Evidence map›Paper›PMID 24790767›Full record

ArticleInternational journal of inflammation2014

The Serum S100B Level as a Biomarker of Enteroglial Activation in Patients with Ulcerative Colitis.

Asuman Celikbilek, Mehmet Celikbilek, Seda Sabah, Nermin Tanık, Elif Borekci, Serkan Dogan, Yavuz Akin, Suleyman Baldane, Kemal Deniz, Neziha Yilmaz and 2 more

Abstract read
In one paragraph

Article in International journal of inflammation, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Observational
  2. Review
  3. The S100B Protein: A Multifaceted Pathogenic Factor More Than a Biomarker.International journal of molecular sciences · 2023
    Review
  4. S100B Affects Gut Microbiota Biodiversity.International journal of molecular sciences · 2023
    Article
  5. S100B Inhibition Attenuates Intestinal Damage and Diarrhea Severity DuringFrontiers in cellular and infection microbiology · 2021
    Article
  6. Potential roles of enteric glia in bridging neuroimmune communication in the gut.American journal of physiology. Gastrointestinal and liver physiology · 2017
    Review
  7. 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

12 authors.

Asuman CelikbilekDepartment of Neurology, Medical School, Bozok University, 66200 Yozgat, Turkey.ORCID 0000-0002-2367-1128
Mehmet CelikbilekDepartment of Gastroenterology, Medical School, Bozok University, 66200 Yozgat, Turkey.ORCID 0000-0001-8890-3885
Seda SabahDepartment of Medical Biology, Medical School, Bozok University, 66200 Yozgat, Turkey.
Nermin TanıkDepartment of Neurology, Medical School, Bozok University, 66200 Yozgat, Turkey.
Elif BorekciDepartment of Internal Medicine, Medical School, Bozok University, 66200 Yozgat, Turkey.
Serkan DoganDepartment of Gastroenterology, Medical School, Erciyes University, 38039 Kayseri, Turkey.
Yavuz AkinDepartment of Internal Medicine, Medical School, Erciyes University, 38039 Kayseri, Turkey.
Suleyman BaldaneDepartment of Internal Medicine, Medical School, Erciyes University, 38039 Kayseri, Turkey.
Kemal DenizDepartment of Pathology, Medical School, Erciyes University, 38039 Kayseri, Turkey.
Neziha YilmazDepartment of Infectious Diseases and Microbiology, Medical School, Bozok University, 66200 Yozgat, Turkey.
Omer OzbakirDepartment of Gastroenterology, Medical School, Erciyes University, 38039 Kayseri, Turkey.
Mehmet YucesoyDepartment of Gastroenterology, Medical School, Erciyes University, 38039 Kayseri, Turkey.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective. Recent studies have demonstrated that enteric glial cells (EGC) participate in the homeostasis of the gastrointestinal tract. This study investigated whether enteroglial markers, including S100B protein and glial fibrillary acidic protein (GFAP), can serve as noninvasive indicators of EGC activation and disease activity in UC patients. Methods. This clinical prospective study included 35 patients with UC and 40 age- and sex-matched controls. The diagnosis of UC was based on standard clinical, radiological, endoscopic, and histological criteria. Clinical disease activity was evaluated using the Modified Truelove-Witts Severity Index. Serum samples were analyzed for human GFAP and S100B using commercial enzyme-linked immunosorbent assay kits. Results. GFAP was not detected in the serum of either UC patients or controls (P > 0.05). However, we found a significant (P < 0.001) decrease in the serum S100B levels in the UC patients. No correlation between the serum S100B level and the disease activity or duration was observed (P > 0.05). The serum S100B levels did not differ between UC patients with active disease (24 patients, 68.6%) or in remission (11 patients, 31.4%) (P > 0.05). Conclusions. Ulcerative colitis patients had significantly lower serum S100B levels, while GFAP was of no diagnostic value in UC patients.

Identifiers

PMID24790767
PMCPMC3985341

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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.