Evidence map›Paper›PMID 29546280›Full record

Trial reportThe Journal of clinical endocrinology and metabolism2018

Metabolic Inflexibility Is an Early Marker of Bed-Rest-Induced Glucose Intolerance Even When Fat Mass Is Stable.

Floriane Rudwill, Donal O'Gorman, Etienne Lefai, Isabelle Chery, Alexandre Zahariev, Sylvie Normand, Allan F Pagano, Angèle Chopard, Anthony Damiot, Claire Laurens and 11 more

Open access · bronzeAbstract readRandomized Controlled Trial
In one paragraph

Trial report in The Journal of clinical endocrinology and metabolism, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed, 2 pooled it
2.6field-weighted citation impact, top 10% 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

39 citing papers in PubMed, 2 syntheses or guidelines pooled it, 58 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

21 authors at 13 institutions in 5 countries.

Floriane RudwillUniversité de Strasbourg, CNRS, IPHC UMR 7178, Strasbourg, France.
Donal O'Gorman3U Diabetes Consortium, Dublin City University, Dublin, Ireland.
Etienne LefaiCarmen INSERM U1060, University of Lyon, INRA U1235, Lyon, France.
Isabelle CheryUniversité de Strasbourg, CNRS, IPHC UMR 7178, Strasbourg, France.
Alexandre ZaharievUniversité de Strasbourg, CNRS, IPHC UMR 7178, Strasbourg, France.
Sylvie NormandHuman Nutrition Research Centre of Rhône-Alpes, Hospices Civils de Lyon, Lyon, France.
Allan F PaganoUniversité de Montpellier, INRA, UMR 866 Dynamique Musculaire et Métabolisme, Montpellier, France.
Angèle ChopardUniversité de Montpellier, INRA, UMR 866 Dynamique Musculaire et Métabolisme, Montpellier, France.
Anthony DamiotUniversité de Strasbourg, CNRS, IPHC UMR 7178, Strasbourg, France.
Claire LaurensUniversité de Strasbourg, CNRS, IPHC UMR 7178, Strasbourg, France.
Leanne HodsonOxford Centre for Diabetes, Endocrinology and Metabolism, University of Oxford, Oxford, United Kingdom.
Emmanuelle Canet-SoulasCarmen INSERM U1060, University of Lyon, INRA U1235, Lyon, France.
Martina HeerInstitute of Nutritional and Food Sciences, Human Nutrition, University of Bonn, Bonn, Germany.
Petra Frings MeuthenGerman Aerospace Center (DLR), Institute of Aerospace Medicine, Cologne, Germany.
Judith BuehlmeierGerman Aerospace Center (DLR), Institute of Aerospace Medicine, Cologne, Germany.
Natalie BaeckerGerman Aerospace Center (DLR), Institute of Aerospace Medicine, Cologne, Germany.
Laure MeillerCarmen INSERM U1060, University of Lyon, INRA U1235, Lyon, France.
Guillemette Gauquelin-KochCentre National d'Etudes Spatiales, Paris, France.
Stéphane BlancUniversité de Strasbourg, CNRS, IPHC UMR 7178, Strasbourg, France.
Chantal SimonCarmen INSERM U1060, University of Lyon, INRA U1235, Lyon, France.
Audrey BergouignanUniversité de Strasbourg, CNRS, IPHC UMR 7178, Strasbourg, France.
Centre National de la Recherche Scientifique · FRDeutsches Zentrum für Luft- und Raumfahrt e. V. (DLR) · DEUniversité Claude Bernard Lyon 1 · FRDynamique Musculaire et MétabolismeInstitut Pluridisciplinaire Hubert Curien · FRCentre National d'Études Spatiales · FRHealth Service Executive · IEHospices Civils de Lyon · FRLaboratoire CarMeN · FRUniversité de Strasbourg · FRUniversity of Bonn · DEUniversity of Colorado Anschutz Medical Campus · USUniversity of Oxford · GB

Funding

PILOT STUDY--SUBSTRATE METABOLISM IN EXTREMELY LOW BIRTH WEIGHT INFANTSP30DK048520 · NIDDK · UNIVERSITY OF COLORADO DENVER · PI Edward L Melanson · 1995 to 2026
$32.6M
NIDDK NIH HHS P30 DK048520
6 · The paper itself

Abstract

Context: The effects of energy-balanced bed rest on metabolic flexibility have not been thoroughly examined. Objective: We investigated the effects of 21 days of bed rest, with and without whey protein supplementation, on metabolic flexibility while maintaining energy balance. We hypothesized that protein supplementation mitigates metabolic inflexibility by preventing muscle atrophy. Design and Setting: Randomized crossover longitudinal study conducted at the German Aerospace Center, Cologne, Germany. Participants and Interventions: Ten healthy men were randomly assigned to dietary countermeasure or isocaloric control diet during a 21-day bed rest. Outcome Measures: Before and at the end of the bed rest, metabolic flexibility was assessed during a meal test. Secondary outcomes were glucose tolerance by oral glucose tolerance test, body composition by dual energy X-ray absorptiometry, ectopic fat storage by magnetic resonance imaging, and inflammation and oxidative stress markers. Results: Bed rest decreased the ability to switch from fat to carbohydrate oxidation when transitioning from fasted to fed states (i.e., metabolic inflexibility), antioxidant capacity, fat-free mass (FFM), and muscle insulin sensitivity along with greater fat deposition in muscle (P < 0.05 for all). Changes in fasting insulin and inflammation were not observed. However, glucose tolerance was reduced during acute overfeeding. Protein supplementation did not prevent FFM loss and metabolic alterations. Conclusions: Physical inactivity triggers metabolic inflexibility, even when energy balance is maintained. Although reduced insulin sensitivity and increased fat deposition were observed at the muscle level, systemic glucose intolerance was detected only in response to a moderately high-fat meal. This finding supports the role of physical inactivity in metabolic inflexibility and suggests that metabolic inflexibility precedes systemic glucose intolerance.

Indexed as

Adipose TissueAdiposityAdultBed RestBiomarkersBody CompositionCross-Over StudiesDietEarly DiagnosisEnergy MetabolismGlucose IntoleranceHumansInsulin ResistanceLongitudinal StudiesMaleTime FactorsBiomarkers

Identifiers

PMID29546280
PMCPMC7263792
OpenAlexW2792573235

What OpenQuestion holds

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LicenceCC BY-NC
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.