Evidence map›Paper›PMID 21791560›Full record

ArticleEndocrinology2011

Differential effects of growth hormone versus insulin-like growth factor-I on the mouse plasma proteome.

Juan Ding, Edward O List, Brian D Bower, John J Kopchick

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in Endocrinology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
1.2field-weighted citation impact, top 22% 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, 1 synthesis or guideline pooled it, 11 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Clinical development of ghrelin axis-derived molecules for cancer cachexia treatment.Current opinion in supportive and palliative care · 2013
    Review
  6. Article
  7. Age- and sex-associated plasma proteomic changes in growth hormone receptor gene-disrupted mice.The journals of gerontology. Series A, Biological sciences and medical sciences · 2012
    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

4 authors at 2 institutions in 1 country.

Juan DingEdison Biotechnology Institute, College of Osteopathic Medicine, Ohio University, Athens, Ohio 45701, USA.
Edward O List
Brian D Bower
John J Kopchick
Biotechnology Institute · USOhio University · US

Funding

The Somatotropic Axis and Health Aging: A Search for MechanismsP01AG031736 · NIA · SOUTHERN ILLINOIS UNIVERSITY SCH OF MED · PI KIRKLAND, JAMES L. · 2009 to 2013
$8.4M
Longevity genes and calorie restriction: early post-natal effectsR01AG019899 · NIA · SOUTHERN ILLINOIS UNIVERSITY SCH OF MED · PI BARTKE, ANDRZEJ · 2001 to 2016
$6.1M
Involvement of CIDE-A in the development of liver steatosisR15DK083729 · NIDDK · OHIO UNIVERSITY ATHENS · PI KELDER, BRUCE · 2010 to 2010
$221k
NIA NIH HHS AG019899NIA NIH HHS AG031736NIA NIH HHS P01 AG031736NIA NIH HHS R01 AG019899NIDDK NIH HHS DK083729NIDDK NIH HHS R15 DK083729
6 · The paper itself

Abstract

The GH/IGF-I axis has both pre- and postpubertal metabolic effects. However, the differential effects of GH and/or IGF-I on animal physiology or the plasma proteome are still being unraveled. In this report, we analyzed several physiological effects along with the plasma proteome after treatment of mice with recombinant bovine GH or recombinant human IGF-I. GH and IGF-I showed similar effects in increasing body length, body weight, lean and fluid masses, and organ weights including muscle, kidney, and spleen. However, GH significantly increased serum total cholesterol, whereas IGF-I had no effect on it. Both acute and longer-term effects on the plasma proteome were determined. Proteins found to be significantly changed by recombinant bovine GH and/or recombinant human IGF-I injections were identified by mass spectrometry (MS) and MS/MS. The identities of these proteins were further confirmed by Western blotting analysis. Isoforms of apolipoprotein A4, apolipoprotein E, serum amyloid protein A-1, clusterin, transthyretin, and several albumin fragments were found to be differentially regulated by GH vs. IGF-I in mouse plasma. Thus, we have identified several plasma protein biomarkers that respond specifically and differentially to GH or IGF-I and may represent new physiological targets of these hormones. These findings may lead to better understanding of the independent biological effects of GH vs. IGF-I. In addition, these novel biomarkers may be useful for the development of tests to detect illicit use of GH or IGF-I.

Indexed as

AnimalsApolipoproteins ABlood ProteinsBlotting, WesternGrowth HormoneInsulin-Like Growth Factor IMaleMiceMice, Inbred C57BLProteomeRecombinant ProteinsSerum Amyloid A Proteinapolipoprotein A-IVApolipoproteins ABlood ProteinsGrowth HormoneInsulin-Like Growth Factor IProteomeRecombinant ProteinsSAA1 protein, humanSerum Amyloid A Protein

Identifiers

PMID21791560
PMCPMC3176651
OpenAlexW2038247719

What OpenQuestion holds

Textmetadata
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.