Evidence map›Paper›PMID 29180837›Full record

ReviewMediators of inflammation2017

IL-33-ST2 Axis in Liver Disease: Progression and Challenge.

Zijian Sun, Binxia Chang, Miaomiao Gao, Jiyuan Zhang, Zhengsheng Zou

Abstract 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 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing 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

26 citing papers in PubMed.

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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

5 authors.

Zijian SunCenter of Non-Infectious Liver Diseases, Peking University 302 Clinical Medical School, Beijing, China.
Binxia ChangCenter of Non-Infectious Liver Diseases, Beijing 302 Hospital, Beijing, China.
Miaomiao GaoCenter of Non-Infectious Liver Diseases, Peking University 302 Clinical Medical School, Beijing, China.
Jiyuan ZhangTreatment and Research Center for Infectious Diseases, Beijing 302 Hospital, Beijing, China.ORCID 0000-0003-4781-4477
Zhengsheng ZouCenter of Non-Infectious Liver Diseases, Peking University 302 Clinical Medical School, Beijing, China.ORCID 0000-0002-1778-269X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The new member of the IL-1 family, interleukin-33 (IL-33), participates in the progression of a variety of diseases through binding with its receptor ST2. Recently, much clinical evidence and experimental data have indicated that IL-33 is associated with various liver diseases. This review primarily addresses the relationship between IL-33 and several hepatic diseases. IL-33 can alleviate high-fat diet- (HFD-) induced hepatic steatosis and insulin resistance, and IL-33 acts as an alarmin, which quickly triggers the immune system to respond to virus invasion and toxic damage to the liver. However, when liver injury is chronic, IL-33 promotes Th2 reactions and hepatic stellate cell (HSC) activity, facilitating progression to liver fibrosis. The complicated functions of IL-33 should be considered before its clinical application.

Indexed as

Diet, High-FatHumansInterleukin-33Liver CirrhosisLiver DiseasesSignal TransductionIL33 protein, humanInterleukin-33

Identifiers

PMID29180837
PMCPMC5664344

What OpenQuestion holds

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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.