Literature DB >> 11720895

Systemic ghrelin levels in subjects with growth hormone deficiency are not modified by one year of growth hormone replacement therapy.

J A Janssen1, F M van der Toorn, L J Hofland, P van Koetsveld, F Broglio, E Ghigo, S W Lamberts, A Jan van der Lely.   

Abstract

OBJECTIVE: Ghrelin stimulates growth hormone (GH) secretion both in vivo and in vitro. Ghrelin is mainly produced in and released from the stomach but it is probably also produced in the hypothalamic arcuate nucleus. Whether pituitary GH release is under the control of ghrelin from the stomach and/or from the arcuate nucleus is not known. Moreover, no data on the feedback of GH on systemic ghrelin concentrations are available. It has recently been suggested that ghrelin may induce obesity.
DESIGN: In this study, we addressed the following two questions: a) are circulating ghrelin levels increased in human GH deficiency (GHD), and b) does GH treatment modify ghrelin levels in human GHD?
METHODS: The study group consisted of 23 patients with GHD. Eighteen had developed adult-onset GHD and five had developed GHD in their childhood (childhood-onset GHD). Ghrelin was measured with a commercially available radioimmunoassay. All measurements were performed twice, first at baseline, before the start of GH replacement therapy, and then again after one year of therapy. GH doses were adjusted every 3 months, targeting serum total IGF-I levels within the normal gender- and age-related reference values for the healthy population. Maintenance doses were continued once the target serum total IGF-I levels were reached.
RESULTS: The sum of skinfolds and body water increased significantly, body fat mass and percentage body fat decreased significantly and body mass index and waist-hip ratio were not significantly changed by one year of GH replacement therapy. Before the start of GH replacement therapy, mean value and range for fasting ghrelin in the studied GHD subjects tended to be lower in comparison with healthy subjects in the control group although the difference did not reach significance (GHD ghrelin mean 67.8 pmol/l, range 37.6-116.3 pmol/l; control mean 83.8 pmol/l, range 35.4-132 pmol/l; P=0.11). One year of GH replacement therapy did not modify circulating ghrelin levels (ghrelin before GH therapy: 67.8 pmol/l, range 37.6-116.3 pmol/l; after GH therapy: 65.3 pmol/l, range 35.8-112.6; P=0.56).
CONCLUSIONS: We did not observe elevated ghrelin levels in adult GHD subjects and GH replacement therapy did not modify circulating ghrelin levels, despite significant decreases in body fat mass and percentage body fat. It is conceivable that the lack of ghrelin modifications after long-term GH therapy was due to the reduction of adiposity and insulin on one hand, and increased GH secretion on the other. However, it is still possible that systemic ghrelin is involved in the development of obesity, both in normal and GHD subjects.

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Year:  2001        PMID: 11720895     DOI: 10.1530/eje.0.1450711

Source DB:  PubMed          Journal:  Eur J Endocrinol        ISSN: 0804-4643            Impact factor:   6.664


  16 in total

1.  The negative association between plasma ghrelin and IGF-I is modified by obesity, insulin resistance and type 2 diabetes.

Authors:  S M Pöykkö; O Ukkola; H Kauma; E Kellokoski; S Hörkkö; Y A Kesäniemi
Journal:  Diabetologia       Date:  2005-02-02       Impact factor: 10.122

2.  Plasma peptide YY and ghrelin levels in infants and children with Prader-Willi syndrome.

Authors:  Merlin G Butler; Douglas C Bittel; Zohreh Talebizadeh
Journal:  J Pediatr Endocrinol Metab       Date:  2004-09       Impact factor: 1.634

3.  Plasma obestatin and ghrelin levels in subjects with Prader-Willi syndrome.

Authors:  Merlin G Butler; Douglas C Bittel
Journal:  Am J Med Genet A       Date:  2007-03-01       Impact factor: 2.802

4.  Growth hormone and somatostatin directly inhibit gastric ghrelin secretion. An in vitro organ culture system.

Authors:  L M Seoane; O Al-Massadi; F Barreiro; C Dieguez; F F Casanueva
Journal:  J Endocrinol Invest       Date:  2007-10       Impact factor: 4.256

5.  Circulating ghrelin levels in newborns are not associated to gender, body weight and hormonal parameters but depend on the type of delivery.

Authors:  S Bellone; A Rapa; D Vivenza; A Vercellotti; A Petri; G Radetti; J Bellone; F Broglio; E Ghigo; G Bona
Journal:  J Endocrinol Invest       Date:  2003-04       Impact factor: 4.256

6.  Integrating GHS into the Ghrelin System.

Authors:  Johannes D Veldhuis; Cyril Y Bowers
Journal:  Int J Pept       Date:  2010-03-18

7.  Serum ghrelin levels in growth hormone-sufficient and growth hormone-deficient patients during growth hormone-releasing hormone plus arginine test.

Authors:  B Tarantini; C Ciuoli; S Checchi; A Montanaro; V Bonato; A Theodoropoulou; L Pasqui; F Pacini
Journal:  J Endocrinol Invest       Date:  2009-04       Impact factor: 4.256

8.  The role of ghrelin in the energy homeostasis of elderly people: a population-based study.

Authors:  M Serra-Prat; X Fernández; E Burdoy; J Mussoll; R Casamitjana; M Puig-Domingo
Journal:  J Endocrinol Invest       Date:  2007-06       Impact factor: 4.256

9.  Ghrelin concentrations in Prader-Willi syndrome (PWS) infants and children: changes during development.

Authors:  Andrea M Haqq; Steven C Grambow; Michael Muehlbauer; Christopher B Newgard; Laura P Svetkey; Aaron L Carrel; Jack A Yanovski; Jonathan Q Purnell; Michael Freemark
Journal:  Clin Endocrinol (Oxf)       Date:  2008-08-15       Impact factor: 3.478

Review 10.  Ghrelin: integrative neuroendocrine peptide in health and disease.

Authors:  James T Wu; John G Kral
Journal:  Ann Surg       Date:  2004-04       Impact factor: 12.969

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