Evidence map›Paper›PMID 26244428›Full record

Trial reportScientific reports2015

Arteriovenous Blood Metabolomics: A Readout of Intra-Tissue Metabostasis.

Julijana Ivanisevic, Darlene Elias, Hiroshi Deguchi, Patricia M Averell, Michael Kurczy, Caroline H Johnson, Ralf Tautenhahn, Zhengjiang Zhu, Jeramie Watrous, Mohit Jain and 3 more

Abstract readClinical Trial
In one paragraph

Trial report in Scientific reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing 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

42 citing papers in PubMed.

  1. Article
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  7. Review
  8. Impact of acute stress on murine metabolomics and metabolic flux.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  9. Review
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  14. Review
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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

13 authors.

Julijana IvanisevicCenter for Metabolomics and Mass Spectrometry, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, California 92037, United States.
Darlene Elias1] Department of Molecular and Experimental Medicine, The Scripps Research Institute, 10550 North Torrey Pines Road, MEM-180, La Jolla, California 92037, United States [2] Anticoagulation Services, Scripps Clinic and Scripps Green Hospital, 10666 North Torrey Pines Road, W207, La Jolla, California 92037, United States.
Hiroshi DeguchiDepartment of Molecular and Experimental Medicine, The Scripps Research Institute, 10550 North Torrey Pines Road, MEM-180, La Jolla, California 92037, United States.
Patricia M AverellAnticoagulation Services, Scripps Clinic and Scripps Green Hospital, 10666 North Torrey Pines Road, W207, La Jolla, California 92037, United States.
Michael KurczyCenter for Metabolomics and Mass Spectrometry, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, California 92037, United States.
Caroline H JohnsonCenter for Metabolomics and Mass Spectrometry, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, California 92037, United States.
Ralf TautenhahnCenter for Metabolomics and Mass Spectrometry, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, California 92037, United States.
Zhengjiang ZhuCenter for Metabolomics and Mass Spectrometry, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, California 92037, United States.
Jeramie WatrousDepartments of Medicine and Pharmacology, University of California, 9500 Gilman Drive, MC 0613, La Jolla, California 92037, United States.
Mohit JainDepartments of Medicine and Pharmacology, University of California, 9500 Gilman Drive, MC 0613, La Jolla, California 92037, United States.
John GriffinDepartment of Molecular and Experimental Medicine, The Scripps Research Institute, 10550 North Torrey Pines Road, MEM-180, La Jolla, California 92037, United States.
Gary J PattiDepartments of Chemistry, Genetics, and Medicine, Washington University, One Brookings Drive, St. Louis, Missouri 63130, United States.
Gary Siuzdak1] Center for Metabolomics and Mass Spectrometry, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, California 92037, United States [2] Departments of Chemistry, Molecular and Computational Biology, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, California 92037, United States.

Funding

Scripps Translational Science InstituteUL1TR001114 · NCATS · SCRIPPS RESEARCH INSTITUTE, THE · PI TOPOL, ERIC JEFFREY · 2013 to 2017
$24.0M
SCRIPPS TRANSLATIONAL SCIENCE INSTITUTE (UL1)UL1RR025774 · NCRR · SCRIPPS RESEARCH INSTITUTE, THE · PI TOPOL, ERIC JEFFREY · 2008 to 2011
$16.3M
Structure and Function of Protein CR01HL052246 · NHLBI · SCRIPPS RESEARCH INSTITUTE, THE · PI GRIFFIN, JOHN H · 2005 to 2017
$9.6M
PROTEINS OF COAGULATION PATHWAYSR01HL021544 · NHLBI · SCRIPPS RESEARCH INSTITUTE, THE · PI GRIFFIN, JOHN H · 1985 to 2014
$7.5M
Griffin: Venous Thromboembolism and mass spectrometry-based untargeted metabolomiRC1HL101034 · NHLBI · SCRIPPS RESEARCH INSTITUTE, THE · PI DEGUCHI, HIROSHI, GRIFFIN, JOHN H · 2009 to 2010
$952k
NCATS NIH HHS UL1 TR001114NCRR NIH HHS UL1 RR025774NCRR NIH HHS UL1RR025774NHLBI NIH HHS HL021544NHLBI NIH HHS HL101034NHLBI NIH HHS R01 HL021544NHLBI NIH HHS R01 HL052246NHLBI NIH HHS RC1 HL101034
6 · The paper itself

Abstract

The human circulatory system consists of arterial blood that delivers nutrients to tissues, and venous blood that removes the metabolic by-products. Although it is well established that arterial blood generally has higher concentrations of glucose and oxygen relative to venous blood, a comprehensive biochemical characterization of arteriovenous differences has not yet been reported. Here we apply cutting-edge, mass spectrometry-based metabolomic technologies to provide a global characterization of metabolites that vary in concentration between the arterial and venous blood of human patients. Global profiling of paired arterial and venous plasma from 20 healthy individuals, followed up by targeted analysis made it possible to measure subtle (<2 fold), yet highly statistically significant and physiologically important differences in water soluble human plasma metabolome. While we detected changes in lactic acid, alanine, glutamine, and glutamate as expected from skeletal muscle activity, a number of unanticipated metabolites were also determined to be significantly altered including Krebs cycle intermediates, amino acids that have not been previously implicated in transport, and a few oxidized fatty acids. This study provides the most comprehensive assessment of metabolic changes in the blood during circulation to date and suggests that such profiling approach may offer new insights into organ homeostasis and organ specific pathology.

Indexed as

MetabolomicsAdultAmino AcidsBlood GlucoseFemaleHumansLactic AcidMaleOxygenAmino AcidsBlood GlucoseLactic AcidOxygen

Identifiers

PMID26244428
PMCPMC4525490

What OpenQuestion holds

Textmetadata
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.