Evidence map›Paper›PMID 25468473›Full record

ReviewBurns : journal of the International Society for Burn Injuries2015

Effects of pharmacological interventions on muscle protein synthesis and breakdown in recovery from burns.

Eva C Diaz, David N Herndon, Craig Porter, Labros S Sidossis, Oscar E Suman, Elisabet Børsheim

Registry-linked trialAbstract readReview
In one paragraph

Review in Burns : journal of the International Society for Burn Injuries, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03678233 (Efficacy of Testosterone Gel to Restore Normal Serum Values of Testosterone During the Acute Phase of Critical Illness in Adult ICU Patients), which is not on this map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
5.8field-weighted citation impact, top 4% 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.

NCT03678233 phase2unknown statusnot on this mapstarted 2019, after this paper: background citation

Efficacy of Testosterone Gel to Restore Normal Serum Values of Testosterone During the Acute Phase of Critical Illness in Adult ICU Patients

TypeinterventionalSponsorUniversity Hospital, Clermont-FerrandRan2019 to 2025Enrolled30ConditionsHypermetabolism in ICU, Loss of Muscle Mass, Functional Disability After ICU, ICU Acquired HypogonadismArmsAndroGel 16.2 mg/L
3 · Its place in the literature

Who cites it

26 citing papers in PubMed, 65 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Trial
  4. Review
  5. Article
  6. Review
  7. Review
  8. Burn-induced hypermetabolism and skeletal muscle dysfunction.American journal of physiology. Cell physiology · 2021
    Review
  9. Article
  10. Glucose Metabolism in Burns-What Happens?International journal of molecular sciences · 2021
    Review
  11. Article
  12. Anabolic and anticatabolic agents used in burn care: What is known and what is yet to be learned.Burns : journal of the International Society for Burn Injuries · 2020
    Review
  13. Review
  14. Article
  15. Modulating Metabolism to Improve Cancer-Induced Muscle Wasting.Oxidative medicine and cellular longevity · 2018
    Review
  16. Review
  17. The Role of Mitochondrial Stress in Muscle Wasting Following Severe Burn Trauma.Journal of burn care & research : official publication of the American Burn Association · 2018
    Review
  18. Body Composition Changes in Severely Burned Children During ICU Hospitalization.Pediatric critical care medicine : a journal of the Society of Critical Care Medicine and the World Federation of Pediatric Intensive and Critical Care Societies · 2017
    Article
  19. The biochemical alterations underlying post-burn hypermetabolism.Biochimica et biophysica acta. Molecular basis of disease · 2017
    Review
  20. Observational
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

6 authors at 3 institutions in 1 country.

Eva C DiazMetabolism Unit, Shriners Hospitals for Children, 815, Market Street, Galveston, TX 77550, USA; Department of Surgery, University of Texas Medical Branch, 301 University Blvd, Galveston, TX 77555, USA; Arkansas Children's Nutrition Center, Arkansas Children's Hospital Research Institute, and Dept. of Pediatrics, University of Arkansas for Medical Sciences, 15 Children's Way, Little Rock, AR 72202, USA. Electronic address: ecdiazfuentes@uams.edu.
David N HerndonMetabolism Unit, Shriners Hospitals for Children, 815, Market Street, Galveston, TX 77550, USA; Department of Surgery, University of Texas Medical Branch, 301 University Blvd, Galveston, TX 77555, USA. Electronic address: dherndon@utmb.edu.
Craig PorterMetabolism Unit, Shriners Hospitals for Children, 815, Market Street, Galveston, TX 77550, USA; Department of Surgery, University of Texas Medical Branch, 301 University Blvd, Galveston, TX 77555, USA. Electronic address: cr2porte@utmb.edu.
Labros S SidossisMetabolism Unit, Shriners Hospitals for Children, 815, Market Street, Galveston, TX 77550, USA; Department of Internal Medicine, University of Texas Medical Branch, 301 University Blvd, Galveston, TX 77555, USA. Electronic address: lasidoss@utmb.edu.
Oscar E SumanMetabolism Unit, Shriners Hospitals for Children, 815, Market Street, Galveston, TX 77550, USA; Department of Surgery, University of Texas Medical Branch, 301 University Blvd, Galveston, TX 77555, USA. Electronic address: oesuman@utmb.edu.
Elisabet BørsheimMetabolism Unit, Shriners Hospitals for Children, 815, Market Street, Galveston, TX 77550, USA; Department of Surgery, University of Texas Medical Branch, 301 University Blvd, Galveston, TX 77555, USA; Arkansas Children's Nutrition Center, Arkansas Children's Hospital Research Institute, and Dept. of Pediatrics, University of Arkansas for Medical Sciences, 15 Children's Way, Little Rock, AR 72202, USA. Electronic address: EBorsheim@uams.edu.
Shriners Hospitals for Children - Galveston · USThe University of Texas Medical Branch at Galveston · USArkansas Children's Nutrition Center · US

