Evidence map›Paper›PMID 31217358›Full record

ArticleJCI insight2019

Development of a 2-dimensional atlas of the human kidney with imaging mass cytometry.

Nikhil Singh, Zachary M Avigan, Judith A Kliegel, Brian M Shuch, Ruth R Montgomery, Gilbert W Moeckel, Lloyd G Cantley

Open access · goldAbstract readValidation Study
In one paragraph

Article in JCI insight, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
2.8field-weighted citation impact, top 8% 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

33 citing papers in PubMed, 50 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. IDOTransplantation direct · 2024
    Article
  9. Article
  10. Precision Medicine in Nephrology: An Integrative Framework of Multidimensional Data in the Kidney Precision Medicine Project.American journal of kidney diseases : the official journal of the National Kidney Foundation · 2024
    Article
  11. Review
  12. Review
  13. Review
  14. Article
  15. Review
  16. Article
  17. Article
  18. FTO-mediated mClinical and translational medicine · 2022
    Article
  19. Cellular and molecular interrogation of kidney biopsy specimens.Current opinion in nephrology and hypertension · 2022
    Review
  20. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 2 institutions in 1 country.

Nikhil SinghSection of Nephrology, Department of Internal Medicine.
Zachary M AviganSection of Nephrology, Department of Internal Medicine.
Judith A KliegelSection of Nephrology, Department of Internal Medicine.
Brian M ShuchDepartment of Urology.
Ruth R MontgomerySection of Rheumatology, Department of Internal Medicine, and.
Gilbert W MoeckelDepartment of Pathology, Yale University School of Medicine, New Haven, Connecticut, USA.
Lloyd G CantleySection of Nephrology, Department of Internal Medicine.
Center for Rheumatology · USYale University · US

Funding

Yale Clinical and Translational Science Award (U Component)UL1TR001863 · NCATS · YALE UNIVERSITY · PI John H. Krystal, LUCILA OHNO-MACHADO · 2016 to 2026
$102.9M
Renal Physiology and Phenotyping CoreP30DK079310 · NIDDK · YALE UNIVERSITY · PI PARIKH, CHIRAG R · 2008 to 2022
$16.8M
PATHOPHYSIOLOGY OF ACUTE AND CHRONIC RENAL DISEASET32DK007276 · NIDDK · YALE UNIVERSITY · PI ARONSON, PETER S., CANTLEY, LLOYD G · 1986 to 2022
$9.3M
Genomic Heterogeneity and the Small Renal MassK08CA207845 · NCI · YALE UNIVERSITY · PI SHUCH, BRIAN · 2016 to 2019
$682k
NCATS NIH HHS UL1 TR001863NCI NIH HHS K08 CA207845NIDDK NIH HHS P30 DK079310NIDDK NIH HHS T32 DK007276
6 · The paper itself

Abstract

An incomplete understanding of the biology of the human kidney, including the relative abundances of and interactions between intrinsic and immune cells, has long constrained the development of therapies for kidney disease. The small amount of tissue obtained by renal biopsy has previously limited the ability to use patient samples for discovery purposes. Imaging mass cytometry (IMC) is an ideal technology for quantitative interrogation of scarce samples, permitting concurrent analysis of more than 40 markers on a single tissue section. Using a validated panel of metal-conjugated antibodies designed to confer unique signatures on the structural and infiltrating cells comprising the human kidney, we performed simultaneous multiplexed imaging with IMC in 23 channels on 16 histopathologically normal human samples. We devised a machine-learning pipeline (Kidney-MAPPS) to perform single-cell segmentation, phenotyping, and quantification, thus creating a spatially preserved quantitative atlas of the normal human kidney. These data define selected baseline renal cell types, respective numbers, organization, and variability. We demonstrate the utility of IMC coupled to Kidney-MAPPS to qualitatively and quantitatively distinguish individual cell types and reveal expected as well as potentially novel abnormalities in diseased versus normal tissue. Our studies define a critical baseline data set for future quantitative analysis of human kidney disease.

Indexed as

Atlases as TopicModels, AnatomicAdultAgedAntibodiesFemaleHumansImage CytometryKidneyKidney NeoplasmsMachine LearningMaleMiddle AgedReproducibility of ResultsAntibodiesCellular immune responseChronic kidney diseaseNephrology

Identifiers

PMID31217358
PMCPMC6629112
OpenAlexW2949884735

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.