<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Kakarala SE</submitter><funding>NCATS NIH HHS</funding><funding>National Institute of Nursing Research</funding><funding>NIA NIH HHS</funding><funding>NIMH NIH HHS</funding><funding>NINR NIH HHS</funding><funding>NIMHD NIH HHS</funding><funding>National Cancer Institute</funding><funding>NCI NIH HHS</funding><funding>National Institute of Mental Health</funding><funding>National Center for Advancing Translation Sciences</funding><funding>National Institute of Minority Health Disparities</funding><funding>National Institute on Aging</funding><pagination>111135</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7442719</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>303</volume><pubmed_abstract>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.</pubmed_abstract><journal>Psychiatry research. Neuroimaging</journal><pubmed_title>The neurobiological reward system in Prolonged Grief Disorder (PGD): A systematic review.</pubmed_title><pmcid>PMC7442719</pmcid><funding_grant_id>AG049666</funding_grant_id><funding_grant_id>UL1 TR002384</funding_grant_id><funding_grant_id>R01 CA106370</funding_grant_id><funding_grant_id>P30 CA008748</funding_grant_id><funding_grant_id>T32 CA009461</funding_grant_id><funding_grant_id>CA106370</funding_grant_id><funding_grant_id>NR018693</funding_grant_id><funding_grant_id>R21 MH121886</funding_grant_id><funding_grant_id>R01 MD007652</funding_grant_id><funding_grant_id>P30 AG022845</funding_grant_id><funding_grant_id>R21 NR018693</funding_grant_id><funding_grant_id>T32 AG049666</funding_grant_id><funding_grant_id>R01 MH063892</funding_grant_id><funding_grant_id>P30CA008748</funding_grant_id><funding_grant_id>R35 CA197730</funding_grant_id><funding_grant_id>CA218313</funding_grant_id><funding_grant_id>R21 CA218313</funding_grant_id><funding_grant_id>MD007652</funding_grant_id><funding_grant_id>MH095378</funding_grant_id><funding_grant_id>R21 MH095378</funding_grant_id><funding_grant_id>CA197730</funding_grant_id><funding_grant_id>CA009461</funding_grant_id><pubmed_authors>Coats T</pubmed_authors><pubmed_authors>Roberts KE</pubmed_authors><pubmed_authors>Maciejewski PK</pubmed_authors><pubmed_authors>Falzarano F</pubmed_authors><pubmed_authors>Avery J</pubmed_authors><pubmed_authors>Rogers M</pubmed_authors><pubmed_authors>Chilov M</pubmed_authors><pubmed_authors>Prigerson HG</pubmed_authors><pubmed_authors>Kakarala SE</pubmed_authors><pubmed_authors>Lichtenthal WG</pubmed_authors><pubmed_authors>Gang J</pubmed_authors></additional><is_claimable>false</is_claimable><name>The neurobiological reward system in Prolonged Grief Disorder (PGD): A systematic review.</name><description>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.</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 Sep</publication><modification>2024-10-15T02:04:43.914Z</modification><creation>2022-02-11T11:36:22.429Z</creation></dates><accession>S-EPMC7442719</accession><cross_references><pubmed>32629197</pubmed><doi>10.1016/j.pscychresns.2020.111135</doi></cross_references></HashMap>