Evidence map›Paper›PMID 28316376›Full record

ReviewMediators of inflammation2017

The Role of Intestinal Alkaline Phosphatase in Inflammatory Disorders of Gastrointestinal Tract.

Jan Bilski, Agnieszka Mazur-Bialy, Dagmara Wojcik, Janina Zahradnik-Bilska, Bartosz Brzozowski, Marcin Magierowski, Tomasz Mach, Katarzyna Magierowska, Tomasz Brzozowski

Open access · goldAbstract readReview
In one paragraph

Review in Mediators of inflammation, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 86 papers.

0numbers the graph read from it
0cells of the map it votes in
86citing papers in PubMed
9.2field-weighted citation impact, top 2% 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

86 citing papers in PubMed, 160 citations in OpenAlex.

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  17. Surface layer proteins fromTissue barriers · 2024
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26 more citing papers are in PubMed but not listed here.

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

9 authors at 1 institution in 1 country.

Jan BilskiDepartment of Ergonomics and Exercise Physiology, Faculty of Health Sciences, Jagiellonian University Medical College, Cracow, Poland.ORCID 0000-0002-2699-3798
Agnieszka Mazur-BialyDepartment of Ergonomics and Exercise Physiology, Faculty of Health Sciences, Jagiellonian University Medical College, Cracow, Poland.ORCID 0000-0003-1056-8276
Dagmara WojcikDepartment of Physiology, Faculty of Medicine, Jagiellonian University Medical College, Cracow, Poland.
Janina Zahradnik-BilskaGastroenterology and Hepatology Clinic, The University Hospital, Jagiellonian University Medical College, Cracow, Poland.
Bartosz BrzozowskiGastroenterology and Hepatology Clinic, The University Hospital, Jagiellonian University Medical College, Cracow, Poland.ORCID 0000-0003-4207-9231
Marcin MagierowskiDepartment of Physiology, Faculty of Medicine, Jagiellonian University Medical College, Cracow, Poland.ORCID 0000-0003-0175-5600
Tomasz MachGastroenterology and Hepatology Clinic, The University Hospital, Jagiellonian University Medical College, Cracow, Poland.
Katarzyna MagierowskaDepartment of Physiology, Faculty of Medicine, Jagiellonian University Medical College, Cracow, Poland.ORCID 0000-0002-4866-1102
Tomasz BrzozowskiDepartment of Physiology, Faculty of Medicine, Jagiellonian University Medical College, Cracow, Poland.ORCID 0000-0002-5805-0065
Jagiellonian University · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Over the past few years, the role of intestinal alkaline phosphatase (IAP) as a crucial mucosal defence factor essential for maintaining gut homeostasis has been established. IAP is an important apical brush border enzyme expressed throughout the gastrointestinal tract and secreted both into the intestinal lumen and into the bloodstream. IAP exerts its effects through dephosphorylation of proinflammatory molecules including lipopolysaccharide (LPS), flagellin, and adenosine triphosphate (ATP) released from cells during stressful events. Diminished activity of IAP could increase the risk of disease through changes in the microbiome, intestinal inflammation, and intestinal permeability. Exogenous IAP exerts a protective effect against intestinal and systemic inflammation in a variety of diseases and represents a potential therapeutic agent in diseases driven by gut barrier dysfunction such as IBD. The intestinal protective mechanisms are impaired in IBD patients due to lower synthesis and activity of endogenous IAP, but the pathomechanism of this enzyme deficiency remains unclear. IAP has been safely administered to humans and the human recombinant form of IAP has been developed. This review was designed to provide an update in recent research on the involvement of IAP in intestinal inflammatory processes with focus on IBD in experimental animal models and human patients.

Indexed as

Alkaline PhosphataseAnimalsGastrointestinal TractHumansInflammationIntestinesAlkaline Phosphatase

Identifiers

PMID28316376
PMCPMC5339520
OpenAlexW2590939865

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.