Antenatal maternal anxiety is related to HPA-axis dysregulation and self-reported depressive symptoms in adolescence: A prospective study on the fetal origins of depressed mood

被引:318
作者
van den Bergh, Bea R. H. [1 ]
van Calster, Ben [2 ]
Smits, Tim [3 ]
van Huffel, Sabine
Lagae, Lieven [4 ]
机构
[1] Katholieke Univ Leuven, Dept Psychol, B-3000 Louvain, Belgium
[2] Katholieke Univ Leuven, Dept Elect Engn, ESAT SISTA, B-3000 Louvain, Belgium
[3] Katholieke Univ Leuven, Ctr Eth, B-3000 Louvain, Belgium
[4] Katholieke Univ Leuven, Dept Paediat Neurol, B-3000 Louvain, Belgium
关键词
fetal programming; HPA-axis; cortisol; depressive disorder; adolescence; antenatal maternal anxiety;
D O I
10.1038/sj.npp.1301450
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Depressive symptomatology can proceed from altered hypothalamic-pituitary-adrenocortex (HPA)-axis function. Some authors stress the role that early life stress (ELS) may play in the pathophysiology of depressive symptoms. However, the involvement of the HPA-axis in linking prenatal ELS with depressive symptoms has not been tested in a prospective-longitudinal study extending until after puberty in humans. Therefore, we examined whether antenatal maternal anxiety is associated with disturbances in HPA-axis regulation and whether the HPA-axis dysregulation mediates the association between antenatal maternal anxiety and depressive symptoms in post-pubertal adolescents. As part of a prospective-longitudinal study, we investigated maternal anxiety at 12-22, 23-32, and 32-40 weeks of pregnancy (wp) with the State Trait Anxiety Inventory (STAI). In the 14-15- year-old offspring (n = 58) HPA-axis function was measured through establishing a saliva cortisol day-time profile. Depressive symptoms were measured with the Children's Depression symptoms Inventory (CDI). Results of regression analyses showed that antenatal exposure to maternal anxiety at 12-22 wp was in both sexes associated with a high, flattened cortisol day-time profile (P = 0.0463) which, in female adolescents only, was associated with depressive symptoms (P = 0.0077). All effects remained after controlling for maternal smoking, birth weight, obstetrical optimality, maternal postnatal anxiety and puberty phase. Our prospective study demonstrates, for the first time, the involvement of the HPA-axis in the link between antenatal maternal anxiety/prenatal ELS and depressive symptoms for post-pubertal female adolescents.
引用
收藏
页码:536 / 545
页数:10
相关论文
共 84 条
[1]   Puberty and depression: the roles of age, pubertal status and pubertal timing [J].
Angold, A ;
Costello, EJ ;
Worthman, CM .
PSYCHOLOGICAL MEDICINE, 1998, 28 (01) :51-61
[2]   THE MODERATOR MEDIATOR VARIABLE DISTINCTION IN SOCIAL PSYCHOLOGICAL-RESEARCH - CONCEPTUAL, STRATEGIC, AND STATISTICAL CONSIDERATIONS [J].
BARON, RM ;
KENNY, DA .
JOURNAL OF PERSONALITY AND SOCIAL PSYCHOLOGY, 1986, 51 (06) :1173-1182
[3]   Prevention of childhood depression: Recent findings and future prospects [J].
Beardslee, WR ;
Gladstone, TRG .
BIOLOGICAL PSYCHIATRY, 2001, 49 (12) :1101-1110
[4]   A healthy body in a healthy mind -: and vice versa -: The damaging power of "uncontrollable" stress [J].
Chrousos, GP ;
Gold, PW .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1998, 83 (06) :1842-1845
[5]   Editorial: Glucocorticoid action networks - An introduction to systems biology [J].
Chrousos, GP ;
Charmandari, E ;
Kino, T .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2004, 89 (02) :563-564
[6]   Stressors, stress, and neuroendocrine integration of the adaptive response - The 1997 Hans Selye Memorial Lecture [J].
Chrousos, GP .
STRESS OF LIFE: FROM MOLECULES TO MAN, 1998, 851 :311-335
[7]  
Claes SJ, 2005, THEORY AND TREATMENT OF DEPRESSION: TOWARD A DYNAMIC INTERACTIONISM MODEL, P227
[8]   CRH, stress, and major depression: A psychobiological interplay [J].
Claes, SJ .
VITAMINS AND HORMONES - ADVANCES IN RESEARCH AND APPLICATIONS, VOL 69, 2004, 69 :117-150
[9]   Prenatal stress diminishes neurogenesis in the dentate gyrus of juvenile rhesus monkeys [J].
Coe, CL ;
Kramer, M ;
Czéh, B ;
Gould, E ;
Reeves, AJ ;
Kirschbaum, C ;
Fuchs, E .
BIOLOGICAL PSYCHIATRY, 2003, 54 (10) :1025-1034
[10]  
Cohen J., 2013, APPL MULTIPLE REGRES, DOI [DOI 10.1002/0471264385.WEI0219, 10.4324/ 9780203774441, DOI 10.4324/9780203774441, 10.1002/0471264385.wei0219]