Evidence map›Paper›PMID 30890654›Full record

ReviewClinical science (London, England : 1979)2019

Potential therapeutic targets for atherosclerosis in sphingolipid metabolism.

Zemou Yu, Qing Peng, Yining Huang

Open access · hybridAbstract readReview
In one paragraph

Review in Clinical science (London, England : 1979), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

25 citing papers in PubMed, 45 citations in OpenAlex.

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  15. Sphingolipids in Atherosclerosis: Chimeras in Structure and Function.International journal of molecular sciences · 2022
    Review
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  17. 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

3 authors at 1 institution in 1 country.

Zemou YuDepartment of Neurology, Peking University First Hospital, Beijing, China.ORCID 0000-0002-9658-4869
Qing PengDepartment of Neurology, Peking University First Hospital, Beijing, China.
Yining HuangDepartment of Neurology, Peking University First Hospital, Beijing, China ynhuang@bjmu.edu.cn.
Peking University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sphingolipids, such as sphingomyelins, ceramides, glycosphingolipids, and sphingosine-1-phosphates (S1P) are a large group of structurally and functionally diverse molecules. Some specific species are found associated with atherogenesis and provide novel therapeutic targets. Herein, we briefly review how sphingolipids are implicated in the progression of atherosclerosis and related diseases, and then we discuss the potential therapy options by targetting several key enzymes in sphingolipid metabolism.

Indexed as

AtherosclerosisCardiovascular AgentsCeramidesHumansMolecular Targeted TherapySphingolipidsSphingomyelin PhosphodiesteraseSphingomyelinsCardiovascular AgentsCeramidesSphingolipidsSphingomyelin PhosphodiesteraseSphingomyelinsAtherosclerosisCeramideSphingolipids

Identifiers

PMID30890654
PMCPMC6422862
OpenAlexW2923289796

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.