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Affective lability in offspring of parents with major depressive disorder, bipolar disorder and schizophrenia

  • Alyson Zwicker
  • Vladislav Drobinin
  • Lynn E. MacKenzie
  • Emily Howes Vallis
  • Victoria C. Patterson
  • Jill Cumby
  • Lukas Propper
  • Sabina Abidi
  • Alexa Bagnell
  • Barbara Pavlova
  • Martin Alda
  • Rudolf UherEmail author
Original Contribution

Abstract

Affective lability, defined as the propensity to experience excessive and unpredictable changes in mood, has been proposed as a potential transdiagnostic predictor of major mood and psychotic disorders. A parental diagnosis of bipolar disorder has been associated with increased affective lability in offspring. However, the association between affective lability and family history of other mood and psychotic disorders has not been examined. We measured affective lability using the self- and parent-reported Children’s Affective Lability Scale in a cohort of 320 youth aged 6–17 years, including 137 offspring of a parent with major depressive disorder, 68 offspring of a parent with bipolar disorder, 24 offspring of a parent with schizophrenia, and 91 offspring of control parents. We tested differences in affective lability between groups using mixed-effects linear regression. Offspring of a parent with major depressive disorder (β = 0.46, 95% CI 0.17–0.76, p = 0.002) or bipolar disorder (β = 0.47, 95% CI 0.12–0.81, p = 0.008) had significantly higher affective lability scores than control offspring. Affective lability did not differ significantly between offspring of a parent with schizophrenia and offspring of control parents. Our results suggest that elevated affective lability during childhood is a marker of familial risk for mood disorders.

Keywords

Severe mental illness Mood lability Cohort study High-risk offspring Developmental psychopathology Antecedent 

Notes

Acknowledgements

The work leading to this publication has been supported by funding from the Canada Research Chairs Program (Award Number 231397), the Canadian Institutes of Health Research (Grant reference numbers 124976, 142738 and 148394), the Brain & Behavior Research Foundation (NARSAD) Independent Investigator Grant 24684, Nova Scotia Health Research Foundation (Grants 275319, 1716 and 353892) and the Dalhousie Medical Research Foundation. Ms. Zwicker has been supported by the Lindsay Family Graduate Studentship. Mr. Drobinin was supported by the CIHR Doctoral Award (157975).

Compliance with ethical standards

Conflict of interest

The authors have no conflicts of interest to declare.

Supplementary material

787_2019_1355_MOESM1_ESM.docx (16 kb)
Supplementary material 1 (DOCX 15 kb)

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Copyright information

© Springer-Verlag GmbH Germany, part of Springer Nature 2019

Authors and Affiliations

  • Alyson Zwicker
    • 1
    • 2
  • Vladislav Drobinin
    • 1
    • 3
  • Lynn E. MacKenzie
    • 1
    • 4
  • Emily Howes Vallis
    • 1
    • 5
  • Victoria C. Patterson
    • 1
    • 4
  • Jill Cumby
    • 1
  • Lukas Propper
    • 5
    • 6
  • Sabina Abidi
    • 5
    • 6
  • Alexa Bagnell
    • 5
    • 6
  • Barbara Pavlova
    • 1
    • 5
  • Martin Alda
    • 1
    • 5
  • Rudolf Uher
    • 1
    • 2
    • 3
    • 4
    • 5
    • 6
    • 7
    Email author
  1. 1.Nova Scotia Health AuthorityHalifaxCanada
  2. 2.Department of PathologyDalhousie UniversityHalifaxCanada
  3. 3.Department of Medical NeuroscienceDalhousie UniversityHalifaxCanada
  4. 4.Department of Psychology and NeuroscienceDalhousie UniversityHalifaxCanada
  5. 5.Department of PsychiatryDalhousie UniversityHalifaxCanada
  6. 6.IWK Health CentreHalifaxCanada
  7. 7.Institute of Psychiatry, Psychology and NeuroscienceKing’s College LondonLondonUK

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