Evidence map›Paper›PMID 28667255›Full record

ArticleScientific reports2017

Circulating Biomarkers to Identify Responders in Cardiac Cell therapy.

Jesse V Jokerst, Nicholas Cauwenberghs, Tatiana Kuznetsova, Francois Haddad, Timothy Sweeney, Jiayi Hou, Yael Rosenberg-Hasson, Eric Zhao, Robert Schutt, Roberto Bolli and 7 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. 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 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.0field-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

14 citing papers in PubMed, 25 citations in OpenAlex.

  1. Gene Therapy for Heart Failure.Journal of cardiovascular translational research · 2026
    Review
  2. Article
  3. [Diagnostics (Basel, Switzerland) · 2023
    Article
  4. Article
  5. Review
  6. Review
  7. Review
  8. Article
  9. Review
  10. Artificial Intelligence for Cardiac Imaging-Genetics Research.Frontiers in cardiovascular medicine · 2019
    Review
  11. Engineering molecular imaging strategies for regenerative medicine.Bioengineering & translational medicine · 2018
    Review
  12. Review
  13. Review
  14. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

17 authors at 10 institutions in 2 countries.

Jesse V JokerstDepartment of NanoEngineering, University of California, San Diego, USA. jjokerst@ucsd.edu.
Nicholas CauwenberghsResearch Unit of Hypertension and Cardiovascular Epidemiology, Department of Cardiovascular Sciences, University of Leuven, Leuven, Belgium.ORCID 0000-0001-8059-7692
Tatiana KuznetsovaResearch Unit of Hypertension and Cardiovascular Epidemiology, Department of Cardiovascular Sciences, University of Leuven, Leuven, Belgium.
Francois HaddadDepartment of Medicine, Stanford University, Stanford, USA.
Timothy SweeneyDepartment of Medicine, Stanford University, Stanford, USA.ORCID 0000-0002-3596-1093
Jiayi HouClinical and Translational Research Institute, University of California, San Diego, USA.
Yael Rosenberg-HassonDepartment of Medicine, Stanford University, Stanford, USA.
Eric ZhaoDepartment of NanoEngineering, University of California, San Diego, USA.
Robert SchuttHouston Methodist Hospital, Houston, USA.
Roberto BolliSchool of Medicine, University of Louisville, Louisville, USA.
Jay H TraverseMinneapolis Heart Institute Foundation at Abbott Northwestern Hospital, Minneapolis, USA.
Carl J PepineUniversity of Florida College of Medicine, Gainesville, USA.
Timothy D HenryCedars-Sinai Heart Institute, Los Angeles, USA.
Ivonne H SchulmanInterdisciplinary Stem Cell Institute, University of Miami Miller School of Medicine, Miami, USA.
Lem MoyéUniversity of Texas School of Public Health, University of Texas Health Science Center, Houston, USA.
Doris A TaylorTexas Heart Institute, CHI St. Luke's Health Baylor College of Medicine Medical Center, Houston, USA.
Phillip C YangDepartment of Medicine, Stanford University, Stanford, USA.
Stanford University · USUniversity of California San Diego · USKU Leuven · BEAbbott Northwestern Hospital · USBaylor College of Medicine · USMethodist Hospital · USThe University of Texas Health Science Center at Houston · USUniversity of Florida · USUniversity of Louisville · USUniversity of Miami · US

Funding

Data Coordinating Center For The Cardiovascular Cell Therapy Research NetworkUM1HL087318 · NHLBI · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI DAVIS, BARRY R · 2012 to 2018
$29.8M
Cardiovascular Cell Therapy Research Network - Data Coordinating CenterU01HL087318 · NHLBI · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI MOYE, LEMUEL A. · 2007 to 2011
$17.6M
Cell Characterization and Imaging for Regenerative Therapies in Ischemic DiseasesUM1HL113456 · NHLBI · STANFORD UNIVERSITY · PI YANG, PHILLIP CHUNG-MING · 2012 to 2018
$3.3M
A Therapeutic Tool for Ultrasound-Guided Stem Cell TherapyR00HL117048 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI JOKERST, JESSE VINCENT · 2015 to 2017
$747k
Patient Oriented Research in Cardiovascular RegenerationK24HL130553 · NHLBI · STANFORD UNIVERSITY · PI YANG, PHILLIP CHUNG-MING · 2016 to 2020
$584k
A Therapeutic Tool for ULtrasound-Guided Stem Cell TherapyK99HL117048 · NHLBI · STANFORD UNIVERSITY · PI JOKERST, JESSE VINCENT · 2014 to 2015
$265k
NHLBI NIH HHS K24 HL130553NHLBI NIH HHS K99 HL117048NHLBI NIH HHS R00 HL117048NHLBI NIH HHS U01 HL087318NHLBI NIH HHS UM1 HL087318NHLBI NIH HHS UM1 HL113456
6 · The paper itself

Abstract

Bone marrow mononuclear cell (BM-MNC) therapy in ST-elevation acute myocardial infarction (STEMI) has no biological inclusion criteria. Here, we analyzed 63 biomarkers and cytokines in baseline plasma samples from 77 STEMI patients treated with BM-MNCs in the TIME and Late-TIME trials as well as 61 STEMI patients treated with placebo. Response to cell therapy was defined by changes in left ventricular ejection fraction, systolic/diastolic volumes, and wall motion indexes. We investigated the clinical value of circulating proteins in outcome prediction using significance testing, partial least squares discriminant analysis, and receiver operating characteristic (ROC) analysis. Responders had higher biomarker levels (76-94% elevated) than non-responders. Several biomarkers had values that differed significantly (P < 0.05) between responders and non-responders including stem cell factor, platelet-derived growth factor, and interleukin-15. We then used these lead candidates for ROC analysis and found multiple biomarkers with values areas under the curve >0.70 including interleukin 15. These biomarkers were not involved in the placebo-treated subjects suggesting that they may have predictive power. We conclude that plasma profiling after STEMI may help identify patients with a greater likelihood of response to cell-based treatment. Prospective trials are needed to assess the predictive value of the circulating biomarkers.

Identifiers

PMID28667255
PMCPMC5493650
OpenAlexW2629764646

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.