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首页> 外文期刊>JAMA psychiatry >Striatal response to reward anticipation evidence for a systems-level intermediate phenotype for schizophrenia
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Striatal response to reward anticipation evidence for a systems-level intermediate phenotype for schizophrenia

机译:纹状体对精神分裂症的系统水平中间表型的奖励预期证据的反应

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Attenuated ventral striatal response during reward anticipation is a core feature of schizophrenia that is seen in prodromal, drug-naive, and chronic schizophrenic patients. Schizophrenia is highly heritable, raising the possibility that this phenotype is related to the genetic risk for the disorder. OBJECTIVE To examine a large sample of healthy first-degree relatives of schizophrenic patients and compare their neural responses to reward anticipation with those of carefully matched controls without a family psychiatric history. To further support the utility of this phenotype, we studied its test-retest reliability, its potential brain structural contributions, and the effects of a protective missense variant in neuregulin 1 (NRG1) linked to schizophrenia by meta-analysis (ie, rs10503929). DESIGN, SETTING, AND PARTICIPANTS Examination of awell-established monetary reward anticipation paradigm during functional magnetic resonance imaging at a university hospital; voxel-based morphometry; test-retest reliability analysis of striatal activations in an independent sample of 25 healthy participants scanned twice with the same task; and imaging genetics analysis of the control group. A total of 54 healthy first-degree relatives of schizophrenic patients and 80 controls matched for demographic, psychological, clinical, and task performance characteristics were studied. MAIN OUTCOMES AND MEASURES Blood oxygen level-dependent response during reward anticipation, analysis of intraclass correlations of functional contrasts, and associations between striatal gray matter volume and NRG1 genotype. RESULTS Compared with controls, healthy first-degree relatives showed a highly significant decrease in ventral striatal activation during reward anticipation (familywise error-corrected P < .03 for multiple comparisons across the whole brain). Supplemental analyses confirmed that the identified systems-level functional phenotype is reliable (with intraclass correlation coefficients of 0.59-0.73), independent of local gray matter volume (with no corresponding group differences and no correlation to function, and with all uncorrected P values.05), and affected by the NRG1 genotype (higher striatal responses in controls with the protective rs10503929 C allele; familywise error-corrected P < .03 for ventral striatal response). CONCLUSIONS AND RELEVANCE Healthy first-degree relatives of schizophrenic patients show altered striatal activation during reward anticipation in a directionality and localization consistent with prior patient findings. This provides evidence for a functional neural system mechanism related to familial risk. The phenotype can be assessed reliably, is independent of alterations in striatal structure, and is influenced by a schizophrenia candidate gene variant in NRG1. These data encourage us to further investigate the genetic and molecular contributions to this phenotype.
机译:奖励预期期间减弱的腹部纹状体反应是精神分裂症的核心特征,在前驱性,单纯药物和慢性精神分裂症患者中可见。精神分裂症是高度遗传的,增加了这种表型与疾病遗传风险相关的可能性。目的检查精神分裂症患者健康一级亲属的大量样本,并比较他们的神经反应对预期的奖励和与没有家庭精神病史的经过仔细匹配的对照组的反应。为了进一步支持该表型的实用性,我们通过荟萃分析(即rs10503929)研究了其重测信度,潜在的脑结构贡献以及神经调节蛋白1(NRG1)与精神分裂症相关的保护性错义变体的影响。设计,设置和参与者在大学医院进行功能性磁共振成像时检查完善的金钱奖励预期范式;基于体素的形态学;对25名健康参与者进行相同任务扫描两次的独立样本中的纹状体激活的重新测试可靠性分析;对照组的成像遗传学分析。研究人员对54名健康的精神分裂症患者的一级亲属和80名对照进行了人口统计学,心理,临床和任务执行特征的匹配研究。主要结果和措施奖励预期期间的血氧水平依赖性反应,功能对比的组内相关性分析以及纹状体灰质量与NRG1基因型之间的关联。结果与对照组相比,健康的一级亲属在奖励预期期间腹侧纹状体激活显着降低(对于整个大脑的多次比较,家庭错误校正后的P <.03)。补充分析证实,所确定的系统级功能表型是可靠的(类内相关系数为0.59-0.73),独立于局部灰质体积(没有相应的组差异,也不与功能相关,并且所有未经校正的P值。05) ),并受到NRG1基因型的影响(在具有保护性rs10503929 C等位基因的对照组中,纹状体反应较高;腹侧纹状体反应的家庭误差校正P <.03)。结论和相关性精神分裂症患者的健康一级亲属在奖励预期期间在定向和定位方面显示出与先前患者发现一致的纹状体激活改变。这提供了与家族风险有关的功能性神经系统机制的证据。该表型可以可靠地评估,独立于纹状体结构的变化,并受NRG1中精神分裂症候选基因变异的影响。这些数据鼓励我们进一步研究遗传和分子对该表型的贡献。

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