Department of Psychiatry, University of Pittsburgh, Pittsburgh, Pennsylvania.
JAMA Psychiatry. 2019 Sep 1;76(9):958-965. doi: 10.1001/jamapsychiatry.2019.0864.
Anhedonia is a symptom of multiple psychiatric conditions in young adults that is associated with poorer mental health and psychosocial function and abnormal ventral striatum reward processing. Aberrant function of neural reward circuitry is well documented in anhedonia and other psychiatric disorders. Longitudinal studies to identify potential biomarkers associated with a reduction in anhedonia are necessary for the development of novel treatment targets.
To identify neural reward-processing factors associated with improved psychiatric symptoms and psychosocial function in a naturalistic, observational context.
DESIGN, SETTING, AND PARTICIPANTS: A longitudinal cohort follow-up study was conducted from March 1, 2014, to June 5, 2018, at the University of Pittsburgh Medical Center after baseline functional magnetic resonance imaging in 52 participants between the ages of 18 and 25 years who were experiencing psychological distress.
Participants were evaluated at baseline and 6 months. At baseline, participants underwent functional magnetic resonance imaging during a card-guessing monetary reward task. Participants completed measures of affective symptoms and psychosocial function at each visit. Neural activation during reward prediction error (RPE), a measure of reward learning, was determined using Statistical Parametric Mapping software. Neural reward regions with significant RPE activation were entered as regions associated with future symptoms in multiple linear regression models.
A total of 52 young adults (42 women and 10 men; mean [SD] age, 21.4 [2.2] years) completed the study. Greater RPE activation in the left ventral striatum was associated with a decrease in anhedonia symptoms during a 6-month period (β = -6.152; 95% CI, -11.870 to -0.433; P = .04). The decrease in anhedonia between baseline and 6 months mediated the association between left ventral striatum activation to RPE and improvement in life satisfaction between baseline and 6 months (total [c path] association: β = 0.245; P = .01; direct [c' path] association: β = 0.133; P = .16; and indirect [ab path] association: 95% CI, 0.026-0.262). Results were not associated with psychotropic medication use.
Greater left ventral striatum responsiveness to RPE may serve as a biomarker or potential target for novel treatments to improve the severity of anhedonia, overall mental health, and psychosocial function.
快感缺失是年轻成年人多种精神疾病的症状,与较差的心理健康和心理社会功能以及腹侧纹状体奖赏处理异常有关。神经奖赏回路的异常功能在快感缺失和其他精神疾病中得到了很好的证明。在自然观察环境中,需要进行识别与快感缺失减少相关的潜在生物标志物的纵向研究,以开发新的治疗靶点。
在自然观察环境中,识别与改善精神症状和心理社会功能相关的神经奖赏处理因素。
设计、地点和参与者:这是一项纵向队列随访研究,于 2014 年 3 月 1 日至 2018 年 6 月 5 日在匹兹堡大学医学中心进行,研究对象为 52 名年龄在 18 至 25 岁之间的参与者,他们在基线时经历了心理困扰,基线时进行了功能磁共振成像,基线后 6 个月进行了随访。
参与者在基线和 6 个月时进行评估。基线时,参与者在卡片猜谜货币奖励任务中接受了功能磁共振成像。每次就诊时,参与者都完成了情感症状和心理社会功能的测量。使用统计参数映射软件确定奖励预测误差(RPE)期间的神经激活,这是衡量奖励学习的一个指标。具有显著 RPE 激活的神经奖励区域被输入到多个线性回归模型中,作为与未来症状相关的区域。
共有 52 名年轻人(42 名女性和 10 名男性;平均[标准差]年龄,21.4[2.2]岁)完成了这项研究。左侧腹侧纹状体的 RPE 激活越大,6 个月期间快感缺失症状的下降幅度越大(β=-6.152;95%CI,-11.870 至-0.433;P=0.04)。基线和 6 个月之间快感缺失的减少介导了左侧腹侧纹状体激活到 RPE 与基线和 6 个月之间生活满意度改善之间的关联(总[c 路径]关联:β=0.245;P=0.01;直接[c'路径]关联:β=0.133;P=0.16;间接[ab 路径]关联:95%CI,0.026-0.262)。结果与精神药物的使用无关。
对 RPE 的更大左侧腹侧纹状体反应可能作为生物标志物或潜在的治疗靶点,以改善快感缺失的严重程度、整体心理健康和心理社会功能。