Aberrant limbic brain structures in young individuals at risk for mental illness.

Saved in:
Bibliographic Details
Title: Aberrant limbic brain structures in young individuals at risk for mental illness.
Authors: Nogovitsyn, Nikita (AUTHOR), Souza, Roberto (AUTHOR), Muller, Meghan (AUTHOR), Srajer, Amelia (AUTHOR), Metzak, Paul D. (AUTHOR), Hassel, Stefanie (AUTHOR), Ismail, Zahinoor (AUTHOR), Protzner, Andrea (AUTHOR), Bray, Signe L. (AUTHOR), Lebel, Catherine (AUTHOR), MacIntosh, Bradley J. (AUTHOR), Goldstein, Benjamin I. (AUTHOR), Wang, JianLi (AUTHOR), Kennedy, Sidney H. (AUTHOR), Addington, Jean (AUTHOR), MacQueen, Glenda M. (AUTHOR)
Source: Psychiatry & Clinical Neurosciences. May2020, Vol. 74 Issue 5, p294-302. 9p. 1 Color Photograph, 2 Charts, 2 Graphs.
Subjects: Mental illness, Mental illness risk factors, Limbic system, Thalamus, Adolescent psychiatry
Abstract: Aim: Alterations in limbic structures may be present before the onset of serious mental illness, but whether subfield‐specific limbic brain changes parallel stages in clinical risk is unknown. To address this gap, we compared the hippocampus, amygdala, and thalamus subfield‐specific volumes in adolescents at various stages of risk for mental illness. Methods: MRI scans were obtained from 182 participants (aged 12–25 years) from the Canadian Psychiatric Risk and Outcome study. The sample comprised of four groups: asymptomatic youth at risk due to family history of mental illness (Stage 0, n = 32); youth with early symptoms of distress (Stage 1a, n = 41); youth with subthreshold psychotic symptoms (Stage 1b, n = 72); and healthy comparison participants with no family history of serious mental illness (n = 37). Analyses included between‐group comparisons of brain measurements and correlational analyses that aimed to identify significant associations between neuroimaging and clinical measurements. A machine‐learning technique examined the discriminative properties of the clinical staging model. Results: Subfield‐specific limbic volume deficits were detected at every stage of risk for mental illness. A machine‐learning classifier identified volume deficits within the body of the hippocampus, left amygdala nuclei, and medial‐lateral nuclei of the thalamus that were most informative in differentiating between risk stages. Conclusion: Aberrant subfield‐specific changes within the limbic system may serve as biological evidence to support transdiagnostic clinical staging in mental illness. Differential patterns of volume deficits characterize those at risk for mental illness and may be indicative of a risk‐stage progression. [ABSTRACT FROM AUTHOR]
Copyright of Psychiatry & Clinical Neurosciences is the property of Wiley-Blackwell and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)
Database: Psychology and Behavioral Sciences Collection
Full text is not displayed to guests.
FullText Links:
  – Type: pdflink
Text:
  Availability: 1
Header DbId: pbh
DbLabel: Psychology and Behavioral Sciences Collection
An: 143042627
AccessLevel: 6
PubType: Academic Journal
PubTypeId: academicJournal
PreciseRelevancyScore: 0
IllustrationInfo
Items – Name: Title
  Label: Title
  Group: Ti
  Data: Aberrant limbic brain structures in young individuals at risk for mental illness.
– Name: Author
  Label: Authors
  Group: Au
  Data: <searchLink fieldCode="AR" term="%22Nogovitsyn%2C+Nikita%22">Nogovitsyn, Nikita</searchLink> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Souza%2C+Roberto%22">Souza, Roberto</searchLink> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Muller%2C+Meghan%22">Muller, Meghan</searchLink> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Srajer%2C+Amelia%22">Srajer, Amelia</searchLink> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Metzak%2C+Paul+D%2E%22">Metzak, Paul D.</searchLink> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Hassel%2C+Stefanie%22">Hassel, Stefanie</searchLink> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Ismail%2C+Zahinoor%22">Ismail, Zahinoor</searchLink> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Protzner%2C+Andrea%22">Protzner, Andrea</searchLink> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Bray%2C+Signe+L%2E%22">Bray, Signe L.</searchLink> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Lebel%2C+Catherine%22">Lebel, Catherine</searchLink> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22MacIntosh%2C+Bradley+J%2E%22">MacIntosh, Bradley J.</searchLink> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Goldstein%2C+Benjamin+I%2E%22">Goldstein, Benjamin I.</searchLink> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Wang%2C+JianLi%22">Wang, JianLi</searchLink> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Kennedy%2C+Sidney+H%2E%22">Kennedy, Sidney H.</searchLink> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Addington%2C+Jean%22">Addington, Jean</searchLink> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22MacQueen%2C+Glenda+M%2E%22">MacQueen, Glenda M.</searchLink> (AUTHOR)
– Name: TitleSource
  Label: Source
  Group: Src
  Data: <searchLink fieldCode="JN" term="%22Psychiatry+%26+Clinical+Neurosciences%22">Psychiatry & Clinical Neurosciences</searchLink>. May2020, Vol. 74 Issue 5, p294-302. 9p. 1 Color Photograph, 2 Charts, 2 Graphs.
