Evidence map›Paper›PMID 31857618›Full record

ArticleScientific reports2019

Differential expression of circulating exosomal microRNAs in refractory intracranial atherosclerosis associated with antiangiogenesis.

Hao Jiang, Juan F Toscano, Shlee S Song, Konrad H Schlick, Oana M Dumitrascu, Jianwei Pan, Patrick D Lyden, Jeffrey L Saver, Nestor R Gonzalez

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
3.5field-weighted citation impact, top 6% 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

30 citing papers in PubMed, 39 citations in OpenAlex.

  1. Article
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  6. Development of stem cell therapy for atherosclerosis.Molecular and cellular biochemistry · 2024
    Review
  7. Article
  8. Atherosclerosis and Its Related Laboratory Biomarkers.International journal of molecular sciences · 2023
    Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 3 institutions in 2 countries.

Hao JiangDepartment of Neurosurgery, Neurovascular Laboratory, Cedars-Sinai Medical Center, Los Angeles, CA, USA.
Juan F ToscanoDepartment of Neurosurgery, Neurovascular Laboratory, Cedars-Sinai Medical Center, Los Angeles, CA, USA.
Shlee S SongDepartment of Neurology, Cedars-Sinai Medical Center, Los Angeles, CA, USA.
Konrad H SchlickDepartment of Neurology, Cedars-Sinai Medical Center, Los Angeles, CA, USA.
Oana M DumitrascuDepartment of Neurology, Cedars-Sinai Medical Center, Los Angeles, CA, USA.ORCID http://orcid.org/0000-0002-1031-9184
Jianwei PanDepartment of Neurosurgery, The First Affiliated Hospital of Zhejiang University, School of Medicine, Hangzhou, China.
Patrick D LydenDepartment of Neurology, Cedars-Sinai Medical Center, Los Angeles, CA, USA.
Jeffrey L SaverDepartment of Neurology, University of California, Los Angeles, Los Angeles, CA, USA.
Nestor R GonzalezDepartment of Neurosurgery, Neurovascular Laboratory, Cedars-Sinai Medical Center, Los Angeles, CA, USA. nestor.gonzalez@cshs.org.
Cedars-Sinai Medical Center · USFirst Affiliated Hospital Zhejiang University · CNUniversity of California, Los Angeles · US

Funding

Surgical Indirect Revascularization For Symptomatic Intracranial Aterial StenosisK23NS079477 · NINDS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI GONZALEZ, NESTOR RAUL · 2013 to 2017
$842k
NINDS NIH HHS K23 NS079477
6 · The paper itself

Abstract

Intracranial atherosclerotic disease (ICAD) is a common cause of stroke with high rates of ischemic recurrence. We aimed to investigate the role of circulating exosomal microRNAs (e-miRNAs) in recurrent ischemic events in ICAD. Consecutive patients with severe ICAD undergoing intensive medical management (IMM) were prospectively enrolled. Those with recurrent ischemic events despite IMM during 6-month follow up were algorithmically matched to IMM responders. Baseline blood e-miRNA expression levels of the matched patients were measured using next generation sequencing. A total of 122 e-miRNAs were isolated from blood samples of 10 non-responders and 11 responders. Thirteen e-miRNAs predicted IMM failure with 90% sensitivity and 100% specificity. Ingenuity pathway analysis (IPA) determined 10 of the 13 e-miRNAs were significantly associated with angiogenesis-related biological functions (p < 0.025) and angiogenic factors that have been associated with recurrent ischemic events in ICAD. These e-miRNAs included miR-122-5p, miR-192-5p, miR-27b-3p, miR-16-5p, miR-486-5p, miR-30c-5p, miR-10b-5p, miR-10a-5p, miR-101-3p, and miR-24-3p. As predicted by IPA, the specific expression profiles of these 10 e-miRNAs in non-responders had a net result of inhibition of the angiogenesis-related functions and up expression of the antiangiogenic factors. This study revealed distinct expression profiles of circulating e-miRNAs in refractory ICAD, suggesting an antiangiogenic mechanism underlying IMM failure.

Indexed as

Gene Expression ProfilingAngiogenesis InhibitorsBase SequenceCirculating MicroRNAExosomesFemaleHumansIntracranial ArteriosclerosisMaleMiddle AgedNeovascularization, PhysiologicPrincipal Component AnalysisAngiogenesis InhibitorsCirculating MicroRNA

Identifiers

PMID31857618
PMCPMC6923371
OpenAlexW2995206239

What OpenQuestion holds

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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.