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Evidence Review
Copyright: ©Author(s) 2026.
World J Gastrointest Pathophysiol. Sep 22, 2026; 17(3): 122786
Published online Sep 22, 2026. doi: 10.4291/wjgp.122786
Table 1 Human studies investigating micro- and nanoplastic burden in inflammatory bowel disease
Ref.
Publication status
Number
Population
Study design
Biospecimen
Analytical method
Main findings
Yan et al[107], 2022Full article52 IBD; 50 healthy controlsAdults with IBD and healthy controlsCross sectional case-controlled studyFecesRaman spectrometryFecal MNP concentration was higher in IBD than controls (41.8 items/g dry matter vs 28.0 items/g dry matter). Fecal MP burden correlated with IBD severity
Lykkemark et al[108], 2025Abstract4 CD; 7 non-IBDPregnant patients in third trimester with and without CDProspective pilot studyFecesμFTIRMNPs > 10 μm were detected in all stool samples, with counts ranging 34 particles/g to 410 particles/g dry weight. MNPs count correlated positively with fecal calprotectin, after adjusting for IBD status (Spearman r = 0.65, P = 0.04)
Wu et al[110], 2025Full article10 CD patients (32 tissue samples)CD patients undergoing intestinal resection for CD complicationCross sectional paired tissue studySurgical specimens: Paired involved ileum, uninvolved ileum, creeping fat and mesenteric adiposeLaser infrared spectroscopyMNPs were detected in fibrotic intestine and adjacent mesenteric adipose tissue. MNPs concentrations correlated positively with fibrosis severity, and fibrotic sites showed significantly greater accumulation than surrounding tissue. Approximately 31.96% of detected particles were 20-50 μm in size
Huang et al[109], 2026Abstract241 CD patients; 43 healthy controlsAdults with CD and healthy controlsTwo centers, prospective; cross sectional baseline analysis with longitudinal follow upSerumPy-GC-MSSerum total MNPs were higher in CD than controls (90.7 ± 33.7 μg/g vs 32.8 ± 12.5 μg/g; P < 0.001). MNPs burden associated with more severe endoscopic or MRE inflammation, and with structuring or penetrating phenotype (OR = 2.65, 95%CI: 1.41-5.11). High MNPs baseline concentration associated with disease progression (45.7% vs 25.8%) and independently increased progression risk (HR = 2.95, 95%CI: 1.57-5.57)
Table 2 Planned and ongoing human studies evaluating micro- and nanoplastic burden in inflammatory bowel disease
Study title
Ref.
Trial acronym
Registry ID
Study design
Key population
Planned biospecimen
Outcomes
Target enrollment
Microplastic Analysis in Pediatric Inflammatory Bowel DiseaseMarszk[111]MAP-IBDNCT07141238Observational case-controlled study; single centerChildren < 18 years undergoing clinically indicated colonoscopy, with and without a previous diagnosis of UC or CDIntestinal mucosal biopsies, stool, urine and bloodDetect and quantify MNPs in intestinal biopsies40 (20 IBD + 20 controls)
The Presence of Microplastics and Nanoplastics in the Humans Ileum, Colon, and Rectum and Their Relation With Inflammatory Bowel DiseaseSileri[112]MATISSENCT06525558Cross sections observational case controlledAdults undergoing planned surgical resection involving ileum, colon or rectum with and without IBDResected bowel specimensDetermine presence and characterization of MNPs in bowel tissue and assess correlation with IBD; exploratory metabolomics/proteomics and plastic-exposure assessment102 (25 UC + 26 CD + 51 healthy controls)
Pregnant Women With and Without Crohn’s Disease to Explore the Role of Plastics and Toxins in Intestinal InflammationAgrawal[113]PLANETNCT06001450Prospective observational maternal-infant cohortWomen > 18 years old who are pregnant or planning pregnancy with and without a diagnosis of CDMaternal stool & saliva; placenta; cord blood; breast milk; infant stoolMeasuring the concentration, size and shape distributions of MNPs in stool samples of women with CD, healthy controls and any relatives. Microbiome characterization and fecal calprotectin46


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