# Effects of probiotics on lipid metabolism, oxidation, and inflammation in coronary heart disease: a systematic review and meta-analysis

**Authors:** Xinyu Yang, Yunfeng Yu, Xiangning Huang, Juan Huang, Qin Xiang, Rong Yu

PMC · DOI: 10.3389/fnut.2025.1681230 · Frontiers in Nutrition · 2026-01-16

## TL;DR

This study finds that probiotics may help reduce inflammation and oxidative stress in coronary heart disease patients, but their effect on cholesterol is not clinically significant.

## Contribution

A systematic review and meta-analysis evaluating the impact of probiotics on lipid metabolism, oxidation, and inflammation in coronary heart disease patients.

## Key findings

- Probiotics significantly reduced LDL-C, malondialdehyde, and inflammatory markers like hs-CRP, TLR4, and IL-6.
- Probiotics increased HDL-C, glutathione, and total antioxidant capacity, but lipid changes were not clinically meaningful.
- TSA confirmed robustness of most outcomes except malondialdehyde, with no significant publication bias detected.

## Abstract

This meta-analysis and trial sequential analysis (TSA) aimed to evaluate the effects of probiotics on lipid metabolism, oxidative stress, and inflammation in patients with coronary heart disease (CHD).

Six databases were systematically searched for relevant studies published before May 1, 2025. Basic study characteristics, outcome data, and risk of bias were extracted. Meta-analyses were performed using RevMan 5.3, TSA was conducted using TSA 0.9.5.10 beta, and publication bias was assessed using Egger’s test.

Eight randomized controlled trials involving 296 patients were included. Compared with the placebo, probiotics significantly reduced the low-density lipoprotein cholesterol (LDL-C) [mean difference (MD) −11.07 mg/dL, 95% confidence interval (CI) −19.94 to −2.20], malondialdehyde [standardized mean difference (SMD) −0.57, 95% CI −1.01 to −0.13], high-sensitivity C-reactive protein (MD −0.81 ng/mL, 95% CI −1.31 to −0.30), Toll-like receptor 4 (MD −4.13 ng/mL, 95% CI −5.39 to −2.88), and interleukin-6 (MD −3.22 ng/mL, 95% CI −4.01 to −2.44). Meanwhile, they increased the high-density lipoprotein cholesterol (HDL-C) (MD 2.79 mg/dL, 95% CI 0.95 to 4.63), glutathione (MD 104.66 μmol/L, 95% CI 53.74 to 155.58), and total antioxidant capacity (MD 69.51 mmol/L, 95% CI 44.64 to 94.38). However, the effects on LDL-C and HDL-C were not robust in sensitivity analyses, and neither outcome reached the minimal clinically important difference, indicating that lipid modulation is not clinically meaningful. Additionally, no significant differences were observed in very low-density lipoprotein cholesterol, total cholesterol, triglycerides, tumor necrosis factor-alpha and adverse event rate. TSA confirmed the robustness of all significant outcomes except for malondialdehyde, and Egger’s tests revealed no significant publication bias.

Probiotics exert moderate anti-inflammatory and antioxidative effects, supporting their potential as an complementary strategy for CHD. In contrast, their influence on lipid metabolism appears uncertain and clinically negligible. Given the limited certainty of evidence and the geographic concentration of available trials, high-quality multicenter studies are required to confirm these findings.

## Linked entities

- **Proteins:** IL6 (interleukin 6)
- **Chemicals:** malondialdehyde (PubChem CID 10964), glutathione (PubChem CID 124886)
- **Diseases:** coronary heart disease (MONDO:0005010)

## Full-text entities

- **Genes:** TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, TLR4 (toll like receptor 4) [NCBI Gene 7099] {aka ARMD10, CD284, TLR-4, TOLL}
- **Diseases:** inflammation (MESH:D007249), CHD (MESH:D003327)
- **Chemicals:** cholesterol (MESH:D002784), malondialdehyde (MESH:D008315), triglycerides (MESH:D014280), glutathione (MESH:D005978), lipid (MESH:D008055)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12858250/full.md

## Figures

8 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12858250/full.md

## References

45 references — full list in the complete paper: https://tomesphere.com/paper/PMC12858250/full.md

---
Source: https://tomesphere.com/paper/PMC12858250