Assessment of Placental Cortisol Pathway Gene Expression in Term Pregnant Women with Anxiety.


Journal

Neuropsychobiology
ISSN: 1423-0224
Titre abrégé: Neuropsychobiology
Pays: Switzerland
ID NLM: 7512895

Informations de publication

Date de publication:
2019
Historique:
received: 31 01 2018
accepted: 27 05 2018
pubmed: 16 8 2018
medline: 12 12 2018
entrez: 16 8 2018
Statut: ppublish

Résumé

The aim of this study was to expand on this field of work by examining, within a cohort of pregnant women with diagnosed clinical anxiety, the mRNA expression of a panel of genes associated with the cortisol pathway and comparing them to controls. Placental samples were obtained from 24 pregnant women, 12 with a diagnosed anxiety disorder and 12 with no psychiatric history, within 30 min of delivery. Differential expression analysis of 85 genes known to be involved in glucocorticoid synthesis, metabolism or signalling was conducted for the: (1) full sample, (2) those at term without labour (5 cases, 7 controls) and (3) those at term with labour (7 cases, 5 controls). Correlation analyses between gene expression and measures of anxiety and depressive symptom severity were also conducted. No robust difference in placental gene expression between pregnant women with and without anxiety disorder was found nor did we detect robust differences by labour status. However, correlational analyses putatively showed a decrease in PER1 expression was associated with an increase in anxiety symptom severity, explaining up to 32% of the variance in anxiety symptom severity. Overall, the strongest correlation was found between a decrease in placental PER1 expression and increased anxiety scores. Labour status was found to have a profound effect on mRNA expression. The placental samples obtained from women following labour produced greater numbers of significant differences in mRNA species expression suggesting that in long-standing anxiety the placenta may respond differently under conditions of chronic stress.

Identifiants

pubmed: 30110692
pii: 000490428
doi: 10.1159/000490428
doi:

Substances chimiques

PER1 protein, human 0
Period Circadian Proteins 0
Hydrocortisone WI4X0X7BPJ

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1-7

Informations de copyright

© 2018 S. Karger AG, Basel.

Auteurs

Penelope M Sheehan (PM)

Pregnancy Research Centre, Royal Women's Hospital, Parkville, Victoria, Australia.

Chad Bousman (C)

Department of Psychiatry, Royal Melbourne Hospital, University of Melbourne, Parkville, Victoria, Australia.

Angela Komiti (A)

Department of Psychiatry, Royal Melbourne Hospital, University of Melbourne, Parkville, Victoria, Australiaangelaak@unimelb.edu.au.

Fiona Judd (F)

Department of Psychiatry, Royal Melbourne Hospital, University of Melbourne, Parkville, Victoria, Australia.
Centre for Women's Mental Health, Royal Women's Hospital, Parkville, Victoria, Australia.

Louise Newman (L)

Department of Psychiatry, Royal Melbourne Hospital, University of Melbourne, Parkville, Victoria, Australia.
Centre for Women's Mental Health, Royal Women's Hospital, Parkville, Victoria, Australia.

Bruce Tonge (B)

Centre for Developmental Psychiatry and Psychology, Monash Medical Centre, Monash University, Clayton, Victoria, Australia.

David Castle (D)

Department of Psychiatry, Royal Melbourne Hospital, University of Melbourne, Parkville, Victoria, Australia.
Department of Psychiatry, St. Vincent's Hospital, Fitzroy, Victoria, Australia.

Ian Everall (I)

Department of Psychiatry, Royal Melbourne Hospital, University of Melbourne, Parkville, Victoria, Australia.

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Classifications MeSH