Evidence map›Paper›PMID 32525525›Full record

Trial reportThe Journal of clinical endocrinology and metabolism2020

Metabolic Effects of Late Dinner in Healthy Volunteers-A Randomized Crossover Clinical Trial.

Chenjuan Gu, Nga Brereton, Amy Schweitzer, Matthew Cotter, Daisy Duan, Elisabet Børsheim, Robert R Wolfe, Luu V Pham, Vsevolod Y Polotsky, Jonathan C Jun

2 registry-linked trialsOpen access · bronzeAbstract readRandomized Controlled Trial
In one paragraph

Trial report in The Journal of clinical endocrinology and metabolism, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 73 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
73citing papers in PubMed, 1 pooled it
8.3field-weighted citation impact, top 2% 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.

NCT04671797 nacompletednot on this mapstarted 2021, after this paper: background citation

Dinner Time 2: Effect of Delayed Eating or Sleeping on Metabolism

TypeinterventionalSponsorJohns Hopkins UniversityRan2021 to 2025Enrolled41ConditionsHealthyArmsEarly dinner, Late Dinner, Late Dinner + Late Sleep
NCT05745441 narecruitingnot on this mapstarted 2023, after this paper: background citation

Dinner Time for Obesity and Prediabetes

TypeinterventionalSponsorJohns Hopkins UniversityRan2023 to 2028Enrolled32ConditionsPreDiabetes, Obesity, HealthyArmsEarly Dinner, Late Dinner, Early Dinner tracer, Late Dinner tracer
3 · Its place in the literature

Who cites it

73 citing papers in PubMed, 1 synthesis or guideline pooled it, 125 citations in OpenAlex.

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  16. 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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13 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 3 institutions in 1 country.

Chenjuan GuDivision of Pulmonary and Critical Care, Department of Medicine, Johns Hopkins University, Baltimore, Maryland.
Nga BreretonInstitute for Clinical and Translational Research, Johns Hopkins University, Baltimore, Maryland.
Amy SchweitzerInstitute for Clinical and Translational Research, Johns Hopkins University, Baltimore, Maryland.
Matthew CotterArkansas Children's Nutrition Center, Arkansas Children's Research Institute, Little Rock, Arkansas.
Daisy DuanDivision of Endocrinology, Diabetes and Metabolism, Department of Medicine, Johns Hopkins University, Baltimore, Maryland.
Elisabet BørsheimArkansas Children's Nutrition Center, Arkansas Children's Research Institute, Little Rock, Arkansas.
Robert R WolfeDepartment of Pediatrics, The University of Arkansas for Medical Sciences, Little Rock, Arkansas.
Luu V PhamDivision of Pulmonary and Critical Care, Department of Medicine, Johns Hopkins University, Baltimore, Maryland.
Vsevolod Y PolotskyDivision of Pulmonary and Critical Care, Department of Medicine, Johns Hopkins University, Baltimore, Maryland.
Jonathan C JunDivision of Pulmonary and Critical Care, Department of Medicine, Johns Hopkins University, Baltimore, Maryland.
Johns Hopkins University · USArkansas Children's Nutrition Center · USUniversity of Arkansas for Medical Sciences · US

Funding

Clinical Research&Epidemiology in Diabetes&EndocrinologyT32DK062707 · NIDDK · JOHNS HOPKINS UNIVERSITY · PI TODD T BROWN, Wendy Lynet Bennett · 2002 to 2026
$7.3M
Lipolysis during sleep and cardiometabolic consequences of sleep apneaR01HL135483 · NHLBI · JOHNS HOPKINS UNIVERSITY · PI JUN, JONATHAN C. · 2018 to 2022
$4.3M
Pilot Study of Beta Adrenergic Blockade to Prevent Metabolic Consequences of Sleep ApneaR03HL138068 · NHLBI · JOHNS HOPKINS UNIVERSITY · PI JUN, JONATHAN C. · 2017 to 2018
$164k
NHLBI NIH HHS R01 HL135483NHLBI NIH HHS R03 HL138068NIDDK NIH HHS T32 DK062707
6 · The paper itself

Abstract

contextConsuming calories later in the day is associated with obesity and metabolic syndrome. We hypothesized that eating a late dinner alters substrate metabolism during sleep in a manner that promotes obesity.

objectiveThe objective of this work is to examine the impact of late dinner on nocturnal metabolism in healthy volunteers. DESIGN AND

settingThis is a randomized crossover trial of late dinner (LD, 22:00) vs routine dinner (RD, 18:00), with a fixed sleep period (23:00-07:00) in a laboratory setting.

participantsParticipants comprised 20 healthy volunteers (10 male, 10 female), age 26.0 ± 0.6 years, body mass index 23.2 ± 0.7 kg/m2, accustomed to a bedtime between 22:00 and 01:00.

interventionsAn isocaloric macronutrient diet was administered on both visits. Dinner (35% daily kcal, 50% carbohydrate, 35% fat) with an oral lipid tracer ([2H31] palmitate, 15 mg/kg) was given at 18:00 with RD and 22:00 with LD.

main outcome measuresMeasurements included nocturnal and next-morning hourly plasma glucose, insulin, triglycerides, free fatty acids (FFAs), cortisol, dietary fatty acid oxidation, and overnight polysomnography.

resultsLD caused a 4-hour shift in the postprandial period, overlapping with the sleep phase. Independent of this shift, the postprandial period following LD was characterized by higher glucose, a triglyceride peak delay, and lower FFA and dietary fatty acid oxidation. LD did not affect sleep architecture, but increased plasma cortisol. These metabolic changes were most pronounced in habitual earlier sleepers determined by actigraphy monitoring.

conclusionLD induces nocturnal glucose intolerance, and reduces fatty acid oxidation and mobilization, particularly in earlier sleepers. These effects might promote obesity if they recur chronically.

Indexed as

AdolescentAdultBlood GlucoseCross-Over StudiesFatty Acids, NonesterifiedFeeding BehaviorFemaleGlucose IntoleranceHealthy VolunteersHumansHydrocortisoneInsulinMaleMealsObesityOxidation-ReductionBlood GlucoseFatty Acids, NonesterifiedHydrocortisoneInsulinTriglyceridescortisolfatty acid oxidationglucoselate eatinglipidssleep

Identifiers

PMID32525525
PMCPMC7337187
OpenAlexW3033969188

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.