Evidence map›Paper›PMID 38891023›Full record

ReviewCells2024

Normal and Dysregulated Sphingolipid Metabolism: Contributions to Podocyte Injury and Beyond.

Matthew Tolerico, Sandra Merscher, Alessia Fornoni

Abstract readReview
In one paragraph

Review in Cells, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Trial
  2. Review
  3. Review
  4. Review
  5. The Life of a Kidney Podocyte.Acta physiologica (Oxford, England) · 2025
    Review
  6. Article
  7. Inflammation in glomerular diseases.Frontiers in immunology · 2025
    Review
  8. Review
  9. Review
  10. Sphingolipids and Chronic Kidney Disease.Journal of clinical medicine · 2024
    Review
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

3 authors.

Matthew TolericoPeggy and Harold Katz Family Drug Discovery Center, Miller School of Medicine, University of Miami, Miami, FL 33136, USA.
Sandra MerscherPeggy and Harold Katz Family Drug Discovery Center, Miller School of Medicine, University of Miami, Miami, FL 33136, USA.ORCID 0000-0002-4757-7494
Alessia FornoniPeggy and Harold Katz Family Drug Discovery Center, Miller School of Medicine, University of Miami, Miami, FL 33136, USA.

Funding

Training Program in Clinical & Translationa Research in Human Glomerular DiseaseU54DK083912 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI KRETZLER, MATTHIAS · 2009 to 2023
$20.3M
Miami Clinical and Translational Science InstituteUM1TR004556 · NCATS · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI Olveen Carrasquillo, ERIN N KOBETZ · 2023 to 2026
$16.0M
CureGNU24DK100845 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI CRYSTAL A. GADEGBEKU, Laura H Mariani · 2019 to 2026
$12.1M
1/13 ApoL1 Genotypes in Kidney Donors and Long-Term Outcomes in Kidney Transplant Recipients Clinical CenterU01DK116101 · NIDDK · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI ALESSIA FORNONI, Mariella Cecilia Ortigosa-goggins · 2017 to 2026
$2.4M
APOM deficiency contributes to renal failure in glomerular diseasesR01DK136679 · NIDDK · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI ALESSIA FORNONI · 2023 to 2026
$1.9M
Workshops and Coaching to Foster Career Skills in Newly Funded NIDDK ScholarsUE5DK137308 · NIDDK · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI Ashutosh Agarwal, ALESSIA FORNONI · 2023 to 2026
$648k
The contribution of the APOM/S1P signaling axis to podocyte injuryF31DK137425 · NIDDK · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI Matthew Robert Tolerico · 2024 to 2026
$126k
Crosstalk between lipid droplets and other organelles in podocytesR56DK104753 · NIDDK · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI FORNONI, ALESSIA · 2023 to 2023
$100k
Department of Defense HT9425-23-1-0054NCATS NIH HHS UM1 TR004556NIDDK NIH HHS F31 DK137425NIDDK NIH HHS R01 DK136679NIDDK NIH HHS R56 DK104753NIDDK NIH HHS U01 DK116101NIDDK NIH HHS U24 DK100845NIDDK NIH HHS U54 DK083912NIDDK NIH HHS UE5 DK137308NIH HHS 1R01DK136679-27A1NIH HHS 1UE5DK137308-28A1NIH HHS 1UM1DK004556-24A1NIH HHS 1UM1TR004556-24A1NIH HHS 2R56DK104753-24A9NIH HHS 2U01DK116101-28A6NIH HHS 3U24DK100845-24S1NIH HHS 5U54DK083912-24A15
6 · The paper itself

Abstract

Podocyte health is vital for maintaining proper glomerular filtration in the kidney. Interdigitating foot processes from podocytes form slit diaphragms which regulate the filtration of molecules through size and charge selectivity. The abundance of lipid rafts, which are ordered membrane domains rich in cholesterol and sphingolipids, near the slit diaphragm highlights the importance of lipid metabolism in podocyte health. Emerging research shows the importance of sphingolipid metabolism to podocyte health through structural and signaling roles. Dysregulation in sphingolipid metabolism has been shown to cause podocyte injury and drive glomerular disease progression. In this review, we discuss the structure and metabolism of sphingolipids, as well as their role in proper podocyte function and how alterations in sphingolipid metabolism contributes to podocyte injury and drives glomerular disease progression.

Indexed as

PodocytesSphingolipidsAnimalsHumansKidney DiseasesLipid MetabolismMembrane MicrodomainsSphingolipidsceramidecerebrosidegangliosideglomerular diseaselipid raftspodocytepodocytopathiessphingolipidsphingosine-1-phosphate

Identifiers

PMID38891023
PMCPMC11171506

What OpenQuestion holds

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LicenceCC BY
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.