Evidence map›Paper›PMID 28181420›Full record

ArticleClinical and translational science2017

Hypoxia Inducible Factor 1: A Urinary Biomarker of Kidney Disease.

S Movafagh, D Raj, M Sanaei-Ardekani, D Bhatia, K Vo, M Mahmoudieh, R Rahman, E H Kim, A F Harralson

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in Clinical and translational science, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02791880 (Genomic and Biomarker Predictors of Acute Kidney Injury and Other Post-Procedural Outcomes Following Transcatheter Aortic Valve Replacement), which is not on this map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.8field-weighted citation impact, top 32% 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.

NCT02791880 active not recruitingnot on this map

Genomic and Biomarker Predictors of Acute Kidney Injury and Other Post-Procedural Outcomes Following Transcatheter Aortic Valve Replacement

TypeobservationalSponsorUniversity of Texas Southwestern Medical CenterRan2016 to 2031Enrolled62ConditionsAcute Kidney Injury, Renal Insufficiency, Chronic, Heart Failure, Myocardial InfarctionArmsTranscatheter Aortic Valve Replacement
3 · Its place in the literature

Who cites it

11 citing papers in PubMed, 14 citations in OpenAlex.

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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

9 authors at 3 institutions in 1 country.

S MovafaghDepartment of Pharmacogenomics, Bernard J. Dunn School of Pharmacy, Shenandoah University, Ashburn, Virginia, USA.
D RajDepartment of Nephrology, George Washington University Division of Kidney Diseases and Hypertension, Washington, DC, USA.
M Sanaei-ArdekaniKidney and Hypertension Specialists, Manassas, Virginia, USA.
D BhatiaDepartment of Pharmacogenomics, Bernard J. Dunn School of Pharmacy, Shenandoah University, Ashburn, Virginia, USA.
K VoBernard J. Dunn School of Pharmacy, Shenandoah University, Ashburn, Virginia, USA.
M MahmoudiehBernard J. Dunn School of Pharmacy, Shenandoah University, Ashburn, Virginia, USA.
R RahmanKidney and Hypertension Specialists, Manassas, Virginia, USA.
E H KimKidney and Hypertension Specialists, Manassas, Virginia, USA.
A F HarralsonDepartment of Pharmacogenomics, Bernard J. Dunn School of Pharmacy, Shenandoah University, Ashburn, Virginia, USA.
Shenandoah University · USTidewater Kidney Specialists · USGeorge Washington University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Identifying noninvasive biomarkers of kidney disease is valuable for diagnostic and therapeutic purposes. Hypoxia inducible factor 1 (HIF-1) expression is known to be elevated in the kidneys in several renal disease pathologies. We hypothesized that the urinary HIF-1a mRNA level may be a suitable biomarker for expression of this protein in chronic kidney disease (CKD). We compared HIF-1a mRNA levels from urine pellets of CKD and healthy subjects. To ensure that urinary HIF-1a mRNA is of kidney origin, we examined colocalization of HIF-1a mRNA with two kidney specific markers in urine cells. We found that HIF-1a mRNA is readily quantifiable in urine pellets and its expression was significantly higher in CKD patients compared with healthy adults. We also showed that the urinary HIF-1a mRNA comes primarily from cells of renal origin. Our data suggest that urinary HIF-1a mRNA is a potential biomarker in CKD and can be noninvasively assessed in patients.

Indexed as

AdultAgedBiomarkersCadherinsCreatinineDemographyFemaleGenes, EssentialHepatitis A Virus Cellular Receptor 1HumansHypoxia-Inducible Factor 1In Situ Hybridization, FluorescenceKidneyMaleReference StandardsRenal Insufficiency, ChronicBiomarkersCadherinsCreatinineHAVCR1 protein, humanHepatitis A Virus Cellular Receptor 1Hypoxia-Inducible Factor 1RNA, Messenger

Identifiers

PMID28181420
PMCPMC5421733
OpenAlexW2587758174

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

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.