Evidence map›Paper›PMID 40607434›Full record

ArticleFrontiers in immunology2025

Inflammation-driven periostin in ECRS has contrasting effects on tissue structural integrity and osteitis.

Soo-In Kim, Min-Seok Rha, Jinsun Kim, Sang Hyeon Ahn, Ji-Hwan Ryu, Hyung-Ju Cho, Chang-Hoon Kim

Abstract read
In one paragraph

Article in Frontiers in immunology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Soo-In KimThe Airway Mucus Institute, Yonsei University College of Medicine, Seoul, Republic of Korea.
Min-Seok RhaThe Airway Mucus Institute, Yonsei University College of Medicine, Seoul, Republic of Korea.
Jinsun KimThe Airway Mucus Institute, Yonsei University College of Medicine, Seoul, Republic of Korea.
Sang Hyeon AhnThe Airway Mucus Institute, Yonsei University College of Medicine, Seoul, Republic of Korea.
Ji-Hwan RyuThe Airway Mucus Institute, Yonsei University College of Medicine, Seoul, Republic of Korea.
Hyung-Ju ChoThe Airway Mucus Institute, Yonsei University College of Medicine, Seoul, Republic of Korea.
Chang-Hoon KimThe Airway Mucus Institute, Yonsei University College of Medicine, Seoul, Republic of Korea.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Eosinophilic chronic rhinosinusitis (ECRS) is a severe form of chronic rhinosinusitis characterized by type 2 inflammation, tissue remodeling, and bone thickening, known as osteitis. Periostin, a matricellular protein involved in extracellular matrix (ECM) regulation and T helper 2 (Th2)-mediated inflammation, is markedly elevated in patients with ECRS; however, its pathophysiological role remains unclear. Methods: We investigated the role of periostin in inflammation and tissue remodeling in ECRS using samples from ECRS patients, human nasal epithelial cells and fibroblasts, as well as an ECRS mouse model including periostin knockout mice. Results: Periostin levels were elevated in ECRS tissues and modestly correlated with osteitis scores. Th2 cytokines increased periostin expression, particularly in nasal fibroblasts. Conditioned medium containing periostin promoted osteogenic differentiation Discussion: These findings demonstrate that periostin contributes to osteogenesis and maintenance of structural stability in the inflamed sinonasal mucosa. Periostin may be a potential therapeutic target for controlling chronic inflammation and tissue remodeling in ECRS.

Indexed as

Cell Adhesion MoleculesEosinophiliaOsteitisRhinitisSinusitisAnimalsChronic DiseaseDisease Models, AnimalFemaleFibroblastsHumansInflammationMaleMiceMice, KnockoutNasal MucosaCell Adhesion MoleculesPeriostinPOSTN protein, humanPostn protein, mouseeosinophilic chronic rhinosinusitisosteitisperiostinTh2 inflammationtissue remodeling

Identifiers

PMID40607434
PMCPMC12213678

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.