Computational phenotyping of effort-based decision-making in type-2 diabetes on and off semaglutide

IF 7.6 1区 医学 Q1 NEUROSCIENCES
Sara Z. Mehrhof, Hugo Fleming, Camilla L. Nord
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Abstract

Motivation plays a fundamental role in human behaviour. Dopaminergic pathways have long been implicated in individual differences in motivation. Emerging evidence suggests such neural mechanisms interact with metabolic processes to coordinate energy expenditure with energy resources, thereby linking motivation with metabolic health. We ask whether a cognitive-computational index of motivation—reliably linked to neuropsychiatric symptoms—is altered in the context of type-2 diabetes and treatment with a GLP-1 agonist (semaglutide). In a pre-registered experiment, we quantified computational effort-based decision-making parameters in participants with diabetes on (N = 58) or off (N = 54) semaglutide treatment, compared to two groups of matched controls without diabetes (N = 58 each). Subjects with type-2 diabetes showed a blunted acceptance bias, a computational parameter describing the bias to accept effort for reward. This effect was not driven by neuropsychiatric comorbidity or antidepressant use. Across all participants, we found that increasing diabetes risk linearly predicted reduced acceptance bias. Participants with diabetes treated with semaglutide did not show restored motivation. Metabolic ill-health is associated with reduced acceptance bias during motivational decision-making. This blunting mirrors—but is largely independent of—neuropsychiatric motivational deficits. This suggests metabolic ill-health is accompanied by a cognitive shift towards energy conservation, potentially contributing to comorbidity between metabolic ill-health and mental illness.
使用和停用西马鲁肽的2型糖尿病患者基于努力的决策的计算表型。
动机在人类行为中起着基本的作用。长期以来,多巴胺能通路与动机的个体差异有关。新出现的证据表明,这些神经机制与代谢过程相互作用,协调能量消耗和能量资源,从而将动力与代谢健康联系起来。我们的问题是,在2型糖尿病和使用GLP-1激动剂(semaglutide)治疗的情况下,是否会改变与神经精神症状可靠相关的动机的认知计算指数。在一项预先注册的实验中,我们量化了接受(N = 58)或不接受(N = 54)西马鲁肽治疗的糖尿病参与者的基于计算努力的决策参数,与两组匹配的无糖尿病对照组(N = 58)相比。2型糖尿病患者表现出迟钝的接受偏差,这是一个计算参数,描述了为了回报而接受努力的偏差。这种影响不是由神经精神合并症或抗抑郁药的使用引起的。在所有参与者中,我们发现糖尿病风险的增加线性预测了接受偏差的降低。接受西马鲁肽治疗的糖尿病患者没有表现出恢复的动力。代谢性疾病与动机决策过程中接受偏差的减少有关。这种钝化反映了神经精神上的动机缺陷,但在很大程度上是独立的。这表明代谢性疾病伴随着对能量节约的认知转变,可能导致代谢性疾病和精神疾病之间的共病。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Neuropsychopharmacology
Neuropsychopharmacology 医学-精神病学
CiteScore
15.00
自引率
2.60%
发文量
240
审稿时长
2 months
期刊介绍: Neuropsychopharmacology is a reputable international scientific journal that serves as the official publication of the American College of Neuropsychopharmacology (ACNP). The journal's primary focus is on research that enhances our knowledge of the brain and behavior, with a particular emphasis on the molecular, cellular, physiological, and psychological aspects of substances that affect the central nervous system (CNS). It also aims to identify new molecular targets for the development of future drugs. The journal prioritizes original research reports, but it also welcomes mini-reviews and perspectives, which are often solicited by the editorial office. These types of articles provide valuable insights and syntheses of current research trends and future directions in the field of neuroscience and pharmacology.
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