# Effects of probiotics on blood lipids, glucose and pressure in patients with coronary heart disease: a systematic review and meta-analysis

**Authors:** Yan Zhong, Xinyu Yang, Weiming Kong, Yaru Shi, Weixiong Jian

PMC · DOI: 10.3389/fcvm.2026.1707408 · Frontiers in Cardiovascular Medicine · 2026-02-06

## TL;DR

This study finds that probiotics can lower LDL cholesterol and insulin in coronary heart disease patients, but effects on other factors are unclear.

## Contribution

The study provides a meta-analysis of probiotic effects on blood lipids and glucose in coronary heart disease patients.

## Key findings

- Probiotics significantly reduced LDL-C and insulin levels in CHD patients.
- No significant effects were observed on blood pressure or triglycerides.
- Trial sequential analysis confirmed sufficient evidence for LDL-C and insulin.

## Abstract

This study aims to investigate the effects of probiotic supplementation on blood glucose, lipids and pressure in patients with coronary heart disease (CHD) through systematic review and meta-analysis, combined with sequential trial analysis, and to assess its safety.

A systematic search was conducted across five English-language databases: PubMed, Embase, Cochrane Library, Web of Science, and MEDLINE. The search period spanned from the inception of each database to May 31, 2,025. The baseline characteristics and data from the included studies were extracted and analyzed. Meta-analysis and trial sequential analysis (TSA) were performed using RevMan 5.3 and TSA 0.9.5.10 beta, respectively.

A total of nine studies involving 478 patients were included in this meta-analysis. The pooled results demonstrated that, compared with the placebo group, probiotic supplementation significantly reduced levels of low-density lipoprotein cholesterol (LDL-C) [mean difference [MD] −11.16, 95% confidence interval [CI] −18.82 to −3.50, P = 0.004], total cholesterol (TC) (MD −9.32, 95% CI −18.01 to −0.63, P = 0.04), fasting blood glucose (FBG) (MD −7.82, 95% CI −15.60 to −0.04, P = 0.05), and insulin (MD −2.47, 95% CI −4.16 to −0.78, P = 0.004), and increased high-density lipoprotein cholesterol (HDL-C) levels (MD 2.24, 95% CI 0.61 to 3.87, P = 0.007). No significant effects were observed on very-low-density lipoprotein cholesterol (VLDL-C) (MD −2.89, 95% CI −6.83 to 1.05, P = 0.15), triglyceride (TG) (MD −13.45, 95% CI −28.60 to 1.70, P = 0.08), homeostasis model assessment of insulin resistance (HOMA-IR) (MD −0.43, 95% CI −1.13 to 0.28, P = 0.23), QUICK (MD 0.00, 95% CI −0.00 to 0.01, P = 0.25), systolic blood pressure (SBP) (MD −1.99, 95% CI −4.97 to 1.00, P = 0.19), diastolic blood pressure (DBP) (MD −1.23, 95% CI −3.32 to 0.86, P = 0.25), or the incidence of adverse events (MD 2.00, 95% CI 0.20 to 20.49, P = 0.56). Trial sequential analysis confirmed that the evidence for LDL-C and insulin was sufficient to reach firm conclusions.

Probiotics have been shown to significantly reduce LDL-C and insulin levels in patients with CHD without increasing the risk of adverse events. However, the impact of probiotics on other metabolic parameters such as TC, FBG, and HDL-C remains inconclusive and requires further investigation through well-designed studies.

https://www.crd.york.ac.uk/PROSPERO/ PROSPERO CRD420251272111.

