Global reward processing deficits predict negative symptoms transdiagnostically and transphasically in a severe mental illness-spectrum sample.

IF 3.5 3区 医学 Q1 CLINICAL NEUROLOGY European Archives of Psychiatry and Clinical Neuroscience Pub Date : 2024-10-01 Epub Date: 2023-12-05 DOI:10.1007/s00406-023-01714-7
Lauren Luther, Sierra A Jarvis, Michael J Spilka, Gregory P Strauss
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Abstract

Reward processing impairments are a key factor associated with negative symptoms in those with severe mental illnesses. However, past findings are inconsistent regarding which reward processing components are impaired and most strongly linked to negative symptoms. The current study examined the hypothesis that these mixed findings may be the result of multiple reward processing pathways (i.e., equifinality) to negative symptoms that cut across diagnostic boundaries and phases of illness. Participants included healthy controls (n = 100) who served as a reference sample and a severe mental illness-spectrum sample (n = 92) that included psychotic-like experiences, clinical high-risk for psychosis, bipolar disorder, and schizophrenia participants. All participants completed tasks measuring four RDoC Positive Valence System constructs: value representation, reinforcement learning, effort-cost computation, and hedonic reactivity. A k-means cluster analysis of the severe mental illness-spectrum samples identified three clusters with differential reward processing profiles that were characterized by: (1) global reward processing deficits (22.8%), (2) selective impairments in hedonic reactivity alone (40.2%), and (3) preserved reward processing (37%). Elevated negative symptoms were only observed in the global reward processing cluster. All clusters contained participants from each clinical group, and the distribution of these groups did not significantly differ among the clusters. Findings identified one pathway contributing to negative symptoms that was transdiagnostic and transphasic. Future work further characterizing divergent pathways to negative symptoms may help to improve symptom trajectories and personalized treatments.

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在严重精神疾病谱系样本中,整体奖赏加工缺陷可预测跨诊断和跨症状的消极症状。
奖赏处理障碍是与严重精神疾病患者的消极症状相关的一个关键因素。然而,过去的研究结果并不一致,不知道哪种奖赏加工过程会受损,也不知道哪种奖赏加工过程与消极症状的关系最密切。本研究提出了一个假设,即这些混杂的研究结果可能是多种奖赏加工途径(即等效性)导致的消极症状的结果,这些途径跨越诊断界限和疾病阶段。参与者包括作为参照样本的健康对照组(n = 100)和严重精神疾病谱样本(n = 92),后者包括精神病样经历、精神病临床高风险、双相情感障碍和精神分裂症参与者。所有参与者都完成了测量四个 RDoC 正价系统结构的任务:价值表征、强化学习、努力成本计算和享乐反应性。对重度精神疾病谱系样本进行的 k-means 聚类分析发现了三个具有不同奖赏加工特征的聚类,它们的特点是(1) 整体奖赏处理缺陷(22.8%),(2) 单纯享乐反应性的选择性损伤(40.2%),(3) 保留奖赏处理(37%)。只有在全面奖赏加工群组中才观察到消极症状的增加。所有群组中都有来自各临床群组的参与者,这些群组的分布在各群组中没有显著差异。研究结果确定了一种导致消极症状的途径,这种途径具有跨诊断性和跨phasic性。未来的工作将进一步确定导致消极症状的不同途径,这将有助于改善症状轨迹和个性化治疗。
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来源期刊
CiteScore
8.80
自引率
4.30%
发文量
154
审稿时长
6-12 weeks
期刊介绍: The original papers published in the European Archives of Psychiatry and Clinical Neuroscience deal with all aspects of psychiatry and related clinical neuroscience. Clinical psychiatry, psychopathology, epidemiology as well as brain imaging, neuropathological, neurophysiological, neurochemical and moleculargenetic studies of psychiatric disorders are among the topics covered. Thus both the clinician and the neuroscientist are provided with a handy source of information on important scientific developments.
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