Literature DB >> 20128787

Short-term isotretinoin treatment decreases insulin-like growth factor-1 and insulin-like growth factor binding protein-3 levels: does isotretinoin affect growth hormone physiology?

A S Karadag1, D T Ertugrul, E Tutal, K O Akin.   

Abstract

BACKGROUND: Isotretinoin is an effective treatment for acne vulgaris. However, it has numerous side-effects. It was previously reported that serum growth hormone (GH) levels decreased with isotretinoin treatment.
OBJECTIVES: To analyse whether isotretinoin has any effects on insulin-like growth factor-1 (IGF-1), insulin-like growth factor binding protein-3 (IGFBP3) and GH levels.
METHODS: Forty-seven patients aged 21.5 +/- 5.1 years (mean +/- SD) with acne vulgaris were included in this study. Isotretinoin therapy was initiated at a dose of 0.5-0.75 mg kg(-1) daily and then adjusted to 0.88 mg kg(-1) daily as maintenance dosage after 1 month. Screening for biochemical and hormonal parameters was performed just before initiation and after 3 months of isotretinoin treatment.
RESULTS: IGF-1 and IGFBP3 levels decreased significantly after treatment (P < 0.01), while GH levels did not change. Post-treatment, significant increases were seen in aspartate aminotransferase, total cholesterol, low-density lipoprotein cholesterol, triglycerides and low-density lipoprotein cholesterol/high-density lipoprotein cholesterol ratio (P < 0.0001) while high-density lipoprotein cholesterol levels were significantly decreased (P < 0.0001).
CONCLUSIONS: Isotretinoin therapy may have an effect on GH physiology, and further studies are needed to understand this association.

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Year:  2010        PMID: 20128787     DOI: 10.1111/j.1365-2133.2009.09618.x

Source DB:  PubMed          Journal:  Br J Dermatol        ISSN: 0007-0963            Impact factor:   9.302


  9 in total

1.  Isotretinoin and FoxO1: A scientific hypothesis.

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Journal:  Dermatoendocrinol       Date:  2011-07-01

2.  [Isotretinoin. How should it be used?].

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Journal:  Hautarzt       Date:  2013-04       Impact factor: 0.751

3.  Dietary intervention in acne: Attenuation of increased mTORC1 signaling promoted by Western diet.

Authors:  Bodo Melnik
Journal:  Dermatoendocrinol       Date:  2012-01-01

4.  Oral toxicity of isotretinoin, misoprostol, methotrexate, mifepristone and levonorgestrel as pregnancy category X medications in female mice.

Authors:  Seong-Kwan Kim; Soo-Jeong Shin; Yohan Yoo; Na-Hyun Kim; Dong-Soon Kim; Dan Zhang; Jin-A Park; Hee Yi; Jin-Suk Kim; Ho-Chul Shin
Journal:  Exp Ther Med       Date:  2015-01-22       Impact factor: 2.447

Review 5.  Linking diet to acne metabolomics, inflammation, and comedogenesis: an update.

Authors:  Bodo C Melnik
Journal:  Clin Cosmet Investig Dermatol       Date:  2015-07-15

6.  Isotretinoin Induced Hyperlipidemia and Impact of Leptin Gene rs 7799039 Polymorphism in Safety of Acne Patients.

Authors:  Amal A Mohamed; Alshymaa Hassnine; Amr Elsayed; Mahmoud Montaser; Yasmeen Ismail; Ahmed El-Demery; Eman Sultan; Rania S Abdel Aziz; Eman Eldemiry; Radwa Hagag; Amal A El-Kholy; Eman Salah
Journal:  Pharmgenomics Pers Med       Date:  2021-12-24

7.  The influence of Mediterranean diet in acne pathogenesis and the correlation with insulin-like growth factor-1 serum levels: Implications and results.

Authors:  Mariabeatrice Bertolani; Eleonora Rodighiero; Roberta Saleri; Giuseppe Pedrazzi; Simona Bertoli; Alessandro Leone; Claudio Feliciani; Torello Lotti; Francesca Satolli
Journal:  Dermatol Reports       Date:  2021-12-17

8.  Potential role of FoxO1 and mTORC1 in the pathogenesis of Western diet-induced acne.

Authors:  Bodo C Melnik; Christos C Zouboulis
Journal:  Exp Dermatol       Date:  2013-05       Impact factor: 3.960

9.  Effects of isotretinoin on body mass index, serum adiponectin, leptin, and ghrelin levels in acne vulgaris patients.

Authors:  Bengu Cevirgen Cemil; Havva Hilal Ayvaz; Gulfer Ozturk; Can Ergin; Havva Kaya Akıs; Muzeyyen Gonul; Ercan Arzuhal
Journal:  Postepy Dermatol Alergol       Date:  2016-08-16       Impact factor: 1.837

  9 in total

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