Prenatal developmental origins of behavior and mental health: The influence of maternal stress in pregnancy
•Maternal psychological distress, life event stress, and objective exposure affect offspring outcome.•Functional and structural brain changes underlie the problems observed in the offspring.•Alterations in stress system, immune system, and gut microbiome play a significant role.•Epigenetic and telom...
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| Published in | Neuroscience and biobehavioral reviews Vol. 117; pp. 26 - 64 |
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| Main Authors | , , , , , , , , , , |
| Format | Journal Article |
| Language | English |
| Published |
United States
Elsevier Ltd
01.10.2020
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| Subjects | |
| Online Access | Get full text |
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| Abstract | •Maternal psychological distress, life event stress, and objective exposure affect offspring outcome.•Functional and structural brain changes underlie the problems observed in the offspring.•Alterations in stress system, immune system, and gut microbiome play a significant role.•Epigenetic and telomere biology mechanisms are beginning to be explored.•Interventions focused on offspring also need to be guided by knowledge of changes in biological systems.
Accumulating research shows that prenatal exposure to maternal stress increases the risk for behavioral and mental health problems later in life. This review systematically analyzes the available human studies to identify harmful stressors, vulnerable periods during pregnancy, specificities in the outcome and biological correlates of the relation between maternal stress and offspring outcome. Effects of maternal stress on offspring neurodevelopment, cognitive development, negative affectivity, difficult temperament and psychiatric disorders are shown in numerous epidemiological and case-control studies. Offspring of both sexes are susceptible to prenatal stress but effects differ. There is not any specific vulnerable period of gestation; prenatal stress effects vary for different gestational ages possibly depending on the developmental stage of specific brain areas and circuits, stress system and immune system. Biological correlates in the prenatally stressed offspring are: aberrations in neurodevelopment, neurocognitive function, cerebral processing, functional and structural brain connectivity involving amygdalae and (pre)frontal cortex, changes in hypothalamo-pituitary-adrenal (HPA)-axis and autonomous nervous system. |
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| AbstractList | Accumulating research shows that prenatal exposure to maternal stress increases the risk for behavioral and mental health problems later in life. This review systematically analyzes the available human studies to identify harmful stressors, vulnerable periods during pregnancy, specificities in the outcome and biological correlates of the relation between maternal stress and offspring outcome. Effects of maternal stress on offspring neurodevelopment, cognitive development, negative affectivity, difficult temperament and psychiatric disorders are shown in numerous epidemiological and case-control studies. Offspring of both sexes are susceptible to prenatal stress but effects differ. There is not any specific vulnerable period of gestation; prenatal stress effects vary for different gestational ages possibly depending on the developmental stage of specific brain areas and circuits, stress system and immune system. Biological correlates in the prenatally stressed offspring are: aberrations in neurodevelopment, neurocognitive function, cerebral processing, functional and structural brain connectivity involving amygdalae and (pre)frontal cortex, changes in hypothalamo-pituitary-adrenal (HPA)-axis and autonomous nervous system.Accumulating research shows that prenatal exposure to maternal stress increases the risk for behavioral and mental health problems later in life. This review systematically analyzes the available human studies to identify harmful stressors, vulnerable periods during pregnancy, specificities in the outcome and biological correlates of the relation between maternal stress and offspring outcome. Effects of maternal stress on offspring neurodevelopment, cognitive development, negative affectivity, difficult temperament and psychiatric disorders are shown in numerous epidemiological and case-control studies. Offspring of both sexes are susceptible to prenatal stress but effects differ. There is not any specific vulnerable period of gestation; prenatal stress effects vary for different gestational ages possibly depending on the developmental stage of specific brain areas and circuits, stress system and immune system. Biological correlates in the prenatally stressed offspring are: aberrations in neurodevelopment, neurocognitive function, cerebral processing, functional and structural brain connectivity involving amygdalae and (pre)frontal cortex, changes in hypothalamo-pituitary-adrenal (HPA)-axis and autonomous nervous system. Accumulating research shows that prenatal exposure to maternal stress increases the risk for behavioral and mental health problems later in life. This review systematically analyzes the available human studies to identify harmful stressors, vulnerable periods during pregnancy, specificities in the outcome and biological correlates of the relation between maternal stress and offspring outcome. Effects of maternal stress on offspring neurodevelopment, cognitive development, negative affectivity, difficult temperament and psychiatric disorders are shown in numerous epidemiological and case-control studies. Offspring of both sexes are susceptible to prenatal stress but effects differ. There is not any specific vulnerable period of gestation; prenatal stress effects vary for different gestational ages possibly depending on the developmental stage of specific brain areas and circuits, stress system and immune system. Biological correlates in the prenatally stressed offspring are: aberrations in neurodevelopment, neurocognitive function, cerebral processing, functional and structural brain connectivity involving amygdalae and (pre)frontal cortex, changes in hypothalamo-pituitary-adrenal (HPA)-axis and autonomous nervous system. •Maternal psychological distress, life event stress, and objective exposure affect offspring outcome.