BACKGROUND: HOS in children with structural hypothalamic lesions is characterised by weight gain refractory to standard lifestyle interventions. Disruption of hypothalamic function results in hyperphagia, hyperinsulinemia and possible reduction of energy expenditure. Metformin induces anorectic effects, but its role in these patients has not been studied. OBJECTIVE: To compare BMI of patients with HOS before and after treatment with Metformin. METHOD: BMI of 6 children with HOS unresponsive to demonstrable change in lifestyle measures was compared before and after treatment with metformin by converting BMI to BMI standard deviation scores (SDS). Tolerance to metformin was assessed. RESULTS: There were 6 females. [Hypothalamic hamartoma (N = 2), craniopharyngioma (N = 2), hypothalamic astrocytoma (N = 2)]. Treatment included surgery (N = 5), primary fractionated radiotherapy (N = 1), additional proton beam radiotherapy (N = 1) and chemotherapy (N = 1). Results are given as median (range). Age at diagnosis was 10.1years (1.3-13.8). Metformin was introduced at 12.5years of age (4.5-18.1). The change in BMI SDS was +0.42/year (+0.06 to +3.6) after 4.3 years (0.2 to 7.1). The change in BMI SDS between commencement of metformin and the final assessment was +0.15/year (-0.31 to +0.22) after follow up of 1.9 years (1.3-5.4). The rate of change in BMI SDS before and after introduction of metformin is statistically significant (p= 0.043). CONCLUSION: Use of metformin in addition to lifestyle change is associated with control of obesity in patients with HOS and structural disease where lifestyle change alone was not successful. A prospective study is warranted to rigorously examine its role in this difficult group of patients.
. 2016 May 30;18(Suppl 3):iii130–iii131. doi: 10.1093/neuonc/now078.18
NS-18: ROLE OF METFORMIN IN THE TREATMENT OF HYPOTHALAMIC OBESITY SYNDROME (HOS)
Arundoss Gangadharan
1, Aliki Bogiatzopoulou
1, Joanne Blair
1, Barry Pizer
2, Lisa Howell
2, James Hayden
2, Conor Mallucci
3, Benedetta Pettorini
3, Mohammed Didi
1
Arundoss Gangadharan
1Department of Endocrinology, Alder Hey Children's Hospital, Liverpool, UK
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Aliki Bogiatzopoulou
1Department of Endocrinology, Alder Hey Children's Hospital, Liverpool, UK
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Joanne Blair
1Department of Endocrinology, Alder Hey Children's Hospital, Liverpool, UK
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Barry Pizer
2Department of Oncology, Alder Hey Children's Hospital, Liverpool, UK
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Lisa Howell
2Department of Oncology, Alder Hey Children's Hospital, Liverpool, UK
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James Hayden
2Department of Oncology, Alder Hey Children's Hospital, Liverpool, UK
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Conor Mallucci
3Department of Neurosurgery, Alder Hey Children's Hospital, Liverpool, UK
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Benedetta Pettorini
3Department of Neurosurgery, Alder Hey Children's Hospital, Liverpool, UK
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Mohammed Didi
1Department of Endocrinology, Alder Hey Children's Hospital, Liverpool, UK
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1Department of Endocrinology, Alder Hey Children's Hospital, Liverpool, UK
2Department of Oncology, Alder Hey Children's Hospital, Liverpool, UK
3Department of Neurosurgery, Alder Hey Children's Hospital, Liverpool, UK
Issue date 2016 Jun.
© the author(s) 2016. published by oxford university press on behalf of the society for neuro-oncology. all rights reserved. for permissions, please e-mail: journals.permissions@oup.com
PMCID: PMC4903693
