Evidence map›Paper›PMID 31580528›Full record

ArticleJournal of diabetes investigation2020

Analysis of urinary sphingolipids using liquid chromatography-tandem mass spectrometry in diabetic nephropathy.

Yoshifumi Morita, Makoto Kurano, Eri Sakai, Takako Nishikawa, Masako Nishikawa, Motoji Sawabe, Junken Aoki, Yutaka Yatomi

Open access · goldAbstract read
In one paragraph

Article in Journal of diabetes investigation, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

27 citing papers in PubMed, 35 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Sphingolipid signaling in kidney diseases.American journal of physiology. Renal physiology · 2025
    Review
  6. Article
  7. Article
  8. Article
  9. Sphingolipids and Chronic Kidney Disease.Journal of clinical medicine · 2024
    Review
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Implications of Sphingolipid Metabolites in Kidney Diseases.International journal of molecular sciences · 2022
    Review
  18. Review
  19. Article
  20. 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

8 authors at 3 institutions in 1 country.

Yoshifumi MoritaDepartment of Clinical Laboratory, The University of Tokyo Hospital, Tokyo, Japan.
Makoto KuranoDepartment of Clinical Laboratory, The University of Tokyo Hospital, Tokyo, Japan.ORCID https://orcid.org/0000-0002-2596-1145
Eri SakaiDepartment of Clinical Laboratory, The University of Tokyo Hospital, Tokyo, Japan.
Takako NishikawaDepartment of Clinical Laboratory, The University of Tokyo Hospital, Tokyo, Japan.
Masako NishikawaDepartment of Clinical Laboratory, The University of Tokyo Hospital, Tokyo, Japan.
Motoji SawabeDepartment of Molecular Pathology, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University, Tokyo, Japan.
Junken AokiLaboratory of Molecular and Cellular Biochemistry, Graduate School of Pharmaceutical Sciences, Tohoku University, Miyagi, Japan.
Yutaka YatomiDepartment of Clinical Laboratory, The University of Tokyo Hospital, Tokyo, Japan.
University of Tokyo Hospital · JPTokyo Medical and Dental University · JPTohoku University · JP

Funding

Grant-in-Aid for Scientific Research on Innovative Areas 15H05906Japan Agency for Medical Research and Development Leading Advanced Projects for medical innovation (Japan Society for the Promotion of Science a Grant-in-Aid for Scientific Research on InnovatiJapan Society for the Promotion of Science JSPS KAKENHI Grant Number 16H06236JSPS KAKENHI 16H06236Leading Advanced Projects for Medical Innovation (LEAP)the Charitable Trust Laboratory Medicine Research Foundation of Japan N/A
6 · The paper itself

Abstract

AIMS/

introductionSphingolipids, such as ceramides and sphingosine, are involved in the pathogenesis of diabetes; however, the modulation of urinary sphingolipids in diabetic nephropathy has not been fully elucidated. Therefore, we aimed to develop a simultaneous measurement system for urinary sphingolipids using liquid chromatography-tandem mass spectrometry and to elucidate the modulation of urinary sphingolipids in diabetic nephropathy. MATERIALS AND

methodsWe established a simultaneous measurement system for the urinary sphingosine, dihydrosphingosine, and six ceramide species (Cer d18:1/16:0, Cer d18:1/18:0, Cer d18:1/18:1, Cer d18:1/20:0, Cer d18:1/22:0 and Cer d18:1/24:0), and we examined the urinary sphingolipids in 64 type 2 diabetes patients and 15 control participants.

resultsThe established measurement system for the urinary sphingolipids showed good precision for Cer d18:1/16:0, Cer d18:1/20:0, Cer d18:1/22:0 and Cer d18:1/24:0. We observed that the urinary levels of Cer d18:1/16:0, Cer d18:1/18:0, Cer d18:1/20:0, Cer d18:1/22:0 and Cer d18:1/24:0 were elevated in patients with stage 3 of diabetic nephropathy, and were correlated with urinary biomarkers, such as albumin and N-acetyl-β-d-glucosaminidase, and sediment score.

conclusionsOur method is useful for the measurement of ceramide in urine specimens, and urinary ceramides might be associated with the pathological condition of diabetic nephropathy, such as renal tubular injury.

Indexed as

AgedBiomarkersCeramidesChromatography, LiquidDiabetes Mellitus, Type 2Diabetic NephropathiesFemaleHumansMaleMiddle AgedSphingolipidsTandem Mass SpectrometryBiomarkersCeramidesSphingolipidsCeramideTandem mass spectrometryUrine

Identifiers

PMID31580528
PMCPMC7078086
OpenAlexW2977896635

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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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.