Evidence map›Paper›PMID 37732475›Full record

ArticleThe Journal of physiology2024

Temporal optimization of exercise to lower fasting glucose levels.

Jill A Kanaley, J W Porter, N C Winn, G Lastra, A Chockalingam, R J Pettit-Mee, G F Petroski, C Cobelli, M Schiavon, E J Parks

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of physiology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.2field-weighted citation impact, top 21% 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.

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

7 citing papers in PubMed, 7 citations in OpenAlex.

  1. Trial
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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

10 authors at 3 institutions in 2 countries.

Jill A KanaleyDepartment of Nutrition and Exercise Physiology, University of Missouri, Columbia, Missouri, USA.
J W PorterDepartment of Nutrition and Exercise Physiology, University of Missouri, Columbia, Missouri, USA.
N C WinnDepartment of Molecular Physiology & Biophysics, Vanderbilt University, Nashville, Tennessee, USA.ORCID 0000-0002-5276-0592
G LastraDepartment of Endocrinology, Internal Medicine, University of Missouri, Columbia, Missouri, USA.
A ChockalingamDepartment of Cardiology, University of Missouri, Columbia, Missouri, USA.
R J Pettit-MeeDepartment of Nutrition and Exercise Physiology, University of Missouri, Columbia, Missouri, USA.ORCID 0000-0003-0870-0215
G F PetroskiOffice of Medical Research, Biostatistics Unit, University of Missouri, Columbia, Missouri, USA.
C CobelliDepartment of Women's and Children's Health, University of Padova, Padova, Italy.
M SchiavonDepartment of Information Engineering, University of Padova, Padova, Italy.ORCID 0000-0003-0590-2399
E J ParksDepartment of Nutrition and Exercise Physiology, University of Missouri, Columbia, Missouri, USA.
University of Missouri · USUniversity of Padua · ITVanderbilt University · US

Funding

Translational Analysis CoreP30DK058404 · NIDDK · VANDERBILT UNIVERSITY MEDICAL CENTER · PI RICHARD M. PEEK · 2002 to 2026
$29.9M
Dawn Phenomena: Lowering Impaired Fasting Glucose Levels with Exercise (LIFE)R01DK101513 · NIDDK · UNIVERSITY OF MISSOURI-COLUMBIA · PI KANALEY, JILL A · 2016 to 2020
$2.0M
NIDDK NIH HHS P30 DK058404NIDDK NIH HHS R01 DK101513
6 · The paper itself

Abstract

Exercise stimulates glucose uptake and increases insulin sensitivity acutely. Temporally optimizing exercise timing may minimize the nocturnal rise in glucose levels. This study examined the effect of exercise timing on evening and overnight glucose concentrations in individuals who were non-obese with normal fasting glucose levels (Non-Ob; n = 18) and individuals with obesity (OB) with impaired fasting glucose levels (OB+IFG) and without (n = 16 and n = 18, respectively). Subjects were studied on three occasions (no exercise (NOEX)), morning exercise (AMEX; 0700 h) and evening exercise (PMEX; 2000 h). The evening meal was provided (1800 h) and blood samples were taken from 1740 to 0700 h and morning endogenous glucose production (EGP) was measured. Glucose and insulin concentrations increased with the dinner meal with peak concentrations being higher in OB+IFG than in OB and Non-Ob (P = 0.04). In OB+IFG, evening glucose concentrations rose above baseline levels at about 2300 h, with the glucose concentrations staying somewhat lower with AMEX and PMEX until ∼0500 h than with NOEX. In OB+IFG, insulin concentrations decreased following the dinner meal and waned throughout the night, despite the rising glucose concentrations. In the OB and Non-Ob individuals following the dinner meal, no increase in glucose concentrations occurred in the evening period and insulin levels mirrored this. No difference was observed in the morning fasting glucose levels between study days or between groups. Regardless of time of day, exercise delays the evening rise in glucose concentrations in adults with OB+IFG but does not lower morning fasting glucose levels or improve the synchrony between glucose and insulin concentrations. KEY POINTS: Insulin resistance and type 2 diabetes have been linked to disturbances of the core clock, and glucose tolerance demonstrates a diurnal rhythm in healthy humans with better glucose tolerance in the morning than in the afternoon and evening. Skeletal muscle is a primary site for insulin resistance in people with impaired glucose tolerance. In individuals with obesity and impaired fasting glucose levels (OB+IFG), following a dinner meal, glucose concentrations started to rise and continues throughout the night, resulting in elevated glucose levels, while concomitantly, insulin levels are waning. Exercise, regardless of the time of day, suppressed the rise in glucose levels in OB+IFG for many hours during the night but did not lower morning fasting glucose levels. Morning exercise was not quite as effective as evening exercise.

Indexed as

Blood GlucoseExerciseFastingInsulinObesityAdultCircadian RhythmFemaleHumansInsulin ResistanceMaleMiddle AgedTime FactorsBlood GlucoseInsulindawn phenomenonendogenous glucose productionobesitytime of daytype 2 diabetes

Identifiers

PMID37732475
PMCPMC10954586
OpenAlexW4386909821

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

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.