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Published on: March 8, 2018
Impaired set-shifting in drug-naïve patients with borderline personality disorder: an event-related potentials study
Chang Xi1, Zhaoxia Liu1, Mingtian Zhong2
1Medical Psychological Center, the Second Xiangya Hospital, Central South University, Changsha, China; Medical Psychological Institute, Central South University, Changsha, China.
Background:
Neurocognitive impairments might play a key role in the development of Borderline Personality Disorder (BPD), however, the pathophysiological mechanism underlying cognitive impairment of BPD is largely unknown. This study was aimed to examine the electrophysiological mechanism of deficits in set-shifting processing in patients with BPD.
Methods:
Twenty-seven drug-naïve patients with BPD and twenty-four healthy controls were recruited. Demographic variables and clinical characteristics of all subjects were collected. Behavioral data and event-related potentials (ERPs) were recorded when subjects were performing the task-switching paradigm, which was applied to investigate the set-shifting function. The P2, N2 and P3 components in the task-switching paradigm would be analyzed.
Results:
Patients with BPD had significantly higher level of impulsivity, depression and anxiety than healthy controls. When performing the switching task, the BPD group had lower P2 amplitude and higher N2 amplitude than the control group. In the BPD group, the P2 latency at Fz electrode in repeat task was correlated positively with the level of depression, and P2 latency at Pz electrode in repeat task and switch task both had significantly negative relationships with the the level of anxiety.
Limitations:
This cross-sectional designed study did not clarify the causal relationship of the electrophysiological characteristics and the development of BPD.
Conclusions:
Patients with BPD might have abnormal brain activities when overcoming the inhibition of current task and inhibiting the effects of prior task, and their top-down control function might be impaired. These findings provide some useful clues for the underlying pathophysiological mechanism of BPD.
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