Vulnerability to Depression in Youth: Advances From Affective Neuroscience

被引:89
|
作者
Kujawa, Autumn [1 ]
Burkhouse, Katie L. [2 ]
机构
[1] Penn State Coll Med, Dept Psychiat, 22 Northeast Dr, Hershey, PA 17033 USA
[2] Univ Illinois, Dept Psychiat, Chicago, IL 60612 USA
关键词
Affective neuroscience; Depression; Developmental psychopathology; EEG/ERP; fMRI; Risk; EVENT-RELATED POTENTIALS; GENERALIZED ANXIETY DISORDER; FRONTAL EEG ASYMMETRY; NEURAL RESPONSE; EMOTIONAL FACES; YOUNG-CHILDREN; BRAIN ACTIVITY; ELECTROCORTICAL REACTIVITY; PUPILLARY REACTIVITY; ATTENTIONAL BIASES;
D O I
10.1016/j.bpsc.2016.09.006
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Vulnerability models of depression posit that individual differences in trait-like vulnerabilities emerge early in life and increase risk for the later development of depression. In this review, we summarize advances from affective neuroscience using neural measures to assess vulnerabilities in youth at high risk for depression due to parental history of depression or temperament style, as well as prospective designs evaluating the predictive validity of these vulnerabilities for symptoms and diagnoses of depression across development. Evidence from multiple levels of analysis indicates that healthy youth at high risk for depression exhibit abnormalities in components of the Research Domain Criteria positive valence systems, including blunted activation in the striatum during reward anticipation and feedback, and that some of these measures can be used to predict later symptoms. In addition, alterations in components of the Research Domain Criteria negative valence systems, including neural processing of sadness, loss, and threat, have been observed in risk for depression, though effects appear to be more task and method dependent. Within the social processes domain, preliminary evidence indicates that neural processing of social feedback, including heightened reactivity to exclusion and blunted response to social reward, may be related to depression vulnerability. These studies indicate that affective neuroscience can inform understanding of developmental pathways to depression and identify altered emotional processing among youth at high risk. We provide an integrated summary of replicated findings from this literature, along with recommendations for future directions and implications for early intervention.
引用
收藏
页码:28 / 37
页数:10
相关论文
共 50 条
  • [21] Clinical Affective Neuroscience
    Penner, Anne E.
    Stoddard, Joel
    JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY, 2018, 57 (12): : 906 - 908
  • [22] Affective neuroscience and addiction
    Charland, Louis C.
    AMERICAN JOURNAL OF BIOETHICS, 2007, 7 (01): : 20 - 21
  • [23] Affective neuroscience and psychiatry
    Harrison, Neil A.
    Critchley, Hugo D.
    BRITISH JOURNAL OF PSYCHIATRY, 2007, 191 : 192 - 194
  • [24] The Affective Neuroscience of Aging
    Mather, Mara
    ANNUAL REVIEW OF PSYCHOLOGY, VOL 67, 2016, 67 : 213 - 238
  • [25] Affective neuroscience and psychiatry
    Walter, H
    NERVENHEILKUNDE, 1999, 18 (03) : 116 - 126
  • [26] The Philosophy of Affective Neuroscience
    Gabriel, Rami
    Panksepp, Jaak
    Asma, Stephen
    Curran, Glennon
    COGNITION IN FLUX, 2010, : 507 - 508
  • [27] THE AFFECTIVE NEUROSCIENCE OF AGING
    Samanez-Larkin, G.
    Nielsen, L.
    GERONTOLOGIST, 2008, 48 : 621 - 621
  • [28] Affective disorders and sexual function: from neuroscience to clinic
    Barata, Bernardo C.
    CURRENT OPINION IN PSYCHIATRY, 2017, 30 (06) : 396 - 401
  • [29] Anxiety Regulation: From Affective Neuroscience to Clinical Practice
    Grecucci, Alessandro
    Sigirci, Huseyin
    Lapomarda, Gaia
    Amodeo, Letizia
    Messina, Irene
    Frederickson, Jon
    BRAIN SCIENCES, 2020, 10 (11) : 1 - 11
  • [30] The "Anhedonia Paradox" in Schizophrenia: Insights from Affective Neuroscience
    Pizzagalli, Diego A.
    BIOLOGICAL PSYCHIATRY, 2010, 67 (10) : 899 - 901