Brain volumes in late life: gender, hormone treatment, and estrogen receptor variants

dc.contributor.authorRyan, Joanne
dc.contributor.authorArtero, Sylvaine
dc.contributor.authorCarrière, Isabelle
dc.contributor.authorScali, Jacqueline
dc.contributor.authorMaller, Jerome J.
dc.contributor.authorMeslin, Chantal
dc.contributor.authorRitchie, Karen
dc.contributor.authorScarabin, Pierre-Yves
dc.contributor.authorAncelin, Marie-Laure
dc.date.accessioned2015-12-10T23:31:36Z
dc.date.issued2014
dc.date.updated2015-12-10T11:15:22Z
dc.description.abstractStructural imaging studies suggest gender differences in brain volumes; however, whether hormone treatment (HT) can protect against age-related structural changes remains unknown, and no prior neuroimaging study has investigated potential interactions between HT and estrogen receptor (ESR) polymorphisms. Magnetic resonance imaging was used to measure gray and white matter, hippocampal volume, corpus callosum, cerebrospinal fluid (CSF), total intracranial volume (ICV) and white matter lesions (WML) in 582 non-demented older adults. In multivariable analysis, when compared to women who had never used HT, men and women currently on treatment, but not past users, had significantly smaller ratios of gray matter to ICV and increased atrophy (CSF/ICV ratio). Hippocampal and white matter volume as well as the corpus callosum area were not significantly different across groups. ESR2 variants were not significantly associated with brain measures, but women with the ESR1 rs2234693 C allele had significantly smaller WML. Furthermore this association was modified by HT use. Our results do not support a beneficial effect of HT on brain volumes in older women, but suggest the potential involvement of ESR1 in WML.
dc.identifier.issn0197-4580
dc.identifier.urihttp://hdl.handle.net/1885/68705
dc.publisherElsevier
dc.sourceNeurobiology of Aging
dc.titleBrain volumes in late life: gender, hormone treatment, and estrogen receptor variants
dc.typeJournal article
local.bibliographicCitation.issue3
local.bibliographicCitation.lastpage654
local.bibliographicCitation.startpage645
local.contributor.affiliationRyan, Joanne, Université Montpellier 1
local.contributor.affiliationArtero, Sylvaine, Université Montpellier 1
local.contributor.affiliationCarrière, Isabelle, Université Montpellier 1
local.contributor.affiliationScali, Jacqueline, Université Montpellier 1
local.contributor.affiliationMaller, Jerome J., The Alfred & Monash University
local.contributor.affiliationMeslin, Chantal, College of Medicine, Biology and Environment, ANU
local.contributor.affiliationRitchie, Karen, Imperial College, London
local.contributor.affiliationScarabin, Pierre-Yves, Université Paris Sud 11
local.contributor.affiliationAncelin, Marie-Laure, French National Institute of Medical Research (INSERM)
local.contributor.authoruidMeslin, Chantal, u4028155
local.description.embargo2037-12-31
local.description.notesImported from ARIES
local.identifier.absfor110999 - Neurosciences not elsewhere classified
local.identifier.absseo920502 - Health Related to Ageing
local.identifier.absseo920112 - Neurodegenerative Disorders Related to Ageing
local.identifier.ariespublicationU3488905xPUB1803
local.identifier.citationvolume35
local.identifier.doi10.1016/j.neurobiolaging.2013.09.026
local.identifier.scopusID2-s2.0-84889563344
local.identifier.thomsonID000328655700022
local.type.statusPublished Version

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