Evidence map›Paper›PMID 31929564›Full record

ArticlePloS one2020

Serum galectins as potential biomarkers of inflammatory bowel diseases.

Tony B Yu, Susanna Dodd, Lu-Gang Yu, Sreedhar Subramanian

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
2.0field-weighted citation impact, top 12% of its field
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

26 citing papers in PubMed, 45 citations in OpenAlex.

  1. Trial
  2. Review
  3. Article
  4. Age-Related Transcriptomic Changes in the Vermiform Appendix.International journal of molecular sciences · 2025
    Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Review
  11. Dichotomous effects of Galectin-9 in disease modulation in murine models of inflammatory bowel disease.Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie · 2025
    Article
  12. Article
  13. Galectin-8 Contributes to Human Trophoblast Cell Invasion.International journal of molecular sciences · 2024
    Article
  14. Article
  15. Article
  16. Galectin-2 in Health and Diseases.International journal of molecular sciences · 2022
    Review
  17. Review
  18. Article
  19. Article
  20. 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

4 authors at 1 institution in 1 country.

Tony B YuEdinburgh Medical School, University of Edinburgh, Edinburgh, Scotland, United Kingdom.
Susanna DoddDepartment of Biostatistics, University of Liverpool, Liverpool, England, United Kingdom.ORCID 0000-0003-2851-3337
Lu-Gang YuGastroenterology Research Unit, Institute of Translational Medicine, University of Liverpool, Liverpool, England, United Kingdom.ORCID 0000-0001-9641-3712
Sreedhar SubramanianGastroenterology Research Unit, Institute of Translational Medicine, University of Liverpool, Liverpool, England, United Kingdom.ORCID 0000-0002-6483-1730
University of Liverpool · GB

Funding

Wellcome TrustWellcome Trust 201871/Z/16/Z
6 · The paper itself

Abstract

The inflammatory bowel diseases (IBD), which include mainly Crohn's disease (CD) and ulcerative colitis (UC), are common chronic inflammatory conditions of the digestive system. The diagnosis of IBD relies on the use of a combination of factors including symptoms, endoscopy and levels of serum proteins such as C-reactive protein (CRP) or faecal calprotectin. Currently there is no single reliable biomarker to determine IBD. Galectins are a family of galactoside-binding proteins that are commonly altered in the circulation of disease conditions such as cancer and inflammation. This study investigated serum galectin levels as possible biomarkers in determining IBD and IBD disease activity. Levels of galectins-1, -2, -3, -4, -7 and -8 were analysed in 208 samples from ambulant IBD patients (97 CD, 71 UC) patients and 40 from healthy people. Disease activity was assessed using Harvey-Bradshaw Index for CD and simple clinical colitis activity index for UC. The relationship of each galectin in determining IBD and IBD disease activity were analysed and compared with current IBD biomarker CRP. It was found that serum level of galectin-1 and -3, but not galectins-2, -4, -7 and -8, were significantly higher in IBD patients than in healthy people. At cut-off of 4.1ng/ml, galectin-1 differentiated IBD from healthy controls with 71% sensitivity and 87% specificity. At cut-off of 38.5ng/ml, galectin-3 separated IBD from healthy controls with 53% sensitivity and 87% specificity. None of the galectins however were able to distinguish active disease from remission in UC or CD. Thus, levels of galectins-1 and -3 are significantly elevated in both UC and CD patients compared to healthy people. Although the increased galectin levels are not able to separate active and inactive UC and CD, they may have the potential to be developed as useful biomarkers for IBD diagnosis either alone or in combination with other biomarkers.

Indexed as

AdultBiomarkersBlood ProteinsColitis, UlcerativeC-Reactive ProteinCrohn DiseaseFemaleGalectin 1Galectin 3GalectinsGastrointestinal TractHumansInflammatory Bowel DiseasesMaleMiddle AgedBiomarkersBlood ProteinsC-Reactive ProteinGalectin 1Galectin 3GalectinsLGALS1 protein, humanLGALS3 protein, human

Identifiers

PMID31929564
PMCPMC6957193
OpenAlexW2999834211

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LicenceCC BY
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Registered trials

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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.