Multifinality in the development of personality disorders: A Biology x Sex x Environment interaction model of antisocial and borderline traits

被引:183
作者
Beauchaine, Theodore P. [1 ]
Klein, Daniel N. [2 ]
Crowell, Sheila E. [1 ]
Derbidge, Christina [1 ]
Gatzke-Kopp, Lisa [3 ]
机构
[1] Univ Washington, Dept Psychol, Seattle, WA 98195 USA
[2] SUNY Stony Brook, Stony Brook, NY 11794 USA
[3] Penn State Univ, University Pk, PA 16802 USA
关键词
ATTENTION-DEFICIT/HYPERACTIVITY DISORDER; DEFICIT HYPERACTIVITY DISORDER; DISRUPTIVE BEHAVIOR DISORDERS; NATIONAL EPIDEMIOLOGIC SURVEY; CATECHOL-O-METHYLTRANSFERASE; EMPIRICALLY BASED CLASSIFICATION; MAJOR DEPRESSIVE DISORDER; BRAIN-STIMULATION REWARD; DOPAMINE-RECEPTOR GENE; AXIS-I DISORDERS;
D O I
10.1017/S0954579409000418
中图分类号
B844 [发展心理学(人类心理学)];
学科分类号
040202 ;
摘要
Although antisocial personality disorder (ASPD) is more common among males and borderline PD (BPD) is more common among females, some authors have suggested that the two disorders reflect multifinal outcomes of a single etiology. This assertion is based on several overlapping symptoms and features, including trait impulsivity, emotional lability, high rates of depression and suicide, and a high likelihood of childhood abuse and/or neglect. Furthermore, rates of ASPD are elevated in the first degree relatives of those with BPD, and concurrent comorbidity rates for the two disorders are high. In this article, we present a common model of antisocial and borderline personality development. We begin by reviewing issues and problems with diagnosing and studying PDs in children and adolescents. Next, we discuss dopaminergic and serotonergic mechanisms of trait impulsivity as predisposing vulnerabilities to ASPD and BPD. Finally, we extend shared risk models for ASPD and BPD by specifying genetic loci that may confer differential vulnerability to impulsive aggression and mood dysregulation among males and impulsive self-injury and mood dysregulation among females. Although the precise mechanisms of these sex-moderated genetic vulnerabilities remain poorly understood, they appear to inter-act with environmental risk factors including adverse rearing environments to potentiate the development of ASPD and BPD.
引用
收藏
页码:735 / 770
页数:36
相关论文
共 311 条
[21]   Population and familial association between the D4 dopamine receptor gene and measures of novelty seeking [J].
Benjamin, J ;
Li, L ;
Patterson, C ;
Greenberg, BD ;
Murphy, DL ;
Hamer, DH .
NATURE GENETICS, 1996, 12 (01) :81-84
[22]  
Berman A., 2006, ADOLESCENT SUICIDE, V2nd
[23]   D2 dopamine receptor gene polymorphism discriminates two kinds of novelty seeking [J].
Berman, S ;
Ozkaragoz, T ;
Young, RM ;
Noble, EP .
PERSONALITY AND INDIVIDUAL DIFFERENCES, 2002, 33 (06) :867-882
[24]  
BERNSTEIN DP, 1993, AM J PSYCHIAT, V150, P1237
[25]   Pleasures of the brain [J].
Berridge, KC .
BRAIN AND COGNITION, 2003, 52 (01) :106-128
[26]   Neurocognitive models of aggression, the antisocial personality disorders, and psychopathy [J].
Blair, RJR .
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 2001, 71 (06) :727-731
[27]   The roles of orbital frontal cortex in the modulation of antisocial behavior [J].
Blair, RJR .
BRAIN AND COGNITION, 2004, 55 (01) :198-208
[28]   Diagnostic efficiency and hierarchical functioning of the DSM-IV borderline personality disorder criteria [J].
Blais, MA ;
Hilsenroth, MJ ;
Fowler, JC .
JOURNAL OF NERVOUS AND MENTAL DISEASE, 1999, 187 (03) :167-173
[29]   THE EFFECTS OF CHANGING AXIS-II DIAGNOSTIC-CRITERIA [J].
BLASHFIELD, R ;
BLUM, N ;
PFOHL, B .
COMPREHENSIVE PSYCHIATRY, 1992, 33 (04) :245-252
[30]   LOW VERSUS HIGH PROLACTIN RESPONDERS TO FENFLURAMINE CHALLENGE - MARKER OF BEHAVIORAL-DIFFERENCES IN ADULT MALE CYNOMOLGUS MACAQUES [J].
BOTCHIN, MB ;
KAPLAN, JR ;
MANUCK, SB ;
MANN, JJ .
NEUROPSYCHOPHARMACOLOGY, 1993, 9 (02) :93-99