# Effects of Antibiotics and Anti-Inflammatory Drugs on Enamel Development: A Systematic Review with Quantitative Synthesis

**Authors:** Nadia Zamri, Hien Ngo, Elizabeth Court, Lakshman Samaranayake, Kausar Sadia Fakhruddin, Bennett Tochukwu Amaechi, Saniya Khani

PMC · DOI: 10.1016/j.identj.2026.109478 · International Dental Journal · 2026-03-12

## TL;DR

This review finds that antibiotics and anti-inflammatory drugs may harm enamel development in animals, suggesting a need for more human studies.

## Contribution

A systematic review and quantitative synthesis of experimental effects of antibiotics and NSAIDs on enamel development.

## Key findings

- Amoxicillin exposure was linked to reduced enamel thickness in animal studies.
- NSAIDs were associated with qualitative disturbances in enamel mineralization.
- Altered ameloblast function and enamel matrix abnormalities were commonly observed.

## Abstract

To investigate the effects of commonly prescribed antibiotics and nonsteroidal anti-inflammatory drugs (NSAIDs) during early life on enamel development through a systematic review with quantitative synthesis.

PubMed, Web of Science, Embase, CINAHL, and Scopus were searched for English-language studies published between 1995 and 2024. In vitro and in vivo experimental studies evaluating antibiotics and/or NSAIDs during tooth development were included. Quantitative meta-analysis was restricted to in vivo animal studies reporting comparable outcomes for enamel thickness or mineral content, while in vitro studies contributed to qualitative mechanistic synthesis. Studies focusing solely on dentine, using questionnaires, lacking extractable data, or classified as grey literature or reviews were excluded.

Experimental exposure to antibiotics and NSAIDs was associated with alterations in ameloblast morphology and function, including changes in tight junction proteins, MMP-20, KLK4, COX-2, and Runx2 expression. Enamel matrix abnormalities such as vacuolar changes and cyst-like lesions were frequently reported. Quantitative synthesis indicated a moderate-to-large pooled effect estimate for reduced enamel thickness associated with amoxicillin exposure (Cohen’s d = 0.79, 95% CI: 0.40-1.36), with a trend toward larger effect sizes at higher experimental doses; these estimates were interpreted cautiously due to substantial heterogeneity. NSAIDs were primarily associated with qualitative disturbances in enamel mineralization. Pooled effect estimates for calcium (Cohen’s d = 0.52, 95% CI: −0.21 to 1.46) and phosphorus (Cohen’s d = 0.46, 95% CI: −0.31 to 1.75) were inconsistent and imprecise.

Certain antibiotics and NSAIDs may disrupt ameloblast integrity and enamel biomineralization in experimental animal models. These findings are hypothesis-generating, and further well-designed human observational and mechanistic studies are required before clinical translation. Clinical Relevance: This systematic review synthesizes experimental evidence on the biological vulnerability of developing enamel to pharmacological exposure, highlighting potential mechanisms underlying enamel thinning and hypomineralization while underscoring the need for cautious interpretation when extrapolating animal data to human clinical contexts.

PROSPERO Registration No.: CRD42025606606.

## Linked entities

- **Chemicals:** antibiotics (PubChem CID 46874763), amoxicillin (PubChem CID 33613), calcium (PubChem CID 5460341), phosphorus (PubChem CID 139579)

## Full-text entities

- **Genes:** Mmp20 (matrix metallopeptidase 20 (enamelysin)) [NCBI Gene 30800], OCLN (occludin) [NCBI Gene 100506658] {aka BLCPMG, PPP1R115, PTORCH1}, KLK4 (kallikrein related peptidase 4) [NCBI Gene 9622] {aka AI2A1, ARM1, EMSP, EMSP1, KLK-L1, PRSS17}, Ptgs2 (prostaglandin-endoperoxide synthase 2) [NCBI Gene 29527] {aka COX-2, Cox2, PGHS-2, PHS II, Pghs2}, CLDN4 (claudin 4) [NCBI Gene 1364] {aka CPE-R, CPER, CPETR, CPETR1, WBSCR8, hCPE-R}, COX1 (cytochrome c oxidase subunit I) [NCBI Gene 26195] {aka COI}, COX2 (cytochrome c oxidase subunit II) [NCBI Gene 4513] {aka COII, MTCO2}, PTGS2 (prostaglandin-endoperoxide synthase 2) [NCBI Gene 5743] {aka COX-2, COX2, GRIPGHS, PGG/HS, PGHS-2, PHS-2}, COX2 (cytochrome c oxidase subunit II) [NCBI Gene 17709], Klk4 (kallikrein related-peptidase 4 (prostase, enamel matrix, prostate)) [NCBI Gene 56640] {aka ESMP1, KLK-L1, PSTS, Prss17}, CLDN1 (claudin 1) [NCBI Gene 9076] {aka CLD1, ILVASC, SEMP1}, MMP20 (matrix metallopeptidase 20) [NCBI Gene 9313] {aka AI2A2, MMP-20}, Cpox (coproporphyrinogen oxidase) [NCBI Gene 304024], RUNX2 (RUNX family transcription factor 2) [NCBI Gene 860] {aka AML3, CBF-alpha-1, CBFA1, CCD, CCD1, CLCD}
- **Diseases:** cyst (MESH:D003560), platelet aggregation (MESH:D001791), infection (MESH:D007239), trauma (MESH:D014947), enamel defects (MESH:D000094602), inflammatory drugs (MESH:D000081015), enamel hypoplasia (MESH:D003744), sepsis (MESH:D018805), dental anomalies (OMIM:614188), congenital heart disease (MESH:D006330), inflammation (MESH:D007249), rheumatic fever (MESH:D012213), fever (MESH:D005334), dental disease (MESH:D009057), necrosis (MESH:D009336)
- **Chemicals:** oxygen (MESH:D010100), NM (MESH:D008466), Amoxicillin (MESH:D000658), Azithromycin (MESH:D017963), Acetaminophen (MESH:D000082), Celecoxib (MESH:D000068579), prostaglandins (MESH:D011453), Ca (MESH:D002118), nitric oxide (MESH:D009569), Ca2+ (-), ibuprofen (MESH:D007052), amoxicillin+clavulanic acid (MESH:D019980), Ampicillin (MESH:D000667), hydroxyapatite (MESH:D017886), Fluoride (MESH:D005459), prostacyclin (MESH:D011464), penicillin (MESH:D010406), arachidonic acid (MESH:D016718), NaF (MESH:D012969), Indomethacin (MESH:D007213), Macrolides (MESH:D018942), phosphate (MESH:D010710), Erythromycin (MESH:D004917), Gentamicin (MESH:D005839), Clavulanate (MESH:D019818), P (MESH:D010758), Tetracycline (MESH:D013752)
- **Species:** Bacteria Latreille et al. 1825 (Bacteria stick insect, genus) [taxon 629395], Mus musculus (house mouse, species) [taxon 10090], Homo sapiens (human, species) [taxon 9606], Rattus norvegicus (brown rat, species) [taxon 10116]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12997327/full.md

## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12997327/full.md

## References

55 references — full list in the complete paper: https://tomesphere.com/paper/PMC12997327/full.md

---
Source: https://tomesphere.com/paper/PMC12997327