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The Methylation of Clock Genes in Perinatal Depression

Which Role for Oxytocin

Bibliographic Data

ID15528508
AuthorsSimona Iodice (0000-0001-5594-8761, University of Milan), Martina Di Paolo (Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, corresponding author), Jennifer L Barkin (0000-0002-8364-4260, Mercer University), Letizia Tarantini (University of Milan), Silvia Grassi (0000-0002-2102-9713, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico), Marta Redaelli (Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico), Marta Serati (0000-0002-6502-7154, Aziende Socio Sanitaria Territoriale Rhodense), Virginia Favalli, Luisa Cirella (Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico), Valentina Bollati (0000-0002-0370-9598, University of Milan), Massimiliano Buoli (0000-0003-3359-3191, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico)
Year2021
Volume12
Pages734825-734825
Publication date2021-09-28
Open AccessYes
TypeARTICLE
VenueFrontiers in Psychiatry (JOURNAL)
Journal identifiersISSN: 1664-0640 • E-ISSN: 1664-0640
PublisherFrontiers Media (PUBLISHER • CH)
DOI10.3389/fpsyt.2021.734825
PMID34650456
OpenAlexW3203760160
LanguageEN
Citations received1
References cited33

Background: Perinatal Depression (PD) is a widespread disabling condition that is hypothesized to be associated with abnormalities in circadian rhythms and neuropeptide release including oxytocin (OXT). Methods: Fourty-four pregnant women (28 with PD, and 16 controls) were evaluated through the Edinburgh Postnatal Depression Scale (EPDS), the State/Trait Anxiety Inventory Form Y (STAI-Y), and the Prenatal Attachment Inventory (PAI). A blood sample was collected from all participants, and OXT plasma levels, DNA methylation of clock genes, as well as of FOXp3 and HERV-W were measured. Linear regression analyses were performed to assess the effect of oxytocin on the methylation of selected genes. Continuous ordinal regression models was further applied to see if the score of rating scales was associated to gene methylation, adjusting for oxytocin-methylation interaction. Results: OXT plasma levels were positively associated with CRY1 methylation. Women with higher OXT plasma levels showed an association between higher degree of CRY2 methylation (thus, reduced expression) and lower EPDS ( OR = 0.21; P = 0.043) and STAI-S scores ( OR = 6.96; P = 0.019). Finally, with high OXT levels, hypermethylation of CRY1 was associated to higher scores on the PAI ( OR = 2.74; P = 0.029) while higher methylation of HERV-W related to lower PAI scores ( OR = 0.273; P = 0.019). Conclusion: Our results suggest a possible protective role played by oxytocin in the development of PD by promoting a favorable methylation profile characterized by reduced expression of CRY1 and CRY2. Moreover, oxytocin strengthens the association between maternal prenatal attachment with a favorable pattern of methylation of clock genes and HERV-W, which is essential for pregnancy outcomes

Anxiety · Biology · Depression (economics · Depressive symptoms · DNA methylation · Edinburgh Postnatal Depression Scale · Gene · Gene expression · Methylation · Oxytocin · Oxytocin receptor · Psychiatry · Attachment and Relationship Dynamics · Maternal Mental Health During Pregnancy and Postpartum · Medicine · Neuroendocrine regulation and behavior · Psychology · Endocrinology · Genetics · Internal Medicine

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    Norma I Gavin, Bradley N Gaynes et al.•Obstetrics and Gynecology•2005

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Citations per year1
Citation span2026 - 2026 (1)
Highly citedNo

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