Evidence map›Paper›PMID 25027794›Full record

ArticleNutrition & diabetes2014

Specific appetite, energetic and metabolomics responses to fat overfeeding in resistant-to-bodyweight-gain constitutional thinness.

N Germain, B Galusca, D Caron-Dorval, J-F Martin, E Pujos-Guillot, Y Boirie, Y Khalfallah, Y Ling, J S Minnion, S R Bloom and 2 more

Open access · goldAbstract read
In one paragraph

Article in Nutrition & diabetes, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed, 2 pooled it
1.7field-weighted citation impact, top 17% 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

26 citing papers in PubMed, 2 syntheses or guidelines pooled it, 56 citations in OpenAlex.

  1. Pooled it
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  10. Persistent thinness and anorexia nervosa differ on a genomic level.European journal of human genetics : EJHG · 2024
    Article
  11. Article
  12. Article
  13. Review
  14. Physiological protection against weight gain: evidence from overfeeding studies and future directions.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2023
    Review
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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

12 authors at 9 institutions in 3 countries.

N Germain1] Division of Endocrinology, Diabetes, Metabolism and Eating disorders, CHU Saint-Etienne, Saint-Etienne Cedex, France [2] Laboratory of Exercise Physiology (LPE EA 4338), University of Lyon, Saint-Etienne Cedex 2, France.
B Galusca1] Division of Endocrinology, Diabetes, Metabolism and Eating disorders, CHU Saint-Etienne, Saint-Etienne Cedex, France [2] Laboratory of Exercise Physiology (LPE EA 4338), University of Lyon, Saint-Etienne Cedex 2, France.
D Caron-Dorval1] Division of Endocrinology, Diabetes, Metabolism and Eating disorders, CHU Saint-Etienne, Saint-Etienne Cedex, France [2] Laboratory of Exercise Physiology (LPE EA 4338), University of Lyon, Saint-Etienne Cedex 2, France.
J-F MartinUMR 1019, Human Nutrition Unit, INRA, Research Center Clermont-Ferrand, Clermont-Ferrand, France.
E Pujos-GuillotUMR 1019, Human Nutrition Unit, INRA, Research Center Clermont-Ferrand, Clermont-Ferrand, France.
Y BoirieUMR 1019, Human Nutrition Unit, INRA, Research Center Clermont-Ferrand, Clermont-Ferrand, France.
Y KhalfallahDivision of Endocrinology, Diabetes, Metabolism and Eating disorders, CHU Saint-Etienne, Saint-Etienne Cedex, France.
Y Ling1] Division of Endocrinology, Diabetes, Metabolism and Eating disorders, CHU Saint-Etienne, Saint-Etienne Cedex, France [2] Laboratory of Exercise Physiology (LPE EA 4338), University of Lyon, Saint-Etienne Cedex 2, France.
J S MinnionDivision of Diabetes, Endocrinology and Metabolism, Imperial College, London, UK.
S R BloomDivision of Diabetes, Endocrinology and Metabolism, Imperial College, London, UK.
J EpelbaumUMR 894, INSERM, Psychiatry and Neurosciences Center, Paris Descartes University, Paris, France.
B Estour1] Division of Endocrinology, Diabetes, Metabolism and Eating disorders, CHU Saint-Etienne, Saint-Etienne Cedex, France [2] Laboratory of Exercise Physiology (LPE EA 4338), University of Lyon, Saint-Etienne Cedex 2, France.
Laboratoire Interuniversitaire de Biologie de la Motricité · FRUnité de Nutrition Humaine · FRUnité de recherche sur les maladies cardiovasculaires et métaboliques · FRCentre Hospitalier Universitaire de Saint-Étienne · FRDélégation Paris 5 · FRImperial College London · GBInstitut National de Recherche pour l'Agriculture, l'Alimentation et l'Environnement · FROxford Centre for Diabetes, Endocrinology and Metabolism · GBUniversité Claude Bernard Lyon 1 · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundContrasting with obesity, constitutional thinness (CT) is a rare condition of natural low bodyweight. CT exhibits preserved menstruation in females, no biological marker of undernutrition, no eating disorders but a bodyweight gain desire. Anorexigenic hormonal profile with high peptide tyrosine tyrosine (PYY) was shown in circadian profile. CT could be considered as the opposite of obesity, where some patients appear to resist diet-induced bodyweight loss.

objectiveThe objective of this study was to evaluate appetite regulatory hormones in CTs in an inverse paradigm of diet-induced weight loss.

methodsA 4-week fat overfeeding (2640 kJ excess) was performed to compare eight CT women (body mass index (BMI)<17.5 kg m(-)(2)) to eight female controls (BMI 18.5-25 kg m(-)(2)). Appetite regulatory hormones profile after test meal, food intake, bodyweight, body composition, energy expenditure and urine metabolomics profiles were monitored before and after overfeeding.

resultsAfter overfeeding, fasting total and acylated ghrelin were significantly lower in CTs than in controls (P=0.01 and 0.03, respectively). After overfeeding, peptide tyrosine tyrosine (PYY) and glucagon-like-peptide 1 both presented earlier (T15 min vs T30 min) and higher post-meal responses (incremental area under the curve) in CTs compared with controls. CTs failed to increase bodyweight (+0.22±0.18 kg, P=0.26 vs baseline), contrasting with controls (+0.72±0.26 kg, P=0.03 vs baseline, P=0.01 vs CTs). Resting energy expenditure increased in CTs only (P=0.031 vs baseline). After overfeeding, a significant negative difference between total energy expenditure and food intake was noticed in CTs only (-2754±720 kJ, P=0.01).

conclusionCTs showed specific adaptation to fat overfeeding: overall increase in anorexigenic hormonal profile, enhanced post prandial GLP-1 and PYY and inverse to controls changes in urine metabolomics. Overfeeding revealed a paradoxical positive energy balance contemporary to a lack of bodyweight gain, suggesting yet unknown specific energy expenditure pathways in CTs.

Identifiers

PMID25027794
PMCPMC5189928
OpenAlexW2088160643

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

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.