Evidence map›Paper›PMID 23357545›Full record

Trial reportJournal of cystic fibrosis : official journal of the European Cystic Fibrosis Society2013

Dietary essential amino acids are highly anabolic in pediatric patients with cystic fibrosis.

Mariëlle P K J Engelen, Gulnur Com, Robert R Wolfe, Nicolaas E P Deutz

Open access · bronzeAbstract readComparative StudyRandomized Controlled Trial
In one paragraph

Trial report in Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
3.8field-weighted citation impact, top 6% 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

20 citing papers in PubMed, 42 citations in OpenAlex.

  1. Trial
  2. Trial
  3. High anabolic potential of essential amino acid mixtures in advanced nonsmall cell lung cancer.Annals of oncology : official journal of the European Society for Medical Oncology · 2015
    Trial
  4. Trial
  5. Trial
  6. Article
  7. Review
  8. Review
  9. Article
  10. Review
  11. Article
  12. Article
  13. Update on maximal anabolic response to dietary protein.Clinical nutrition (Edinburgh, Scotland) · 2018
    Review
  14. Personalizing protein nourishment.Critical reviews in food science and nutrition · 2017
    Review
  15. Article
  16. Article
  17. Article
  18. Review
  19. Article
  20. 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

4 authors at 3 institutions in 1 country.

Mariëlle P K J EngelenCenter for Translational Research in Aging & Longevity, Dept. of Geriatrics, University of Arkansas for Medical Sciences, Little Rock, AR, USA. mpkj.engelen@ctral.org
Gulnur Com
Robert R Wolfe
Nicolaas E P Deutz
Texas A&M University · USArkansas Children's Hospital · USUniversity of Arkansas for Medical Sciences · US

Funding

TSQ Vantage Bundle with Acquity UltraPerformance LCS10RR027047 · NCRR · UNIV OF ARKANSAS FOR MED SCIS · PI DEUTZ, NICOLAAS E · 2010 to 2010
$398k
NCRR NIH HHS S10 RR027047NCRR NIH HHS S10RR027047
6 · The paper itself

Abstract

backgroundCurrent nutritional approaches have been partially successful in Cystic Fibrosis (CF). Essential amino acids mixtures with high Leucine levels (EAA) have anabolic properties in catabolic conditions, however data in CF are lacking.

methodsOn two days according a randomized crossover design, 15 pediatric CF patients ingested 6.7 g EAA versus mixture of total amino acids as present in whey. Whole body protein and Arginine metabolism (as EAA lack Arginine) were assessed by stable isotope methodology.

resultsProtein synthesis (P<0.05) but not protein breakdown was higher after EAA and 70% higher values for net anabolism (P<0.001)were found both in patients with and without nutritional failure. Arginine turnover was lower (P<0.001) and de novo Arginine synthesis tended lower (P=0.09) after EAA. Nitric oxide synthesis was not different.

conclusionsCF patients are highly responsive to EAA intake independent of their nutritional status. Addition of Arginine to the EAA mixture may be warranted in CF.

Indexed as

DietAdolescentAmino Acids, EssentialChildCross-Over StudiesCystic FibrosisFemaleHumansMaleYoung AdultAmino Acids, EssentialArginine productionbalanced mixture of essential and non-essential amino acidsBMIbody mass indexCFcTTRCystic Fibrosisde novo Arginine productiondual-energy X-ray absorptiometryDXAEAAessential amino acidsEssential amino acidsfat-free massfat massFEV(1)FFMFMforced expiratory volume in 1sforced vital capacityFVCnet protein synthesisNetPSnitric oxidenitric oxide productionNitric oxide synthesisNONutritional failureQ Arginine to CitrullineQ Citrulline to ArginineRarate of appearanceSEstandard errorTAAtracer tracee ratiotracer–tracee ratios of amino acids corrected for their baseline valueTTRWbPBWbPSWhole body protein anabolismwhole body protein breakdownwhole body protein synthesis

Identifiers

PMID23357545
PMCPMC3640686
OpenAlexW2072095946

What OpenQuestion holds

Textmetadata
LicenceTDM
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.