Evidence map›Paper›PMID 28126408›Full record

Observational studyResuscitation2017

Characterization of mitochondrial injury after cardiac arrest (COMICA).

Michael W Donnino, Xiaowen Liu, Lars W Andersen, Jon C Rittenberger, Benjamin S Abella, David F Gaieski, Joseph P Ornato, Raúl J Gazmuri, Anne V Grossestreuer, Michael N Cocchi and 6 more

Open access · greenAbstract readMulticenter StudyObservational Study
In one paragraph

Observational study in Resuscitation, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 2 pooled it
3.2field-weighted citation impact, top 8% 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

17 citing papers in PubMed, 2 syntheses or guidelines pooled it, 34 citations in OpenAlex.

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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

16 authors at 7 institutions in 2 countries.

Michael W DonninoBeth Israel Deaconess Medical Center, Department of Emergency Medicine, Boston, MA, United States; Beth Israel Deaconess Medical Center, Department of Medicine, Division of Pulmonary, Critical Care, and Sleep Medicine, Boston, MA, United States. Electronic address: mdonnino@bidmc.harvard.edu.
Xiaowen LiuBeth Israel Deaconess Medical Center, Department of Emergency Medicine, Boston, MA, United States.
Lars W AndersenBeth Israel Deaconess Medical Center, Department of Emergency Medicine, Boston, MA, United States; Aarhus University Hospital, Research Center for Emergency Medicine, Aarhus, Denmark; Aarhus University Hospital, Department of Anesthesiology,, Aarhus, Denmark.
Jon C RittenbergerUniversity of Pittsburgh School of Medicine, Pittsburgh, United States.
Benjamin S AbellaUniversity of Pennsylvania, Center for Resuscitation Science, Philadelphia, PA, United States.
David F GaieskiThomas Jefferson University Hospital, Department of Emergency Medicine, Philadelphia, PA, United States.
Joseph P OrnatoVirginia Commonwealth University, Department of Emergency Medicine, Richmond, VA, United States.
Raúl J GazmuriRosalind Franklin University of Medicine and Science, Resuscitation Institute and Division of Critical Care Medicine, North Chicago, IL, United States.
Anne V GrossestreuerBeth Israel Deaconess Medical Center, Department of Emergency Medicine, Boston, MA, United States.
Michael N CocchiBeth Israel Deaconess Medical Center, Department of Emergency Medicine, Boston, MA, United States; Beth Israel Deaconess Medical Center, Department of Anesthesia Critical Care, Division of Critical Care, Boston, MA, United States.
Antonio AbbateVirginia Commonwealth University, Department of Internal Medicine, Richmond, VA, United States.
Amy UberBeth Israel Deaconess Medical Center, Department of Emergency Medicine, Boston, MA, United States.
John CloreVirginia Commonwealth University, Department of Internal Medicine, Richmond, VA, United States.
Mary Anne PeberdyVirginia Commonwealth University, Department of Internal Medicine and Emergency Medicine, Richmond, VA, United States.
Clifton W CallawayUniversity of Pittsburgh School of Medicine, Pittsburgh, United States.
National Post Arrest Research Consortium (NPARC) Investigators
Beth Israel Deaconess Medical Center · USVirginia Commonwealth University · USUniversity of Pittsburgh · USAarhus University Hospital · DKRosalind Franklin University of Medicine and Science · USThomas Jefferson University Hospital · USUniversity of Pennsylvania · US

Funding

Center for Clinical and Translational ResearchUL1TR000058 · NCATS · VIRGINIA COMMONWEALTH UNIVERSITY · PI MOELLER, FREDERICK GERARD · 2012 to 2015
$12.5M
Thaimine as an adjunct metabolic resuscitator in cardiac arrestK24HL127101 · NHLBI · BETH ISRAEL DEACONESS MEDICAL CENTER · PI DONNINO, MICHAEL WILLIAM · 2015 to 2024
$1.2M
Effect of Thiamine on Pyruvate Dehydrogenase Activity in Septic ShockK02HL107447 · NHLBI · BETH ISRAEL DEACONESS MEDICAL CENTER · PI DONNINO, MICHAEL WILLIAM · 2012 to 2014
$309k
NCATS NIH HHS UL1 TR000058NHLBI NIH HHS K02 HL107447NHLBI NIH HHS K24 HL127101
6 · The paper itself

Abstract

introductionMitochondrial injury post-cardiac arrest has been described in pre-clinical settings but the extent to which this injury occurs in humans remains largely unknown. We hypothesized that increased levels of mitochondrial biomarkers would be associated with mortality and neurological morbidity in post-cardiac arrest subjects.

methodsWe performed a prospective multicenter study of post-cardiac arrest subjects. Inclusion criteria were comatose adults who suffered an out-of-hospital cardiac arrest. Mitochondrial biomarkers were measured at 0, 12, 24, 36 and 48h after return of spontaneous circulation as well as in healthy controls.

resultsOut of 111 subjects enrolled, 102 had evaluable samples at 0h. Cardiac arrest subjects had higher baseline cytochrome c levels compared to controls (2.18ng/mL [0.74, 7.74] vs. 0.16ng/mL [0.03, 0.91], p<0.001), and subjects who died had higher 0h cytochrome c levels compared to survivors (3.66ng/mL [1.40, 14.9] vs. 1.27ng/mL [0.16, 2.37], p<0.001). There were significantly higher Ribonuclease P (RNaseP) (3.3 [1.2, 5.7] vs. 1.2 [0.8, 1.2], p<0.001) and Beta-2microglobulin (B2M) (12.0 [1.0, 22.9], vs. 0.6 [0.6, 1.3], p<0.001) levels in cardiac arrest subjects at baseline compared to the control subjects. There were no differences between survivors and non-survivors for mitochondrial DNA, nuclear DNA, or cell free DNA.

conclusionsCytochrome c was increased in post- cardiac arrest subjects compared to controls, and in post-cardiac arrest non-survivors compared to survivors. Nuclear DNA and cell free DNA was increased in plasma of post-cardiac arrest subjects. There were no differences in mitochondrial DNA, nuclear DNA, or cell free DNA between survivors and non-survivors. Mitochondrial injury markers showed mixed results in the post-cardiac arrest period. Future research needs to investigate these differences.

Indexed as

ComaNervous System DiseasesAgedCardiopulmonary ResuscitationCytochromes cDNA, MitochondrialFemaleHeart ArrestHumansMaleMiddle AgedMitochondriaRibonuclease PStatistics as TopicSurvival AnalysisSurvivorsCytochromes cDNA, MitochondrialRibonuclease PCardiac arrestCytochrome cDNAMitochondriaMortalityPost-cardiac arrest

Identifiers

PMID28126408
PMCPMC5497747
OpenAlexW2582043308

What OpenQuestion holds

Textmetadata
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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.