A broad search approach was applied to obtain pertinent articles from both domestic and international databases, covering publications up to 31 December 2024. Using RevMan software (Version 5.4), a systematic review and meta-analysis were conducted to assess the efficacy and safety of CHM in treating CHD patients with CIS.

In the meta-analysis, 18 trails were analyzed, encompassing 2,202 patients in total. The aggregated findings indicated that the utilization of CHM improved the overall effective rate, ECG performance and TCM scores significantly. Furthermore, the CHM therapy demonstrated significant improvements in LVEF, MMSE, and NIHSS. Additionally, the CHMs therapy positively influenced lipid profiles, specifically TC, TG, LDL-C, and HDL-C. Notably, the application of CHM during the intervention was particularly effective in reducing blood viscosity, fibrinogen and platelet aggregation. Importantly, the CHM therapy was found to provide comparable safety profile to that of conventional western medicine treatment (WM) alone.

The CHM demonstrated superior efficacy in the management of CHD patients with CIS. Concurrently, the CHM showed potential for improving neurological damage, lipid profiles, and positively affecting hemorheological parameters, all while minimizing the risk of adverse effects. Even so, because of the limitations in study quality and the potential for reporting bias, it is crucial that these findings require to be further validated through rigorous, large-scale, and high-quality RCT in future research.

## Linked entities

- **Diseases:** coronary heart disease (MONDO:0005010)

## Full-text entities

- **Genes:** COX-2 [NCBI Gene 18126272], FGB (fibrinogen beta chain) [NCBI Gene 2244] {aka HEL-S-78p}
- **Diseases:** hematological abnormalities (MESH:D006402), dizziness (MESH:D004244), infections (MESH:D007239), liver problems (MESH:D017093), hypercoagulable (MESH:D019851), myocardial ischemia (MESH:D017202), Cardio-cerebrovascular disease (MESH:D002561), cardiovascular and cerebrovascular diseases (MESH:D002318), CHM (MESH:C562377), NIHSS (MESH:C538175), dyslipidemia (MESH:D050171), cerebral ischemia (MESH:D002545), inflammatory (MESH:D007249), hematuria (MESH:D006417), cerebral edema (MESH:D001929), neurological damage (MESH:D020196), coagulation (MESH:D001778), Disease (MESH:D004194), gastrointestinal discomfort (MESH:D005767), brain infarction (MESH:D020520), arterial stenosis (MESH:D012078), platelet aggregation (MESH:D001791), stomach issues (MESH:D013272), headaches (MESH:D006261), atherosclerotic plaque (MESH:D058226), atherosclerosis (MESH:D050197), skin redness (MESH:D012871), deaths (MESH:D003643), cognitive dysfunction (MESH:D003072), CHD (MESH:D003327), cerebral infarction (MESH:D002544), ischemic brain injury (MESH:D001930), palpitations (MESH:D006331), functional deficits (MESH:D001289), reperfusion injury (MESH:D015427), CIS (MESH:D020521), allergic reactions (MESH:D004342), bleeding (MESH:D006470)
- **Chemicals:** PGI2 (MESH:D011464), hydrogen (MESH:D006859), danshensu (MESH:C035055), Chinese Herbal Medicine (-), TG (MESH:D013866), salvianolic acid B (MESH:C076944), ferulic acid (MESH:C004999), TC (MESH:D013667), HSYA (MESH:C085278), clopidogrel (MESH:D000077144), lipid (MESH:D008055), TG (MESH:D014280), cholesterol (MESH:D002784)
- **Species:** Salvia miltiorrhiza (Chinese salvia, species) [taxon 226208], Paeonia veitchii (species) [taxon 40722], Carthamus tinctorius (safflower, species) [taxon 4222], Olivierus martensii (Chinese scorpion, species) [taxon 34649], Homo sapiens (human, species) [taxon 9606], Panax ginseng (Asiatic ginseng, species) [taxon 4054], Citrus reticulata (mandarin orange, species) [taxon 85571]
- **Mutations:** rs20551

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12307363/full.md

## Figures

14 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12307363/full.md

## References

61 references — full list in the complete paper: https://tomesphere.com/paper/PMC12307363/full.md

---
Source: https://tomesphere.com/paper/PMC12307363