# Age‐related variations in prostaglandin E‐major urinary metabolite values in Japanese children

**Authors:** Takatoshi Maeyama, Ayaka Takashiba, Ayaha Hata, Keinosuke Hizuka, Ryutaro Saura, Yuri Etani, Shin‐ichiro Hagiwara

PMC · DOI: 10.1111/ped.70355 · 2026-03-04

## TL;DR

This study establishes normal reference ranges for a urinary biomarker in healthy Japanese children, showing that younger children have higher values than older children and adults.

## Contribution

The study provides the first reference values for PGE-MUM in healthy children, highlighting age-related differences important for clinical interpretation.

## Key findings

- Young children (2–6 years) had higher PGE-MUM values (18.4–58.7 μg/g·Cr) compared to older children (7–14 years, 12.4–50.3 μg/g·Cr).
- PGE-MUM values decreased with age but showed no significant sex-related differences.
- Healthy children have higher PGE-MUM values than healthy adults, emphasizing the need for age-specific reference ranges.

## Abstract

Prostaglandin E‐major urinary metabolite (PGE‐MUM) is an emerging noninvasive biomarker used to evaluate clinical and endoscopic activity in patients with inflammatory bowel disease. Previous studies have shown that PGE‐MUM values correlate with colonic inflammation in pediatric ulcerative colitis; however, reference values for children without inflammation have not been defined yet. This study aimed to determine the normal reference values of PGE‐MUM in healthy pediatric subjects without inflammatory conditions.

Between December 2018 and January 2022, we prospectively enrolled 221 participants (cross‐sectional study, aged 0–15 years) who were undergoing growth hormone stimulation testing for diagnostic purposes and exhibited no symptoms of inflammation or elevated C‐reactive protein levels at a single pediatric center in Japan. PGE‐MUM values were measured using a chemiluminescent enzyme immunoassay and assessed for age‐ and sex‐related differences.

A total of 218 participants were included in the analysis. Based on age, the participants were classified as young children (2–6 years, n = 147) and older children (7–14 years, n = 66); the reference ranges for the two groups were identified as 18.4–58.7 μg/g·Cr and 12.4–50.3 μg/g·Cr, respectively. The PGE‐MUM values tended to decrease with increasing age; however, no significant sex‐related differences were observed (median 29.1 μg/g·Cr for boys versus 30.4 μg/g·Cr for girls).

Healthy pediatric subjects generally have higher PGE‐MUM values than healthy adults, with particularly elevated values in young children (2–6 years). These observations suggest that age‐related variability must be taken into account when using PGE‐MUM as a biomarker in young children with ulcerative colitis.

## Linked entities

- **Chemicals:** PGE-MUM (PubChem CID 161468)
- **Diseases:** inflammatory bowel disease (MONDO:0005265), ulcerative colitis (MONDO:0005101)
- **Species:** Homo sapiens (taxon 9606)

## Full-text entities

- **Genes:** COX1 (cytochrome c oxidase subunit I) [NCBI Gene 4512] {aka COI, MTCO1}, COX8A (cytochrome c oxidase subunit 8A) [NCBI Gene 1351] {aka COX, COX8, COX8-2, COX8L, MC4DN15, VIII}, GH1 (growth hormone 1) [NCBI Gene 2688] {aka GH, GH-N, GHB5, GHN, IGHD1A, IGHD1B}, CBR1 (carbonyl reductase 1) [NCBI Gene 873] {aka CBR, PG-9-KR, SDR21C1, hCBR1}, SLCO2A1 (solute carrier organic anion transporter family member 2A1) [NCBI Gene 6578] {aka MATR1, OATP2A1, PGT, PHOAD, PHOAR2, SLC21A2}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, HPGD (15-hydroxyprostaglandin dehydrogenase) [NCBI Gene 3248] {aka 15-PGDH, PGDH, PGDH1, PHOAR1, SDR36C1}, COX2 (cytochrome c oxidase subunit II) [NCBI Gene 4513] {aka COII, MTCO2}
- **Diseases:** IBD (MESH:D015212), UC (MESH:D003093), FGIDs (MESH:D005767), proteinuria (MESH:D011507), colonic inflammation (MESH:D007249), pulmonary disorders (MESH:D008171), diabetes (MESH:D003920)
- **Chemicals:** steroid (MESH:D013256), creatinine (MESH:D003404), 7-hydroxy-5,11-diketotetranorprosta-1,16-dioic acid (-), Cr (MESH:D002857), PGE2 (MESH:D015232), arachidonic acid (MESH:D016718), sennosides (MESH:D000081226), prostaglandin (MESH:D011453), PGE (MESH:D011458)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12961369/full.md

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Source: https://tomesphere.com/paper/PMC12961369