Evidence map›Paper›PMID 19820031›Full record

Trial reportThe Journal of clinical endocrinology and metabolism2009

Impact of growth hormone receptor blockade on substrate metabolism during fasting in healthy subjects.

Louise Moller, Helene Norrelund, Niels Jessen, Allan Flyvbjerg, Steen B Pedersen, Bruce D Gaylinn, Jianhua Liu, Michael O Thorner, Niels Moller, Jens Otto Lunde Jorgensen

Registry-linked trialOpen access · bronzeAbstract readRandomized Controlled Trial
In one paragraph

Trial report in The Journal of clinical endocrinology and metabolism, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02152124 (Growth Hormone, IGF-1 and Medical Treatment in Acromegaly), which is not on this map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
3.0field-weighted citation impact, top 9% 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.

NCT02152124 completednot on this mapstarted 2014, after this paper: background citation

Growth Hormone, IGF-1 and Medical Treatment in Acromegaly: Are There Effects on Gut Hormone Physiology and Postprandial Substrate Metabolism?

TypeobservationalSponsorUniversity Hospital, GhentRan2014 to 2017Enrolled21ConditionsAcromegaly
3 · Its place in the literature

Who cites it

17 citing papers in PubMed, 42 citations in OpenAlex.

  1. Reduction in visceral adiposity is associated with an improved metabolic profile in HIV-infected patients receiving tesamorelin.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2012
    Trial
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  11. Review
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  14. Extra-hepatic Acromegaly.European endocrinology · 2013
    Review
  15. Article
  16. Review
  17. 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

10 authors at 3 institutions in 2 countries.

Louise MollerMedical Department M, Medical Research Laboratories, Clinical Institute, Aarhus University Hospital, Aarhus Sygehus, DK-8000 Aarhus C, Denmark. louisem@dadlnet.dk
Helene Norrelund
Niels Jessen
Allan Flyvbjerg
Steen B Pedersen
Bruce D Gaylinn
Jianhua Liu
Michael O Thorner
Niels Moller
Jens Otto Lunde Jorgensen
Aarhus University Hospital · DKUniversity of Virginia Health System · USRegionshospitalet Viborg · DK

Funding

Ghrelin Regulation: Implications for Understanding ObesityR01DK076037 · NIDDK · UNIVERSITY OF VIRGINIA · PI THORNER, MICHAEL O · 2008 to 2012
$2.7M
NIDDK NIH HHS DK076037NIDDK NIH HHS R01 DK076037
6 · The paper itself

Abstract

contextExperimental studies in GH-deficient patients and in healthy subjects receiving somatostatin-infusion suggest that GH is an important regulator of substrate metabolism during fasting. These models may not adequately reflect the selective effects of GH, and GH receptor (GHR) blockade offers a new model to define the metabolic role of GH.

objectiveThe aim of this study was to investigate the impact of GHR blockade on substrate metabolism and insulin sensitivity during fasting.

designWe conducted a randomized, placebo-controlled, crossover study in 10 healthy young men.

interventionAfter 36 h of fasting with saline or pegvisomant (GHR blockade), the subjects were studied during a 4-h basal period and 2.5-h hyperinsulinemic euglycemic clamp. MAIN OUTCOME: We measured whole-body and forearm glucose, lipid, and protein metabolism, peripheral insulin sensitivity, and acyl and desacyl ghrelin.

resultsGHR blockade significantly suppressed circulating free fatty acids (1226 +/- 83 vs. 1074 +/- 65 micromol/liter; P = 0.03) and ketone bodies (3080 +/- 271 vs. 2015 +/- 235 micromol/liter; P <or= 0.01), as well as forearm uptake of free fatty acids (0.341 +/- 0.150 vs. 0.004 +/- 0.119 micromol/100 ml x min; P < 0.01) and lipid oxidation (1.3 +/- 0.1 vs. 1.2 +/- 0.1 mg/kg x min; P = 0.03) in the basal period. By contrast, IGF-I levels in either serum or peripheral tissues were not impacted by GHR blockade, and protein metabolism was also unaffected. Basal glucose levels were elevated by GHR blockade, but insulin sensitivity was similar; this was associated with an increased acyl/desacyl ghrelin ratio.

conclusionGHR blockade, without changes in circulating or tissue IGF-I levels, selectively suppresses lipid mobilization and oxidation after short-term fasting. This supports the notion that stimulation of lipolysis is a primary and important effect of GH.

Indexed as

Blood GlucoseBody Mass IndexCross-Over StudiesFastingFatty Acids, NonesterifiedGlucose Clamp TechniqueGrowth HormoneHuman Growth HormoneHumansInsulin-Like Growth Factor IMiddle AgedPhenylalaninePlacebosReceptors, SomatotropinReference ValuesSingle-Blind MethodBlood GlucoseFatty Acids, NonesterifiedGrowth HormoneHuman Growth HormoneInsulin-Like Growth Factor IpegvisomantPhenylalaninePlacebosReceptors, SomatotropinTyrosineUrea

Identifiers

PMID19820031
PMCPMC2775657
OpenAlexW2087447921

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.