# Harmful Effects of Microplastics and Nanoplastics in Human Body Systems: A Systematic Review

**Authors:** Precious Patrick Edet, Amal K. Mitra, Melissa Dennis, Md S. Zaman

PMC · DOI: 10.3390/diseases14030088 · 2026-02-27

## TL;DR

This paper reviews how microplastics and nanoplastics in the human body are linked to health issues in multiple organ systems.

## Contribution

It provides a systematic review of MNP exposure and health effects in humans, highlighting organ-specific impacts and cellular mechanisms.

## Key findings

- MNPs were detected in human blood, thrombi, feces, and tissues.
- Higher MNP levels correlated with increased disease severity in multiple organ systems.
- In vitro studies showed MNPs cause oxidative stress, DNA damage, and apoptosis in human cells.

## Abstract

Background: Microplastics and nanoplastics (MNPs) are ubiquitous environmental contaminants from plastic degradation, leading to human exposure through ingestion, inhalation, and dermal contact. While emerging evidence suggests potential health effects, comprehensive human-specific data remain limited. Objective: To systematically review evidence on MNP exposure and health impacts across human organ systems. Methods: Following PRISMA guidelines, we searched Embase, Environment Complete, MEDLINE, and Scopus for peer-reviewed English-language studies published between 2020 and 2025 that reported MNP exposure in adult human populations and addressed at least one organ system. Thirty studies met inclusion criteria, and all clinical studies were assessed for risk of bias using the Newcastle–Ottawa Scale (NOS) Results: Clinical studies consistently detected MNPs in human blood, thrombi, feces, and respiratory and reproductive tissues. Higher MNP burdens correlated with increased disease severity across cardiovascular, gastrointestinal, respiratory, musculoskeletal, and reproductive systems. In vitro studies using human-derived cell lines demonstrated that MNPs penetrate cells and disrupt cellular processes, inducing oxidative stress, cytotoxicity, mitochondrial dysfunction, inflammation, DNA damage, and apoptosis. Toxic effects were size-, polymer-, and concentration-dependent, with smaller particles exhibiting greater cellular uptake and toxicity. Conclusions: Human MNP exposure is widespread and associated with adverse biological effects across multiple organ systems. Further interdisciplinary research is needed to establish causal relationships and inform risk assessment and regulatory frameworks for plastic-associated contaminants. Other: This research received no external funding. The research protocol was registered with PROSPERO (Registration ID number CRD420261284559).

