# Chinese herbal medicine treatment and the association with long-term major adverse cardiac events in patients with chronic kidney disease: A propensity-score matched cohort study

**Authors:** Yuan-Ching Liao, Mei-Yao Wu, Cheng-Li Lin, Chiz-Tzung Chang, Peter K. Mayer, Hung-Rong Yen

PMC · DOI: 10.37796/2211-8039.1699 · BioMedicine · 2026-03-01

## TL;DR

This study finds that Chinese herbal medicine may reduce cardiovascular risks in patients with chronic kidney disease.

## Contribution

The study provides empirical evidence linking Chinese herbal medicine use to reduced major adverse cardiac events in CKD patients.

## Key findings

- CHM use was associated with a 23%–31% reduction in cardiovascular outcomes and mortality.
- Ji-Sheng-Shen-Qi-Wan and Danshen were the most commonly used CHM treatments.
- Findings suggest CHM could help mitigate cardiovascular risks in CKD patients.

## Abstract

Cardiovascular disease (CVD) represents the leading cause of mortality among individuals with chronic kidney disease (CKD). While Chinese herbal medicine (CHM) is commonly used by CKD patients in Taiwan, the impact of CHM use on cardiovascular outcomes in this population remains insufficiently understood.

This study aimed to evaluate the association between CHM use and the long-term risk of major adverse cardiac events (MACEs) in patients with CKD.

Data were obtained from the Taiwan National Health Insurance Research Database to identify patients aged over 20 years with newly diagnosed CKD. A 1:1 propensity score matching was performed based on age, sex, comorbidities, medication use, and CHM exposure, resulting in 6351 matched pairs. Participants were followed from 2000 to 2017 to assess the incidence of MACEs, including heart failure (HF), myocardial infarction (MI), ischemic stroke (IS), cardiovascular death, and all-cause mortality.

The CHM group comprised 56.4 % females with a mean age of 49.4 ± 15.3 years. After matching, CHM use was associated with a statistically significant reduction of 23 %–31 % in the adjusted hazard ratios for various cardiovascular outcomes and all-cause mortality (P < 0.001). The most commonly prescribed CHM formula and single herb were Ji-Sheng-Shen-Qi-Wan (JSSQW) and Danshen (Salviae Miltiorrhizae), respectively.

The use of CHM as an adjunct therapy in CKD patients was associated with a significantly lower risk of MACEs and all-cause mortality. These findings support the potential of CHM in cardiovascular risk mitigation among CKD patients and highlight the need for future clinical and ethnopharmacological investigations.

## Linked entities

- **Diseases:** chronic kidney disease (MONDO:0005300), cardiovascular disease (MONDO:0004995), heart failure (MONDO:0005252), myocardial infarction (MONDO:0005068), ischemic stroke (MONDO:1060198)

## Full-text entities

- **Genes:** REN (renin) [NCBI Gene 5972] {aka ADTKD4, HNFJ2, RTD}, EPO (erythropoietin) [NCBI Gene 2056] {aka DBAL, ECYT5, EP, MVCD2}, GLP1R (glucagon like peptide 1 receptor) [NCBI Gene 2740] {aka GLP-1, GLP-1-R, GLP-1R}, DPP4 (dipeptidyl peptidase 4) [NCBI Gene 1803] {aka ADABP, ADCP2, CD26, DPPIV, TP103}, INS (insulin) [NCBI Gene 3630] {aka IDDM, IDDM1, IDDM2, ILPR, IRDN, MODY10}, SLC5A2 (solute carrier family 5 member 2) [NCBI Gene 6524] {aka SGLT2}
- **Diseases:** bradycardia (MESH:D001919), iron deficiency (MESH:D000090463), chronic (MESH:D002908), proteinuria (MESH:D011507), premature ventricular contractions (MESH:D018879), kidney and liver-related diseases (MESH:D000077733), diabetic nephropathy (MESH:D003928), cardiac (MESH:D006331), strokes (MESH:D020521), cardiac remodeling (MESH:D020257), CHM (MESH:C562377), obesity (MESH:D009765), impaired kidney function (MESH:D007674), autoimmune disease (MESH:D001327), HF (MESH:D006333), PKD (MESH:C537180), T2DM (MESH:D003924), CKD (MESH:D051436), lactic acidosis (MESH:D000140), IS (MESH:D002544), endocrine and metabolic diseases (MESH:D004700), cancer (MESH:D009369), diabetes (MESH:D003920), myocardial hypertrophy (MESH:D006984), cerebral ischemic injuries (MESH:D017202), infections (MESH:D007239), CVD (MESH:D002318), MI (MESH:D009203), alcoholism (MESH:D000437), Catastrophic Illness (MESH:D002388), death (MESH:D003643), hypertension (MESH:D006973), hyperlipidemia (MESH:D006949), inflammatory (MESH:D007249), glomerulonephritis (MESH:D005921), Anemia (MESH:D000740), injury (MESH:D014947)
- **Chemicals:** blood sugar (MESH:D001786), cholesterol (MESH:D002784), creatinine (MESH:D003404), Fuzi (MESH:C575009), digoxin (MESH:D004077), lipid (MESH:D008055), metformin (MESH:D008687), tetrahydroxystilbene glucoside (MESH:C489707), aspirin (MESH:D001241), thiazolidinedione (MESH:C089946), potassium (MESH:D011188), phosphorus (MESH:D010758), nitrates (MESH:D009566), aristolochic acid (MESH:C000228), -blockers (-), clopidogrel (MESH:D000077144)
- **Species:** Plantago (ribworts, genus) [taxon 26867], Astragalus membranaceus (species) [taxon 649199], Homo sapiens (human, species) [taxon 9606], Rheum officinale (yao yong da huang, species) [taxon 137220], Aconitum carmichaelii (species) [taxon 85363], Pleuropterus multiflorus (fo ti, species) [taxon 76025], Rheum palmatum (species) [taxon 137221]

## Full text

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## References

40 references — full list in the complete paper: https://tomesphere.com/paper/PMC12962764/full.md

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Source: https://tomesphere.com/paper/PMC12962764