The neurobiological reward system in Prolonged Grief Disorder (PGD): A systematic review

被引:46
作者
Kakarala, S. E. [1 ]
Roberts, K. E. [2 ]
Rogers, M. [1 ]
Coats, T. [2 ]
Falzarano, F. [1 ]
Gang, J. [1 ]
Chilov, M. [3 ]
Avery, J. [5 ]
Maciejewski, P. K. [1 ,5 ]
Lichtenthal, W. G. [2 ,4 ]
Prigerson, H. G. [1 ,6 ]
机构
[1] Weill Cornell Med, Cornell Ctr Res End Of Life Care, 420 E 70th St, New York, NY 10021 USA
[2] Mem Sloan Kettering Canc Ctr, Dept Psychiat & Behav Sci, 1275 York Ave, New York, NY 10065 USA
[3] Mem Sloan Kettering Canc Ctr, Med Lib, 1275 York Ave, New York, NY 10065 USA
[4] Weill Cornell Med, Dept Psychiat, 525 E 68th St, New York, NY 10065 USA
[5] Weill Cornell Med, Dept Radiol, 1305 York Ave, New York, NY 10021 USA
[6] Weill Cornell Med, Dept Med, 1320 York Ave, New York, NY 10021 USA
关键词
Bereavement; Prolonged Grief Disorder (PGD); Complicated Grief (CG); Neuroimaging; Nneurobiology; QUALITY-OF-LIFE; NUCLEUS-ACCUMBENS; COMPLICATED GRIEF; ORBITOFRONTAL CORTEX; POSTERIOR CINGULATE; ATTENTIONAL BIAS; TRAUMATIC GRIEF; DRUG-USE; ADDICTION; COGNITION;
D O I
10.1016/j.pscychresns.2020.111135
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Prolonged Grief Disorder (PGD) is a debilitating condition affecting between 7% and 10% of bereaved individuals. Past imaging and psychological studies have proposed links between PGD's characteristic symptoms in particular, profound yearning -and the neural reward system. We conducted a systematic review to investigate this connection. On December 19, 2019, we searched six bibliographic databases for data on the neurobiology of grief and disordered grief. We excluded studies of the hypothalamic-pituitary-adrenal (HPA) axis, animal studies, and reviews. After abstract and full-text screening, twenty-four studies were included in the final review. We found diverse evidence for the activation of several reward-related regions of the brain in PGD. The data reviewed suggest that compared to normative grief, PGD involves a differential pattern of activity in the amygdala and orbitofrontal cortex (OFC); likely differential activity in the posterior cingulate cortex (PCC), rostral or subgenual anterior cingulate cortex (ACC), and basal ganglia overall, including the nucleus accumbens (NAc); and possible differential activity in the insula. It also appears that oxytocin signaling is altered in PGD, though the exact mechanism is unclear. Our findings appear to be consistent with, though not confirmative of, conceptualizing PGD as a disorder of reward, and identify directions for future research.
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页数:19
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