Evidence map›Paper›PMID 36357929›Full record

ArticleJournal of biomedical science2022

Dynamic modulations of urinary sphingolipid and glycerophospholipid levels in COVID-19 and correlations with COVID-19-associated kidney injuries.

Makoto Kurano, Daisuke Jubishi, Koh Okamoto, Hideki Hashimoto, Eri Sakai, Yoshifumi Morita, Daisuke Saigusa, Kuniyuki Kano, Junken Aoki, Sohei Harada and 4 more

Open access · diamondAbstract read
In one paragraph

Article in Journal of biomedical science, 2022. 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
1.9field-weighted citation impact, top 13% 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

10 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
  2. Article
  3. Sphingolipid signaling in kidney diseases.American journal of physiology. Renal physiology · 2025
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  5. Article
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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

14 authors at 3 institutions in 1 country.

Makoto KuranoDepartment of Clinical Laboratory Medicine, Graduate School of Medicine, The University of Tokyo, 7-3-1 Hongo, Bunkyo-Ku, Tokyo, 113-8655, Japan. kurano-tky@umin.ac.jp.ORCID http://orcid.org/0000-0002-2596-1145
Daisuke JubishiDepartment of Infectious Diseases, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
Koh OkamotoDepartment of Infectious Diseases, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
Hideki HashimotoDepartment of Infectious Diseases, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
Eri SakaiDepartment of Clinical Laboratory, The University of Tokyo Hospital, Tokyo, Japan.
Yoshifumi MoritaDepartment of Clinical Laboratory, The University of Tokyo Hospital, Tokyo, Japan.
Daisuke SaigusaLaboratory of Biomedical and Analytical Sciences, Faculty of Pharma-Science, Teikyo University, Tokyo, Japan.
Kuniyuki KanoDepartment of Health Chemistry, Graduate School of Pharmaceutical Sciences, The University of Tokyo, Tokyo, Japan.
Junken AokiDepartment of Health Chemistry, Graduate School of Pharmaceutical Sciences, The University of Tokyo, Tokyo, Japan.
Sohei HaradaDepartment of Infection Control and Prevention, The University of Tokyo, Tokyo, Japan.
Shu OkugawaDepartment of Infectious Diseases, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
Kent DoiDepartment of Emergency and Critical Care Medicine, The University of Tokyo Hospital, Tokyo, Japan.
Kyoji MoriyaDepartment of Infectious Diseases, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
Yutaka YatomiDepartment of Clinical Laboratory Medicine, Graduate School of Medicine, The University of Tokyo, 7-3-1 Hongo, Bunkyo-Ku, Tokyo, 113-8655, Japan.
The University of Tokyo · JPUniversity of Tokyo Hospital · JPTeikyo University · JP

Funding

Japan Agency for Medical Research and Development LEAPJapan Society for the Promotion of Science 20H03573
6 · The paper itself

Abstract

backgroundAmong various complications of coronavirus disease 2019 (COVID-19), caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), renal complications, namely COVID-19-associated kidney injuries, are related to the mortality of COVID-19.

methodsIn this retrospective cross-sectional study, we measured the sphingolipids and glycerophospholipids, which have been shown to possess potent biological properties, using liquid chromatography-mass spectrometry in 272 urine samples collected longitudinally from 91 COVID-19 subjects and 95 control subjects without infectious diseases, to elucidate the pathogenesis of COVID-19-associated kidney injuries.

resultsThe urinary levels of C18:0, C18:1, C22:0, and C24:0 ceramides, sphingosine, dihydrosphingosine, phosphatidylcholine, lysophosphatidylcholine, lysophosphatidic acid, and phosphatidylglycerol decreased, while those of phosphatidylserine, lysophosphatidylserine, phosphatidylethanolamine, and lysophosphatidylethanolamine increased in patients with mild COVID-19, especially during the early phase (day 1-3), suggesting that these modulations might reflect the direct effects of infection with SARS-CoV-2. Generally, the urinary levels of sphingomyelin, ceramides, sphingosine, dihydrosphingosine, dihydrosphingosine L-phosphate, phosphatidylcholine, lysophosphatidic acid, phosphatidylserine, lysophosphatidylserine, phosphatidylethanolamine, lysophosphatidylethanolamine, phosphatidylglycerol, lysophosphatidylglycerol, phosphatidylinositol, and lysophosphatidylinositol increased, especially in patients with severe COVID-19 during the later phase, suggesting that their modulations might result from kidney injuries accompanying severe COVID-19.

conclusionsConsidering the biological properties of sphingolipids and glycerophospholipids, an understanding of their urinary modulations in COVID-19 will help us to understand the mechanisms causing COVID-19-associated kidney injuries as well as general acute kidney injuries and may prompt researchers to develop laboratory tests for predicting maximum severity and/or novel reagents to suppress the renal complications of COVID-19.

Indexed as

COVID-19SphingolipidsCeramidesCross-Sectional StudiesGlycerophospholipidsHumansKidneyPhosphatidylcholinesPhosphatidylethanolaminesPhosphatidylglycerolsPhosphatidylserinesRetrospective StudiesSARS-CoV-2SphingosineCeramidesGlycerophospholipidsPhosphatidylcholinesPhosphatidylethanolaminesPhosphatidylglycerolsPhosphatidylserinessafingolSphingolipidsSphingosineCOVID-19-associated kidney injuriesGlycerophospholipidsLipidomicsSphingolipidsUrine

Identifiers

PMID36357929
PMCPMC9647768
OpenAlexW4309244417

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.