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dc.contributor.authorDeligiannidis, Kristina M.
dc.contributor.authorFales, Christina L.
dc.contributor.authorKroll-Desrosiers, Aimee
dc.contributor.authorShaffer, Scott A.
dc.contributor.authorVillamarin, Vanessa
dc.contributor.authorTan, Yanglan
dc.contributor.authorHall, Janet E.
dc.contributor.authorFrederick, Blaise B.
dc.contributor.authorSikoglu, Elif M.
dc.contributor.authorEdden, Richard A.
dc.contributor.authorRothschild, Anthony J.
dc.contributor.authorMoore, Constance M.
dc.date2022-08-11T08:10:31.000
dc.date.accessioned2022-08-23T17:11:38Z
dc.date.available2022-08-23T17:11:38Z
dc.date.issued2019-02-01
dc.date.submitted2019-08-29
dc.identifier.citation<p>Neuropsychopharmacology. 2019 Feb;44(3):546-554. doi: 10.1038/s41386-018-0242-2. Epub 2018 Oct 17. <a href="https://doi.org/10.1038/s41386-018-0242-2">Link to article on publisher's site</a></p>
dc.identifier.issn0893-133X (Linking)
dc.identifier.doi10.1038/s41386-018-0242-2
dc.identifier.pmid30327498
dc.identifier.urihttp://hdl.handle.net/20.500.14038/46323
dc.description.abstractPostpartum depression (PPD) is associated with abnormalities in resting-state functional connectivity (RSFC) but the underlying neurochemistry is unclear. We hypothesized that peripartum GABAergic neuroactive steroids (NAS) are related to cortical GABA concentrations and RSFC in PPD as compared to healthy comparison women (HCW). To test this, we measured RSFC with fMRI and GABA+/Creatine (Cr) concentrations with proton magnetic resonance spectroscopy ((1)H MRS) in the pregenual anterior cingulate (pgACC) and occipital cortices (OCC) and quantified peripartum plasma NAS. We examined between-group differences in RSFC and the relationship between cortical GABA+/Cr concentrations with RSFC. We investigated the relationship between NAS, RSFC and cortical GABA+/Cr concentrations. Within the default mode network (DMN) an area of the dorsomedial prefrontal cortex (DMPFC) had greater connectivity with the rest of the DMN in PPD (peak voxel: MNI coordinates (2, 58, 32), p = 0.002) and was correlated to depression scores (peak HAM-D17 voxel: MNI coordinates (0, 60, 34), p = 0.008). pgACC GABA+/Cr correlated positively with DMPFC RSFC in a region spanning the right anterior/posterior insula and right temporal pole (r = +0.661, p = 0.000). OCC GABA+/Cr correlated positively with regions spanning both amygdalae (right amygdala: r = +0.522, p = 0.000; left amygdala: r = +0.651, p = 0.000) as well as superior parietal areas. Plasma allopregnanolone was higher in PPD (p = 0.03) and positively correlated with intra DMPFC connectivity (r = +0.548, p = 0.000) but not GABA+/Cr. These results provide initial evidence that PPD is associated with altered DMN connectivity; cortical GABA+/Cr concentrations are associated with postpartum RSFC and allopregnanolone is associated with postpartum intra-DMPFC connectivity.
dc.language.isoen_US
dc.relation<p><a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=30327498&dopt=Abstract">Link to Article in PubMed</a></p>
dc.relation.urlhttps://doi.org/10.1038/s41386-018-0242-2
dc.subjectGonadal hormones
dc.subjectPrefrontal cortex
dc.subjectBiochemistry
dc.subjectEndocrine System
dc.subjectFemale Urogenital Diseases and Pregnancy Complications
dc.subjectHormones, Hormone Substitutes, and Hormone Antagonists
dc.subjectNervous System
dc.subjectNeuroscience and Neurobiology
dc.subjectPharmacology, Toxicology and Environmental Health
dc.subjectPsychiatry
dc.subjectPsychiatry and Psychology
dc.subjectReproductive and Urinary Physiology
dc.subjectWomen's Health
dc.titleResting-state functional connectivity, cortical GABA, and neuroactive steroids in peripartum and peripartum depressed women: a functional magnetic resonance imaging and spectroscopy study
dc.typeJournal Article
dc.source.journaltitleNeuropsychopharmacology : official publication of the American College of Neuropsychopharmacology
dc.source.volume44
dc.source.issue3
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/psych_pp/880
dc.identifier.contextkey15233902
html.description.abstract<p>Postpartum depression (PPD) is associated with abnormalities in resting-state functional connectivity (RSFC) but the underlying neurochemistry is unclear. We hypothesized that peripartum GABAergic neuroactive steroids (NAS) are related to cortical GABA concentrations and RSFC in PPD as compared to healthy comparison women (HCW). To test this, we measured RSFC with fMRI and GABA+/Creatine (Cr) concentrations with proton magnetic resonance spectroscopy ((1)H MRS) in the pregenual anterior cingulate (pgACC) and occipital cortices (OCC) and quantified peripartum plasma NAS. We examined between-group differences in RSFC and the relationship between cortical GABA+/Cr concentrations with RSFC. We investigated the relationship between NAS, RSFC and cortical GABA+/Cr concentrations. Within the default mode network (DMN) an area of the dorsomedial prefrontal cortex (DMPFC) had greater connectivity with the rest of the DMN in PPD (peak voxel: MNI coordinates (2, 58, 32), p = 0.002) and was correlated to depression scores (peak HAM-D17 voxel: MNI coordinates (0, 60, 34), p = 0.008). pgACC GABA+/Cr correlated positively with DMPFC RSFC in a region spanning the right anterior/posterior insula and right temporal pole (r = +0.661, p = 0.000). OCC GABA+/Cr correlated positively with regions spanning both amygdalae (right amygdala: r = +0.522, p = 0.000; left amygdala: r = +0.651, p = 0.000) as well as superior parietal areas. Plasma allopregnanolone was higher in PPD (p = 0.03) and positively correlated with intra DMPFC connectivity (r = +0.548, p = 0.000) but not GABA+/Cr. These results provide initial evidence that PPD is associated with altered DMN connectivity; cortical GABA+/Cr concentrations are associated with postpartum RSFC and allopregnanolone is associated with postpartum intra-DMPFC connectivity.</p>
dc.identifier.submissionpathpsych_pp/880
dc.contributor.departmentCenter for Comparative Neuroimaging
dc.contributor.departmentDepartment of Biochemistry and Molecular Pharmacology
dc.contributor.departmentMass Spectrometry Facility
dc.contributor.departmentDepartment of Quantitative Health Sciences
dc.contributor.departmentDepartment of Psychiatry, Center for Psychopharmacologic Research and Treatment
dc.source.pages546-554


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