Expert meeting report: epidemiology and management of acquired hypothalamic obesity

Acquired hypothalamic obesity (aHO) is a disease characterized by rapid, clinically significant, and persistent weight gain resulting from damage to hypothalamic structures. aHO is associated with substantial morbidity, increased mortality, and marked impairment in quality of life. Etiologies include craniopharyngioma and other space-occupying lesions of the sellar/parasellar region, neurosurgical procedures, cranial irradiation, and traumatic brain injury. A multidisciplinary panel comprising ten specialists in neuroendocrinology, neurooncology, and neurosurgery from Germany, Austria, and Switzerland convened in Frankfurt am Main, Germany, on November 10, 2025, to discuss contemporary challenges and advances in this field. aHO should be conceptualized and treated within the broader clinical entity of hypothalamic syndrome, a complex disorder involving multiple neuroendocrine deficiencies, disturbances of circadian regulation, impaired control of hunger, satiety, and thirst, altered thermoregulation, and a range of cognitive, sleep-related, and psychosocial dysfunctions. Long-term outcomes for affected individuals are frequently unfavorable, largely due to increased risks of metabolic syndrome, cardiovascular disease, profound reductions in health-related quality of life, and elevated rates of premature mortality. The management of hypothalamic syndrome remains particularly challenging. Pharmacological strategies, including dextroamphetamine and glucagon-like peptide-1 receptor agonists, have demonstrated potential benefits for weight and hyperphagia-related outcomes. Recently, preliminary findings from a prospective, randomized, placebo-controlled clinical trial (TRANSCEND) provided encouraging evidence for the efficacy of setmelanotide, a melanocortin-4 receptor agonist. This perspectives report reviews clinical advances in epidemiology, diagnostics, treatment, and follow-up of patients with aHO and outlines key directions for future research aimed at improving outcomes in this vulnerable population.

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Publication Details

Journal
Frontiers in Endocrinology
Published
2026-04-15
DOI
https://doi.org/10.3389/fendo.2026.1798619
Primary Topic
Pituitary Gland Disorders and Treatments
Type
article
Field-Weighted Citation Impact
0.00

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article

Expert meeting report: epidemiology and management of acquired hypothalamic obesity

Christian Denzer, Hermann L. Müller, Katrin Scheinemann, Johannes Gojo et al.
Frontiers in Endocrinology
Pituitary Gland Disorders and Treatments
article

Expert meeting report: epidemiology and management of acquired hypothalamic obesity

Christian Denzer, Hermann L. Müller, Katrin Scheinemann, Johannes Gojo, Ulrich Dischinger, Annette Richter-Unruh, Katharina Schilbach, Carsten Friedrich, Jörg Flitsch, Ute K. Bartels
article en

Abstract

Acquired hypothalamic obesity (aHO) is a disease characterized by rapid, clinically significant, and persistent weight gain resulting from damage to hypothalamic structures. aHO is associated with substantial morbidity, increased mortality, and marked impairment in quality of life. Etiologies include craniopharyngioma and other space-occupying lesions of the sellar/parasellar region, neurosurgical procedures, cranial irradiation, and traumatic brain injury. A multidisciplinary panel comprising ten specialists in neuroendocrinology, neurooncology, and neurosurgery from Germany, Austria, and Switzerland convened in Frankfurt am Main, Germany, on November 10, 2025, to discuss contemporary challenges and advances in this field. aHO should be conceptualized and treated within the broader clinical entity of hypothalamic syndrome, a complex disorder involving multiple neuroendocrine deficiencies, disturbances of circadian regulation, impaired control of hunger, satiety, and thirst, altered thermoregulation, and a range of cognitive, sleep-related, and psychosocial dysfunctions. Long-term outcomes for affected individuals are frequently unfavorable, largely due to increased risks of metabolic syndrome, cardiovascular disease, profound reductions in health-related quality of life, and elevated rates of premature mortality. The management of hypothalamic syndrome remains particularly challenging. Pharmacological strategies, including dextroamphetamine and glucagon-like peptide-1 receptor agonists, have demonstrated potential benefits for weight and hyperphagia-related outcomes. Recently, preliminary findings from a prospective, randomized, placebo-controlled clinical trial (TRANSCEND) provided encouraging evidence for the efficacy of setmelanotide, a melanocortin-4 receptor agonist. This perspectives report reviews clinical advances in epidemiology, diagnostics, treatment, and follow-up of patients with aHO and outlines key directions for future research aimed at improving outcomes in this vulnerable population.

Frontiers in EndocrinologyVol. 17
Universität Hamburg (DE), University of Lucerne (CH), German Cancer Research Center (DE), Heidelberg University (DE), Diabetes Australia (AU), LMU Klinikum (DE), Comprehensive Cancer Center Vienna (AT), University Medical Center Hamburg-Eppendorf (DE), Klinikum Oldenburg (DE), Hopp Children's Cancer Center Heidelberg (DE), Zentrum Überleben (DE), Universitätsklinikum Würzburg (DE), Ostschweizer Kinderspital (CH), Medical University of Vienna (AT), Ludwig-Maximilians-Universität München (DE)
Deutsche Kinderkrebsstiftung
Zero hunger
Openalex Percentile: Top 27%
Pituitary Gland Disorders and Treatments
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