Serotonin transporter polymorphism predicts waking cortisol in young girls

被引:46
作者
Chen, Michael C. [1 ]
Joormann, Jutta [2 ]
Hallmayer, Joachim [3 ]
Gotlib, Ian H. [1 ]
机构
[1] Stanford Univ, Dept Psychol, Stanford, CA 94305 USA
[2] Univ Miami, Dept Psychol, Coral Gables, FL 33124 USA
[3] Stanford Univ, Sch Med, Stanford, CA 94305 USA
关键词
Serotonin transporter; 5-HTTLPR; Diurnal cortisol; HPA-axis; Depression; Stress; STRUCTURED CLINICAL INTERVIEW; SALIVARY CORTISOL; MAJOR DEPRESSION; STRESS; ASSOCIATION; COMORBIDITY; RELIABILITY; MECHANISM; CHILDREN; 5-HTTLPR;
D O I
10.1016/j.psyneuen.2008.11.006
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Major Depressive Disorder (MDD) is one of the most prevalent and costly of all psychiatric disorders. The hypothalamic pituitary adrenal (HPA)-axis, which regulates the hormonal response to stress, has been found to be disrupted in depression. HPA dysregulation may represent an important risk factor for depression. To examine a possible genetic underpinning of this risk factor without the confound of current or lifetime depression, we genotyped 84 never-disordered young girls, over a third of whom were at elevated risk for depression, to assess the association between a polymorphism in the promoter region of the serotonin transporter (5-HTT) gene and diurnal variation in HPA-axis activity. This 5-HTT-linked polymorphic region (5-HTTLPR) has been previously found to interact with stress to increase risk for depression. We found 5-HTTLPR to be significantly associated with diurnal cortisol levels: girls who were homozygous for the short-allele had higher levels of waking (but not afternoon or evening) cortisol than did their long-allele counterparts. This finding suggests that genetic susceptibility to HPA-axis dysregulation, especially apparent in levels of waking cortisol, is detectable in individuals as young as 9 years of age. (C) 2008 Elsevier Ltd. All rights reserved.
引用
收藏
页码:681 / 686
页数:6
相关论文
共 42 条
[1]   Heritability of daytime cortisol levels in children [J].
Bartels, M ;
de Geus, EJC ;
Kirschbaum, C ;
Sluyter, F ;
Boomsma, DI .
BEHAVIOR GENETICS, 2003, 33 (04) :421-433
[2]  
Beck A. T., 1996, MANUAL BECK DEPRESSI, P115, DOI DOI 10.1037/T00742-000
[3]   Increased salivary cortisol after waking in depression [J].
Bhagwagar, Z ;
Hafizi, S ;
Cowen, PJ .
PSYCHOPHARMACOLOGY, 2005, 182 (01) :54-57
[4]   Timing the end of nocturnal sleep [J].
Born, J ;
Hansen, K ;
Marshall, L ;
Mölle, M ;
Fehm, HL .
NATURE, 1999, 397 (6714) :29-30
[5]   Influence of life stress on depression: Moderation by a polymorphism in the 5-HTT gene [J].
Caspi, A ;
Sugden, K ;
Moffitt, TE ;
Taylor, A ;
Craig, IW ;
Harrington, H ;
McClay, J ;
Mill, J ;
Martin, J ;
Braithwaite, A ;
Poulton, R .
SCIENCE, 2003, 301 (5631) :386-389
[6]   24-HOUR CORTISOL MEASURES IN ADOLESCENTS WITH MAJOR DEPRESSION - A CONTROLLED-STUDY [J].
DAHL, RE ;
RYAN, ND ;
PUIGANTICH, J ;
NGUYEN, NA ;
ALSHABBOUT, M ;
MEYER, VA ;
PEREL, J .
BIOLOGICAL PSYCHIATRY, 1991, 30 (01) :25-36
[7]   Population-based study of first onset and chronicity in major depressive disorder [J].
Eaton, William W. ;
Shao, Huibo ;
Nestadt, Gerald ;
Lee, Ben Hochang ;
Bienvenu, O. Joseph ;
Zandi, Peter .
ARCHIVES OF GENERAL PSYCHIATRY, 2008, 65 (05) :513-520
[8]  
First M. B., 2015, User's Guide for the SCID-5-PD (Structured Clinical Interview for DSM-5 Personality Disorder)
[9]  
Gadow KD, 2002, DEV MED CHILD NEUROL, V44, P330
[10]   Hypercortisolemia and depression [J].
Gillespie, CF ;
Nemeroff, CB .
PSYCHOSOMATIC MEDICINE, 2005, 67 :S26-S28