Chang Jeryn, Teo Annissa H, Shaw Thomas B, Dupuis Luc, Ngo Shyuan T, Steyn Frederik J
School of Biomedical Sciences, Faculty of Health, Medicine and Behavioural Sciences, The University of Queensland, QLD, 4072, Australia.
School of Electrical Engineering and Computer Science, The University of Queensland, QLD, 4072, Australia.
EBioMedicine. 2025 Jul 11;118:105845. doi: 10.1016/j.ebiom.2025.105845.
Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease with highly heterogeneous clinical presentations. Among the non-motor features increasingly recognised as clinically relevant is the dysregulation of energy balance, with weight loss-particularly due to fat mass loss-emerging as a significant modifier of disease risk, progression, and survival. In this context, the hypothalamus-a key regulator of homeostatic and metabolic processes-has gained attention for its potential role in ALS pathophysiology. This Review synthesises emerging evidence of hypothalamic involvement in ALS, including neuronal loss, proteinopathy, and volume loss observed through histological and neuroimaging studies. We critically examine current imaging approaches and their technical limitations and explore neuroendocrine dysfunction across the hypothalamic-pituitary axes. Collectively, these findings suggest that hypothalamic dysfunction may contribute to clinically relevant metabolic, sleep, behavioural, and cognitive changes in ALS, adding to our understanding of ALS as a multisystem disease. Continued investigation of the hypothalamus may reveal novel biomarkers, inform risk stratification, and identify therapeutic opportunities to address disease heterogeneity and improve clinical outcomes.
肌萎缩侧索硬化症(ALS)是一种致命的神经退行性疾病,临床表现高度异质。在越来越被认为具有临床相关性的非运动特征中,能量平衡失调是其中之一,体重减轻——尤其是由于脂肪量减少——已成为疾病风险、进展和生存的重要调节因素。在此背景下,下丘脑——稳态和代谢过程的关键调节者——因其在ALS病理生理学中的潜在作用而受到关注。本综述综合了下丘脑参与ALS的新证据,包括通过组织学和神经影像学研究观察到的神经元丢失、蛋白病和体积减小。我们批判性地审视了当前的成像方法及其技术局限性,并探讨了下丘脑-垂体轴的神经内分泌功能障碍。总体而言,这些发现表明下丘脑功能障碍可能导致ALS患者出现具有临床相关性的代谢、睡眠、行为和认知变化,这加深了我们对ALS作为一种多系统疾病的理解。对下丘脑的持续研究可能会揭示新的生物标志物,为风险分层提供信息,并确定应对疾病异质性和改善临床结果的治疗机会。