Evidence map›Paper›PMID 29907353›Full record

Observational studyClinical nutrition (Edinburgh, Scotland)2019

Determinants of skeletal muscle protein turnover following severe burn trauma in children.

Ioannis Malagaris, David N Herndon, Efstathia Polychronopoulou, Victoria G Rontoyanni, Clark R Andersen, Oscar E Suman, Craig Porter, Labros S Sidossis

Open access · greenAbstract readObservational Study
In one paragraph

Observational study in Clinical nutrition (Edinburgh, Scotland), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.0field-weighted citation impact, top 24% 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

6 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. [Roles of adenosine monophosphate activated protein kinase in skeletal muscle atrophy in rats with severe scald].Zhonghua shao shang za zhi = Zhonghua shaoshang zazhi = Chinese journal of burns · 2021
    Article
  6. Burn-induced hypermetabolism and skeletal muscle dysfunction.American journal of physiology. Cell physiology · 2021
    Review
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 2 institutions in 1 country.

Ioannis MalagarisRehabilitation Sciences, University of Texas Medical Branch, Galveston, TX, USA; Metabolism Unit, Shriners Hospitals for Children, Galveston, Texas, USA.
David N HerndonDepartment of Surgery, University of Texas Medical Branch, Galveston, TX, USA; Metabolism Unit, Shriners Hospitals for Children, Galveston, Texas, USA; Institute of Translational Sciences, University of Texas Medical Branch, Galveston, TX, USA. Electronic address: dherndon@UTMB.edu.
Efstathia PolychronopoulouRehabilitation Sciences, University of Texas Medical Branch, Galveston, TX, USA; Metabolism Unit, Shriners Hospitals for Children, Galveston, Texas, USA.
Victoria G RontoyanniDepartment of Surgery, University of Texas Medical Branch, Galveston, TX, USA; Metabolism Unit, Shriners Hospitals for Children, Galveston, Texas, USA.
Clark R AndersenDepartment of Surgery, University of Texas Medical Branch, Galveston, TX, USA.
Oscar E SumanDepartment of Surgery, University of Texas Medical Branch, Galveston, TX, USA; Metabolism Unit, Shriners Hospitals for Children, Galveston, Texas, USA.
Craig PorterDepartment of Surgery, University of Texas Medical Branch, Galveston, TX, USA; Metabolism Unit, Shriners Hospitals for Children, Galveston, Texas, USA; Institute of Translational Sciences, University of Texas Medical Branch, Galveston, TX, USA.
Labros S SidossisDepartment of Surgery, University of Texas Medical Branch, Galveston, TX, USA; Metabolism Unit, Shriners Hospitals for Children, Galveston, Texas, USA.
Shriners Hospitals for Children - Galveston · USThe University of Texas Medical Branch at Galveston · US

Funding

UTMB Clinical and Translational Science AwardUL1TR001439 · NCATS · UNIVERSITY OF TEXAS MED BR GALVESTON · PI URBAN, RANDALL J · 2015 to 2024
$40.0M
Project 9: The role of androgen/corticosteroid in fat, muscle and glucose metabolism of burn victimsP50GM060338 · NIGMS · UNIVERSITY OF TEXAS MEDICAL BR GALVESTON · PI HERNDON, DAVID N. · 2000 to 2017
$24.2M
MODULATION OF THE POSTBURN HYPERMETABOLIC RESPONSER01GM056687 · NIGMS · UNIVERSITY OF TEXAS MEDICAL BR GALVESTON · PI HERNDON, DAVID N. · 1998 to 2017
$9.0M
Oxandrolone and Exercise: A potent therapy in the rehabilitation from burnsR01HD049471 · NICHD · UNIVERSITY OF TEXAS MED BR GALVESTON · PI SUMAN-VEJAS, OSCAR E. · 2006 to 2019
$5.8M
UTMB Clinical and Translational Science AwardKL2TR001441 · NCATS · UNIVERSITY OF TEXAS MED BR GALVESTON · PI AMEREDES, BILL T · 2015 to 2024
$4.0M
POSTDOCTORAL TRAINING IN TRAUMA &BURNST32GM008256 · NIGMS · UNIVERSITY OF TEXAS MEDICAL BR GALVESTON · PI Celeste Campbell Finnerty, Oscar E. Suman-Vejas · 1990 to 2026
$4.0M
Physiological Adaptations to Exercise in Burned ChildrenK01HL070451 · NHLBI · UNIVERSITY OF TEXAS MEDICAL BR GALVESTON · PI SUMAN, OSCAR E · 2002 to 2006
$639k
NCATS NIH HHS KL2 TR001441NCATS NIH HHS UL1 TR001439NHLBI NIH HHS K01 HL070451NICHD NIH HHS R01 HD049471NIGMS NIH HHS P50 GM060338NIGMS NIH HHS R01 GM056687NIGMS NIH HHS T32 GM008256
6 · The paper itself

Abstract

BACKGROUND &

aimsBurns remain the fifth cause of non-fatal pediatric injuries globally, with muscle cachexia being a hallmark of the stress response to burns. Burn-induced muscle wasting is associated with morbidity, yet the determinants of muscle protein catabolism in response to burn trauma remains unclear. Our objective was to determine the effect of patient and injury characteristics on muscle protein kinetics in burn patients.

methodsThis retrospective, observational study was performed using protein kinetic data from pediatric patients who had severe burns (>30% of the total body surface area burned) and underwent cross-limb stable isotope infusions between 1999 and 2008 as part of prospective clinical trials. Mixed multiple regression models were used to assess associations between patient/injury characteristics and muscle protein fractional synthesis rate (FSR), net balance (NB), and rates of phenylalanine appearance (Ra; index of protein breakdown) and disappearance (Rd; index of protein synthesis) across the leg.

resultsA total of 268 patients who underwent 499 studies were analyzed. Increasing time post injury was associated with greater FSR (p < 0.001) and NB (p = 0.01). Males were more catabolic than females (as indicated by lower NB, p = 0.04 and greater Ra, p = 0.008), a consequence of higher protein breakdown rather than lower synthesis. Increasing burn size was associated with higher protein synthesis rate (as indicated by higher FSR, p = 0.019) and higher protein breakdown rates (as indicated by greater Ra, p = 0.001). FSR was negatively associated with age (p < 0.001).

conclusionsData from this large patient cohort show that injury severity, sex, and time post injury influence skeletal muscle wasting in burned children. These findings suggest that individual patient characteristics should be considered when devising therapies to improve the acute care and rehabilitation of burn survivors.

Indexed as

BurnsChildFemaleHumansMaleMuscle ProteinsMuscle, SkeletalMuscular AtrophyProspective StudiesProtein BiosynthesisRetrospective StudiesSeverity of Illness IndexSex FactorsMuscle ProteinsAmino acid kineticsBurnsMuscle metabolismPediatricStable isotope

Identifiers

PMID29907353
PMCPMC6279601
OpenAlexW2805932547

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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.