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dc.contributor.authorKeller, Jenniferen_US
dc.contributor.authorGomez, Rowenaen_US
dc.contributor.authorWilliams, Gordonen_US
dc.contributor.authorLembke, Annaen_US
dc.contributor.authorLazzeroni, Lauraen_US
dc.contributor.authorMurphy, Greer M.en_US
dc.contributor.authorSchatzberg, Alan F.en_US
dc.date.accessioned2017-03-28T23:49:41Z
dc.date.issued2016en_US
dc.identifier.citationKeller, Jennifer, Rowena Gomez, Gordon Williams, Anna Lembke, Laura Lazzeroni, Greer M. Murphy, and Alan F. Schatzberg. 2016. “HPA Axis in Major Depression: Cortisol, Clinical Symptomatology, and Genetic Variation Predict Cognition.” Molecular psychiatry :10.1038/mp.2016.120. doi:10.1038/mp.2016.120. http://dx.doi.org/10.1038/mp.2016.120.en
dc.identifier.issnen
dc.identifier.urihttp://nrs.harvard.edu/urn-3:HUL.InstRepos:31731754
dc.description.abstractThe Hypothalamic Pituitary Adrenal (HPA) axis has been implicated in the pathophysiology of a variety of mood and cognitive disorders. Neuroendocrine studies have demonstrated HPA axis overactivity in major depression, a relationship of HPA axis activity to cognitive performance, and a potential role of HPA axis genetic variation in cognition. The present study investigated the simultaneous roles HPA axis activity, clinical symptomatology, and HPA genetic variation play in cognitive performance. Patients with major depression with psychosis (PMD) and without psychosis (NPMD) and healthy controls (HC) were studied. All participants underwent a diagnostic interview and psychiatric ratings, a comprehensive neuropsychological battery, overnight hourly blood sampling for cortisol, and genetic assessment. Cognitive performance differed as a function of depression subtype. Across all subjects, cognitive performance was negatively correlated with higher cortisol, and PMD patients had higher cortisol than did NPMDs and HCs. Cortisol, clinical symptoms, and variation in genes, NR3C1 (glucocorticoid receptor - GR) and NR3C2 (minercorticoid receptor – MR) that encode for glucocorticoid and mineralcorticoid receptors, predicted cognitive performance. Beyond the effects of cortisol, demographics, and clinical symptoms, NR3C1 variation predicted attention and working memory, whereas NR3C2 polymorphisms predicted memory performance. These findings parallel the distribution of GR and MR in primate brain and their putative roles in specific cognitive tasks. HPA axis genetic variation and activity were important predictors of cognition across the entire sample of depressed subjects and healthy controls. GR and MR genetic variation predicted unique cognitive functions, beyond the influence of cortisol and clinical symptoms. GR genetic variation was implicated in attention and working memory, whereas MR was implicated in verbal memory.en
dc.language.isoen_USen
dc.relation.isversionofdoi:10.1038/mp.2016.120en
dc.relation.hasversionhttp://www.ncbi.nlm.nih.gov/pmc/articles/PMC5313380/pdf/en
dash.licenseLAAen_US
dc.subjectMajor depressionen
dc.subjectpsychosisen
dc.subjectcortisolen
dc.subjectglucocorticoid genesen
dc.subjectHPA axisen
dc.subjectcognitionen
dc.titleHPA Axis in Major Depression: Cortisol, Clinical Symptomatology, and Genetic Variation Predict Cognitionen
dc.typeJournal Articleen_US
dc.description.versionVersion of Recorden
dc.relation.journalMolecular psychiatryen
dash.depositing.authorWilliams, Gordonen_US
dc.date.available2017-03-28T23:49:41Z
dc.identifier.doi10.1038/mp.2016.120*
dash.contributor.affiliatedWilliams, Gordon


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