Literature DB >> 15080777

Raloxifene decreases serum IGF-I in male patients with active acromegaly.

Eleni V Dimaraki1, Kathleen V Symons, Ariel L Barkan.   

Abstract

OBJECTIVE: Most patients with acromegaly require additional treatments after trans-sphenoidal surgery. Although traditional methods of treatment aim at suppressing GH hypersecretion from the pituitary tumor, recent studies on the use of the GH receptor antagonist have shown that targeting the action of GH on peripheral tissues may be more effective. Estrogens and the selective estrogen receptor modulator tamoxifen have been used previously to suppress circulating IGF-I levels in patients with acromegaly. Positive effects of raloxifene in women with active acromegaly have been reported recently. This study was designed to examine the potential role of raloxifene in the treatment of acromegaly in male patients.
DESIGN: We studied eight men with active acromegaly despite the fact that they were receiving traditional treatments. All subjects were treated with raloxifene (60 mg twice a day) for a median of 5 weeks.
METHODS: The effects of raloxifene on GH secretion were assessed by obtaining 24-h GH profiles and studying the response of GH to various stimuli before and after treatment with raloxifene. Serum IGF-I was measured before and after raloxifene treatment.
RESULTS: Raloxifene did not affect basal GH secretion or response of GH to TRH, GHRH or glucose, but it decreased circulating IGF-I by 16+/-4% (P=0.001), and normalized plasma IGF-I in two patients. No changes in clinical parameters were observed. Prolactin levels, the prolactin response to TRH and free testosterone levels remained unchanged. Raloxifene was well tolerated.
CONCLUSION: Raloxifene might be useful in the treatment of male patients with active acromegaly, but longer term studies are clearly needed.

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Year:  2004        PMID: 15080777     DOI: 10.1530/eje.0.1500481

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


  15 in total

Review 1.  GH receptor antagonist: mechanism of action and clinical utility.

Authors:  Sowmya K Surya; Ariel L Barkan
Journal:  Rev Endocr Metab Disord       Date:  2005-01       Impact factor: 6.514

Review 2.  Pharmacological treatment of acromegaly: its place in the overall therapeutic approach.

Authors:  Evgenia Korytnaya; Ariel Barkan
Journal:  J Neurooncol       Date:  2014-01-18       Impact factor: 4.130

Review 3.  Estrogens and selective estrogen receptor modulators in acromegaly.

Authors:  Felipe H Duarte; Raquel S Jallad; Marcello D Bronstein
Journal:  Endocrine       Date:  2016-10-04       Impact factor: 3.633

Review 4.  Estrogen treatment for acromegaly.

Authors:  Ilan Shimon; Ariel Barkan
Journal:  Pituitary       Date:  2012-12       Impact factor: 4.107

5.  Tamoxifen enhances the control of acromegaly treated with somatostatin analog lanreotide.

Authors:  Jean-Christophe Maiza; Stéphane Castillo-Ros; Maria Matta; Antoine Bennet; Philippe Caron
Journal:  Pituitary       Date:  2012-12       Impact factor: 4.107

Review 6.  Estrogen and selective estrogen receptor modulators (SERMs) for the treatment of acromegaly: a meta-analysis of published observational studies.

Authors:  Jennifer C Stone; Justin Clark; Ross Cuneo; Anthony W Russell; Suhail A R Doi
Journal:  Pituitary       Date:  2014-06       Impact factor: 4.107

Review 7.  Medical therapy: options and uses.

Authors:  John D Carmichael; Vivien S Bonert
Journal:  Rev Endocr Metab Disord       Date:  2008-03       Impact factor: 6.514

8.  Aromatase enzyme expression in acromegaly and its possible relationship with disease prognosis.

Authors:  Alev Selek; Berrin Cetinarslan; Yesim Gurbuz; Ilhan Tarkun; Zeynep Canturk; Burak Cabuk
Journal:  Endocrine       Date:  2014-10-10       Impact factor: 3.633

9.  Tamoxifen as a therapeutic agent in acromegaly.

Authors:  Irida Balili; Ariel Barkan
Journal:  Pituitary       Date:  2014-12       Impact factor: 4.107

10.  Effects of fulvestrant on biological activity and Wnt expression in rat GH3 cells.

Authors:  Jiwei Bai; Yan Wang; Chuzhong Li; Yazhuo Zhang
Journal:  Neural Regen Res       Date:  2012-02-05       Impact factor: 5.135

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