# Effect of evolocumab on the gut microbiota in patients with acute myocardial infarction

**Authors:** Jie Zou, Yunzhu Peng, Hongyan Cai, Qinghua Zhong, Na Zhu, Wenyi Gu, Fazhi Yang, Tao Shi, Sirui Yang, Lixing Chen

PMC · DOI: 10.1099/jmm.0.002114 · Journal of Medical Microbiology · 2026-01-13

## TL;DR

This study found that evolocumab, a drug used for heart disease, can shift gut bacteria in patients with heart attacks toward a healthier balance.

## Contribution

First study to investigate the effect of evolocumab on gut microbiota in acute myocardial infarction patients.

## Key findings

- Evolocumab treatment increased the abundance of beneficial bacteria like Odoribacter and Parabacteroides.
- Firmicutes decreased while Bacteroidota increased in patients after evolocumab treatment.
- No significant differences in gut microbiota diversity were observed between groups.

## Abstract

Introduction. Growing evidence indicates significant interactions between the intestinal microflora and drugs commonly used to treat coronary heart disease.

Hypothesis/Gap Statement. Despite this, research specifically investigating the relationship between proprotein convertase subtilisin/kexin type 9 inhibitors and alterations in the gut microbiota has not been previously published.

Aim. This study aimed to identify changes in the gut microbiota potentially associated with evolocumab use in patients with acute myocardial infarction (AMI).

Methodology. In this prospective study, 26 AMI patients receiving statins (≥8 weeks) were administered evolocumab (420 mg/4 weeks) alongside standard therapy. Eighteen age-matched healthy volunteers served as controls. 16S rRNA sequencing (NCBI SRA: PRJNA1154993) was subsequently performed on samples from these groups to analyse the gut microbiota community.

Results. No significant α-diversity differences were observed among groups (P>0.05). Firmicutes dominated AMI-evolocumab baseline (0 W: 76.32%) versus post-treatment (8 W: 65.22%) and controls (60.40%), while Bacteroidota increased post-treatment (0 W: 15.07%→8 W: 19.99%; control: 27.11%). The second most abundant phyla were Proteobacteria and Actinobacteria. In addition, the differences in the microbial structure among the three groups were as follows: at the genus level, the results of the genus difference analysis revealed significant differences in the abundances of nine types of bacteria among the three groups. Compared with those in the AMI-evolocumab (0 W) group, the abundances of beneficial bacteria, such as Odoribacter and Parabacteroides, were increased in the AMI-evolocumab (8 W) group.

Conclusion. Our research showed that evolocumab can regulate the gut microbiota of patients with AMI to promote a healthier state, which is beneficial for patients with AMI.

## Linked entities

- **Diseases:** acute myocardial infarction (MONDO:0004781), coronary heart disease (MONDO:0005010)

## Full-text entities

- **Genes:** MB (myoglobin) [NCBI Gene 4151] {aka MYOSB, PVALB}, FFAR3 (free fatty acid receptor 3) [NCBI Gene 2865] {aka FFA3R, GPR41}, TLR4 (toll like receptor 4) [NCBI Gene 7099] {aka ARMD10, CD284, TLR-4, TOLL}, SIRT3 (sirtuin 3) [NCBI Gene 23410] {aka SIR2L3}, PCSK9 (proprotein convertase subtilisin/kexin type 9) [NCBI Gene 255738] {aka FH3, FHCL3, HCHOLA3, LDLCQ1, NARC-1, NARC1}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, LDLR (low density lipoprotein receptor) [NCBI Gene 3949] {aka LDLCQ2}, HP (haptoglobin) [NCBI Gene 3240] {aka HP2ALPHA2, HPA1S}, FFAR2 (free fatty acid receptor 2) [NCBI Gene 2867] {aka FFA2R, GPR43}, GPT (glutamic--pyruvic transaminase) [NCBI Gene 2875] {aka AAT1, ALT, ALT1, GPT1, SGPT}
- **Diseases:** STEMI (MESH:D000072657), obesity (MESH:D009765), autoimmune diseases (MESH:D001327), cognitive and psychiatric disorders (MESH:D001523), hypertension (MESH:D006973), malignant neoplasms (MESH:D009369), infectious diseases (MESH:D003141), gastroenteritis (MESH:D005759), atherogenesis (MESH:D050197), depression (MESH:D003866), gastrointestinal diseases (MESH:D005767), insulin resistance (MESH:D007333), diabetes mellitus (MESH:D003920), coronary heart disease (MESH:D003327), dysbiosis (MESH:D064806), heart failure (MESH:D006333), liver diseases (MESH:D008107), cardiovascular diseases (MESH:D002318), ischaemia (MESH:D007511), AMI (MESH:D009203), endothelial dysfunction (MESH:D014652), microvascular obstruction (MESH:D017566), CAD (MESH:D003324), myocardial necrosis (MESH:D009336), inflammation (MESH:D007249), TMAO (MESH:C536108), kidney diseases (MESH:D007674)
- **Chemicals:** butyrate (MESH:D002087), lipid (MESH:D008055), nitrogen (MESH:D009584), choline (MESH:D002794), glucose (MESH:D005947), agarose (MESH:D012685), Odoribacter (-), creatinine (MESH:D003404), Butyric acid (MESH:D020148), nitrates (MESH:D009566), atorvastatin (MESH:D000069059), SCFA (MESH:D005232), uric acid (MESH:D014527), carnitine (MESH:D002331), TMAO (MESH:C005855), aspirin (MESH:D001241), carbohydrate (MESH:D002241), steroids (MESH:D013256), cholesterol (MESH:D002784), ezetimibe (MESH:D000069438), bile acids (MESH:D001647), triglyceride (MESH:D014280), rosuvastatin (MESH:D000068718), polysaccharides (MESH:D011134), LPS (MESH:D008070), Evolocumab (MESH:C577155)
- **Species:** Agathobacter (genus) [taxon 1766253], Tyzzerella (genus) [taxon 1506577], Granulicatella (genus) [taxon 117563], Bacteria Latreille et al. 1825 (Bacteria stick insect, genus) [taxon 629395], Alistipes (genus) [taxon 239759], Actinomycetota (actinobacteria, phylum) [taxon 201174], Blautia (genus) [taxon 572511], Faecalibacterium (genus) [taxon 216851], Prevotella (genus) [taxon 838], Roseburia (genus) [taxon 841], Soehngenia (genus) [taxon 253255], Allisonella [taxon 209879], Desulfovibrio (genus) [taxon 872], Dialister (genus) [taxon 39948], Acidaminococcus (genus) [taxon 904], Mogibacterium (genus) [taxon 86331], Pseudomonadota (proteobacteria, phylum) [taxon 1224], Mus musculus (house mouse, species) [taxon 10090], Streptococcus (genus) [taxon 1301], Parabacteroides (genus) [taxon 375288], Eubacterium ventriosum (species) [taxon 39496], Bacteroides (genus) [taxon 816], Homo sapiens (human, species) [taxon 9606], Tissierella (genus) [taxon 41273], Holdemanella (genus) [taxon 1573535], Lactobacillus (genus) [taxon 1578], Akkermansia muciniphila (species) [taxon 239935], Pseudobutyrivibrio (genus) [taxon 46205], gut metagenome (species) [taxon 749906], Bacillota (clostridial firmicutes, phylum) [taxon 1239], Odoribacter (genus) [taxon 283168], Rothia (genus) [taxon 508215]

## Full text

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## Figures

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## References

34 references — full list in the complete paper: https://tomesphere.com/paper/PMC12799316/full.md

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Source: https://tomesphere.com/paper/PMC12799316