Evidence map›Paper›PMID 25870289›Full record

Trial reportProceedings of the National Academy of Sciences of the United States of America2015

Endogenous circadian system and circadian misalignment impact glucose tolerance via separate mechanisms in humans.

Christopher J Morris, Jessica N Yang, Joanna I Garcia, Samantha Myers, Isadora Bozzi, Wei Wang, Orfeu M Buxton, Steven A Shea, Frank A J L Scheer

4 registry-linked trialsOpen access · bronzeAbstract readClinical TrialMulticenter Study
In one paragraph

Trial report in Proceedings of the National Academy of Sciences of the United States of America, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 4 registered trials, which are not on this map. Cited by 308 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
308citing papers in PubMed, 3 pooled it
15.5field-weighted citation impact, top 1% 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.

NCT03647306 naactive not recruitingnot on this mapstarted 2018, after this paper: background citation

Behavioral Chronotype: Impact on Sleep and Metabolism

TypeinterventionalSponsorUniversity of ChicagoRan2018 to 2027Enrolled200ConditionsType2 Diabetes Mellitus, Cardiovascular DiseasesArmsEarly Total Caloric Intake, Late Total Caloric Intake, Extended Overnight Fast
NCT06887543 naterminatednot on this mapstarted 2025, after this paper: background citation

The Impact of Time Restricted Eating on Type 2 Diabetes Study

TypeinterventionalSponsorRockefeller UniversityRan2025 to 2025Enrolled2ConditionsType 2 DiabetesArmsMeal timing, Time restricted eating, Usual feeding pattern.
NCT06916039 naenrolling by invitationnot on this mapstarted 2025, after this paper: background citation

Randomized Controlled Nutrition Trial on Breakfast Glycaemic Index on the Course of Memory and Attention Among Young Adults - Relevance of Chronotype

TypeinterventionalSponsorAnette BuykenRan2025 to 2027Enrolled177ConditionsHealthyArmsimmediate verbal memory after high GI breakfast, immediate verbal memory after low glycemic index breakfast
NCT06941740 naenrolling by invitationnot on this mapstarted 2025, after this paper: background citation

Randomized Controlled Nutrition Trial on Reactive Hypoglycaemia on the Course of Memory and Attention Among Young Adults - Relevance of Chronotype

TypeinterventionalSponsorAnette BuykenRan2025 to 2027Enrolled177ConditionsHealthyArmsimmediate verbal memory after low glycemic index breakfast inducing no reactive hypoglycaemia, immediate verbal memory after low glycemic index breakfast causing reactive hypoglycaemia
3 · Its place in the literature

Who cites it

308 citing papers in PubMed, 3 syntheses or guidelines pooled it, 474 citations in OpenAlex.

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248 more citing papers are in PubMed but not listed here.

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 4 institutions in 1 country.

Christopher J MorrisMedical Chronobiology Program, Division of Sleep and Circadian Disorders, Brigham and Women's Hospital, Boston, MA 02115; Division of Sleep Medicine, Harvard Medical School, Boston, MA 02115; cjmorris@partners.org fscheer@rics.bwh.harvard.edu.
Jessica N YangMedical Chronobiology Program, Division of Sleep and Circadian Disorders, Brigham and Women's Hospital, Boston, MA 02115;
Joanna I GarciaMedical Chronobiology Program, Division of Sleep and Circadian Disorders, Brigham and Women's Hospital, Boston, MA 02115;
Samantha MyersMedical Chronobiology Program, Division of Sleep and Circadian Disorders, Brigham and Women's Hospital, Boston, MA 02115;
Isadora BozziMedical Chronobiology Program, Division of Sleep and Circadian Disorders, Brigham and Women's Hospital, Boston, MA 02115;
Wei WangMedical Chronobiology Program, Division of Sleep and Circadian Disorders, Brigham and Women's Hospital, Boston, MA 02115; Division of Sleep Medicine, Harvard Medical School, Boston, MA 02115;
Orfeu M BuxtonMedical Chronobiology Program, Division of Sleep and Circadian Disorders, Brigham and Women's Hospital, Boston, MA 02115; Division of Sleep Medicine, Harvard Medical School, Boston, MA 02115; Department of Biobehavioral Health, Pennsylvania State University, University Park, PA 16802; and.
Steven A SheaMedical Chronobiology Program, Division of Sleep and Circadian Disorders, Brigham and Women's Hospital, Boston, MA 02115; Division of Sleep Medicine, Harvard Medical School, Boston, MA 02115; Oregon Institute of Occupational Health Sciences, Oregon Health & Science University, Portland, OR 97239.
Frank A J L ScheerMedical Chronobiology Program, Division of Sleep and Circadian Disorders, Brigham and Women's Hospital, Boston, MA 02115; Division of Sleep Medicine, Harvard Medical School, Boston, MA 02115; cjmorris@partners.org fscheer@rics.bwh.harvard.edu.
Brigham and Women's Hospital · USCircadian (United States) · USHarvard University · USOregon Health & Science University · US

