Reward systems and cognitions in Major Depressive Disorder

被引:43
作者
Clery-Melin, Marie-Laure [1 ,2 ]
Jollant, Fabrice [1 ,2 ]
Gorwood, Philip [1 ,2 ]
机构
[1] Univ Paris 05, Hop Sainte Anne, CMME, 100 Rue Sante, F-75014 Paris, France
[2] INSERM, Ctr Psychiat & Neurosci, UMR 894, 2 Ter Rue Alesia, F-75014 Paris, France
关键词
anhedonia; cognition; dopamine; endophenotype; liking; motivation; neurotoxicity; reward; striatum; wanting; IMPAIRED DECISION-MAKING; FUNCTIONAL CONNECTIVITY; 1ST-DEGREE RELATIVES; SUICIDAL-BEHAVIOR; HEDONIC CAPACITY; SEROTONIN; BRAIN; MOOD; DEFICITS; SCALE;
D O I
10.1017/S1092852918001335
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
A lack of motivation and anhedonia represent frequent and pervasive symptoms in depression, although with poor specificity. Historically described as a response bias, reward-related impairments in depression may account for the important aspects of the cognitive impairments associated with diagnosis of major depressive disorder. Reward processing is a broad psychological construct that can be parsed into 3 distinct components known as "reinforcement learning" (learning), "reward responsiveness" (liking), and "motivation to obtain a reward" (wanting). Depressed patients respond hyposensitively to reward and maladaptively to punishment: this pattern is related to a dysfunction in the frontostriatal systems modulated by the monoamine systems; seems to be observed in medicated and unmedicated patients with depression and in healthy individuals with high levels of anhedonia; and could be observed in patients with a history of depression, even when in full remission. Considered to be cognitive impairments, reward-related-impairments may also constitute part of an underlying neurobiological vulnerability to major depressive disorder (MDD). For example, the reward-related impairment is state dependent and, more or less, correlated with symptom severity in some studies but has also been proposed as being trait like, with endophenotype characteristics, possibly contributing to the persistence of the disease or treatment resistance. The 3 core aspects of reward processing have specific neurobiological correlates that involve the ventral and dorsal striatum, lateral habenula, ventral tegmental area, orbitofrontal cortex, anterior cingulate cortex, and ventromedial and dorsolateral prefrontal cortex. These structures underline the important role of the dopaminergic mesolimbic pathway, but glutamate and serotonin could also have an important role, at least in some aspects of reward-related impairments.
引用
收藏
页码:64 / 77
页数:14
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