Please use this identifier to cite or link to this item: https://hdl.handle.net/20.500.14279/22637
DC FieldValueLanguage
dc.contributor.authorPampaka, Despina-
dc.contributor.authorPapatheodorou, Stefania-
dc.contributor.authorAlSeaidan, Mohammad-
dc.contributor.authorAl Wotayan, Rihab-
dc.contributor.authorWright, Rosalind J.-
dc.contributor.authorBuring, Julie E-
dc.contributor.authorDockery, Douglas W.-
dc.contributor.authorChristophi, Costas A.-
dc.date.accessioned2021-06-03T08:38:33Z-
dc.date.available2021-06-03T08:38:33Z-
dc.date.issued2021-12-
dc.identifier.citationBMC Pregnancy and Childbirth, 2021, vol. 21, no. 1, articl. no. 313en_US
dc.identifier.issn14712393-
dc.identifier.urihttps://hdl.handle.net/20.500.14279/22637-
dc.description.abstractBackground: The association of antenatal depression with adverse pregnancy, birth, and postnatal outcomes has been an item of scientific interest over the last decades. However, the evidence that exists is controversial or limited. We previously found that one in five women in Kuwait experience antenatal depressive symptoms. Therefore, the aim of this study was to examine whether antenatal depressive symptoms are associated with preterm birth (PTB), small for gestational age (SGA), or large for gestational age (LGA) babies in this population. Methods: This was a secondary analysis based on data collected in the Transgenerational Assessment of Children’s Environmental Risk (TRACER) Study that was conducted in Kuwait. Logistic regression analysis was used to examine whether antenatal depressive symptoms assessed using the Edinburgh Depression Scale (EDS) were associated with preterm birth, small for gestational age, and large for gestational age babies. Results: A total of 1694 women had complete information about the outcomes of interest. Women with depressive symptoms in pregnancy had increased, albeit non-significant, odds of having PTB (OR = 1.41; 95%CI: 0.81, 2.45), SGA babies (OR = 1.26; 0.80, 1.98), or LGA babies (OR = 1.27; 0.90, 1.79). Antenatal depressive symptoms had similar increased odds for the three outcomes even after adjusting for several covariates though none of these reached statistical significance. Conclusions: In the present study, the depressive symptoms in pregnancy did not predict adverse birth outcomes, such as PTB, SGA, and LGA, which adds to the currently non-conclusive literature. However, further research is needed to examine these associations, as the available evidence is quite limited.en_US
dc.formatpdfen_US
dc.language.isoenen_US
dc.relation.ispartofBMC Pregnancy and Childbirthen_US
dc.rights© The Author(s). 2021 Open Accessen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectAntenatal depressive symptomsen_US
dc.subjectPreterm birthen_US
dc.subjectSmall for gestational ageen_US
dc.subjectLarge for gestational ageen_US
dc.subjectAdverse perinatal outcomesen_US
dc.subjectKuwaiten_US
dc.titleAntenatal depressive symptoms and adverse perinatal outcomesen_US
dc.typeArticleen_US
dc.collaborationCyprus University of Technologyen_US
dc.collaborationDasman Diabetes Instituteen_US
dc.collaborationKuwait Primary Health Careen_US
dc.collaborationIcahn School of Medicine at Mount Sinaien_US
dc.collaborationBrigham and Women’s Hospitalen_US
dc.collaborationHarvard Universityen_US
dc.subject.categoryHealth Sciencesen_US
dc.journalsOpen Accessen_US
dc.countryCyprusen_US
dc.countryUnited Statesen_US
dc.countryKuwaiten_US
dc.subject.fieldMedical and Health Sciencesen_US
dc.publicationPeer Revieweden_US
dc.identifier.doi10.1186/s12884-021-03783-9en_US
cut.common.academicyear2021-2022en_US
item.openairetypearticle-
item.cerifentitytypePublications-
item.languageiso639-1en-
item.fulltextWith Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_6501-
item.grantfulltextopen-
crisitem.author.deptCyprus International Institute for Environmental and Public Health-
crisitem.author.deptCyprus International Institute for Environmental and Public Health-
crisitem.author.deptDepartment of Rehabilitation Sciences-
crisitem.author.facultyFaculty of Health Sciences-
crisitem.author.facultyFaculty of Health Sciences-
crisitem.author.facultyFaculty of Health Sciences-
crisitem.author.orcid0000-0002-9451-9094-
crisitem.author.orcid0000-0003-0503-1538-
crisitem.author.parentorgFaculty of Health Sciences-
crisitem.author.parentorgFaculty of Health Sciences-
crisitem.author.parentorgFaculty of Health Sciences-
crisitem.journal.journalissn1471-2393-
crisitem.journal.publisherBioMed Central-
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