Evidence map›Paper›PMID 34540912›Full record

ArticleFrontiers in cardiovascular medicine2021

Peripheral Blood Biomarkers Associated With Improved Functional Outcome in Patients With Chronic Left Ventricular Dysfunction: A Biorepository Evaluation of the FOCUS-CCTRN Trial.

Lourdes Chacon Alberty, Emerson C Perin, James T Willerson, Amir Gahremanpour, Roberto Bolli, Phillip C Yang, Jay H Traverse, Dejian Lai, Carl J Pepine, Doris A Taylor

Abstract read
In one paragraph

Article in Frontiers in cardiovascular medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

10 authors.

Lourdes Chacon AlbertyRegenerative Medicine Department, Texas Heart Institute, Houston, TX, United States.
Emerson C PerinStem Cell Center, Texas Heart Institute, Houston, TX, United States.
James T WillersonStem Cell Center, Texas Heart Institute, Houston, TX, United States.
Amir GahremanpourHospital Corporation of America-Houston Heart, Houston, TX, United States.
Roberto BolliSchool of Medicine, University of Louisville, Louisville, KY, United States.
Phillip C YangStanford University School of Medicine, Stanford, CA, United States.
Jay H TraverseMinneapolis Heart Institute Foundation at Abbott Northwestern Hospital and University of Minnesota School of Medicine, Minneapolis, MN, United States.
Dejian LaiUTHealth School of Public Health, Houston, TX, United States.
Carl J PepineUniversity of Florida College of Medicine, Gainesville, FL, United States.
Doris A TaylorRegenerative Medicine Department, Texas Heart Institute, Houston, TX, United States.

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
UF Clinical and Translational Science AwardUL1TR000064 · NCATS · UNIVERSITY OF FLORIDA · PI NELSON, DAVID R · 2012 to 2014
$12.2M
NCATS NIH HHS UL1 TR000064NHLBI NIH HHS HHSN268201000007CNHLBI NIH HHS HHSN268201000008CNHLBI NIH HHS N01 HB037163NHLBI NIH HHS N01 HB037164NHLBI NIH HHS UM1 HL087318
6 · The paper itself

Abstract

Cell therapy trials for heart failure (HF) have shown modest improvement; however, the mechanisms underlying improvement in some patients but not others are not well understood. Although immune cells are important in the course of HF, our understanding of the immune processes in HF is limited. The objective of this study was to evaluate associations between temporal changes in peripheral blood (PB) cell subpopulations and improved outcome in patients with chronic ischemic cardiomyopathy after bone marrow-derived mononuclear cell therapy or placebo in the FOCUS-CCTRN trial. Peripheral blood was collected at days 0, 1, 30, 90, and 180 from consented participants. We used flow cytometry to compare PB populations in patients with the best (cohort 1) or worst functional outcome (cohort 2) in three primary endpoints: left ventricular (LV) ejection fraction, LV end-systolic volume, and maximal oxygen consumption (VO

Indexed as

B-CellsB-lymphocytescell therapyheartheart failureimmune systemstem cellsventricular dysfunction

Identifiers

PMID34540912
PMCPMC8446350

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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.