Evidence map›Paper›PMID 30183740›Full record

Trial reportPloS one2018

Prolonged fasting-induced metabolic signatures in human skeletal muscle of lean and obese men.

Ann Mosegaard Bak, Mikkel Holm Vendelbo, Britt Christensen, Rikke Viggers, Bo Martin Bibby, Jørgen Rungby, Jens Otto Lunde Jørgensen, Niels Møller, Niels Jessen

Open access · goldAbstract readClinical Trial
In one paragraph

Trial report in PloS one, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed, 2 pooled it
1.9field-weighted citation impact, top 14% 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

22 citing papers in PubMed, 2 syntheses or guidelines pooled it, 37 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

9 authors at 1 institution in 1 country.

Ann Mosegaard BakMedical Research Laboratory, Department of Clinical Medicine, Aarhus University, Aarhus, Denmark.ORCID 0000-0003-3597-8378
Mikkel Holm VendelboMedical Research Laboratory, Department of Clinical Medicine, Aarhus University, Aarhus, Denmark.
Britt ChristensenDepartment of Endocrinology and Internal Medicine (MEA), Aarhus University Hospital, Aarhus, Denmark.
Rikke ViggersMedical Research Laboratory, Department of Clinical Medicine, Aarhus University, Aarhus, Denmark.
Bo Martin BibbyDepartment of Public Health, Aarhus University, Aarhus, Denmark.
Jørgen RungbyDepartment of Biomedicine, Aarhus University, Denmark.
Jens Otto Lunde JørgensenMedical Research Laboratory, Department of Clinical Medicine, Aarhus University, Aarhus, Denmark.
Niels MøllerMedical Research Laboratory, Department of Clinical Medicine, Aarhus University, Aarhus, Denmark.
Niels JessenDepartment of Endocrinology and Internal Medicine (MEA), Aarhus University Hospital, Aarhus, Denmark.
Aarhus University · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Insulin resistance is a well-known physiological adaptation to prolonged fasting in healthy skeletal muscle. Obesity is associated with insulin resistance and metabolic inflexibility in skeletal muscle, and a pronounced increase in the risk of metabolic complications. Under the hypothesis that the metabolic traits of insulin resistance associated with prolonged fasting are different from insulin resistance associated with obesity, we examined nine obese and nine lean participants during 12 and 72h of fasting, respectively. Insulin resistance in obese participants was associated with impaired insulin signaling, and reduced levels of glucose-6-phosphate and TCA-cycle intermediates. 72h of fasting in lean participants reduced insulin-stimulated glucose uptake to levels similar to obese participants fasted for 12h. This was associated with increased lipid oxidation, but not accumulation of diacylglycerol or acylcarnitines and impairment of insulin signaling. Prolonged fasting was associated with pronounced increases in β-hydroxybutyrate and β- hydroxybutyrylcarnitine levels in skeletal muscle suggesting augmented ketone body metabolism. Fasting induced insulin resistance may be a consequence of substrate competition. The underlying mechanism behind insulin resistance in obesity is thus not comparable to the physiological adaptations in skeletal muscle induced by prolonged fasting in lean participants.

Indexed as

FastingInsulin ResistanceSignal TransductionAdultGlucose-6-PhosphateHumansInsulinLipid MetabolismMaleMuscle, SkeletalObesityTime FactorsGlucose-6-PhosphateInsulin

Identifiers

PMID30183740
PMCPMC6124727
OpenAlexW2891954475

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.