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      Hypothalamic Obesity after Craniopharyngioma: Mechanisms, Diagnosis, and Treatment

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          Abstract

          Obesity is a common complication after craniopharyngioma therapy, occurring in up to 75% of survivors. Its weight gain is unlike that of normal obesity, in that it occurs even with caloric restriction, and attempts at lifestyle modification are useless to prevent or treat the obesity. The pathogenesis of this condition involves the inability to transduce afferent hormonal signals of adiposity, in effect mimicking a state of CNS starvation. Efferent sympathetic activity drops, resulting in malaise and reduced energy expenditure, and vagal activity increases, resulting in increased insulin secretion and adipogenesis. Lifestyle intervention is essentially useless in this syndrome, termed “hypothalamic obesity.” Pharmacologic treatment is also difficult, consisting of adrenergics to mimic sympathetic activity, or suppression of insulin secretion with octreotide, or both. Recently, bariatric surgery (Roux-en-Y gastric bypass, laparoscopic gastric banding, truncal vagotomy) have also been attempted with variable results. Early and intensive management is required to mitigate the obesity and its negative consequences.

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          Most cited references74

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          Insulin sensitivity indices obtained from oral glucose tolerance testing: comparison with the euglycemic insulin clamp.

          Several methods have been proposed to evaluate insulin sensitivity from the data obtained from the oral glucose tolerance test (OGTT). However, the validity of these indices has not been rigorously evaluated by comparing them with the direct measurement of insulin sensitivity obtained with the euglycemic insulin clamp technique. In this study, we compare various insulin sensitivity indices derived from the OGTT with whole-body insulin sensitivity measured by the euglycemic insulin clamp technique. In this study, 153 subjects (66 men and 87 women, aged 18-71 years, BMI 20-65 kg/m2) with varying degrees of glucose tolerance (62 subjects with normal glucose tolerance, 31 subjects with impaired glucose tolerance, and 60 subjects with type 2 diabetes) were studied. After a 10-h overnight fast, all subjects underwent, in random order, a 75-g OGTT and a euglycemic insulin clamp, which was performed with the infusion of [3-3H]glucose. The indices of insulin sensitivity derived from OGTT data and the euglycemic insulin clamp were compared by correlation analysis. The mean plasma glucose concentration divided by the mean plasma insulin concentration during the OGTT displayed no correlation with the rate of whole-body glucose disposal during the euglycemic insulin clamp (r = -0.02, NS). From the OGTT, we developed an index of whole-body insulin sensitivity (10,000/square root of [fasting glucose x fasting insulin] x [mean glucose x mean insulin during OGTT]), which is highly correlated (r = 0.73, P < 0.0001) with the rate of whole-body glucose disposal during the euglycemic insulin clamp. Previous methods used to derive an index of insulin sensitivity from the OGTT have relied on the ratio of plasma glucose to insulin concentration during the OGTT. Our results demonstrate the limitations of such an approach. We have derived a novel estimate of insulin sensitivity that is simple to calculate and provides a reasonable approximation of whole-body insulin sensitivity from the OGTT.
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            From lesions to leptin: hypothalamic control of food intake and body weight.

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              Interacting Appetite-Regulating Pathways in the Hypothalamic Regulation of Body Weight

              S P Kalra (1999)
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                Author and article information

                Journal
                Front Endocrinol (Lausanne)
                Front Endocrinol (Lausanne)
                Front. Endocrin.
                Frontiers in Endocrinology
                Frontiers Research Foundation
                1664-2392
                29 August 2011
                03 November 2011
                2011
                : 2
                : 60
                Affiliations
                [1] 1simpleDepartment of Pediatrics, University of California San Francisco San Francisco, CA, USA
                Author notes

                Edited by: Hermann Lothar Mueller, Klinikum Oldenburg gGmbH, Germany

                Reviewed by: Fahrettin Kelestimur, Erciyes University, Turkey; Vera Popovic-Brkic, University Belgrade, Serbia

                *Correspondence: Robert H. Lustig, Division of Pediatric Endocrinology, University of California San Francisco, Box 0434, 500 Parnassus Avenue, San Francisco, CA 94143-0434, USA. e-mail: rlustig@ 123456peds.ucsf.edu

                This article was submitted to Frontiers in Pituitary Endocrinology, a specialty of Frontiers in Endocrinology.

                Article
                10.3389/fendo.2011.00060
                3356006
                22654817
                5827b69f-1565-4983-8901-2c21329a1776
                Copyright © 2011 Lustig.

                This is an open-access article subject to a non-exclusive license between the authors and Frontiers Media SA, which permits use, distribution and reproduction in other forums, provided the original authors and source are credited and other Frontiers conditions are complied with.

                History
                : 29 July 2011
                : 06 October 2011
                Page count
                Figures: 3, Tables: 0, Equations: 0, References: 85, Pages: 8, Words: 6894
                Categories
                Endocrinology
                Review Article

                Endocrinology & Diabetes
                craniopharyngioma,ghrelin,leptin resistance,octreotide,symapthetic nervous system,vagus nerve,hypothalamic obesity,insulin

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