Evidence map›Paper›PMID 31167651›Full record

ArticleBMC nephrology2019

Association of endothelin genetic variants and hospitalized infection complications in end-stage renal disease (ESRD) patients.

Chih-Chin Kao, Shih-Ying Cheng, Yu-Jia Wang, Shu-Chen Chien, Yu-Wen Hsu, Mei-Yi Wu, Hsing-Fang Lu, Sean Nam, Tao Sun, Mai-Szu Wu and 1 more

Open access · goldAbstract read
In one paragraph

Article in BMC nephrology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact, top 94% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. 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

11 authors at 4 institutions in 2 countries.

Chih-Chin KaoGraduate Institute of Clinical Medicine, College of Medicine, Taipei Medical University, Taipei, Taiwan.
Shih-Ying ChengDepartment of Pharmacy, Taipei Medical University Hospital, Taipei, Taiwan.
Yu-Jia WangPh.D. Program for Neural Regenerative Medicine, College of Medical Science and Technology, Taipei Medical University, Taipei, Taiwan.
Shu-Chen ChienDepartment of Pharmacy, Taipei Medical University Hospital, Taipei, Taiwan.
Yu-Wen HsuPh.D. Program for Translational Medicine, College of Medical Science and Technology, Academia Sinica, Taipei Medical University, Taipei, Taiwan.
Mei-Yi WuDivision of Nephrology, Department of Internal Medicine, School of Medicine, College of Medicine, Taipei Medical University, Taipei, Taiwan.
Hsing-Fang LuDepartment of Clinical Pharmacy, School of Pharmacy, College of Pharmacy, Taipei Medical University, Taipei, Taiwan.
Sean NamDepartment of Clinical Pharmacy, School of Pharmacy, College of Pharmacy, Taipei Medical University, Taipei, Taiwan.
Tao SunDepartment of Surgery, University of Chicago, Chicago, IL, USA.
Mai-Szu WuGraduate Institute of Clinical Medicine, College of Medicine, Taipei Medical University, Taipei, Taiwan. maiszuwu@gmail.com.
Wei-Chiao ChangDepartment of Clinical Pharmacy, School of Pharmacy, College of Pharmacy, Taipei Medical University, Taipei, Taiwan. wcc@tmu.edu.tw.
Taipei Medical University · TWAcademia Sinica · TWTaipei Medical University-Shuang Ho Hospital · TWUniversity of Chicago · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundInfection is the second most common cause of mortality for patients with end-stage renal disease (ESRD), accompanying with immune dysfunction. Endothelin (EDN) is known to be related to inflammation; however, it is unknown whether genetic variants of the EDN gene family are associated with increased risk of hospitalized infection events.

methodsNineteen tagging single-nucleotide polymorphisms (tSNPs) of the EDN gene family were selected for genotyping a cohort of 190 ESRD patients. Patient demographics were recorded, the subtypes of infection events were identified, and association analysis between the EDN genetic variants and hospitalized infection events was performed.

resultsIn this study, 106 patients were hospitalized for infection events. The leading events were pneumonia, bacteremia, and cellulitis. The minor allele of rs260741, rs197173, and rs926632 SNPs of EDN3 were found to be associated with reduced risk of hospitalized bacteremia events.

conclusionsThe minor allele of rs260741, rs197173, and rs926632 in EDN3 were associated with reduced risk of hospitalized bacteremia events in ESRD patients.

Indexed as

Cross InfectionKidney Failure, ChronicChinaEndothelin-3FemaleGenetic TestingHospitalizationHumansMaleMiddle AgedPolymorphism, Single NucleotideProtective FactorsEDN3 protein, humanEndothelin-3EndothelinEnd stage renal diseaseInfectionRenal failure

Identifiers

PMID31167651
PMCPMC6549338
OpenAlexW2948765460

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LicenceCC BY
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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.