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腹侧纹状体-海马体在奖励处理过程中的耦合作为精神障碍的分层生物标志物。

Ventral Striatal-Hippocampus Coupling During Reward Processing as a Stratification Biomarker for Psychotic Disorders.

机构信息

Systems Neuroscience in Psychiatry, Department of Psychiatry and Psychotherapy, Central Institute of Mental Health, Medical Faculty Mannheim/Heidelberg University, Mannheim, Germany.

Department of Genetic Epidemiology in Psychiatry, Central Institute of Mental Health, Medical Faculty Mannheim/Heidelberg University, Mannheim, Germany.

出版信息

Biol Psychiatry. 2022 Jan 15;91(2):216-225. doi: 10.1016/j.biopsych.2021.07.016. Epub 2021 Jul 24.

Abstract

BACKGROUND

Altered ventral striatal (vST) activation to reward expectancy is a well-established intermediate phenotype for psychiatric disorders, specifically schizophrenia (SZ). Preclinical research suggests that striatal alterations are related to a reduced inhibition by the hippocampal formation, but its role in human transdiagnostic reward-network dysfunctions is not well understood.

METHODS

We performed functional magnetic resonance imaging during reward processing in 728 individuals including healthy control subjects (n = 396), patients (SZ: n = 46; bipolar disorder: n = 45; major depressive disorder: n = 60), and unaffected first-degree relatives (SZ: n = 46; bipolar disorder: n = 50; major depressive disorder: n = 85). We assessed disorder-specific differences in functional vST-hippocampus coupling and transdiagnostic associations with dimensional measures of positive, negative, and cognitive symptoms. We also probed the genetic underpinning using polygenic risk scores for SZ in a subset of healthy participants (n = 295).

RESULTS

Functional vST-hippocampus coupling was 1) reduced in patients with SZ and bipolar disorder (p < .05, small-volume corrected [SVC]); 2) associated transdiagnostically to dimensional measures of positive (p = .01, SVC) and cognitive (p = .02, SVC), but not negative, (p > .05, SVC) symptoms; and 3) reduced in first-degree relatives of patients with SZ (p = .017, SVC) and linked to the genetic risk for SZ in healthy participants (p = .035).

CONCLUSIONS

We provide evidence that reduced vST-hippocampus coupling during reward processing is an endophenotype for SZ linked to positive and cognitive symptoms, supporting current preclinical models of the emergence of psychosis. Moreover, our data indicate that vST-hippocampus coupling is familial and linked to polygenic scores for SZ, supporting the use of this measure as an intermediate phenotype for psychotic disorders.

摘要

背景

腹侧纹状体(vST)对奖赏预期的激活改变是精神疾病的一个成熟的中间表型,特别是精神分裂症(SZ)。临床前研究表明,纹状体的改变与海马结构的抑制减少有关,但它在人类跨诊断奖赏网络功能障碍中的作用尚不清楚。

方法

我们在 728 名个体(包括健康对照组[ n = 396]、SZ 患者[ n = 46]、双相情感障碍患者[ n = 45]、重性抑郁障碍患者[ n = 60])中进行了奖赏处理的功能磁共振成像。我们评估了功能 vST-海马耦合的障碍特异性差异,并与阳性、阴性和认知症状的维度测量进行了跨诊断关联。我们还使用 SZ 的多基因风险评分在健康参与者的亚组( n = 295)中探测了遗传基础。

结果

功能 vST-海马耦合:1)SZ 和双相情感障碍患者的耦合减少( p <.05,小体积校正[SVC]);2)与阳性( p =.01,SVC)和认知( p =.02,SVC)维度测量的跨诊断相关,但与阴性( p >.05,SVC)维度测量无关;3)SZ 患者一级亲属的耦合减少( p =.017,SVC),与健康参与者的 SZ 遗传风险相关( p =.035)。

结论

我们提供的证据表明,奖赏处理过程中 vST-海马耦合减少是 SZ 的一个内表型,与阳性和认知症状有关,支持当前精神病发生的临床前模型。此外,我们的数据表明 vST-海马耦合是家族性的,与 SZ 的多基因评分相关,支持将该测量作为精神病的中间表型。

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