## Linked entities

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

## Full-text entities

- **Genes:** JAK2 (Janus kinase 2) [NCBI Gene 3717] {aka JTK10}, 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}, NFKB1 (nuclear factor kappa B subunit 1) [NCBI Gene 4790] {aka CVID12, EBP-1, KBF1, NF-kB, NF-kB1, NF-kappa-B1}, APOE (apolipoprotein E) [NCBI Gene 348] {aka AD2, APO-E, ApoE4, LDLCQ5, LPG}, REN (renin) [NCBI Gene 5972] {aka ADTKD4, HNFJ2, RTD}, IL18 (interleukin 18) [NCBI Gene 3606] {aka IGIF, IL-18, IL-1g, IL1F4}, NPC1L1 (NPC1 like intracellular cholesterol transporter 1) [NCBI Gene 29881] {aka LDLCQ7, NPC11L1, SLC65A2}, IRS1 (insulin receptor substrate 1) [NCBI Gene 3667] {aka HIRS-1}, IL10 (interleukin 10) [NCBI Gene 3586] {aka CSIF, GVHDS, IL-10, IL10A, TGIF}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, STAT3 (signal transducer and activator of transcription 3) [NCBI Gene 6774] {aka ADMIO, ADMIO1, APRF, HIES}, TLR4 (toll like receptor 4) [NCBI Gene 7099] {aka ARMD10, CD284, TLR-4, TOLL}, IL1B (interleukin 1 beta) [NCBI Gene 3553] {aka IL-1, IL1-BETA, IL1F2, IL1beta}, CD36 (CD36 molecule (CD36 blood group)) [NCBI Gene 948] {aka BDPLT10, CHDS7, FAT, GP3B, GP4, GPIV}, INS (insulin) [NCBI Gene 3630] {aka IDDM, IDDM1, IDDM2, ILPR, IRDN, MODY10}, CCL2 (C-C motif chemokine ligand 2) [NCBI Gene 6347] {aka GDCF-2, HC11, HSMCR30, MCAF, MCP-1, MCP1}
- **Diseases:** liver damage (MESH:D056486), myopathy (MESH:D009135), type 1 diabetes (MESH:D003922), T2DM (MESH:D003924), stomach discomfort (MESH:D013272), atherosclerotic plaque (MESH:D058226), Hypertension (MESH:D006973), deaths (MESH:D003643), atherosclerosis (MESH:D050197), endothelial injury (MESH:D057772), HOMA-IR (MESH:D007333), cardiovascular disease (MESH:D002318), gastrointestinal (MESH:D005767), model (MESH:D004195), CHD (MESH:D003327), gastrointestinal symptoms (MESH:D012817), Chronic inflammation (MESH:D007249), myocardial fibrosis (MESH:D005355), hyperlipidemia (MESH:D006949), platelet aggregation (MESH:D001791), Hyperglycemia (MESH:D006943), AS (MESH:D001161), gut microbial dysbiosis (MESH:D064806), endothelial dysfunction (MESH:D014652), diabetes (MESH:D003920)
- **Chemicals:** LPS (MESH:D008070), lipid (MESH:D008055), polyphenols (MESH:D059808), butyric acid (MESH:D020148), glucose (MESH:D005947), SCFAs (MESH:D005232), reactive oxygen species (MESH:D017382), metoprolol (MESH:D008790), coprostanol (MESH:D004083), atorvastatin (MESH:D000069059), L-carnitine (MESH:D002331), betaine (MESH:D001622), Blood lipid (-), caproic acid (MESH:C037652), valeric acid (MESH:C038780), carbohydrates (MESH:D002241), propionic acid (MESH:C029658), cholesterol (MESH:D002784), nitric oxide (MESH:D009569), isovaleric acid (MESH:C008216), Blood glucose (MESH:D001786), TMA (MESH:C023336), acetic acid (MESH:D019342), TMAO (MESH:C005855), fats (MESH:D005223), TG (MESH:D014280), choline (MESH:D002794), isobutyric acid (MESH:C020380)
- **Species:** Limosilactobacillus fermentum (species) [taxon 1613], Bifidobacterium bifidum (species) [taxon 1681], gut metagenome (species) [taxon 749906], Limosilactobacillus reuteri (species) [taxon 1598], Lactobacillus gasseri (species) [taxon 1596], Lacticaseibacillus casei (species) [taxon 1582], Homo sapiens (human, species) [taxon 9606], Bifidobacterium animalis subsp. lactis (subspecies) [taxon 302911], Lactobacillus acidophilus (species) [taxon 1579], Lactococcus lactis (species) [taxon 1358], Lacticaseibacillus rhamnosus (species) [taxon 47715], Mus musculus (house mouse, species) [taxon 10090]

## Full text

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## Figures

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## References

86 references — full list in the complete paper: https://tomesphere.com/paper/PMC12920485/full.md

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Source: https://tomesphere.com/paper/PMC12920485