Evidence map›Paper›PMID 24650924›Full record

ArticleJournal of the American Heart Association2014

Triiodothyronine facilitates weaning from extracorporeal membrane oxygenation by improved mitochondrial substrate utilization.

Matthew D Files, Masaki Kajimoto, Colleen M O'Kelly Priddy, Dolena R Ledee, Chun Xu, Christine Des Rosiers, Nancy Isern, Michael A Portman

Open access · goldAbstract read
In one paragraph

Article in Journal of the American Heart Association, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 1 pooled it
3.4field-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, 1 synthesis or guideline pooled it, 32 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Review
  5. Article
  6. Article
  7. Review
  8. Quantitative cardiac phosphoproteomics profiling during ischemia-reperfusion in an immature swine model.American journal of physiology. Heart and circulatory physiology · 2017
    Article
  9. Article
  10. Thyroid Hormone in the Pediatric Intensive Care Unit.Journal of pediatric intensive care · 2016
    Review
  11. Review
  12. Review
  13. Article
  14. Article
  15. Article
  16. Role of thyroid hormones in ventricular remodeling.Current heart failure reports · 2015
    Review
  17. 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

8 authors at 4 institutions in 2 countries.

Matthew D FilesDepartment of Cardiology, Seattle Children's Hospital, Seattle, WA.
Masaki Kajimoto
Colleen M O'Kelly Priddy
Dolena R Ledee
Chun Xu
Christine Des Rosiers
Nancy Isern
Michael A Portman
Seattle Children's Hospital · USEnvironmental Molecular Sciences Laboratory · USMontreal Heart Institute · CAUniversity of Washington · US

Funding

Thyroid Regulation in the Developing HeartR01HL060666 · NHLBI · UNIVERSITY OF WASHINGTON · PI PORTMAN, MICHAEL A · 1998 to 2013
$4.7M
NHLBI NIH HHS R01 HL060666NHLBI NIH HHS R01HL60666
6 · The paper itself

Abstract

backgroundExtracorporeal membrane oxygenation (ECMO) provides a bridge to recovery after myocardial injury in infants and children, yet morbidity and mortality remain high. Weaning from the circuit requires adequate cardiac contractile function, which can be impaired by metabolic disturbances induced either by ischemia-reperfusion and/or by ECMO. We tested the hypothesis that although ECMO partially ameliorates metabolic abnormalities induced by ischemia-reperfusion, these abnormalities persist or recur with weaning. We also determined if thyroid hormone supplementation (triiodothyronine) during ECMO improves oxidative metabolism and cardiac function. METHODS AND

resultsNeonatal piglets underwent transient coronary ischemia to induce cardiac injury then were separated into 4 groups based on loading status. Piglets without coronary ischemia served as controls. We infused into the left coronary artery [2-(13)C]pyruvate and [(13)C6, (15)N]l-leucine to evaluate oxidative metabolism by gas chromatography-mass spectroscopy and nuclear magnetic resonance methods. ECMO improved survival, increased oxidative substrate contribution through pyruvate dehydrogenase, reduced succinate and fumarate accumulation, and ameliorated ATP depletion induced by ischemia. The functional and metabolic benefit of ECMO was lost with weaning, yet triiodothyronine supplementation during ECMO restored function, increased relative pyruvate dehydrogenase flux, reduced succinate and fumarate, and preserved ATP stores.

conclusionsAlthough ECMO provides metabolic rest by decreasing energy demand, metabolic impairments persist, and are exacerbated with weaning. Treating ECMO-induced thyroid depression with triiodothyronine improves substrate flux, myocardial oxidative capacity and cardiac contractile function. This translational model suggests that metabolic targeting can improve weaning.

Indexed as

Extracorporeal Membrane OxygenationAnimalsAnimals, NewbornCardiotonic AgentsDisease Models, AnimalEnergy MetabolismMaleMitochondria, HeartMyocardial ContractionMyocardial Reperfusion InjuryMyocardiumRecovery of FunctionSwineTime FactorsTriiodothyronineVentricular Function, LeftCardiotonic AgentsTriiodothyroninecardiac metabolismcongenital heart defectsextracorporeal circulationthyroid hormone

Identifiers

PMID24650924
PMCPMC4187495
OpenAlexW2101993823

What OpenQuestion holds

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LicenceCC BY-NC
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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.