•Functional and structural brain changes underlie the problems observed in the offspring.•Alterations in stress system, immune system, and gut microbiome play a significant role.•Epigenetic and telomere biology mechanisms are beginning to be explored.•Interventions focused on offspring also need to be guided by knowledge of changes in biological systems. Accumulating research shows that prenatal exposure to maternal stress increases the risk for behavioral and mental health problems later in life. This review systematically analyzes the available human studies to identify harmful stressors, vulnerable periods during pregnancy, specificities in the outcome and biological correlates of the relation between maternal stress and offspring outcome. Effects of maternal stress on offspring neurodevelopment, cognitive development, negative affectivity, difficult temperament and psychiatric disorders are shown in numerous epidemiological and case-control studies. Offspring of both sexes are susceptible to prenatal stress but effects differ. There is not any specific vulnerable period of gestation; prenatal stress effects vary for different gestational ages possibly depending on the developmental stage of specific brain areas and circuits, stress system and immune system. Biological correlates in the prenatally stressed offspring are: aberrations in neurodevelopment, neurocognitive function, cerebral processing, functional and structural brain connectivity involving amygdalae and (pre)frontal cortex, changes in hypothalamo-pituitary-adrenal (HPA)-axis and autonomous nervous system. |
| Author | Van den Bergh, Bea R.H. Roseboom, Tessa de Rooij, Susanne R. Lahti, Marius Räikkönen, Katri Schwab, Matthias Hoyer, Dirk Entringer, Sonja King, Suzanne van den Heuvel, Marion I. Braeken, Marijke |
| Author_xml | – sequence: 1 givenname: Bea R.H. surname: Van den Bergh fullname: Van den Bergh, Bea R.H. email: bea.vandenbergh@kuleuven.be organization: Research Group on Health Psychology, Faculty of Psychology and Educational sciences, KU Leuven, Leuven, Belgium – sequence: 2 givenname: Marion I. surname: van den Heuvel fullname: van den Heuvel, Marion I. email: m.vdnheuvel@wayne.edu organization: Merrill Palmer Skillman Institute for Child and Family Development, Wayne State University, Detroit, MI, USA – sequence: 3 givenname: Marius surname: Lahti fullname: Lahti, Marius email: marius.lahti@helsinki.fi organization: Department of Psychology and Logopedics, Faculty of Medicine, University of Helsinki, Helsinki, Finland – sequence: 4 givenname: Marijke surname: Braeken fullname: Braeken, Marijke email: marijke.braeken@uhasselt.be organization: Rehabilitation Research Center, Biomedical Research Institute, Faculty of Medicine and Life Sciences, Hasselt University, Hasselt, Belgium – sequence: 5 givenname: Susanne R. surname: de Rooij fullname: de Rooij, Susanne R. email: s.r.derooij@amc.uva.nl organization: Department of Clinical Epidemiology, Biostatistics and Bioinformatics, Academic Medical Centre, University of Amsterdam, Amsterdam, The Netherlands – sequence: 6 givenname: Sonja surname: Entringer fullname: Entringer, Sonja email: sonja.entringer@charite.de organization: Institute of Medical Psychology, Charité University Medicine Berlin, Berlin, Germany – sequence: 7 givenname: Dirk surname: Hoyer fullname: Hoyer, Dirk email: dirk.hoyer@med.uni-jena.de organization: Biomagnetic Center, Hans Berger Department of Neurology, Jena University Hospital, Jena, Germany – sequence: 8 givenname: Tessa surname: Roseboom fullname: Roseboom, Tessa email: t.j.rooseboom@amc.uva.nl organization: Department of Clinical Epidemiology, Biostatistics and Bioinformatics, Academic Medical Centre, University of Amsterdam, Amsterdam, The Netherlands – sequence: 9 givenname: Katri surname: Räikkönen fullname: Räikkönen, Katri email: katri.raikkonen@helsinki.fi organization: Department of Psychology and Logopedics, Faculty of Medicine, University of Helsinki, Helsinki, Finland – sequence: 10 givenname: Suzanne surname: King fullname: King, Suzanne email: suzanne.king@mcgill.ca organization: Douglas Hospital Research Centre, and Dept. of Psychiatry, McGill University, Montreal, Quebec, Canada – sequence: 11 givenname: Matthias surname: Schwab fullname: Schwab, Matthias email: matthias.schwab@med.uni-jena.de organization: Hans Berger Department of Neurology, Jena University Hospital, Jena, Germany |
| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/28757456$$D View this record in MEDLINE/PubMed |
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| Snippet | •Maternal psychological distress, life event stress, and objective exposure affect offspring outcome.•Functional and structural brain changes underlie the... Accumulating research shows that prenatal exposure to maternal stress increases the risk for behavioral and mental health problems later in life. This review... |
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| SubjectTerms | Anxiety Attention deficit hyperactivity disorder (ADHD) Autism Autonomic nervous system Brain network connectivity Cortisol Depression Disaster exposure EEG Epigenetics Event related potential (ERP) Female Fetal programming Functional magnetic resonance imaging (fMRI) Gut microbiome Heart rate variability HPA-axis Humans Hypothalamo-Hypophyseal System Life events Male Maternal psychological distress Mental Health Objective stress Pituitary-Adrenal System Pregnancy Pregnancy-specific anxiety Prenatal Exposure Delayed Effects Psychiatric disorders Schizophrenia Stress, Psychological Telomere biology |
| Title | Prenatal developmental origins of behavior and mental health: The influence of maternal stress in pregnancy |
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