Funding

ZOLLINGER-ELLISON SYNDROME AND DUODONAL ULCER DISEASEM01RR000073 · NCRR · UNIVERSITY OF TEXAS MEDICAL BR GALVESTON · PI ANDERSON, KARL ELMO · 1985 to 2009
$31.3M
Project 9: The role of androgen/corticosteroid in fat, muscle and glucose metabolism of burn victimsP50GM060338 · NIGMS · UNIVERSITY OF TEXAS MEDICAL BR GALVESTON · PI SZABO, CSABA · 2000 to 2017
$24.2M
UTMB Clinical and Translational Science AwardUL1TR000071 · NCATS · UNIVERSITY OF TEXAS MED BR GALVESTON · PI BRASIER, ALLAN R. · 2012 to 2014
$14.4M
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
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
NCATS NIH HHS UL1 TR000071NCRR NIH HHS M01 RR000073NICHD NIH HHS R01 HD049471NICHD NIH HHS R01-HD049471NIGMS NIH HHS P50 GM060338NIGMS NIH HHS P50-GM060338NIGMS NIH HHS R01 GM056687NIGMS NIH HHS R01-GM056687NIGMS NIH HHS T32 GM008256NIGMS NIH HHS T32-GM008256PHS HHS H133A070026PHS HHS H133A70019
6 · The paper itself

Abstract

objectiveThe pathophysiological response to burn injury disturbs the balance between skeletal muscle protein synthesis and breakdown, resulting in severe muscle wasting. Muscle loss after burn injury is related to increased mortality and morbidity. Consequently, mitigation of this catabolic response has become a focus in the management of these patients. The aim of this review is to discuss the literature pertaining to pharmacological interventions aimed at attenuating skeletal muscle catabolism in severely burned patients. DATA SELECTION: Review of the literature related to skeletal muscle protein metabolism following burn injury was conducted. Emphasis was on studies utilizing stable isotope tracer kinetics to assess the impact of pharmacological interventions on muscle protein metabolism in severely burned patients.

conclusionData support the efficacy of testosterone, oxandrolone, human recombinant growth hormone, insulin, metformin, and propranolol in improving skeletal muscle protein net balance in patients with severe burns. The mechanisms underlying the improvement of protein net balance differ between types and dosages of drugs, but their main effect is on protein synthesis. Finally, the majority of studies have been conducted during the acute hypermetabolic phase of the injury. Except for oxandrolone, the effects of drugs on muscle protein kinetics following discharge from the hospital are largely unknown.

Indexed as

Adrenergic beta-AntagonistsAnabolic AgentsAndrogensBody Surface AreaBurnsHuman Growth HormoneHumansHypoglycemic AgentsInsulinMetforminMuscle ProteinsMuscle, SkeletalOxandrolonePropranololRecombinant ProteinsTestosteroneAdrenergic beta-AntagonistsAnabolic AgentsAndrogensHuman Growth HormoneHypoglycemic AgentsInsulinMetforminMuscle ProteinsOxandrolonePropranololRecombinant ProteinsTestosteroneBurn injuryCatabolismHypermetabolismMuscleProteinStable isotopes

Identifiers

PMID25468473
PMCPMC4417037
OpenAlexW1994333936

What OpenQuestion holds

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Registered trials

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.