Prenatal stress and genetic risk: How prenatal stress interacts with genetics to alter risk for psychiatric illness

被引:75
作者
Abbott, Parker W. [1 ]
Gumusoglu, Serena B. [1 ,2 ]
Bittle, Jada [1 ,2 ]
Beversdorf, David Q. [3 ,4 ,5 ]
Stevens, Hanna E. [1 ,2 ,6 ]
机构
[1] Univ Iowa, Carver Coll Med, Dept Psychiat, 1310 PBDB,169 Newton Rd, Iowa City, IA 52246 USA
[2] Univ Iowa, Interdisciplinary Grad Program Neurosci, 356 Med Res Ctr, Iowa City, IA 52242 USA
[3] Univ Missouri, Dept Radiol, Thompson Ctr Autism & Neurodev Disorders, Interdisciplinary Neurosci Program,Interdisciplin, Columbia, MO USA
[4] Univ Missouri, Dept Neurol, Thompson Ctr Autism & Neurodev Disorders, Interdisciplinary Neurosci Program,Interdisciplin, Columbia, MO USA
[5] Univ Missouri, Dept Psychol Sci, Thompson Ctr Autism & Neurodev Disorders, Interdisciplinary Neurosci Program,Interdisciplin, Columbia, MO USA
[6] Univ Iowa, Carver Coll Med, Iowa Neurosci Inst, 2312 PBDB,169 Newton Rd, Iowa City, IA 52246 USA
关键词
Prenatal stress; Gene-environment interaction; Animal models; Development; Psychiatric illness; SCHIZOPHRENIA-LIKE PHENOTYPE; GLUCOCORTICOID-RECEPTOR GENE; MENTAL-HEALTH OUTCOMES; EARLY-LIFE STRESS; BRAIN-DEVELOPMENT; MATERNAL STRESS; EPIGENETIC MODIFICATIONS; OFFSPRING DEPRESSION; LEARNING-DEFICITS; RESTRAINT STRESS;
D O I
10.1016/j.psyneuen.2018.01.019
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Risk for neuropsychiatric disorders is complex and includes an individual's internal genetic endowment and their environmental experiences and exposures. Embryonic development captures a particularly complex period, in which genetic and environmental factors can interact to contribute to risk. These environmental factors are incorporated differently into the embryonic brain than postnatal one. Here, we comprehensively review the human and animal model literature for studies that assess the interaction between genetic risks and one particular environmental exposure with strong and complex associations with neuropsychiatric outcomes prenatal maternal stress. Gene-environment interaction has been demonstrated for stress occurring during childhood, adolescence, and adulthood. Additional work demonstrates that prenatal stress risk may be similarly complex. Animal model studies have begun to address some underlying mechanisms, including particular maternal or fetal genetic susceptibilities that interact with stress exposure and those that do not. More specifically, the genetic underpinnings of serotonin and dopamine signaling and stress physiology mechanisms have been shown to be particularly relevant to social, attentional, and internalizing behavioral changes, while other genetic factors have not, including some growth factor and hormone-related genes. Interactions have reflected both the diathesis stress and differential susceptibility models. Maternal genetic factors have received less attention than those in offspring, but strongly modulate impacts of prenatal stress. Priorities for future research are investigating maternal response to distinct forms of stress and developing whole-genome methods to examine the contributions of genetic variants of both mothers and offspring, particularly including genes involved in neurodevelopment. This is a burgeoning field of research that will ultimately contribute not only to a broad understanding of psychiatric pathophysiology but also to efforts for personalized medicine.
引用
收藏
页码:9 / 21
页数:13
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