Evidence map›Paper›PMID 30256126›Full record

ArticleAmerican journal of physiology. Renal physiology2018

Automatic glomerular identification and quantification of histological phenotypes using image analysis and machine learning.

Susan M Sheehan, Ron Korstanje

Abstract read
In one paragraph

Article in American journal of physiology. Renal physiology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing 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

15 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Review
  8. Review
  9. Quantification of Glomerular Structural Lesions: Associations With Clinical Outcomes and Transcriptomic Profiles in Nephrotic Syndrome.American journal of kidney diseases : the official journal of the National Kidney Foundation · 2022
    Observational
  10. Review
  11. Deep learning segmentation of glomeruli on kidney donor frozen sections.Journal of medical imaging (Bellingham, Wash.) · 2021
    Article
  12. Article
  13. Article
  14. Revisiting Experimental Models of Diabetic Nephropathy.International journal of molecular sciences · 2020
    Review
  15. 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

2 authors.

Susan M SheehanThe Jackson Laboratory , Bar Harbor, Maine.
Ron KorstanjeThe Jackson Laboratory , Bar Harbor, Maine.ORCID 0000-0002-2808-1610

Funding

The Jackson Laboratory Center for Precision Genetics: From New Models to Novel TherapeuticsU54OD020351 · OD · JACKSON LABORATORY · PI LUTZ, CATHLEEN M · 2015 to 2019
$10.2M
Integrative Biology of Childhood Kidney DiseaseP50DK079306 · NIDDK · MEDICAL COLLEGE OF WISCONSIN · PI AVNER, ELLIS DAVID · 2007 to 2011
$5.1M
Genome-wide fine-mapping of metabolic traits in heterogeneous stock ratsR01DK088975 · NIDDK · MEDICAL COLLEGE OF WISCONSIN · PI SOLBERG WOODS, LEAH CATHERINE · 2010 to 2014
$1.9M
Biotechnology and Biological Sciences Research CouncilNIDDK NIH HHS P50 DK079306NIDDK NIH HHS R01 DK088975NIH HHS U54 OD020351
6 · The paper itself

Abstract

Current methods of scoring histological kidney samples, specifically glomeruli, do not allow for collection of quantitative data in a high-throughput and consistent manner. Neither untrained individuals nor computers are presently capable of identifying glomerular features, so expert pathologists must do the identification and score using a categorical matrix, complicating statistical analysis. Critical information regarding overall health and physiology is encoded in these samples. Rapid comprehensive histological scoring could be used, in combination with other physiological measures, to significantly advance renal research. Therefore, we used machine learning to develop a high-throughput method to automatically identify and collect quantitative data from glomeruli. Our method requires minimal human interaction between steps and provides quantifiable data independent of user bias. The method uses free existing software and is usable without extensive image analysis training. Validation of the classifier and feature scores in mice is highlighted in this work and shows the power of applying this method in murine research. Preliminary results indicate that the method can be applied to data sets from different species after training on relevant data, allowing for fast glomerular identification and quantitative measurements of glomerular features. Validation of the classifier and feature scores are highlighted in this work and show the power of applying this method. The resulting data are free from user bias. Continuous data, such that statistical analysis can be performed, allows for more precise and comprehensive interrogation of samples. These data can then be combined with other physiological data to broaden our overall understanding of renal function.

Indexed as

Machine LearningAnimalsAutomation, LaboratoryBiopsyDiagnosis, Computer-AssistedDisease Models, AnimalFemaleHumansImage Interpretation, Computer-AssistedKidney DiseasesKidney GlomerulusMaleMice, Inbred C57BLMice, TransgenicMicroscopyPattern Recognition, Automateddigital pathologyhistologymachine learning

Identifiers

PMID30256126
PMCPMC6336999

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.