Evidence map›Paper›PMID 31123272›Full record

ArticleScientific reports2019

Analysis of the Ribonuclease A Superfamily of Antimicrobial Peptides in Patients Undergoing Chronic Peritoneal Dialysis.

Neha Dhingra Pottanat, Amy C Brook, Maria Bartosova, Hanna Cortado, Sudipti Gupta, Birong Li, Ashley R Jackson, Martin Vonau, Shira Cohen, Maria Ferrara and 8 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 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
0.8field-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

1 citing paper in PubMed, 5 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

18 authors at 7 institutions in 5 countries.

Neha Dhingra PottanatDivision of Nephrology, Department of Pediatrics, Riley Children's Hospital and Indiana University School of Medicine, Indianapolis, Indiana, USA.
Amy C BrookDivision of Infection and Immunity, School of Medicine and Systems Immunity Research Institute, Cardiff University, Cardiff, CF14 4XN, United Kingdom.ORCID http://orcid.org/0000-0001-8374-2218
Maria BartosovaDivision of Pediatric Nephrology, Center for Pediatric and Adolescent Medicine, University of Heidelberg, Heidelberg, Germany.
Hanna CortadoCenter for Clinical and Translational Research, The Research Institute at Nationwide Children's Hospital, Columbus, OH, USA.
Sudipti GuptaCenter for Clinical and Translational Research, The Research Institute at Nationwide Children's Hospital, Columbus, OH, USA.
Birong LiCenter for Clinical and Translational Research, The Research Institute at Nationwide Children's Hospital, Columbus, OH, USA.
Ashley R JacksonCenter for Clinical and Translational Research, The Research Institute at Nationwide Children's Hospital, Columbus, OH, USA.ORCID http://orcid.org/0000-0002-1571-3906
Martin VonauDepartment of Pediatrics and Internal Medicine, Ohio State University College of Medicine, Columbus, OH, USA.
Shira CohenCenter for Clinical and Translational Research, The Research Institute at Nationwide Children's Hospital, Columbus, OH, USA.
Maria FerraraDivision of Neonatology, Department of Pediatrics, Nationwide Children's Hospital, Columbus, OH, USA.
Christina B ChingCenter for Clinical and Translational Research, The Research Institute at Nationwide Children's Hospital, Columbus, OH, USA.
John David SpencerCenter for Clinical and Translational Research, The Research Institute at Nationwide Children's Hospital, Columbus, OH, USA.
Annelie BraunerDepartment of Microbiology, Tumor and Cell Biology, Division of Clinical Microbiology, Karolinska Institutet and Karolinska University Hospital, Stockholm, Sweden.
Donald J FraserDivision of Infection and Immunity, School of Medicine and Systems Immunity Research Institute, Cardiff University, Cardiff, CF14 4XN, United Kingdom.
Claus Peter SchmittDivision of Pediatric Nephrology, Center for Pediatric and Adolescent Medicine, University of Heidelberg, Heidelberg, Germany.
Matthias EberlDivision of Infection and Immunity, School of Medicine and Systems Immunity Research Institute, Cardiff University, Cardiff, CF14 4XN, United Kingdom.
Rose AyoobDivision of Nephrology, Department of Pediatrics, Charleston, WV, USA. rose.ayoob@hsc.wvu.edu.
Brian BecknellCenter for Clinical and Translational Research, The Research Institute at Nationwide Children's Hospital, Columbus, OH, USA. brian.becknell2@nationwidechildrens.org.
Nationwide Children's Hospital · USInstitute of Infection and Immunity · CAHeidelberg University · DEKarolinska University Hospital · SERiley Hospital for Children · USThe Ohio State University · USWest Virginia University Hospitals · US

Funding

The Contributions of Ribonuclease 4 & 7 to Urinary Tract Antibacterial DefenseR01DK115737 · NIDDK · RESEARCH INST NATIONWIDE CHILDREN'S HOSP · PI John David Spencer · 2018 to 2026
$2.8M
Medical Research Council MR/N023145/1NIDDK NIH HHS R01 DK115737
6 · The paper itself

Abstract

Infectious peritonitis is a common complication in patients undergoing chronic peritoneal dialysis (PD), limiting the duration of PD as a modality for renal replacement therapy and increasing patient morbidity and mortality. Antimicrobial peptides (AMPs) serve critical roles in mucosal defense, but their expression and activity during peritonitis are poorly understood. We hypothesized that AMPs belonging to the Ribonuclease (RNase) A Superfamily are present in peritoneal fluid and increase during peritonitis in patients undergoing chronic PD. In the absence of peritonitis, we detected RNase 3, RNase 6, and RNase 7 in cell-free supernatants and viable cells obtained from peritoneal fluid of chronic PD patients. The cellular sources of these RNases were eosinophils (RNase 3), macrophages (RNase 6), and mesothelial cells (RNase 7). During peritonitis, RNase 3 increased 55-fold and RNase 7 levels increased 3-fold on average, whereas RNase 6 levels were unchanged. The areas under the receiver-operating characteristic curves for RNase 3 and RNase 7 were 0.99 (95% confidence interval (CI): 0.96-1.0) and 0.79 (95% CI: 0.64-0.93), respectively, indicating their potential as biomarkers of peritonitis. Discrete omental reservoirs of these RNases were evident in patients with end stage kidney disease prior to PD initiation, and omental RNase 3 reactive cells increased in patients undergoing PD with a history of peritonitis. We propose that constitutive and inducible pools of antimicrobial RNases form a network to shield the peritoneal cavity from microbial invasion in patients undergoing chronic PD.

Indexed as

AdolescentAdultAgedAged, 80 and overAnti-Bacterial AgentsAnti-Infective AgentsAscitic FluidChildChild, PreschoolFemaleHumansKidney Failure, ChronicMaleMiddle AgedPeptidesPeritoneal DialysisAnti-Bacterial AgentsAnti-Infective AgentsPeptidesRibonuclease, PancreaticRibonucleases

Identifiers

PMID31123272
PMCPMC6533318
OpenAlexW2945226987

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.