Evidence map›Paper›PMID 42324738›Full record

ArticleNutrition bulletin2026

Diurnal Variation and Impairment of Postprandial Glucose-Insulin Responses and Lipid Rhythms in Simulated Shift Work.

Ameena M Khan Sullivan, Cheryl M Isherwood, Hana Hassanin, Debra J Skene, Daan R van der Veen

Abstract read
In one paragraph

Article in Nutrition bulletin, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

5 authors.

Ameena M Khan SullivanSection of Chronobiology, Faculty of Health and Medical Sciences, University of Surrey, Guildford, UK.ORCID https://orcid.org/0000-0002-8806-6412
Cheryl M IsherwoodSection of Chronobiology, Faculty of Health and Medical Sciences, University of Surrey, Guildford, UK.ORCID https://orcid.org/0000-0002-5790-4460
Hana HassaninSurrey Clinical Research Facility, Faculty of Health and Medical Sciences, University of Surrey, Guildford, UK.ORCID https://orcid.org/0000-0002-1492-3653
Debra J SkeneSection of Chronobiology, Faculty of Health and Medical Sciences, University of Surrey, Guildford, UK.ORCID https://orcid.org/0000-0001-8202-6180
Daan R van der VeenSection of Chronobiology, Faculty of Health and Medical Sciences, University of Surrey, Guildford, UK.ORCID https://orcid.org/0000-0001-8037-1407

Funding

Wellcome TrustWellcome Trust 23704/Z/21/Z
6 · The paper itself

Abstract

Shift work is associated with insulin resistance, dyslipidaemia and metabolic syndrome, but how consecutive meals at the same clock times differentially shape postprandial metabolism in day- and night-shifts remains unclear. This study used a unique simulated shift work intervention with four consecutive meals and high-resolution sampling to examine interactions of endogenous rhythms and behavioural timing on postprandial metabolism. Nine healthy non-shift-worker participants (age 21-33 years, 3 females) completed a strictly-controlled laboratory protocol with a day-shift followed by two night-shifts of 10-h delayed sleep and mealtimes. Participants consumed four identical, isoenergetic, mixed-composition meals per shift. Three of four mealtimes (08:00, 18:00, 22:00) were fixed across conditions; the first and last meals were 1 h after waking and before bedtime. Plasma glucose, insulin, triglycerides, HDL-cholesterol and total cholesterol were measured hourly, with continuous interstitial glucose monitoring. Subjective hunger and appetite were assessed throughout. Plasma lipid rhythms shifted with the 10-h delay in sleep-wake times: acrophases delayed ~10-13 h and amplitudes lowered 46%-54% (all p < 0.01). Night-shifts elevated postprandial glucose (+165 mmol/L·min, 95% CI 1.05-34.31, p = 0.05) and insulin (+7678.7 mmol/L·min, 95% CI 3671.02-11686.38, p < 0.01). Time-of-day effects persisted irrespective of shift, with 18:00 meals producing the highest glycaemic responses (+261 mmol/L·min, 95% CI 124.37-398.01, p < 0.01). Insulin dynamics did not fully compensate for elevated glycaemia in night-shifts, indicating lower glucose tolerance and insulin sensitivity. Mistimed meals suggest a mechanism by which circadian disruption may increase metabolic disease risk.

Indexed as

Blood GlucoseCircadian RhythmInsulinLipidsPostprandial PeriodShift Work ScheduleAdultFemaleHumansInsulin ResistanceMaleMealsSleepTriglyceridesYoung AdultBlood GlucoseInsulinLipidsTriglyceridesblood glucosecircadian rhythminsulin resistancemealspostprandial periodshift work schedule

Identifiers

PMID42324738
PMCPMC13522867

What OpenQuestion holds

Textmetadata
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.