Funding

HARVARD CLINICAL AND TRANSLATIONAL SCIENCE CENTER (UL1)UL1RR025758 · NCRR · HARVARD MEDICAL SCHOOL · PI NADLER, LEE MARSHALL · 2008 to 2011
$91.4M
TRANSPLANTATION ANALYSIS OF CIRCADIAN RHYTHMS AND AGINGP01AG009975 · NIA · BRIGHAM AND WOMEN'S HOSPITAL · PI SAPER, CLIFFORD B · 1991 to 2018
$23.1M
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
Chronobiology of cardiovascular and pulmonary diseaseK24HL076446 · NHLBI · OREGON HEALTH & SCIENCE UNIVERSITY · PI SHEA, STEVEN A · 2004 to 2013
$1.5M
NCRR NIH HHS UL1 RR025758NCRR NIH HHS UL1RR025758NHLBI NIH HHS K24 HL076446NHLBI NIH HHS R01 HL094806NHLBI NIH HHS R01 HL118601NIA NIH HHS P01 AG009975NIDDK NIH HHS R01 DK099512
6 · The paper itself

Abstract

Glucose tolerance is lower in the evening and at night than in the morning. However, the relative contribution of the circadian system vs. the behavioral cycle (including the sleep/wake and fasting/feeding cycles) is unclear. Furthermore, although shift work is a diabetes risk factor, the separate impact on glucose tolerance of the behavioral cycle, circadian phase, and circadian disruption (i.e., misalignment between the central circadian pacemaker and the behavioral cycle) has not been systematically studied. Here we show--by using two 8-d laboratory protocols--in healthy adults that the circadian system and circadian misalignment have distinct influences on glucose tolerance, both separate from the behavioral cycle. First, postprandial glucose was 17% higher (i.e., lower glucose tolerance) in the biological evening (8:00 PM) than morning (8:00 AM; i.e., a circadian phase effect), independent of the behavioral cycle effect. Second, circadian misalignment itself (12-h behavioral cycle inversion) increased postprandial glucose by 6%. Third, these variations in glucose tolerance appeared to be explained, at least in part, by different mechanisms: during the biological evening by decreased pancreatic β-cell function (27% lower early-phase insulin) and during circadian misalignment presumably by decreased insulin sensitivity (elevated postprandial glucose despite 14% higher late-phase insulin) without change in early-phase insulin. We explored possible contributing factors, including changes in polysomnographic sleep and 24-h hormonal profiles. We demonstrate that the circadian system importantly contributes to the reduced glucose tolerance observed in the evening compared with the morning. Separately, circadian misalignment reduces glucose tolerance, providing a mechanism to help explain the increased diabetes risk in shift workers.

Indexed as

Circadian RhythmPostprandial PeriodSleepAdultBlood GlucoseDiabetes MellitusFemaleGlucose Tolerance TestHumansInsulin-Secreting CellsMaleMiddle AgedBlood Glucosecircadian disruptiondiabetesglucose metabolismnight workshift work

Identifiers

PMID25870289
PMCPMC4418873
OpenAlexW2081139788

What OpenQuestion holds

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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.