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The 5-HTTLPR Polymorphism modulates the association of serious life events (SLE) and impulsivity in patients with Borderline Personality Disorder
被引:52
|作者:
Wagner, Stefanie
[1
]
Baskaya, Oemuer
[1
]
Lieb, Klaus
[1
]
Dahmen, Norbert
[1
,2
]
Tadic, Andre
[1
]
机构:
[1] Univ Med Ctr Mainz, Dept Psychiat & Psychotherapy, D-55131 Mainz, Germany
[2] Bioglobe Mol Genet Lab, D-22529 Hamburg, Germany
关键词:
Borderline Personality Disorder;
Impulsivity;
Serious life events;
Serotonin transporter (5-HTTLPR);
SEROTONIN TRANSPORTER GENE;
POSTTRAUMATIC-STRESS-DISORDER;
PROMOTER POLYMORPHISM;
MAJOR DEPRESSION;
RISK-FACTORS;
ADOLESCENTS;
EXPERIENCE;
VALIDITY;
VERSION;
TRAUMA;
D O I:
10.1016/j.jpsychires.2009.03.004
中图分类号:
R749 [精神病学];
学科分类号:
100205 ;
摘要:
Background: Impulsivity belongs to the key features of Borderline Personality Disorder (BPD). It has been linked to altered serotoninergic neurotransmission and, genetically, to an over-representation of the short (S) allele of the serotonin transporter promoter-linked polymorphic region polymorphism (5-HTTLPR). On the other hand, serious life events (SLE) are of major importance in the development of BPD. However, the inter-relations between SLEs, impulsivity, and 5-HTTLPR are not understood. Method: 159 BPD patients from Germany were included in this study. Impulsivity was assessed by the Barratt Impulsiveness Scale (BIS). We analysed (1) the effects of SLEs on impulsivity; and (2) modulating effects of the 5-HTTLPR polymorphism on the effects of SLEs on impulsivity. Results: Regression analyses confirmed a decreasing effect of childhood sexual abuse, the cumulative SLE-related reactions and the impairment by SLEs on BIS sum score. Regarding BIS sum score, all SLEs except for rape were associated with a decrease of impulsivity in SS/SL carriers and an increase of BIS sum score in LL carriers. Conclusions: This study analyzing a specific gene x environment interaction in BPD patients suggests an interaction between SLEs and the 5-HTTLPR S/L polymorphism in the development of impulsivity in BPD patients. Clinical and research implications are discussed. (C) 2009 Elsevier Ltd. All rights reserved
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页码:1067 / 1072
页数:6
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