Evidence map›Paper›PMID 24976841›Full record

ReviewHepatitis monthly2014

Portal hypertension as immune mediate disease.

Sara Manti, Lucia Marseglia, Gabriella D'Angelo, Martina Filippelli, Caterina Cuppari, Eloisa Gitto, Claudio Romano, Teresa Arrigo, Carmelo Salpietro

Open access · hybridAbstract readReview
In one paragraph

Review in Hepatitis monthly, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.6field-weighted citation impact, top 30% 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

5 citing papers in PubMed, 9 citations in OpenAlex.

  1. Review
  2. Nonresponse to intramuscular vaccination: An unmet need in hepatitis B vaccination.Saudi journal of gastroenterology : official journal of the Saudi Gastroenterology Association · 2020
    Article
  3. Review
  4. Review
  5. Oxidative stress in obesity: a critical component in human diseases.International journal of molecular sciences · 2014
    Review
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.

Sara MantiDepartment of Pediatric Sciences, Genetics and Pediatric Immunology Unit, University of Messina, Messina, Italy.
Lucia MarsegliaDepartment of Pediatric Sciences, Genetics and Pediatric Immunology Unit, University of Messina, Messina, Italy.
Gabriella D'AngeloDepartment of Pediatric Sciences, Genetics and Pediatric Immunology Unit, University of Messina, Messina, Italy.
Martina FilippelliDepartment of Pediatric Sciences, Genetics and Pediatric Immunology Unit, University of Messina, Messina, Italy.
Caterina CuppariDepartment of Pediatric Sciences, Genetics and Pediatric Immunology Unit, University of Messina, Messina, Italy.
Eloisa GittoDepartment of Pediatric Sciences, Genetics and Pediatric Immunology Unit, University of Messina, Messina, Italy.
Claudio RomanoDepartment of Pediatric Sciences, Genetics and Pediatric Immunology Unit, University of Messina, Messina, Italy.
Teresa ArrigoDepartment of Pediatric Sciences, Genetics and Pediatric Immunology Unit, University of Messina, Messina, Italy.
Carmelo SalpietroDepartment of Pediatric Sciences, Genetics and Pediatric Immunology Unit, University of Messina, Messina, Italy.
University of Messina · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

contextPortal Hypertension (PH) is a progressive complication due to chronic liver disease. In addition to pathophysiologic changes in the micro-circulation, in PH are established fibrous tissue (periportal fibrous septal) and regenerative hyperplastic nodules (from micro- to macro-nodules) promoting hepatic architectural distortion. EVIDENCE ACQUISITION: A literature search of electronic databases was undertaken for the major studies published from 1981 to today. The databases searched were: PubMed, EMBASE, Orphanet, Midline and Cochrane Library. We used the keywords: "portal hypertension, children, immune system, endocrine system, liver fibrosis".

resultsIt is believed that PH results from three "phenotype": ischemia-reperfusion, involving nervous system (NS); edema and oxidative damage, involving immune system; inflammation and angiogenesis, involving endocrine system. However, its exact cause still underdiagnosed and unknown.

conclusionsPH is a dynamic and potentially reversible process. Researchers have tried to demonstrate mechanisms underlying PH and its related-complications. This review focuses on the current knowledge regarding the pathogenesis, and immune, endocrine-metabolic factors of disease. The strong positive association between immune system and development of PH could be efficient to identify non-invasive markers of disease, to modify prognosis of PH, and to development and application of specific and individual anti-inflammatory therapy.

Indexed as

ChildrenEndocrine SystemImmune SystemLiver FibrosisPortal Hypertension

Identifiers

PMID24976841
PMCPMC4071352
OpenAlexW2169513887

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.