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LIBRIS Formathandbok  (Information om MARC21)
FältnamnIndikatorerMetadata
00003953naa a2200409 4500
001oai:DiVA.org:uu-473459
003SwePub
008220427s2022 | |||||||||||000 ||eng|
024a https://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-4734592 URI
024a https://doi.org/10.1038/s41598-022-07109-32 DOI
040 a (SwePub)uu
041 a engb eng
042 9 SwePub
072 7a ref2 swepub-contenttype
072 7a art2 swepub-publicationtype
100a Dubol, Manonu Uppsala universitet,Science for Life Laboratory, SciLifeLab,Comasco: Neuropsykofarmakologi4 aut0 (Swepub:uu)mandu832
2451 0a Grey matter correlates of affective and somatic symptoms of premenstrual dysphoric disorder
264 c 2022-04-09
264 1b Springer Nature,c 2022
338 a electronic2 rdacarrier
500 a Shared last authorship: Inger Sundström-Poromaa and Erika Comasco.
520 a Ovarian hormones fluctuations across the menstrual cycle are experienced by about 58% of women in their fertile age. Maladaptive brain sensitivity to these changes likely leads to the severe psychological, cognitive, and physical symptoms repeatedly experienced by women with Premenstrual Dysphoric Disorder (PMDD) during the late luteal phase of the menstrual cycle. However, the neuroanatomical correlates of these symptoms are unknown. The relationship between grey matter structure and PMDD symptom severity was delineated using structural magnetic resonance imaging during the late luteal phase of fifty-one women diagnosed with PMDD, combined with Voxel- and Surface-Based Morphometry, as well as subcortical volumetric analyses. A negative correlation was found between depression-related symptoms and grey matter volume of the bilateral amygdala. Moreover, the severity of affective and somatic PMDD symptoms correlated with cortical thickness, gyrification, sulcal depth, and complexity metrics, particularly in the prefrontal, cingulate, and parahippocampal gyri. The present findings provide the first evidence of grey matter morphological characteristics associated with PMDD symptomatology in brain regions expressing ovarian hormone receptors and of relevance to cognitive-affective functions, thus potentially having important implications for understanding how structural brain characteristics relate to PMDD symptomatology.
650 7a MEDICIN OCH HÄLSOVETENSKAPx Klinisk medicinx Psykiatri0 (SwePub)302152 hsv//swe
650 7a MEDICAL AND HEALTH SCIENCESx Clinical Medicinex Psychiatry0 (SwePub)302152 hsv//eng
650 7a MEDICIN OCH HÄLSOVETENSKAPx Klinisk medicinx Reproduktionsmedicin och gynekologi0 (SwePub)302202 hsv//swe
650 7a MEDICAL AND HEALTH SCIENCESx Clinical Medicinex Obstetrics, Gynaecology and Reproductive Medicine0 (SwePub)302202 hsv//eng
700a Wikström, Johan,d 1964-u Uppsala universitet,Radiologi4 aut0 (Swepub:uu)jwi06759
700a Lanzenberger, Rupertu Department of Psychiatry and Psychotherapy, Medical University of Vienna, Vienna, Austria4 aut
700a Epperson, C. Neillu Department of Psychiatry, Department of Family Medicine, University of Colorado School of Medicine-Anschutz Medical Campus, Aurora, USA4 aut
700a Sundström Poromaa, Inger,d 1964-u Uppsala universitet,Reproduktiv hälsa4 aut0 (Swepub:uu)inspo702
700a Comasco, Erika,d 1982-u Uppsala universitet,Science for Life Laboratory, SciLifeLab,Comasco: Neuropsykofarmakologi4 aut0 (Swepub:uu)erico267
710a Uppsala universitetb Science for Life Laboratory, SciLifeLab4 org
773t Scientific Reportsd : Springer Natureg 12:1q 12:1x 2045-2322
856u https://doi.org/10.1038/s41598-022-07109-3y Fulltext
856u https://uu.diva-portal.org/smash/get/diva2:1654421/FULLTEXT02.pdfx primaryx Raw objecty fulltext:print
8564 8u https://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-473459
8564 8u https://doi.org/10.1038/s41598-022-07109-3

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