ارتباطات عصبی پردازش احساسات در اختلال شخصیت مرزی
|کد مقاله||سال انتشار||مقاله انگلیسی||ترجمه فارسی||تعداد کلمات|
|33101||2009||8 صفحه PDF||سفارش دهید||محاسبه نشده|
Publisher : Elsevier - Science Direct (الزویر - ساینس دایرکت)
Journal : Psychiatry Research: Neuroimaging, Volume 172, Issue 3, 30 June 2009, Pages 192–199
Emotional instability is a hallmark feature of borderline personality disorder (BPD), yet its biological underpinnings are poorly understood. We employed functional magnetic resonance imaging (fMRI) to compare patterns of regional brain activation in BPD patients and healthy volunteers as they process positive and negative social emotional stimuli. fMRI images were acquired while 19 BPD patients and 17 healthy controls (HC) viewed emotion-inducing pictures from the International Affective Pictures System set. Activation data were analyzed with SPM5 ANCOVA models to derive the effects of diagnosis and stimulus type. BPD patients demonstrated greater differences in activation than controls, when viewing negative pictures compared with rest, in the amygdala, fusiform gyrus, primary visual areas, superior temporal gyrus (STG), and premotor areas, while healthy controls showed greater differences than BPD patients in the insula, middle temporal gyrus and dorsolateral prefrontal cortex (BA46). When viewing positive pictures compared with rest, BPD patients showed greater differences in the STG, premotor cortex, and ventrolateral prefrontal cortex. These findings suggest that BPD patients show greater amygdala activity and heightened activity of visual processing regions relative to findings for HC subjects in the processing of negative social emotional pictures compared with rest. The patients activate neural networks in emotion processing that are phylogeneticall older and more reflexive than those activated by HC subjects.
Emotional instability is one of the most striking features of borderline personality disorder (BPD) and is central to many of the behavioral and interpersonal symptoms of the disorder (Stone, 1988 and Linehan, 1993), including some of the most disabling, even life-threatening, symptoms of BPD, such as suicidality, outbursts of intense anger, stormy relationships, and identity disturbances (Koenigsberg et al., 2001). This emotional instability may be related to a heightened attention or sensitivity to social–emotional cues in interpersonal senarios (Wagner and Linehan, 1999, Meyer et al., 2004, Taylor and Fragopanagos, 2005 and Lynch et al., 2006), a tendency to self-referential emotional processing (Schnell et al., 2007), or to dysregulated emotional processing mechanisms (Phillips et al., 2003b). Understanding the nature of the disturbances in emotion processing in BPD may provide important insights into the mechanisms of affective instability, the underlying pathology of the disorder, understanding disorder, and the relationship between BPD and the Axis I mood disorders, as well as helping to identify endophenotypes that could focus genetic studies of BPD, and target biological or psychological treatments to more specifically address affective instability in BPD. Neuroimaging studies have begun to identify networks that are engaged in emotion processing in healthy individuals and in those with disturbed affect. A number of studies have employed images from the International Affective Pictures System (IAPS; Lang et al., 2001) as emotional stimuli. The IAPS is a set of positive, negative and neutral valence pictures for which normative data for picture valence and arousal level are available. In healthy individuals, viewing of emotional pictures is associated with activation in the visual cortex (Takahashi et al., 2004 and Britton et al., 2006), ventromedial prefrontal cortex and medial orbitofrontal cortex (Northoff et al., 2000, Takahashi et al., 2004, Britton et al., 2006 and Grimm et al., 2006), anterior cingulate (Takahashi et al., 2004 and Grimm et al., 2006), dorsolateral prefrontal cortex (Northoff et al., 2000 and Grimm et al., 2006), amygdala-hippocampal region (Takahashi et al., 2004 and Britton et al., 2006) and basal ganglia (Takahashi et al., 2004). Differences in activation patterns in these regions have been identified in schizophrenic subjects with and without affective flattening (Takahashi et al., 2004), phobics (Goossens et al., 2007), and individuals high in neuroticism (Britton et al., 2007). Little is known about the neurobiological underpinnings of the emotional instability in BPD, but the BPD syndrome itself has been associated with regional hypometabolism and deficits in serotonergic activity (De La Fuente et al., 1997, Siever et al., 1999, Soloff et al., 2000, Leyton et al., 2001, New et al., 2002 and Juengling et al., 2003). Structural magnetic resonance imaging (MRI) studies have found smaller amygdala, hippocampal (Driessen et al., 2000, Schmahl et al., 2003 and Tebartz van Elst et al., 2003), anterior cingulate (Tebartz van Elst et al., 2003 and Hazlett et al., 2005) and orbitofrontal cortex (Tebartz van Elst et al., 2003) volumes in BPD patients compared with controls. Two functional neuroimaging studies of borderline patients performing an emotion-relation task have been reported. In the first, BOLD functional MRI (fMRI) was performed in six BPD patients and controls as they viewed negative or neutral pictures (inanimate objects). Compared with healthy controls, the BPD patients showed an increased activation of the amygdala bilaterally and of the medial and inferolateral prefrontal cortex when viewing the negative versus the neutral images (Herpertz et al., 2001). The second study examined the processing of facial expressions of emotion (Donegan et al., 2003). The BPD patients showed increased left amygdala activation to fearful, sad, happy and neutral faces. The emotional instability in BPD is associated with emotional reactivity to social events (Stiglmayr et al., 2005), yet the neuroimaging studies of emotion processing in BPD have thus far been confined to studies of face perception (Donegan et al., 2003) and to scenes intermixing social and non-social stimuli (e.g. images of attacking animals, offensive insects and reptiles, and disfigured bodies), making it impossible to characterize the processing of social cues in particular. This is a serious limitation since social and non-social emotional stimuli are processed differently in the brain (Britton et al., 2006). The present study represents an important advance because of its focus on social emotional processing in particular.