Evidence map›Paper›PMID 42157106›Full record

ArticleBMC gastroenterology2026

Association between iron status and inflammation markers with GDF15 and BMP6 in inflammatory bowel disease: a single center cross-sectional study.

Yusuf Üstün, Sinan Yanık, Fatma Uçar, Ahmet Yalçın Üstün, Harun Erdal, Yusuf Coşkun, İlhami Yüksel

Abstract read
In one paragraph

Article in BMC gastroenterology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Yusuf ÜstünUniversity of Health Sciences, Dışkapı Yıldırım Beyazıt Education and Research Hospital, Gastroenterology Clinic, Ankara, Turkey. yusufus@hotmail.com.ORCID http://orcid.org/0000-0003-0453-8783
Sinan YanıkUniversity of Health Sciences, Dışkapı Yıldırım Beyazıt Education and Research Hospital, Gastroenterology Clinic, Ankara, Turkey.ORCID http://orcid.org/0000-0003-4026-170X
Fatma UçarUniversity of Health Sciences, Dışkapı Yıldırım Beyazıt Education and Research Hospital, Gastroenterology Clinic, Ankara, Turkey.ORCID http://orcid.org/0000-0001-7354-375X
Ahmet Yalçın ÜstünFaculty of Medicine, Azerbaijan Medical University, Baku, Azerbaijan.ORCID http://orcid.org/0009-0009-4296-4522
Harun ErdalUniversity of Health Sciences, Dışkapı Yıldırım Beyazıt Education and Research Hospital, Gastroenterology Clinic, Ankara, Turkey.ORCID http://orcid.org/0000-0002-3171-8133
Yusuf CoşkunUniversity of Health Sciences, Dışkapı Yıldırım Beyazıt Education and Research Hospital, Gastroenterology Clinic, Ankara, Turkey.ORCID http://orcid.org/0000-0001-6016-6297
İlhami YükselUniversity of Health Sciences, Dışkapı Yıldırım Beyazıt Education and Research Hospital, Gastroenterology Clinic, Ankara, Turkey.ORCID http://orcid.org/0000-0002-9730-2309

Funding

Dışkapı Yıldırım Beyazıt Education and Research Hospital Scientific Research Projects Administration 10.15. 2015/55 resolution
6 · The paper itself

Abstract

backgroundInflammatory bowel diseases (IBD), including Crohn's disease (CD) and ulcerative colitis (UC), are chronic disorders with relapsing and remitting disease courses. Several clinical indicators and biomarkers have been evaluated for their clinical utility in assessing disease prognosis and monitoring disease activity. This study evaluated the utility of growth differentiation factor-15 (GDF15) and bone morphogenetic protein-6 (BMP6) in inflammatory pathways and iron regulation in IBD.

methodsBetween September 2015 and March 2016, this single-center, cross-sectional study included 40 CD patients, 29 UC patients, and 70 healthy controls. The disease activity was measured using the Mayo score and the Crohn's Disease Activity Index (CDAI). Serum iron, hematological indices, inflammatory markers, and the novel biomarkers BMP6 and GDF15 as determined by ELISA were evaluated.

resultsBoth the CD and UC groups showed significantly lower serum iron (p < 0.001), reduced mean corpuscular hemoglobin concentration, and higher red cell distribution width than the control group. Inflammatory markers, including erythrocyte sedimentation rate (ESR) and C-reactive protein (CRP), were elevated in IBD, particularly during active disease, with CRP increasing significantly in active UC compared to remission (p = 0.040). In contrast, BMP6 and GDF15 levels did not differ significantly between the disease groups or activity states. Nonetheless, GDF15 demonstrated moderate positive correlations with serum iron (r = 0.314), hemoglobin (r = 0.320), and mean corpuscular hemoglobin concentration (MCHC) (r = 0.344), suggesting a link to erythropoietic or iron-related processes rather than inflammation.

conclusionsConventional markers reliably confirmed iron deficiency and inflammation in IBD. BMP6 and GDF15 levels did not differ significantly across disease states, indicating limited utility as markers of disease activity. Notably, GDF15 was positively correlated with serum iron, hemoglobin, and MCHC, suggesting its association with iron metabolism rather than active inflammation. Larger longitudinal studies are warranted to validate this potential role.

trial registrationNot applicable.

Indexed as

Bone Morphogenetic Protein 6Colitis, UlcerativeCrohn DiseaseGrowth Differentiation Factor 15IronAdultBiomarkersBlood SedimentationCase-Control StudiesC-Reactive ProteinCross-Sectional StudiesErythrocyte IndicesFemaleHumansInflammationMaleBiomarkersBMP6 protein, humanBone Morphogenetic Protein 6C-Reactive ProteinGDF15 protein, humanGrowth Differentiation Factor 15IronBMP6 proteinCrohn diseaseGDF-15 proteinInflammationInflammatory bowel diseasesIronUlcerative colitis

Identifiers

PMID42157106
PMCPMC13353025

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

None linked

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.