Borderline personality disorder: current drug treatments and future prospects

被引:8
作者
Olabi, Bayanne [1 ]
Hall, Jeremy [1 ]
机构
[1] Univ Edinburgh, Royal Edinburgh Hosp, Sch Mol & Clin Med, Div Psychiat, Edinburgh EH10 5HF, Midlothian, Scotland
关键词
antidepressants; antipsychotic medications; borderline personality disorder; mood stabilizers; epigenetics;
D O I
10.1177/2040622310368455
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Individuals with borderline personality disorder (BPD) suffer from marked affective disturbance, an unstable sense of self, difficulty in interpersonal relationships and heightened impulsivity, leading to high rates of self-harm and suicide. Patients are often refractory to treatment and are at high risk for acute or dangerous presentations, with a serious impact on mental health services. There has been much debate on the effectiveness of pharmacotherapy in treating different facets of the psychopathology of the disorder. Several guidelines recommend the use of antidepressant agents, mood stabilizers for affective dysregulation and impulsive-behavioural dyscontrol, and antipsychotics for cognitive-perceptual symptoms. However, concerns have recently been raised regarding the strength of evidence for these treatment recommendations in BPD. Here, we review the evidence for efficacy of the main psychotropic medications used in BPD, drawing, in particular, on evidence from randomized controlled trials and meta-analyses. Overall, meta-analysis provides little evidence to support the use of antidepressant medication in BPD outside episodes of major depression. However, there is evidence for the use of both mood stabilizers and antipsychotic medications for the treatment of specific aspects of the disorder. Most existing studies have been conducted on small numbers of patients, and there is a requirement for further large-scale trials to substantiate these findings. In addition, given the limitations of current pharmacological treatment of BPD, there is a pressing need to investigate potential new therapeutic targets, including neuropeptides, such as the opioids and vasopressin, and drugs targeted at ameliorating the biological effects of early life stress.
引用
收藏
页码:59 / 66
页数:8
相关论文
共 107 条
[1]   Evidenced-based pharmacologic treatment of borderline personality disorder: A shift from SSRIs to anticonvulsants and atypical antipsychotics? [J].
Abraham, P. Francis ;
Calabrese, Joseph R. .
JOURNAL OF AFFECTIVE DISORDERS, 2008, 111 (01) :21-30
[2]   Borderline Personality Disorder and Childhood Trauma: Evidence for a Causal Relationship [J].
Ball, Jeffrey S. ;
Links, Paul S. .
CURRENT PSYCHIATRY REPORTS, 2009, 11 (01) :63-68
[3]   Efficacy and tolerability of pharmacotherapies for borderline personality disorder [J].
Bellino, Silvio ;
Paradiso, Erika ;
Bogetto, Filippo .
CNS DRUGS, 2008, 22 (08) :671-692
[4]   Low-dose clozapine in acute and continuation treatment of severe borderline personality disorder [J].
Benedetti, F ;
Sforzini, L ;
Colombo, C ;
Maffei, C ;
Smeraldi, E .
JOURNAL OF CLINICAL PSYCHIATRY, 1998, 59 (03) :103-107
[5]   Profound impairment in social recognition and reduction in anxiety-like behavior in vasopressin V1a receptor knockout mice [J].
Bielsky, IF ;
Hu, SB ;
Szegda, KL ;
Westphal, H ;
Young, LJ .
NEUROPSYCHOPHARMACOLOGY, 2004, 29 (03) :483-493
[6]  
Binks CA, 2006, COCHRANE DB SYST REV, V25
[7]   Endogenous opiates and behavior: 2008 [J].
Bodnar, Richard J. .
PEPTIDES, 2009, 30 (12) :2432-2479
[8]  
Bogenschutz MP, 2004, J CLIN PSYCHIAT, V65, P104
[9]  
Bowden Charles L, 2007, Expert Rev Neurother, V7, P9, DOI 10.1586/14737175.7.1.9
[10]   Vasopressin: Behavioral roles of an "original" neuropeptide [J].
Caldwell, Heather K. ;
Lee, Heon-Jin ;
Macbeth, Abbe H. ;
Young, W. Scott, III .
PROGRESS IN NEUROBIOLOGY, 2008, 84 (01) :1-24