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Maternal prenatal anxiety and child brain-derived neurotrophic factor (BDNF) genotype: Effects on internalizing symptoms from 4 to 15 years of age

Published online by Cambridge University Press:  25 November 2014

Kieran J. O'Donnell*
Affiliation:
McGill University
Vivette Glover
Affiliation:
Imperial College London
Joanna D. Holbrook
Affiliation:
Singapore Institute for Clinical Sciences
Thomas G. O'Connor*
Affiliation:
University of Rochester Medical Center
*
Address correspondence and reprint requests to: Kieran O'Donnell, Douglas Mental Health University Institute, Room E-4122, 6875 La Salle Boulevard, Montreal, QC H4H 1R3, Canada; E-mail: kieran.odonnell@mail.mcgill.ca; or Thomas G. O'Connor, Department of Psychiatry, Wynne Center for Family Research, University of Rochester Medical Center, 300 Crittenden Boulevard, Rochester, NY 14642; E-mail: tom_oconnor@urmc.rochester.edu.
Address correspondence and reprint requests to: Kieran O'Donnell, Douglas Mental Health University Institute, Room E-4122, 6875 La Salle Boulevard, Montreal, QC H4H 1R3, Canada; E-mail: kieran.odonnell@mail.mcgill.ca; or Thomas G. O'Connor, Department of Psychiatry, Wynne Center for Family Research, University of Rochester Medical Center, 300 Crittenden Boulevard, Rochester, NY 14642; E-mail: tom_oconnor@urmc.rochester.edu.

Abstract

Multiple behavioral and health outcomes, including internalizing symptoms, may be predicted from prenatal maternal anxiety, depression, or stress. However, not all children are affected, and those that are can be affected in different ways. Here we test the hypothesis that the effects of prenatal anxiety are moderated by genetic variation in the child's brain-derived neurotrophic factor (BDNF) gene, using the Avon Longitudinal Study of Parents and Children population cohort. Internalizing symptoms were assessed from 4 to 13 years of age using the Strengths and Difficulties Questionnaire (n = 8,584); a clinical interview with the adolescents was conducted at age 15 years (n = 4,704). Obstetric and psychosocial risk and postnatal maternal symptoms were included as covariates. Results show that prenatal maternal anxiety predicted internalizing symptoms, including with the diagnostic assessment at 15 years. There was a main effect of two BDNF polymorphisms (rs6265 [val66met] and rs11030104) on internalizing symptoms up to age 13. There was also genetic moderation of the prenatal anxiety effect by different BDNF polymorphisms (rs11030121 and rs7124442), although significant effects were limited to preadolescence. The findings suggest a role for BDNF gene–environment interactions in individual vulnerability to the effects of prenatal anxiety on child internalizing symptoms.

Type
Regular Articles
Copyright
Copyright © Cambridge University Press 2014 

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