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dc.contributor.authorPandey, Ashwini Kumar
dc.contributor.authorArdekani, Babak Assai
dc.contributor.authorKamarajan, Chella
dc.contributor.authorZhang, Jian
dc.contributor.authorChorlian, David Balin
dc.contributor.authorByrne, Kelly Nicole-Helen
dc.contributor.authorPandey, Gayathri
dc.contributor.authorMeyers, Jacquelyn Leigh
dc.contributor.authorKinreich, Sivan
dc.contributor.authorStimus, Arthur
dc.contributor.authorPorjesz, Bernice
dc.date.accessioned2022-12-09T17:38:12Z
dc.date.available2022-12-09T17:38:12Z
dc.date.issued2018-08-17
dc.identifier.citationPandey AK, Ardekani BA, Kamarajan C, Zhang J, Chorlian DB, Byrne KN, Pandey G, Meyers JL, Kinreich S, Stimus A, Porjesz B. Lower Prefrontal and Hippocampal Volume and Diffusion Tensor Imaging Differences Reflect Structural and Functional Abnormalities in Abstinent Individuals with Alcohol Use Disorder. Alcohol Clin Exp Res. 2018 Oct;42(10):1883-1896. doi: 10.1111/acer.13854. Epub 2018 Aug 17. PMID: 30118142; PMCID: PMC6167190.en_US
dc.identifier.eissn1530-0277
dc.identifier.doi10.1111/acer.13854
dc.identifier.pmid30118142
dc.identifier.urihttp://hdl.handle.net/20.500.12648/7938
dc.description.abstractBackground: Alcohol use disorder (AUD) is known to have adverse effects on brain structure and function. Multimodal assessments investigating volumetric, diffusion, and cognitive characteristics may facilitate understanding of the consequences of long-term alcohol use on brain circuitry, their structural impairment patterns, and their impact on cognitive function in AUD. Methods: Voxel- and surface-based volumetric estimations, diffusion tensor imaging (DTI), and neuropsychological tests were performed on 60 individuals: 30 abstinent individuals with AUD (DSM-IV) and 30 healthy controls. Group differences in the volumes of cortical and subcortical regions, fractional anisotropy (FA), axial and radial diffusivities (AD and RD, respectively), and performance on neuropsychological tests were analyzed, and the relationship among significantly different measures was assessed using canonical correlation. Results: AUD participants had significantly smaller volumes in left pars orbitalis, right medial orbitofrontal, right caudal middle frontal, and bilateral hippocampal regions, lower FA in 9 white matter (WM) regions, and higher FA in left thalamus, compared to controls. In AUD, lower FA in 6 of 9 WM regions was due to higher RD and due to lower AD in the left external capsule. AUD participants scored lower on problem-solving ability, visuospatial memory span, and working memory. Positive correlations of prefrontal cortical, left hippocampal volumes, and FA in 4 WM regions with visuospatial memory performance and negative correlation with lower problem-solving ability were observed. Significant positive correlation between age and FA was observed in bilateral putamen. Conclusions: Findings showed specific structural brain abnormalities to be associated with visuospatial memory and problem-solving ability-related impairments observed in AUD. Higher RD in 6 WM regions suggests demyelination, and lower AD in left external capsule suggests axonal loss in AUD. The positive correlation between FA and age in bilateral putamen may reflect accumulation of iron depositions with increasing age.en_US
dc.language.isoenen_US
dc.relation.urlhttps://onlinelibrary.wiley.com/doi/10.1111/acer.13854en_US
dc.rights© 2018 by the Research Society on Alcoholism.
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectAxial and Radial Diffusivityen_US
dc.subjectDiffusion Tensor Imagingen_US
dc.subjectFractional Anisotropyen_US
dc.subjectHippocampal Volumeen_US
dc.subjectNeuropsychological Tasksen_US
dc.titleLower Prefrontal and Hippocampal Volume and Diffusion Tensor Imaging Differences Reflect Structural and Functional Abnormalities in Abstinent Individuals with Alcohol Use Disorder.en_US
dc.typeArticle/Reviewen_US
dc.source.journaltitleAlcoholism, clinical and experimental researchen_US
dc.source.volume42
dc.source.issue10
dc.source.beginpage1883
dc.source.endpage1896
dc.source.countryUnited States
dc.source.countryUnited States
dc.source.countryEngland
dc.description.versionAMen_US
refterms.dateFOA2022-12-09T17:38:13Z
dc.description.institutionSUNY Downstateen_US
dc.description.departmentHenri Begleiter Neurodynamics Laboratoryen_US
dc.description.degreelevelN/Aen_US
dc.identifier.journalAlcoholism, clinical and experimental research


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© 2018 by the Research Society on Alcoholism.
Except where otherwise noted, this item's license is described as © 2018 by the Research Society on Alcoholism.