Evidence map›Paper›PMID 39562547›Full record

ArticleNature communications2024

Profiling of insulin-resistant kidney models and human biopsies reveals common and cell-type-specific mechanisms underpinning Diabetic Kidney Disease.

Abigail C Lay, Van Du T Tran, Viji Nair, Virginie Betin, Jennifer A Hurcombe, Alexandra F Barrington, Robert Jp Pope, Frédéric Burdet, Florence Mehl, Dmytro Kryvokhyzha and 16 more

Abstract read
In one paragraph

Article in Nature communications, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing 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

21 citing papers in PubMed.

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  15. Article
  16. Review
  17. The Life of a Kidney Podocyte.Acta physiologica (Oxford, England) · 2025
    Review
  18. Review
  19. Article
  20. 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

26 authors.

Abigail C LayBristol Renal, Bristol Medical School, University of Bristol, Bristol, UK.ORCID 0000-0001-5923-634X
Van Du T TranVital-IT group, SIB Swiss Institute of Bioinformatics, Lausanne, Switzerland.ORCID 0000-0003-2074-5029
Viji NairDivision of Nephrology, Department of Internal Medicine, University of Michigan, Ann Arbor, MI, USA.
Virginie BetinBristol Renal, Bristol Medical School, University of Bristol, Bristol, UK.
Jennifer A HurcombeBristol Renal, Bristol Medical School, University of Bristol, Bristol, UK.
Alexandra F BarringtonBristol Renal, Bristol Medical School, University of Bristol, Bristol, UK.
Robert Jp PopeBristol Renal, Bristol Medical School, University of Bristol, Bristol, UK.
Frédéric BurdetVital-IT group, SIB Swiss Institute of Bioinformatics, Lausanne, Switzerland.ORCID 0000-0002-2923-827X
Florence MehlVital-IT group, SIB Swiss Institute of Bioinformatics, Lausanne, Switzerland.ORCID 0000-0002-9619-1707
Dmytro KryvokhyzhaDepartment of Clinical Sciences, Lund University Diabetes Centre, Lund University, Malmö, Sweden.ORCID 0000-0001-6498-1977
Abrar AhmadDepartment of Clinical Sciences, Lund University Diabetes Centre, Lund University, Malmö, Sweden.ORCID 0000-0002-6308-952X
Matthew C SintonDivision of Cardiovascular Sciences, Faculty of Biology, Medicine and Health, University of Manchester, Manchester, UK.ORCID 0000-0003-1292-799X
Philip LewisProteomics Facility, University of Bristol, Bristol, UK.
Marieangela C WilsonProteomics Facility, University of Bristol, Bristol, UK.ORCID 0000-0001-6218-3533
Rajasree MenonDivision of Nephrology, Department of Internal Medicine, University of Michigan, Ann Arbor, MI, USA.ORCID 0000-0001-6280-9639
Edgar OttoDivision of Nephrology, Department of Internal Medicine, University of Michigan, Ann Arbor, MI, USA.ORCID 0000-0002-2387-9973
Kate J HeesomProteomics Facility, University of Bristol, Bristol, UK.ORCID 0000-0002-5418-5392
Mark IbbersonVital-IT group, SIB Swiss Institute of Bioinformatics, Lausanne, Switzerland.ORCID 0000-0003-3152-5670
Helen C LookerChronic Kidney Disease Section, National Institute of Diabetes and Digestive and Kidney Diseases, National Institute of Health, Phoenix, AZ, USA.
Robert G NelsonChronic Kidney Disease Section, National Institute of Diabetes and Digestive and Kidney Diseases, National Institute of Health, Phoenix, AZ, USA.
Wenjun JuDivision of Nephrology, Department of Internal Medicine, University of Michigan, Ann Arbor, MI, USA.ORCID 0000-0002-9136-8454
Matthias KretzlerDivision of Nephrology, Department of Internal Medicine, University of Michigan, Ann Arbor, MI, USA.
Simon C SatchellBristol Renal, Bristol Medical School, University of Bristol, Bristol, UK.ORCID 0000-0001-5276-4537
Maria F GomezDepartment of Clinical Sciences, Lund University Diabetes Centre, Lund University, Malmö, Sweden.ORCID 0000-0001-6210-3142
Richard J M CowardBristol Renal, Bristol Medical School, University of Bristol, Bristol, UK. Richard.Coward@bristol.ac.uk.ORCID 0000-0001-6183-2546
BEAt-DKD consortium

