Evidence map›Paper›PMID 35368578›Full record

ArticleKidney3602022

Shroom3, a Gene Associated with CKD, Modulates Epithelial Recovery after AKI.

Aihua Li, Joanna Cunanan, Hadiseh Khalili, Timothy Plageman, Kjetil Ask, Ahsan Khan, Ashmeet Hunjan, Thomas Drysdale, Darren Bridgewater

Open access · diamondAbstract read
In one paragraph

Article in Kidney360, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
0.5field-weighted citation impact, top 37% 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

10 citing papers in PubMed, 1 synthesis or guideline pooled it, 11 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Mapping Shroom3 expression across the adult mouse.Gene expression patterns : GEP · 2025
    Article
  4. Cells · 2025
    Article
  5. Focus on a CKD-Associated Locus:Kidney international reports · 2025
    Article
  6. Review
  7. Article
  8. Review
  9. Review
  10. 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

9 authors at 3 institutions in 2 countries.

Aihua LiDepartment of Pathology and Molecular Medicine, McMaster University, Hamilton, Canada.
Joanna CunananDepartment of Pathology and Molecular Medicine, McMaster University, Hamilton, Canada.ORCID 0000-0001-9587-4533
Hadiseh KhaliliDepartment of Pathology and Molecular Medicine, McMaster University, Hamilton, Canada.
Timothy PlagemanCollege of Optometry, The Ohio State University, Columbus, Ohio.ORCID 0000-0001-6565-2577
Kjetil AskDepartment of Medicine, McMaster University, Hamilton, Canada.ORCID 0000-0002-0202-735X
Ahsan KhanDepartment of Pathology and Molecular Medicine, McMaster University, Hamilton, Canada.
Ashmeet HunjanDepartment of Pathology and Molecular Medicine, McMaster University, Hamilton, Canada.
Thomas DrysdaleDepartment of Physiology and Pharmacology, University of Western Ontario, London, Canada.
Darren BridgewaterDepartment of Pathology and Molecular Medicine, McMaster University, Hamilton, Canada.ORCID 0000-0002-8409-1020
McMaster University · CAThe Ohio State University · USWestern University · CA

Funding

Characterizing the fundamental mechanisms of epithelial invagination during ocular morphogenesisR01EY026910 · NEI · OHIO STATE UNIVERSITY · PI PLAGEMAN, TIMOTHY F · 2016 to 2020
$1.9M
NEI NIH HHS R01 EY026910
6 · The paper itself

Abstract

Background: Ischemia-induced AKI resulting in tubular damage can often progress to CKD and is a common cause of nephrology consultation. After renal tubular epithelial damage, molecular and cellular mechanisms are activated to repair and regenerate the damaged epithelium. If these mechanisms are impaired, AKI can progress to CKD. Even in patients whose kidney function returns to normal baseline are more likely to develop CKD. Genome-wide association studies have provided robust evidence that genetic variants in Shroom3, which encodes an actin-associated protein, are associated with CKD and poor outcomes in transplanted kidneys. Here, we sought to further understand the associations of Shroom3 in CKD. Methods: Kidney ischemia was induced in wild-type (WT) and Results: A 28-minute bilateral ischemia in Conclusion: These findings establish that Shroom3 is required for epithelial repair and redifferentiation through the organization of actomyosin regulators, and could explain why genetic variants in Shroom3 are associated with CKD and allograft rejection.

Indexed as

Acute Kidney InjuryRenal Insufficiency, ChronicAnimalsFibrosisGenome-Wide Association StudyHumansKidneyMiceMicrofilament ProteinsMicrofilament ProteinsShrm protein, mouseSHROOM3 protein, humanacute kidney injurychronic kidney diseaserenal tubular epithelial cellsShroom3

Identifiers

PMID35368578
PMCPMC8967620
OpenAlexW3210070651

What OpenQuestion holds

Textmetadata
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.