Genetic risk, number of previous depressive episodes, and stressful life events in predicting onset of major depression

被引:150
作者
Kendler, KS
Thornton, LM
Gardner, CO
机构
[1] Virginia Inst Psychiat & Behav Genet, Richmond, VA 23298 USA
[2] Virginia Commonwealth Univ, Med Coll Virginia, Dept Psychiat, Richmond, VA 23298 USA
[3] Virginia Commonwealth Univ, Med Coll Virginia, Dept Human Genet, Richmond, VA 23298 USA
关键词
D O I
10.1176/appi.ajp.158.4.582
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
Objective: The association between stressful life events and the onset of major depression decreases as the number of previous depressive episodes increases. How do genetic risk factors for major depression impact on this "kindling" phenomenon? In particular, do those at high genetic risk exhibit an increase in the speed of kindling, or are they "prekindled"? Method: Using discrete-time survival analysis, the authors examined the interaction between genetic risk, number of previous depressive episodes, and life event exposure in the prediction of episodes of major depression in female-female twin pairs from a population-based registry. The twins were interviewed four times over a 9-year period, producing 92,521 person-months of exposure. Results: The decline in the association between stressful life events and risk for major depression as the number of previous depressive episodes increased was strongest in those at low genetic risk and was weak to absent in those at high genetic risk. in the absence of previous depressive episodes, those at high genetic risk frequently experienced depressive episodes without major environmental stressors. Conclusions: Genetic risk factors for depression produce a "prekindling" effect rather than increase the speed of kindling. The "kindled" state, wherein depressive episodes occur with little provocation, may be reached by two pathways: many previous depressive episodes, perhaps driven by multiple adversities, and high genetic risk.
引用
收藏
页码:582 / 586
页数:5
相关论文
共 20 条
[1]  
Allison P.D., 1982, SOCIOL METHODOL, V13, P61, DOI [DOI 10.2307/270718, 10.2307/270718]
[2]  
Allison PD, 1995, Survival analysis using sas: A practical guide, V2nd
[3]  
BROWN GW, 1994, ARCH GEN PSYCHIAT, V51, P525
[4]  
BRUCE ML, 1997, DIVORCE PSYCHOPATHOL, P219
[5]   PSYCHOPATHOLOGY, TEMPERAMENT, AND PAST COURSE IN PRIMARY MAJOR DEPRESSIONS .2. TOWARD A REDEFINITION OF BIPOLARITY WITH A NEW SEMISTRUCTURED INTERVIEW FOR DEPRESSION [J].
CASSANO, GB ;
AKISKAL, HS ;
MUSETTI, L ;
PERUGI, G ;
SORIANI, A ;
MIGNANI, V .
PSYCHOPATHOLOGY, 1989, 22 (05) :278-288
[6]   LIFE EVENTS, DEPRESSION AND HYPOTHALAMIC PITUITARY-ADRENAL AXIS FUNCTION [J].
DOLAN, RJ ;
CALLOWAY, SP ;
FONAGY, P ;
DESOUZA, FVA ;
WAKELING, A .
BRITISH JOURNAL OF PSYCHIATRY, 1985, 147 (OCT) :429-433
[7]   PSYCHOSOCIAL FACTORS AND EPISODE NUMBER IN DEPRESSION [J].
EZQUIAGA, E ;
GUTIERREZ, JLA ;
LOPEZ, AG .
JOURNAL OF AFFECTIVE DISORDERS, 1987, 12 (02) :135-138
[8]   LIFE EVENTS AND THE RECURRENCE OF DEPRESSION [J].
GHAZIUDDIN, M ;
GHAZIUDDIN, N ;
STEIN, GS .
CANADIAN JOURNAL OF PSYCHIATRY-REVUE CANADIENNE DE PSYCHIATRIE, 1990, 35 (03) :239-242
[9]  
KENDLER KS, 1992, ARCH GEN PSYCHIAT, V49, P257
[10]   A population-based twin study of lifetime major depression in men and women [J].
Kendler, KS ;
Prescott, CA .
ARCHIVES OF GENERAL PSYCHIATRY, 1999, 56 (01) :39-44