Evidence map›Paper›PMID 35381220›Full record

ArticleLife sciences2022

Diabetic bladder dysfunction progresses from an overactive to an underactive phenotype in a type-1 diabetic mouse model (Akita female mouse) and is dependent on NLRP3.

Francis M Hughes, Armand Allkanjari, Michael R Odom, Huixia Jin, J Todd Purves

Open access · greenAbstract read
In one paragraph

Article in Life sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

17 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
  2. Therapeutic Potential of Mitochondrial Transplantation with Focus on DBD.International journal of molecular sciences · 2026
    Review
  3. Article
  4. Article
  5. Mitochondrial damage causes inflammation via cGAS-STING signaling in ketamine-induced cystitis.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2025
    Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Review
  12. Article
  13. Association of detrusor underactivity with aging and metabolic syndrome: suggestions from animal models.Journal of smooth muscle research = Nihon Heikatsukin Gakkai kikanshi · 2024
    Review
  14. Article
  15. Article
  16. Article
  17. 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

5 authors at 1 institution in 1 country.

Francis M HughesDivision of Urology, Department of Surgery, Duke University Medical Center, Durham, NC, United States of America. Electronic address: monty.hughes@duke.edu.
Armand AllkanjariDivision of Urology, Department of Surgery, Duke University Medical Center, Durham, NC, United States of America.
Michael R OdomDivision of Urology, Department of Surgery, Duke University Medical Center, Durham, NC, United States of America.
Huixia JinDivision of Urology, Department of Surgery, Duke University Medical Center, Durham, NC, United States of America.
J Todd PurvesDivision of Urology, Department of Surgery, Duke University Medical Center, Durham, NC, United States of America.
Duke Medical Center · US

Funding

Duke KURe ProgramK12DK100024 · NIDDK · DUKE UNIVERSITY · PI Cindy Amundsen · 2013 to 2026
$8.4M
Inflammation and neuropathy drive sex-specific diabetic bladder dysfunction in Akita miceR01DK117890 · NIDDK · DUKE UNIVERSITY · PI J. Todd Purves · 2019 to 2026
$2.5M
NIDDK NIH HHS K12 DK100024NIDDK NIH HHS R01 DK117890
6 · The paper itself

Abstract

aimsDiabetic bladder dysfunction (DBD) is a prevalent diabetic complication thought to progress from overactive (OAB) to underactive (UAB) bladder. Previously we found OAB at 15 weeks in the Akita mouse, a genetic model of Type 1 diabetes. The first aim of this study assesses bladder function at 30 weeks to assess progression. In addition, inflammation triggered by the NLRP3 inflammasome is implicated in DBD. In a second aim we assessed a role for NLRP3 by crossing Akita mice with NLRP3 MAIN

methodsAkita mice were bred with NLRP3 KEY

findingsAt 30 weeks blood glucose of nondiabetics and diabetics was not affected by the presence of absence of NLRP3. Diabetic/NLRP3 SIGNIFICANCE: Akita diabetic mice progress from OAB to UAB. NLRP3 is a possible target to treat DBD.

Indexed as

Diabetes Mellitus, ExperimentalDiabetes Mellitus, Type 1Urinary Bladder, OveractiveAnimalsBlood GlucoseDisease Models, AnimalFemaleHumansInflammasomesInflammationMiceNLR Family, Pyrin Domain-Containing 3 ProteinPhenotypeUrinary BladderBlood GlucoseInflammasomesNLR Family, Pyrin Domain-Containing 3 ProteinNlrp3 protein, mouseBladderComplicationsCystitisDiabetesImmunityUrodynamics

Identifiers

PMID35381220
PMCPMC9112812
OpenAlexW4223925037

What OpenQuestion holds

Textmetadata
LicenceTDM
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.