Evidence map›Paper›PMID 24436105›Full record

ArticleNeurourology and urodynamics2014

What is the role for biomarkers for lower urinary tract disorders? ICI-RS 2013.

Christopher H Fry, Arun Sahai, Bahareh Vahabi, Anthony J Kanai, Lori A Birder

Open access · greenAbstract read
In one paragraph

Article in Neurourology and urodynamics, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
5.1field-weighted citation impact, top 5% 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

12 citing papers in PubMed, 31 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

5 authors at 4 institutions in 2 countries.

Christopher H FryDepartment of Biochemistry and Physiology, University of Surrey, Guildford, Surrey, United Kingdom.
Arun Sahai
Bahareh Vahabi
Anthony J Kanai
Lori A Birder
University of Pittsburgh · USGuy's and St Thomas' NHS Foundation Trust · GBSouthmead Hospital · GBUniversity of Surrey · GB

Funding

Urothelium in Detrusor OveractivityP01DK093424 · NIDDK · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI DEGROAT, WILLIAM C · 2013 to 2017
$7.9M
PDE5 Inhibition of Afferents and Interstitial Cells in Overactive Mouse BladdersR01DK098361 · NIDDK · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI BIRDER, LORI A, KANAI, ANTHONY JOHN · 2014 to 2024
$5.7M
Roles of Nitric Oxide and Superoxide in CystitisR01DK071085 · NIDDK · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI KANAI, ANTHONY JOHN · 2005 to 2017
$3.3M
NIDDK NIH HHS P01 DK093424NIDDK NIH HHS R01 DK071085NIDDK NIH HHS R01 DK098361
6 · The paper itself

Abstract

aimsA biomarker is an entity that measures a normal or pathological process, or the response to an intervention. A biomarker must measure exclusively and be sufficiently sensitive to the process of interest. Alternatively, a biomarker may give clues regarding the underlying pathology of the condition and be a useful research or specialist tool. If a biomarker is to be of practical benefit then it must also be economical and practical to use. This article will consider chemical moieties as biomarkers, although in principle physical markers (e.g., bladder wall thickness) could also be defined as such. RESULTS AND

conclusionsThe validation of a biomarker for detrusor overactivity (DO) must appreciate the fact that the condition is likely to multifactorial and thus no single entity may be sufficiently selective and sensitive. However, more specific conditions, such as bladder pain associated with DO, may make the biomarker search easier. Several prospective agents including antiproliferative factor (APF) and epidermal growth factors (EGF) are discussed. Several urinary biomarkers, including neurotrophins (NGF, BDNF) and cytokines, and a serum marker, C-reactive protein, are considered as reaching the above criteria. All suffer from relatively poor lack of discrimination, as they all change in response to other, often inflammatory, conditions; BDNF may offer the highest expectations. Urinary ATP has also been proposed as a DO/OAB biomarker but requires further evaluation. Finally genetic markers offer potential to understand more about the pathophysiology of DO/OAB. The increasing availability of genome-wide association studies and micro-RNA assays offer genetic markers as a new generation of biomarkers. Neurourol. Urodynam. 33:602-605, 2014. © 2014 Wiley Periodicals, Inc.

Indexed as

BiomarkersBrain-Derived Neurotrophic FactorC-Reactive ProteinCystitis, InterstitialCytokinesEpidermal Growth FactorGenetic MarkersGlycoproteinsHumansIntercellular Signaling Peptides and ProteinsNerve Growth FactorProstaglandinsUrinary Bladder, OveractiveUrinary Incontinenceantiproliferative factor APF, humanBiomarkersBrain-Derived Neurotrophic FactorC-Reactive ProteinCytokinesEpidermal Growth FactorGenetic MarkersGlycoproteinsIntercellular Signaling Peptides and ProteinsNerve Growth FactorProstaglandinsbiomarkerbladder pain syndromecytokinegenetic markersnerve growth factoroveractive bladder

Identifiers

PMID24436105
PMCPMC5517085
OpenAlexW1706583688

What OpenQuestion holds

Textmetadata
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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.