– Name: Subject
  Label: Subjects
  Group: Su
  Data: <searchLink fieldCode="DE" term="%22Mental+illness%22">Mental illness</searchLink><br /><searchLink fieldCode="DE" term="%22Mental+illness+risk+factors%22">Mental illness risk factors</searchLink><br /><searchLink fieldCode="DE" term="%22Limbic+system%22">Limbic system</searchLink><br /><searchLink fieldCode="DE" term="%22Thalamus%22">Thalamus</searchLink><br /><searchLink fieldCode="DE" term="%22Adolescent+psychiatry%22">Adolescent psychiatry</searchLink>
– Name: Abstract
  Label: Abstract
  Group: Ab
  Data: Aim: Alterations in limbic structures may be present before the onset of serious mental illness, but whether subfield‐specific limbic brain changes parallel stages in clinical risk is unknown. To address this gap, we compared the hippocampus, amygdala, and thalamus subfield‐specific volumes in adolescents at various stages of risk for mental illness. Methods: MRI scans were obtained from 182 participants (aged 12–25 years) from the Canadian Psychiatric Risk and Outcome study. The sample comprised of four groups: asymptomatic youth at risk due to family history of mental illness (Stage 0, n = 32); youth with early symptoms of distress (Stage 1a, n = 41); youth with subthreshold psychotic symptoms (Stage 1b, n = 72); and healthy comparison participants with no family history of serious mental illness (n = 37). Analyses included between‐group comparisons of brain measurements and correlational analyses that aimed to identify significant associations between neuroimaging and clinical measurements. A machine‐learning technique examined the discriminative properties of the clinical staging model. Results: Subfield‐specific limbic volume deficits were detected at every stage of risk for mental illness. A machine‐learning classifier identified volume deficits within the body of the hippocampus, left amygdala nuclei, and medial‐lateral nuclei of the thalamus that were most informative in differentiating between risk stages. Conclusion: Aberrant subfield‐specific changes within the limbic system may serve as biological evidence to support transdiagnostic clinical staging in mental illness. Differential patterns of volume deficits characterize those at risk for mental illness and may be indicative of a risk‐stage progression. [ABSTRACT FROM AUTHOR]
– Name: AbstractSuppliedCopyright
  Label:
  Group: Ab
  Data: <i>Copyright of Psychiatry & Clinical Neurosciences is the property of Wiley-Blackwell and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract.</i> (Copyright applies to all Abstracts.)
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=pbh&AN=143042627
RecordInfo BibRecord:
  BibEntity:
    Identifiers:
      – Type: doi
        Value: 10.1111/pcn.12985
    Languages:
      – Code: eng
        Text: English
    PhysicalDescription:
      Pagination:
        PageCount: 9
        StartPage: 294
    Subjects:
      – SubjectFull: Mental illness
        Type: general
      – SubjectFull: Mental illness risk factors
        Type: general
      – SubjectFull: Limbic system
        Type: general
      – SubjectFull: Thalamus
        Type: general
      – SubjectFull: Adolescent psychiatry
        Type: general
    Titles:
      – TitleFull: Aberrant limbic brain structures in young individuals at risk for mental illness.
        Type: main
  BibRelationships:
    HasContributorRelationships:
      – PersonEntity:
          Name:
            NameFull: Nogovitsyn, Nikita
      – PersonEntity:
          Name:
            NameFull: Souza, Roberto
      – PersonEntity:
          Name:
            NameFull: Muller, Meghan
      – PersonEntity:
          Name:
            NameFull: Srajer, Amelia
      – PersonEntity:
          Name:
            NameFull: Metzak, Paul D.
      – PersonEntity:
          Name:
            NameFull: Hassel, Stefanie
      – PersonEntity:
          Name:
            NameFull: Ismail, Zahinoor
      – PersonEntity:
          Name:
            NameFull: Protzner, Andrea
      – PersonEntity:
          Name:
            NameFull: Bray, Signe L.
      – PersonEntity:
          Name:
            NameFull: Lebel, Catherine
      – PersonEntity:
          Name:
            NameFull: MacIntosh, Bradley J.
      – PersonEntity:
          Name:
            NameFull: Goldstein, Benjamin I.
      – PersonEntity:
          Name:
            NameFull: Wang, JianLi
      – PersonEntity:
          Name:
            NameFull: Kennedy, Sidney H.
      – PersonEntity:
          Name:
            NameFull: Addington, Jean
      – PersonEntity:
          Name:
            NameFull: MacQueen, Glenda M.
    IsPartOfRelationships:
      – BibEntity:
          Dates:
            – D: 01
              M: 05
              Text: May2020
              Type: published
              Y: 2020
          Identifiers:
            – Type: issn-print
              Value: 13231316
          Numbering:
            – Type: volume
              Value: 74
            – Type: issue
              Value: 5
          Titles:
            – TitleFull: Psychiatry & Clinical Neurosciences
              Type: main
ResultId 1