## Full-text entities

- **Genes:** SERPINA1 (serpin family A member 1) [NCBI Gene 5265] {aka A1A, A1AT, AAT, PI, PI1, PRO2275}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, NUP62 (nucleoporin 62) [NCBI Gene 23636] {aka IBSN, SNDI, p62}, NLRP3 (NLR family pyrin domain containing 3) [NCBI Gene 114548] {aka AGTAVPRL, AII, AVP, C1orf7, CIAS1, CLR1.1}, CPE (carboxypeptidase E) [NCBI Gene 1363] {aka BDVS, CPH, IDDHH}, NR4A1 (nuclear receptor subfamily 4 group A member 1) [NCBI Gene 3164] {aka GFRP1, HMR, N10, NAK-1, NGFIB, NP10}, LGALS3 (galectin 3) [NCBI Gene 3958] {aka CBP35, GAL3, GALBP, GALIG, L31, LGALS2}, OLR1 (oxidized low density lipoprotein receptor 1) [NCBI Gene 4973] {aka CLEC8A, LOX1, LOXIN, SCARE1, SLOX1}, RUNX2 (RUNX family transcription factor 2) [NCBI Gene 860] {aka AML3, CBF-alpha-1, CBFA1, CCD, CCD1, CLCD}, ROCK1 (Rho associated coiled-coil containing protein kinase 1) [NCBI Gene 6093] {aka P160ROCK, ROCK-I}, NOS2 (nitric oxide synthase 2) [NCBI Gene 4843] {aka HEP-NOS, INOS, NOS, NOS2A}, NFKB1 (nuclear factor kappa B subunit 1) [NCBI Gene 4790] {aka CVID12, EBP-1, KBF1, NF-kB, NF-kB1, NF-kappa-B1}, F2 (coagulation factor II, thrombin) [NCBI Gene 2147] {aka PT, RPRGL2, THPH1}, CASP3 (caspase 3) [NCBI Gene 836] {aka CPP32, CPP32B, SCA-1}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, BCL2 (BCL2 apoptosis regulator) [NCBI Gene 596] {aka Bcl-2, PPP1R50}, BAX (BCL2 associated X, apoptosis regulator) [NCBI Gene 581] {aka BCL2L4}
- **Diseases:** acute myocardial infarction (MESH:D009203), ECAS (MESH:D012078), chronic diseases (MESH:D002908), cancer (MESH:D009369), hypertrophic (MESH:D002312), Crohn's disease (MESH:D003424), fibrosis (MESH:D005355), hypertension (MESH:D006973), hypertrophy (MESH:D006984), colorectal adenocarcinoma (MESH:D003110), NSCAP (MESH:D045169), uterine (MESH:D014591), osteoporosis (MESH:D010024), Cardiotoxic (MESH:D066126), cardiometabolic disease (MESH:D024821), CAP (MESH:D003147), necrosis (MESH:D009336), cardiovascular and respiratory disease (MESH:D012140), carcinogenic (MESH:D011230), colon (MESH:D003108), Chronic inflammation (MESH:D007249), thrombosis (MESH:D013927), PIH (MESH:D046110), IBD (MESH:D015212), acute coronary syndrome (MESH:D054058), unstable angina (MESH:D000789), ischemic stroke (MESH:D002544), injury to (MESH:D014947), damage (MESH:D020263), Cardiovascular toxicity (MESH:D002318), Toxic (MESH:D064420), cervical cancer (MESH:D002583), lung disease (MESH:D008171), endocrine (MESH:D004700), colorectal cancer (MESH:D015179), chronic obstructive pulmonary disease (MESH:D029424), cardiovascular, gastrointestinal, and reproductive pathologies (MESH:D005767), atherosclerosis (MESH:D050197), mitochondrial Ca2+ dysfunction (MESH:D028361), deep vein thrombosis (MESH:D020246), coronary artery disease (MESH:D003324), inflammatory cytokines (MESH:D000080424), arterial and venous thrombi (MESH:C566282), fibroid (MESH:D007889)
- **Chemicals:** phthalates (MESH:C032279), PET (MESH:D011093), polyurethane (MESH:D011140), poly(methyl methacrylate) (MESH:D019904), ROS (MESH:D017382), PVC (MESH:D011143), PP (MESH:D011126), ATP (MESH:D000255), bisphenols (MESH:C543008), water (MESH:D014867), D-mannose (MESH:D008358), calcium (MESH:D002118), plastics (MESH:D010969), polymer (MESH:D011108), PTFE (MESH:D011138), MNP (-), oxygen (MESH:D010100), PE (MESH:D020959), PS (MESH:D011137), PU (MESH:D011005), heavy metals (MESH:D019216), nylon (MESH:D009757), iron (MESH:D007501), MP (MESH:D000080545), amino sugar (MESH:D000606), D- (MESH:D003903), lipids (MESH:D008055), bisphenol A (MESH:C006780)
- **Species:** Enterobacteriaceae (enterobacteria, family) [taxon 543], Homo sapiens (human, species) [taxon 9606], Lactobacillales (order) [taxon 186826], Desulfovibrio (genus) [taxon 872]
- **Cell lines:** Caco-2 — Homo sapiens (Human), Colon adenocarcinoma, Cancer cell line (CVCL_0025), A549 — Homo sapiens (Human), Lung adenocarcinoma, Cancer cell line (CVCL_0023), BEAS-2B — Homo sapiens (Human), Transformed cell line (CVCL_0168), AC16 — Homo sapiens (Human), Transformed cell line (CVCL_HA69), KGN — Homo sapiens (Human), Ovarian granulosa cell tumor, Cancer cell line (CVCL_0375), EA.hy926 — Homo sapiens (Human), Hybrid cell line (CVCL_3901), THLE-2 — Homo sapiens (Human), Transformed cell line (CVCL_3803)

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13024950/full.md

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Source: https://tomesphere.com/paper/PMC13024950