Evidence map›Paper›PMID 41841693›Full record

ArticleThe Journal of clinical endocrinology and metabolism2026

Elevated periostin level in serum of adults with osteogenesis imperfecta is associated with disease severity.

Alexandre Mercier-Guery, Maxime Auroux, Evelyne Gineyts, Olivier Borel, Pawel Szulc, Elisabeth Sornay-Rendu, Elisabeth Fontanges, Martine Croset, Jean-Charles Rousseau, Roland Chapurlat

Abstract read
In one paragraph

Article in The Journal of clinical endocrinology and metabolism, 2026. 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. Article
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

10 authors.

Alexandre Mercier-GueryHospices Civils de Lyon, Hôpital E.Herriot, Service de Rhumatologie et Pathologie Osseuse, Lyon 69003, France.ORCID 0000-0002-7515-9353
Maxime AurouxHospices Civils de Lyon, Hôpital E.Herriot, Service de Rhumatologie et Pathologie Osseuse, Lyon 69003, France.ORCID 0000-0002-3408-0948
Evelyne GineytsUniversité de Lyon, Université Lyon 1, INSERM UMR 1033, LYOS Pathophysiology, Diagnosis & Treatments of Musculoskeletal Disorders, Lyon 69008, France.ORCID 0000-0003-3868-5810
Olivier BorelUniversité de Lyon, Université Lyon 1, INSERM UMR 1033, LYOS Pathophysiology, Diagnosis & Treatments of Musculoskeletal Disorders, Lyon 69008, France.
Pawel SzulcUniversité de Lyon, Université Lyon 1, INSERM UMR 1033, LYOS Pathophysiology, Diagnosis & Treatments of Musculoskeletal Disorders, Lyon 69008, France.ORCID 0000-0003-4168-6697
Elisabeth Sornay-RenduUniversité de Lyon, Université Lyon 1, INSERM UMR 1033, LYOS Pathophysiology, Diagnosis & Treatments of Musculoskeletal Disorders, Lyon 69008, France.ORCID 0000-0002-2573-5316
Elisabeth FontangesHospices Civils de Lyon, Hôpital E.Herriot, Service de Rhumatologie et Pathologie Osseuse, Lyon 69003, France.ORCID 0000-0003-2512-8214
Martine CrosetUniversité de Lyon, Université Lyon 1, INSERM UMR 1033, LYOS Pathophysiology, Diagnosis & Treatments of Musculoskeletal Disorders, Lyon 69008, France.ORCID 0000-0003-0564-7033
Jean-Charles RousseauUniversité de Lyon, Université Lyon 1, INSERM UMR 1033, LYOS Pathophysiology, Diagnosis & Treatments of Musculoskeletal Disorders, Lyon 69008, France.ORCID 0000-0002-3755-2891
Roland ChapurlatHospices Civils de Lyon, Hôpital E.Herriot, Service de Rhumatologie et Pathologie Osseuse, Lyon 69003, France.ORCID 0000-0001-8214-6385

Funding

1033 department's own fundsHospices Civils de LyonINSERMUniversity Hospital of Lyon
6 · The paper itself

Abstract

objectiveIn osteogenesis imperfecta (OI), phenotypic variability and the limited predictive value of genotype-phenotype correlations underscore the need for reliable predictive marker of disease severity. Periostin is a matricellular protein involved in bone formation, remodeling, and response to mechanical stress. It interacts with type I collagen and modulates osteoblast activity via Wnt/β-catenin and TGF-β signaling. Given its established role in other bone disorders, we hypothesized that circulating periostin may be a relevant biomarker in OI.

methodsWe performed a matched case-control analysis of serum periostin levels in 61 adult patients with OI and 61 age-, sex-, and BMI-matched controls. Periostin was measured by ELISA. Associations between periostin levels and clinical variables were assessed using t-tests, Pearson correlations, and multivariable linear regression models.

resultsMean periostin levels were significantly higher in OI patients than in controls (796.5 ± 209 vs 713.6 ± 167 pmol/L, P = .017). Among OI patients, higher periostin level was associated with female sex (P = .01), presence of scoliosis (P = .01), and Sillence type III (P = .05). Positive correlations were observed between periostin and markers of axial skeletal severity as height-wingspan discrepancy (r = 0.30, P = .023). In multivariable analysis, the number of severe fractures (defined as femur/pelvis/humerus/vertebral fractures) was independently associated with higher periostin level (β = 25.6, P = .041), while smoking was negatively associated (β = -269.8, P = .012).

conclusionThis study is the first to report the elevated circulating level of periostin in adults with OI and its association with disease severity.

Indexed as

Cell Adhesion MoleculesOsteogenesis ImperfectaPeriostinAdultBiomarkersCase-Control StudiesFemaleHumansMaleMiddle AgedSeverity of Illness IndexYoung AdultBiomarkersCell Adhesion MoleculesPeriostinPOSTN protein, humanbiomarkerdisease severityosteogenesis imperfectaperiostinrare bone disease

Identifiers

PMID41841693
PMCPMC13466953

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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.