Evidence map›Paper›PMID 29974405›Full record

ReviewInternational urology and nephrology2018

Initiation of the inflammatory response after renal ischemia/reperfusion injury during renal transplantation.

Lijuan Gu, Yu Tao, Cheng Chen, Yingze Ye, Xiaoxing Xiong, Yao Sun

Abstract readReview
PubMed Publisher
In one paragraph

Review in International urology and nephrology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

21 citing papers in PubMed, 32 citations in OpenAlex.

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  16. Observational
  17. Article
  18. Predictors of symptomatic lymphocele after kidney transplantation.International urology and nephrology · 2019
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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

6 authors at 2 institutions in 1 country.

Lijuan GuCentral Laboratory, Renmin Hospital of Wuhan University, Wuhan, 430060, China.
Yu TaoDepartment of Nephrology, Renmin Hospital of Wuhan University, Wuhan, 430060, China.
Cheng ChenDepartment of Nephrology, Renmin Hospital of Wuhan University, Wuhan, 430060, China.
Yingze YeCentral Laboratory, Renmin Hospital of Wuhan University, Wuhan, 430060, China.
Xiaoxing XiongCentral Laboratory, Renmin Hospital of Wuhan University, Wuhan, 430060, China. xiaoxingxiong@whu.edu.cn.
Yao SunKey Laboratory of Pesticides and Chemical Biology, Ministry of Education, International Joint Research Center for Intelligent Biosensor Technology and Health, Hubei International Scientific and Technology Cooperation Base of Pesticide and Green Synthesis, Chemical Biology Center, College of Chemistry, Central China Normal Universtiy, Wuhan, 430079, China. sunyaogbasp@mail.ccnu.edu.cn.
Renmin Hospital of Wuhan University · CNWuhan University · CN

Funding

The National Natural Science Foundation of China 81301019The National Natural Science Foundation of China 81571147The National Natural Science Foundation of China 81771283
6 · The paper itself

Abstract

Ischemia/reperfusion injury (IRI) occurs commonly during renal transplantation. It has been well demonstrated that the inflammatory response has an important role in the pathogenesis and pathological processes of IRI. However, the signaling events that trigger the activation of the inflammatory response are less clear. Accumulated evidence has identified the role of various injury factors released from or exposed in ischemic, damaged, or dying cells, which serve as initiators of the inflammatory response and exacerbate kidney injury after renal IRI. Signaling pathways triggered by these endogenous molecules that activate different pathogen recognition receptors have also been widely investigated. Here, we review the molecular signaling molecules that initiate the inflammatory response during renal IRI and that provide potential therapeutic options for the disease.

Indexed as

HumansInflammationKidney TransplantationNF-kappa BNLR Family, Pyrin Domain-Containing 3 ProteinNLR ProteinsReperfusion InjurySignal TransductionToll-Like ReceptorsNF-kappa BNLR Family, Pyrin Domain-Containing 3 ProteinNLRP3 protein, humanNLR ProteinsToll-Like ReceptorsInflammatory responseIschemia/reperfusion injuryMolecular signaling eventsNod-like receptorsRenal transplantationThe pyrin domain containing protein 3 (NLRP3)

Identifiers

PMID29974405
OpenAlexW2809746813

What OpenQuestion holds

Textmetadata
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.