Evidence map›Paper›PMID 31737931›Full record

ReviewNeurourology and urodynamics2020

New targets for overactive bladder-ICI-RS 2109.

Christopher Henry Fry, Basu Chakrabarty, Hikaru Hashitani, Karl-Erik Andersson, Karen McCloskey, Rita I Jabr, Marcus J Drake

Abstract readReview
In one paragraph

Review in Neurourology and urodynamics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
–field-weighted citation impact
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

14 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
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  5. Article
  6. Review
  7. Article
  8. Review
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  10. Article
  11. Article
  12. Article
  13. Review
  14. Current pharmacotherapy of overactive bladder.International braz j urol : official journal of the Brazilian Society of Urology
    Review
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

7 authors.

Christopher Henry FrySchool of Physiology, Pharmacology and Neuroscience, University of Bristol, Bristol, UK.ORCID 0000-0003-3647-5983
Basu ChakrabartySchool of Physiology, Pharmacology and Neuroscience, University of Bristol, Bristol, UK.ORCID 0000-0002-7320-4931
Hikaru HashitaniDepartment of Cell Physiology, Nagoya City University, Nagoya, Japan.
Karl-Erik AnderssonInstitute of Laboratory Medicine, Lund University, Lund, Sweden.ORCID 0000-0003-0665-3486
Karen McCloskeySchool of Medicine, Dentistry and Biomedical Sciences, Queens University Belfast, Belfast, UK.ORCID 0000-0002-9135-9013
Rita I JabrDivision of Biochemical Sciences, Faculty of Health and Biomedical Sciences, University of Surrey, Guildford, UK.
Marcus J DrakeBristol Medical School, University of Bristol, Bristol, UK.

Funding

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
Medical Research Council MR/M012425/1NIDDK NIH HHS R01 DK098361
6 · The paper itself

Abstract

aimTo review evidence for novel drug targets that can manage overactive bladder (OAB) symptoms.

methodsA think tank considered evidence from the literature and their own research experience to propose new drug targets in the urinary bladder to characterize their use to treat OAB.

resultsFive classes of agents or cellular pathways were considered. (a) Cyclic nucleotide-dependent (cyclic adenosine monophosphate and cyclic guanosine monophosphate) pathways that modulate adenosine triphosphate release from motor nerves and urothelium. (b) Novel targets for β

conclusionsThe specificity of action remains a consideration if particular classes of agents can be considered for future development as receptors or pathways that mediate actions of the above mentioned potential agents are distributed among most organ systems. The tasks are to determine more detail of the pathological changes that occur in the OAB and how the specificity of potential drugs may be directed to bladder pathological changes. An important conclusion was that the storage, not the voiding, phase in the micturition cycle should be investigated and potential targets lie in the whole range of tissue in the bladder wall and not just detrusor.

Indexed as

HumansUrinary Bladder, OveractiveUrinationUrological AgentsUrotheliumUrological Agentscyclic nucleotidesfibrosissmall conductance K+ channelsTRP channelsβ3-agonists

Identifiers

PMID31737931
PMCPMC8114459

What OpenQuestion holds

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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.