Evidence mapPaperPMID 22719910Full record

Trial reportPloS one2012

Effects of meal frequency on metabolic profiles and substrate partitioning in lean healthy males.

Marjet J M Munsters, Wim H M Saris

Registry-linked trialAbstract readRandomized Controlled Trial
In one paragraph

Trial report in PloS one, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01034293 (Effect of Feeding Frequency on Glucose and Insulin Metabolism and Substrate Partitioning), which is not on this map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
field-weighted citation impact
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.

NCT01034293 nacompletednot on this map

Effect of Feeding Frequency on Glucose and Insulin Metabolism and Substrate Partitioning

TypeinterventionalSponsorMaastricht University Medical CenterRan2009 to 2010Enrolled14ConditionsInsulin, Glucose MetabolismArmslow feeding frequency (3x), High feeding frequency (14x)
3 · Its place in the literature

Who cites it

30 citing papers in PubMed.

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  20. Influence of dietary macronutrients on liver fat accumulation and metabolism.Journal of investigative medicine : the official publication of the American Federation for Clinical Research · 2017
    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

2 authors.

Marjet J M MunstersDepartment of Human Biology, Nutrition and Toxicology Research Institute Maastricht, Maastricht University Medical Center, Maastricht, The Netherlands. M.Munsters@maastrichtuniversity.nl
Wim H M Saris

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionThe daily number of meals has an effect on postprandial glucose and insulin responses, which may affect substrate partitioning and thus weight control. This study investigated the effects of meal frequency on 24 h profiles of metabolic markers and substrate partitioning.

methodsTwelve (BMI:21.6 ± 0.6 kg/m(2)) healthy male subjects stayed after 3 days of food intake and physical activity standardization 2 × 36 hours in a respiration chamber to measure substrate partitioning. All subjects randomly received two isoenergetic diets with a Low meal Frequency (3 ×; LFr) or a High meal Frequency (14 ×; HFr) consisting of 15 En% protein, 30 En% fat, and 55 En% carbohydrates. Blood was sampled at fixed time points during the day to measure metabolic markers and satiety hormones.

resultsGlucose and insulin profiles showed greater fluctuations, but a lower AUC of glucose in the LFr diet compared with the HFr diet. No differences between the frequency diets were observed on fat and carbohydrate oxidation. Though, protein oxidation and RMR (in this case SMR + DIT) were significantly increased in the LFr diet compared with the HFr diet. The LFr diet increased satiety and reduced hunger ratings compared with the HFr diet during the day.

conclusionThe higher rise and subsequently fall of insulin in the LFr diet did not lead to a higher fat oxidation as hypothesized. The LFr diet decreased glucose levels throughout the day (AUC) indicating glycemic improvements. RMR and appetite control increased in the LFr diet, which can be relevant for body weight control on the long term.

trial registrationClinicalTrials.gov NCT01034293.

Indexed as

MealsAdolescentAdultArea Under CurveBlood GlucoseCross-Over StudiesHumansInsulinMaleReference ValuesYoung AdultBlood GlucoseInsulin

Identifiers

PMID22719910
PMCPMC3374835

What Socratic holds

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LicenceCC BY
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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 Socratic graph.