TY - JOUR
T1 - Antenatal depression and antidepressants during pregnancy
T2 - Unraveling the complex interactions for the offspring
AU - Olivier, Jocelien D. A.
AU - Akerud, Helena
AU - Poromaa, Inger Sundstrom
N1 - Copyright © 2014 Elsevier B.V. All rights reserved.
PY - 2015/4/15
Y1 - 2015/4/15
N2 - During pregnancy the risk for a woman to develop a depressive episode is as high as 20%. Antenatal depression is not harmless for the developing child as several changes, including neurodevelopmental alterations, have been reported. Sometimes it is unavoidable to treat a pregnant mother with antidepressants, especially when she is suicidal. Currently, selective serotonin reuptake inhibitors (SSRls) are the pharmacological choice of antidepressant treatment. SSRIs do not cause gross teratogenic alterations and are generally considered safe for use in pregnancy. However, although SSRls may relieve the maternal symptoms, they definitively cross the placenta partially influencing the neurodevelopment of the fetus. In this review an overview is given of the effects on the offspring of maternal antenatal depression and the putative neurodevelopmental effects of SSRI treatment during pregnancy. Although we primarily focus on human data, some animal data are discussed to describe possible mechanisms on how SSRls are affecting underlying biological mechanisms associated with depression. In summary, maternal depression may have long-lasting effects on the offspring, whereas prenatal SSRI exposure also increases the risk for long-lasting effects. It remains to be determined whether the effects found after SSRI treatment in pregnant women are only due to the SSRI exposure or if the underlying depression is also contributing to these effects. The possibility of epigenetic alterations as one of the underlying mechanisms that is altered by SSRI exposure is discussed. However much more research in this area is needed to explain the exact role of epigenetic mechanisms in SSRI exposure during pregnancy. (C) 2014 Elsevier BA/. All rights reserved,
AB - During pregnancy the risk for a woman to develop a depressive episode is as high as 20%. Antenatal depression is not harmless for the developing child as several changes, including neurodevelopmental alterations, have been reported. Sometimes it is unavoidable to treat a pregnant mother with antidepressants, especially when she is suicidal. Currently, selective serotonin reuptake inhibitors (SSRls) are the pharmacological choice of antidepressant treatment. SSRIs do not cause gross teratogenic alterations and are generally considered safe for use in pregnancy. However, although SSRls may relieve the maternal symptoms, they definitively cross the placenta partially influencing the neurodevelopment of the fetus. In this review an overview is given of the effects on the offspring of maternal antenatal depression and the putative neurodevelopmental effects of SSRI treatment during pregnancy. Although we primarily focus on human data, some animal data are discussed to describe possible mechanisms on how SSRls are affecting underlying biological mechanisms associated with depression. In summary, maternal depression may have long-lasting effects on the offspring, whereas prenatal SSRI exposure also increases the risk for long-lasting effects. It remains to be determined whether the effects found after SSRI treatment in pregnant women are only due to the SSRI exposure or if the underlying depression is also contributing to these effects. The possibility of epigenetic alterations as one of the underlying mechanisms that is altered by SSRI exposure is discussed. However much more research in this area is needed to explain the exact role of epigenetic mechanisms in SSRI exposure during pregnancy. (C) 2014 Elsevier BA/. All rights reserved,
KW - Antenatal depressro
KW - Antidepressants
KW - SSRI
KW - Pregnancy
KW - Neurodevelopment
KW - Epigenetics
KW - SEROTONIN REUPTAKE INHIBITORS
KW - EXPOSED IN-UTERO
KW - 11-BETA-HYDROXYSTEROID DEHYDROGENASE TYPE-1
KW - CORTICOTROPIN-RELEASING HORMONE
KW - CORTICOSTEROID-BINDING GLOBULIN
KW - MATERNAL PSYCHOLOGICAL DISTRESS
KW - NATIONAL-COMORBIDITY-SURVEY
KW - AUTISM SPECTRUM DISORDERS
KW - PROMOTER GENOTYPE SLC6A4
KW - INFANT TEMPERAMENT
U2 - 10.1016/j.ejphar.2014.07.049
DO - 10.1016/j.ejphar.2014.07.049
M3 - Article
C2 - 25094036
VL - 753
SP - 257
EP - 262
JO - European Journal of Pharmacology
JF - European Journal of Pharmacology
SN - 0014-2999
ER -