Evidence map›Paper›PMID 26028283›Full record

Trial reportMetabolism: clinical and experimental2015

Multipathway modulation of exercise and glucose stress effects upon GH secretion in healthy men.

Johannes D Veldhuis, Thomas P Olson, Paul Y Takahashi, John M Miles, Michael J Joyner, Rebecca J Yang, Jean Wigham

Open access · greenAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Metabolism: clinical and experimental, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.7field-weighted citation impact, top 28% 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

3 citing papers in PubMed, 9 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
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

7 authors at 2 institutions in 1 country.

Johannes D VeldhuisEndocrine Research Unit, Mayo Clinic College of Medicine, Center for Translational Science Activities. Electronic address: veldhuis.johannes@mayo.edu.
Thomas P OlsonCardiovascular Research, Mayo Clinic, Rochester, MN 55905.
Paul Y TakahashiPrimary Care Internal Medicine, Mayo Clinic, Rochester, MN 55905.
John M MilesEndocrine Research Unit, Mayo Clinic College of Medicine, Center for Translational Science Activities.
Michael J JoynerAnesthesia Research, Mayo Clinic, Rochester, MN 55905.
Rebecca J YangEndocrine Research Unit, Mayo Clinic College of Medicine, Center for Translational Science Activities.
Jean WighamEndocrine Research Unit, Mayo Clinic College of Medicine, Center for Translational Science Activities.
Mayo Clinic in Florida · USWinnMed · US

Funding

Mayo Clinic Center for Translational Science ActivitiesUL1TR000135 · NCATS · MAYO CLINIC ROCHESTER · PI KHOSLA, SUNDEEP · 2012 to 2015
$41.2M
Obesity and Energy Metabolism CoreP30DK050456 · NIDDK · UNIVERSITY OF MINNESOTA TWIN CITIES · PI CROW, SCOTT J · 1995 to 2015
$17.0M
Age-Dependent Estrogen-Independent Mechanism of Hyposomatotropism in WomenR01AG029362 · NIA · MAYO CLINIC ROCHESTER · PI VELDHUIS, JOHANNES D · 2007 to 2016
$4.0M
Aging Systems in Geriatrics: the Male Gonadal AxisR01AG031763 · NIA · MAYO CLINIC ROCHESTER · PI VELDHUIS, JOHANNES D · 2010 to 2014
$1.9M
Actions of Testosterone on the Aging Male GH AxisR01AG019695 · NIA · MAYO CLINIC ROCHESTER · PI VELDHUIS, JOHANNES D · 2012 to 2016
$1.9M
NCATS NIH HHS UL1 TR000135NIA NIH HHS R01 AG019695NIA NIH HHS R01 AG029362NIA NIH HHS R01 AG031763NIDDK NIH HHS P30 DK050456
6 · The paper itself

Abstract

objectiveExercise evokes pulsatile GH release followed by autonegative feedback, whereas glucose suppresses GH release followed by rebound-like GH release (feedforward escape). Here we test the hypothesis that age, sex steroids, insulin, body composition and physical power jointly determine these dynamic GH responses.

methodsThis was a prospectively randomized glucose-blinded study conducted in the Mayo Center for Advancing Translational Sciences in healthy men ages 19-77 years (N=23). Three conditions, fasting/rest/saline, fasting/exercise/saline and fasting/rest/iv glucose infusions, were used to drive GH dynamics during 10-min blood sampling for 6h. Linear correlation analysis was applied to relate peak/nadir GH dynamics to age, sex steroids, insulin, CT-estimated abdominal fat and physical power (work per unit time).

resultsCompared with the fasting/rest/saline (control) day, fasting/exercise/saline infusion evoked peak GH within 1h, followed by negative feedback 3-5h later. The dynamic GH excursion was strongly (R(2)=0.634) influenced by (i) insulin negatively (P=0.011), (ii) power positively (P=0.0008), and (iii) E2 positively (P=0.001). Dynamic glucose-modulated GH release was determined by insulin negatively (P=0.0039) and power positively (P=0.0034) (R(2)=0.454). Under rest/saline, power (P=0.031) and total abdominal fat (P=0.012) (R(2)=0.267) were the dominant correlates of GH excursions.

conclusionIn healthy men, dynamic GH perturbations induced by exercise and glucose are strongly related to physical power, insulin, estradiol, and body composition, thus suggesting a network of regulatory pathways.

Indexed as

Abdominal FatAdultAgedAgingBody CompositionExerciseFastingFeedback, PhysiologicalGlucoseGonadal Steroid HormonesHuman Growth HormoneHumansInsulinMaleMiddle AgedMuscle StrengthGlucoseGonadal Steroid HormonesHuman Growth HormoneInsulinAgeBody compositionMetabolicSomatotropin

Identifiers

PMID26028283
PMCPMC4546548
OpenAlexW1653014607

What OpenQuestion holds

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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.