Funding

Regional Pilot And Feasibility Study Grants ProgramP30DK020572 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI DAVID P OLSON · 2013 to 2026
$24.3M
Central Hub for Kidney Precision MedicineU24DK114886 · NIDDK · UNIVERSITY OF WASHINGTON · PI Jonathan Himmelfarb, Matthias Kretzler · 2022 to 2026
$21.1M
ConProject-002U2CDK114886 · NIDDK · UNIVERSITY OF WASHINGTON · PI KRETZLER, MATTHIAS · 2017 to 2021
$21.0M
University of Michigan O'Brien Kidney Translational Core CenterP30DK081943 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI PENNATHUR, SUBRAMANIAM · 2008 to 2022
$12.9M
KPMP Kidney Mapping and Atlas Project (KMAP)U01DK133090 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Jonathan Himmelfarb, Matthias Kretzler · 2022 to 2026
$10.4M
Integrated spatial interrogation of cellular and molecular signatures of human kidney diseaseU01DK114923 · NIDDK · INDIANA UNIVERSITY INDIANAPOLIS · PI Tarek Maurice Ashkar, Pierre C Dagher · 2022 to 2026
$5.4M
Single cell multiomic and spatial atlas of acute and chronic kidney injuryU01DK114933 · NIDDK · WASHINGTON UNIVERSITY · PI Sanjay Jain · 2022 to 2026
$5.0M
Spatial Multi-Omics to Profile Metabolic Pathways for Kidney DiseaseU01DK114920 · NIDDK · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI Christopher R Anderton, Kumar Sharma · 2022 to 2026
$3.9M
Boston Chronic Kidney Disease Research Biopsy CenterU01DK133092 · NIDDK · BOSTON MEDICAL CENTER · PI Sylvia E Rosas, Sushrut S. Waikar · 2022 to 2026
$3.5M
Multimodal Imaging Mass Spectrometry and Spatial Omics for the Human KidneyU01DK133766 · NIDDK · VANDERBILT UNIVERSITY · PI Jeffrey M Spraggins · 2022 to 2026
$3.4M
PREcision Medicine through IntErrogation of Rna in the kidnEy (PREMIERE)U01DK114907 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Nir Hacohen, Jeffrey Benton Hodgin · 2022 to 2026
$3.2M
Spatial Metabolomics for Human KidneysUH3DK114920 · NIDDK · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI SHARMA, KUMAR · 2019 to 2021
$2.7M
EC | Horizon 2020 Framework Programme (EU Framework Programme for Research and Innovation H2020) BEAt DKD 115974Kidney Research UK INT_002_20220705NIDDK NIH HHS P30 DK020572NIDDK NIH HHS P30 DK081943NIDDK NIH HHS U01 DK114866NIDDK NIH HHS U01 DK114907NIDDK NIH HHS U01 DK114908NIDDK NIH HHS U01 DK114920NIDDK NIH HHS U01 DK114923NIDDK NIH HHS U01 DK114933NIDDK NIH HHS U01 DK133081NIDDK NIH HHS U01 DK133090NIDDK NIH HHS U01 DK133091NIDDK NIH HHS U01 DK133092NIDDK NIH HHS U01 DK133093NIDDK NIH HHS U01 DK133095NIDDK NIH HHS U01 DK133097NIDDK NIH HHS U01 DK133113NIDDK NIH HHS U01 DK133766NIDDK NIH HHS U01 DK133768NIDDK NIH HHS U24 DK114886NIDDK NIH HHS U2C DK114886NIDDK NIH HHS UH3 DK114861NIDDK NIH HHS UH3 DK114866NIDDK NIH HHS UH3 DK114870NIDDK NIH HHS UH3 DK114907NIDDK NIH HHS UH3 DK114908NIDDK NIH HHS UH3 DK114915NIDDK NIH HHS UH3 DK114920NIDDK NIH HHS UH3 DK114923NIDDK NIH HHS UH3 DK114926NIDDK NIH HHS UH3 DK114933NIDDK NIH HHS UH3 DK114937RCUK | Medical Research Council (MRC) MR/K010492/1RCUK | Medical Research Council (MRC) MR/T002263/1RCUK | Medical Research Council (MRC) MR/W019582/1
6 · The paper itself

Abstract

Diabetic kidney disease (DKD) is the leading cause of end stage kidney failure worldwide, of which cellular insulin resistance is a major driver. Here, we study key human kidney cell types implicated in DKD (podocytes, glomerular endothelial, mesangial and proximal tubular cells) in insulin sensitive and resistant conditions, and perform simultaneous transcriptomics and proteomics for integrated analysis. Our data is further compared with bulk- and single-cell transcriptomic kidney biopsy data from early- and advanced-stage DKD patient cohorts. We identify several consistent changes (individual genes, proteins, and molecular pathways) occurring across all insulin-resistant kidney cell types, together with cell-line-specific changes occurring in response to insulin resistance, which are replicated in DKD biopsies. This study provides a rich data resource to direct future studies in elucidating underlying kidney signalling pathways and potential therapeutic targets in DKD.

Indexed as

Diabetic NephropathiesInsulin ResistanceKidneyBiopsyGene Expression ProfilingHumansProteomicsSignal TransductionTranscriptome

Identifiers

PMID39562547
PMCPMC11576882

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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.