Evidence map›Paper›PMID 29571565›Full record

Observational studyClinical nutrition (Edinburgh, Scotland)2019

Heritability of the timing of food intake.

Jesus Lopez-Minguez, Hassan S Dashti, Juan J Madrid-Valero, Juan A Madrid, Richa Saxena, Frank A J L Scheer, Juan R Ordoñana, Marta Garaulet

Registry-linked trialAbstract readObservational Study
In one paragraph

Observational study in Clinical nutrition (Edinburgh, Scotland), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03059576 (Circadian System Heritability Assessed in Free Living Conditions in a Twin Mediterranean Population), which is not on this map. Cited by 28 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed, 2 pooled it
–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.

NCT03059576 completednot on this map

Circadian System Heritability Assessed in Free Living Conditions in a Twin Mediterranean Population

TypeobservationalSponsorUniversidad de MurciaRan2012 to 2017Enrolled106ConditionsHealthyArmsChronobiological status of the subjects
3 · Its place in the literature

Who cites it

28 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Food Intake According to Clock Gene Polymorphisms: A Systematic Review.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2025
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  5. Targeting Habitual Fast Eating as a Modifiable Risk Factor for Type 2 Diabetes: A Propensity Score-Matched Analysis.Diabetes therapy : research, treatment and education of diabetes and related disorders · 2026
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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

8 authors.

Jesus Lopez-MinguezDepartment of Physiology, Faculty of Biology, University of Murcia, Spain; Murcia Institute for BioHealth Research (IMIB-Arrixaca-UM), University of Murcia, Spain.
Hassan S DashtiCenter for Genomic Medicine, Massachusetts General Hospital, Boston, MA, USA.
Juan J Madrid-ValeroMurcia Institute for BioHealth Research (IMIB-Arrixaca-UM), University of Murcia, Spain; Department of Human Anatomy and Psychobiology, School of Psychology, University of Murcia, Spain.
Juan A MadridDepartment of Physiology, Faculty of Biology, University of Murcia, Spain; Murcia Institute for BioHealth Research (IMIB-Arrixaca-UM), University of Murcia, Spain.
Richa SaxenaCenter for Genomic Medicine, Massachusetts General Hospital, Boston, MA, USA; Division of Sleep and Circadian Disorders, Brigham and Women's Hospital, Boston, MA, USA.
Frank A J L ScheerDivision of Sleep and Circadian Disorders, Brigham and Women's Hospital, Boston, MA, USA; Division of Sleep Medicine, Harvard Medical School, Boston, MA, USA.
Juan R OrdoñanaMurcia Institute for BioHealth Research (IMIB-Arrixaca-UM), University of Murcia, Spain; Department of Human Anatomy and Psychobiology, School of Psychology, University of Murcia, Spain. Electronic address: ordonana@um.es.
Marta GarauletMurcia Institute for BioHealth Research (IMIB-Arrixaca-UM), University of Murcia, Spain. Electronic address: garaulet@um.es.

Funding

Genetics of chronotype and impact on metabolic diseaseR01DK107859 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI Richa Saxena · 2016 to 2026
$4.0M
Melatonin and Receptor Gene Variant: Linking Circadian System and Type 2 DiabetesR01DK102696 · NIDDK · BRIGHAM AND WOMEN'S HOSPITAL · PI SAXENA, RICHA, SCHEER, FRANK A · 2015 to 2019
$3.8M
Impact of Malatonin, Food Timing and Receptor Variant on Type 2 Diabetes RiskR01DK105072 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI SAXENA, RICHA, SCHEER, FRANK A · 2016 to 2020
$3.2M
Meal Time Effects on Metabolic Health.R01DK099512 · NIDDK · BRIGHAM AND WOMEN'S HOSPITAL · PI SCHEER, FRANK A · 2014 to 2017
$2.8M
Development of countermeasures against adverse metabolic effects of shift workR01HL118601 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI SCHEER, FRANK A · 2014 to 2017
$2.6M
Mechanisms underlying adverse health consequences of shift workR01HL094806 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI SCHEER, FRANK A · 2009 to 2013
$1.6M
NHLBI NIH HHS R01 HL094806NHLBI NIH HHS R01 HL118601NIDDK NIH HHS R01 DK099512NIDDK NIH HHS R01 DK102696NIDDK NIH HHS R01 DK105072NIDDK NIH HHS R01 DK107859
6 · The paper itself

Abstract

BACKGROUND &

aimsWhile environmental factors are presumed to be primary drivers of food timing, preliminary evidence suggests that genetics may be an additional determinant. The aim was to explore the relative contribution of genetics and environmental factors to variation in the timing of food intake in a Spanish twin population. Because chronotype, bedtime and wake time are related to food timing, covariance with food timing was further assessed.

methodsIn this observational study, 53 pairs of adult (mean (SD) = 52 (6.03) years) female twins (28 monozygotic; 25 dizygotic) were recruited from the Murcia Twin Register. Zygosity was determined by DNA-testing. Timing of the three main meals of the day was assessed via 7-day dietary records, and the midpoint of food intake was computed by calculating the midpoint between breakfast and dinner times. Chronotype, bedtime and wake time were self-reported. Heritability of food timing and related traits were estimated by comparing monozygotic and dizygotic twin correlations and fitting genetic structural equation models to measured variables.

resultsWe observed genetic influences for food timing, with highest heritability for the midpoint of food intake (64%) in an overweight/obese population (BMI = 26.01 ± 3.77). Genetic factors contributed to a higher degree to the timing of breakfast (56%) than the timing of lunch (38%) or dinner (n.s.). Similarly, heritability estimates were larger in related behavioral traits earlier on in the day (i.e. wake time, (55%)), than those later on in the day (i.e. bedtime, (38%)). Bivariate analyses revealed a significant genetic overlap between food timing and bedtime and chronotype (rG between 0.78 and 0.91).

conclusionsGenetic influences appear to account for a significant proportion of the variability in food timing, particularly breakfast. Thus, interventions related to food timing may be more effective when targeting afternoon/evening traits, such as lunch or dinner times. Furthermore, our data suggest shared genetic architecture underlying food timing and phenotypically related traits. CLINICAL TRIAL: NCT03059576. https://clinicaltrials.gov/ct2/show/NCT03059576.

Indexed as

AgedDietEatingEnvironmentFeeding BehaviorFemaleHumansMaleMiddle AgedTime FactorsTwins, DizygoticTwins, MonozygoticDietary intakeFood timingHeritabilityTwins

Identifiers

PMID29571565
PMCPMC6135708

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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 OpenQuestion graph.