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. 2021 Jul:87:102035.
doi: 10.1016/j.cpr.2021.102035. Epub 2021 May 3.

Neural reward circuit dysfunction as a risk factor for bipolar spectrum disorders and substance use disorders: A review and integration

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Neural reward circuit dysfunction as a risk factor for bipolar spectrum disorders and substance use disorders: A review and integration

Corinne P Bart et al. Clin Psychol Rev. 2021 Jul.

Abstract

Bipolar spectrum disorders (BSDs) and substance use disorders (SUDs) are associated with neural reward dysfunction. However, it is unclear what pattern of neural reward function underlies pre-existing vulnerability to BSDs and SUDs, or whether neural reward function explains their high co-occurrence. The current paper provides an overview of the separate literatures on neural reward sensitivity in BSDs and SUDs. We provide a systematic review of 35 studies relevant to identifying neural reward function vulnerability to BSDs and SUDs. These studies include those examining neural reward processing on a monetary reward task with prospective designs predicting initial onset of SUDs, familial risk studies that examine unaffected offspring or first-degree relatives of family members with BSDs or SUDs, and studies that examine individuals with BSDs or SUDs who are not currently in an episode of the disorder. Findings from the review highlight that aberrant responding and connectivity across neural regions associated with reward and cognitive control confers risk for the development of BSDs and SUDs. Discussion focuses on limitations of the extant literature. We conclude with an integration and theoretical model for understanding how aberrant neural reward responding may constitute a vulnerability to the development of both BSDs and SUDs.

Keywords: Bipolar spectrum disorder; Monetary incentive delay; Reward processing; Risk; Substance use disorder.

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Conflict of interest statement

Conflict of Interests

All authors declare that they have no conflicts of interest, financial or otherwise.

Figures

Figure 1.
Figure 1.
Flowchart of study selection. Note. Thirty-four distinct articles were identified, consisting of 35 separate studies (Kollman et al., 2017 included results from two separate studies on familial risk and euthymic samples).

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