Migraine associated with early onset postpartum depression in women with major depressive disorder.


Journal

Archives of women's mental health
ISSN: 1435-1102
Titre abrégé: Arch Womens Ment Health
Pays: Austria
ID NLM: 9815663

Informations de publication

Date de publication:
12 2021
Historique:
received: 26 11 2020
accepted: 03 04 2021
pubmed: 22 4 2021
medline: 30 11 2021
entrez: 21 4 2021
Statut: ppublish

Résumé

Major depressive disorder (MDD) and migraine are both more common among women than men. Women's reproductive years are associated with increased susceptibility to recurrence of both conditions, suggesting a potential role of sex hormones in aetiology. We examined associations between comorbid migraine and clinical features of MDD in women, including relationships with lifetime reproductive events such as childbirth. Lifetime clinical characteristics and reproductive events in a well-characterised sample of 222 UK women with recurrent MDD, with (n = 98) and without (n = 124) migraine were compared. Women had all been recruited as part of a UK-based ongoing programme of research into the genetic and non-genetic determinants of mood disorders. Multivariate analysis showed a specific association between the lifetime presence of migraine and postpartum depression (PPD) within 6 weeks of delivery (OR = 2.555; 95% CI: 1.037-6.295, p = 0.041). This association did not extend to a broader definition of PPD with onset up to 6 months postpartum. All other factors included in the analysis were not significantly associated with the presence of migraine: family history of depression, younger age at depression onset, history of suicide attempt and severe premenstrual syndrome symptoms. The finding that women with MDD and comorbid migraine may be particularly sensitive to hormonal changes early in the postpartum period leads to aetiological hypotheses and suggests this group may be useful for future studies attempting to characterise PPD and MDD phenotypes. The refinement of such phenotypes has implications for individualising risk and treatment and for future biological and genetic studies.

Identifiants

pubmed: 33881600
doi: 10.1007/s00737-021-01131-6
pii: 10.1007/s00737-021-01131-6
pmc: PMC8585813
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

949-955

Subventions

Organisme : Wellcome Trust
Pays : United Kingdom
Organisme : Stanley Center for Psychiatric Research, Broad Institute
ID : 6045240-5500000100
Organisme : Wellcome Trust
ID : 078901
Pays : United Kingdom

Informations de copyright

© 2021. The Author(s).

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Auteurs

Katherine Gordon-Smith (K)

Psychological Medicine, University of Worcester, Henwick Grove, Worcester, WR2 6AJ, UK.

Paul Ridley (P)

GP Speciality School, Health Education North West, North West, UK.

Amy Perry (A)

Psychological Medicine, University of Worcester, Henwick Grove, Worcester, WR2 6AJ, UK.

Nicholas Craddock (N)

Division of Psychiatry and Clinical Neurosciences, School of Medicine, Cardiff University, Cardiff, UK.

Ian Jones (I)

Division of Psychiatry and Clinical Neurosciences, School of Medicine, Cardiff University, Cardiff, UK.

Lisa Jones (L)

Psychological Medicine, University of Worcester, Henwick Grove, Worcester, WR2 6AJ, UK. lisa.jones@worc.ac.uk.

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