Evidence map›Paper›PMID 39630889›Full record

ArticleScience advances2024

Renal Angptl4 is a key fibrogenic molecule in progressive diabetic kidney disease.

Swayam Prakash Srivastava, Han Zhou, Rachel Shenoi, Myshal Morris, Begoña Lainez-Mas, Leigh Goedeke, Barani Kumar Rajendran, Ocean Setia, Binod Aryal, Keizo Kanasaki and 7 more

Abstract read
In one paragraph

Article in Science advances, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing 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

30 citing papers in PubMed.

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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

17 authors.

Swayam Prakash SrivastavaDepartment of Pediatrics, Yale University School of Medicine, New Haven, CT, USA.ORCID 0000-0002-7162-3091
Han ZhouDepartment of Pediatrics, Yale University School of Medicine, New Haven, CT, USA.
Rachel ShenoiDepartment of Pediatrics, Yale University School of Medicine, New Haven, CT, USA.
Myshal MorrisDepartment of Pediatrics, Yale University School of Medicine, New Haven, CT, USA.ORCID 0009-0008-7179-1985
Begoña Lainez-MasDepartment of Pediatrics, Yale University School of Medicine, New Haven, CT, USA.ORCID 0000-0003-3991-3512
Leigh GoedekeDepartment of Medicine, Yale University School of Medicine, New Haven, CT, USA.ORCID 0000-0002-7690-1572
Barani Kumar RajendranDepartment of Pharmacology, Yale University School of Medicine, New Haven, CT, USA.ORCID 0000-0001-9675-7718
Ocean SetiaDepartment of Surgery, Yale University School of Medicine, New Haven, CT, USA.
Binod AryalVascular Biology and Therapeutics Program, Yale University, New Haven, CT, USA.
Keizo KanasakiDepartment of Diabetology and Endocrinology, Kanazawa Medical University, Uchinada, Japan.
Daisuke KoyaDepartment of Diabetology and Endocrinology, Kanazawa Medical University, Uchinada, Japan.
Ken InokiLife Sciences Institute, University of Michigan, Ann Arbor, MI, USA.ORCID 0000-0001-8882-444X
Alan DardikVascular Biology and Therapeutics Program, Yale University, New Haven, CT, USA.ORCID 0000-0001-5022-7367
Thomas BellIonis Pharmaceuticals, Carlsbad, CA, USA.
Carlos Fernández-HernandoVascular Biology and Therapeutics Program, Yale University, New Haven, CT, USA.
Gerald I ShulmanDepartment of Medicine, Yale University School of Medicine, New Haven, CT, USA.ORCID 0000-0003-1529-5668
Julie E GoodwinDepartment of Pediatrics, Yale University School of Medicine, New Haven, CT, USA.ORCID 0000-0002-8986-8695

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
Yale Diabetes Research CenterP30DK045735 · NIDDK · YALE UNIVERSITY · PI GERALD I SHULMAN · 1993 to 2026
$44.0M
Regional Pilot And Feasibility Study Grants ProgramP30DK020572 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI DAVID P OLSON · 2013 to 2026
$24.3M
In vivo Pathway Discovery in Autosomal Dominant Polycystic Kidney DiseaseRC2DK120534 · NIDDK · YALE UNIVERSITY · PI CAPLAN, MICHAEL J., SHULMAN, GERALD I · 2019 to 2023
$6.6M
Novel insights into the molecular and cellular mechanism regulating lipid metabolism and atherosclerosisR35HL135820 · NHLBI · YALE UNIVERSITY · PI FERNANDEZ HERNANDO, CARLOS · 2017 to 2023
$6.0M
Manipulating the matrix to improve arteriovenous fistula patencyR01HL144476 · NHLBI · YALE UNIVERSITY · PI Alan Dardik · 2019 to 2026
$5.6M
Endothelial glucocorticoid receptor suppresses vascular inflammationR01HL131952 · NHLBI · YALE UNIVERSITY · PI GOODWIN, JULIE · 2016 to 2025
$4.9M
Yale Center for Metabolic Phenotyping in Live Models of Obesity and DiabetesU2CDK134901 · NIDDK · YALE UNIVERSITY · PI GERALD I SHULMAN · 2023 to 2026
$3.8M
Adaptive immunity regulates arteriovenous fistula remodelingR01HL162580 · NHLBI · YALE UNIVERSITY · PI Alan Dardik · 2023 to 2026
$3.0M
Mechanism of Renal Cortical Insulin ResistanceR01DK133143 · NIDDK · YALE UNIVERSITY · PI SHULMAN, GERALD I · 2022 to 2025
$2.3M
Lysosomal cholesterol-dependent anabolic regulationR01DK124709 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI INOKI, KEN · 2022 to 2025
$2.1M
Molecular mechanism of Rheb-dependent mTORC1 regulationR01GM145631 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI INOKI, KEN · 2022 to 2025
$1.8M
NCATS NIH HHS UL1 TR001863NHLBI NIH HHS R01 HL131952NHLBI NIH HHS R01 HL144476NHLBI NIH HHS R01 HL162580NHLBI NIH HHS R35 HL135820NIDDK NIH HHS P30 DK020572NIDDK NIH HHS P30 DK045735NIDDK NIH HHS R01 DK124709NIDDK NIH HHS R01 DK133143NIDDK NIH HHS RC2 DK120534NIDDK NIH HHS U2C DK134901NIGMS NIH HHS R01 GM145631
6 · The paper itself

Abstract

Angiopoietin-like 4 (ANGPTL4), a key protein involved in lipoprotein metabolism, has diverse effects. There is an association between Angptl4 and diabetic kidney disease; however, this association has not been well investigated. We show that both podocyte- and tubule-specific ANGPTL4 are crucial fibrogenic molecules in diabetes. Diabetes accelerates the fibrogenic phenotype in control mice but not in ANGPTL4 mutant mice. The protective effect observed in ANGPTL4 mutant mice is correlated with a reduction in stimulator of interferon genes pathway activation, expression of pro-inflammatory cytokines, reduced epithelial-to-mesenchymal transition and endothelial-to-mesenchymal transition, lessened mitochondrial damage, and increased fatty acid oxidation. Mechanistically, we demonstrate that podocyte- or tubule-secreted

Indexed as

Angiopoietin-Like Protein 4Diabetic NephropathiesFibrosisPodocytesAnimalsDiabetes Mellitus, ExperimentalDisease Models, AnimalEpithelial-Mesenchymal TransitionHumansIntegrin beta1KidneyMiceAngiopoietin-Like Protein 4ANGPTL4 protein, humanAngptl4 protein, mouseIntegrin beta1

Identifiers

PMID39630889
PMCPMC11616692

What OpenQuestion holds

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Registered trials

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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.