Evidence map›Paper›PMID 26526637›Full record

ArticleBiomarkers in cancer2015

Blood-based Biomarkers at Large Bowel Endoscopy and Prediction of Future Malignancies.

Thomas S Kring, Thomas B Piper, Lars N Jørgensen, Jesper Olsen, Hans B Rahr, Knud T Nielsen, Søren Laurberg, Gerard Davis, Barry Dowell, Julia S Johansen and 3 more

Abstract read
In one paragraph

Article in Biomarkers in cancer, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

13 authors.

Thomas S KringDepartment of Surgical Gastroenterology, Hvidovre Hospital, Hvidovre, Denmark.
Thomas B PiperDepartment of Surgical Gastroenterology, Hvidovre Hospital, Hvidovre, Denmark.
Lars N JørgensenDigestive Disease Center, Bispebjerg Hospital, Copenhagen, Denmark. ; Institute of Clinical Medicine, University of Copenhagen, Copenhagen, Denmark.
Jesper OlsenDepartment of Surgical Gastroenterology, Glostrup Hospital, Glostrup, Denmark.
Hans B RahrDepartment of Surgical Gastroenterology, Odense University Hospital, Odense, Denmark.
Knud T NielsenDepartment of Surgery, Randers Hospital, Randers, Denmark.
Søren LaurbergDepartment of Surgical Gastroenterology, Aarhus Hospital THG, Aarhus, Denmark.
Gerard DavisAbbott Diagnostics Division R&D, Chicago, USA.
Barry DowellAbbott Diagnostics Division R&D, Chicago, USA.
Julia S JohansenDepartment of Oncology, Herlev Hospital, Herlev, Denmark.
Ib J ChristensenDepartment of Surgical Gastroenterology, Hvidovre Hospital, Hvidovre, Denmark.
Nils BrünnerInstitute of Veterinary Disease Biology, Faculty of Health and Medical Sciences, University of Copenhagen, Frederiksberg, Denmark.
Hans J NielsenDepartment of Surgical Gastroenterology, Hvidovre Hospital, Hvidovre, Denmark. ; Institute of Clinical Medicine, University of Copenhagen, Copenhagen, Denmark.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Soluble cancer-related protein biomarker levels may be increased in subjects without findings at large bowel endoscopy performed due to symptoms associated with colorectal cancer. The present study focused on a possible association between increased biomarker levels in such subjects and subsequent development of malignant diseases. In a major study of 4,990 subjects undergoing large bowel endoscopy, 691 were without pathology and comorbidity. Plasma levels of TIMP-1, CEA, CA19-9, and YKL-40 were determined in samples collected just before endoscopy and compared with subsequent development of a malignant disease within a period of 7-8 years. The upper 90% limits of the reference levels of every single protein were used to differentiate between normal and increased levels. The levels were separated into three groups: 0, none of the biomarkers increased; 1, one biomarker increased; 2, two or more biomarkers increased. A total of 43 subjects developed a primary malignant disease in the observation period. Univariatly, increase of all four biomarkers was significantly associated with subsequent development of a malignant disease. A multivariate analysis showed that increased biomarker levels were associated with subsequent development of a malignant disease (P = 0.002). The cumulative risk of developing malignant disease within the first 5 years after endoscopy was group 0, 3.3%; group 1, 5.8%; group 2, 7.8%. It is concluded that increased levels of plasma TIMP-1, CEA, CA19-9, and serum YKL-40 at large bowel endoscopy without findings may be associated with an increased risk of developing a subsequent malignant disease.

Indexed as

CA19-9cancer riskCEAcolorectal cancerendoscopyTIMP-1YKL-40

Identifiers

PMID26526637
PMCPMC4620935

What OpenQuestion holds

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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.