Preattentive dysfunction in patients with bipolar disorder as revealed by the pitch-mismatch negativity: a magnetoencephalography (MEG) study.

BIPOLAR DISORDERS(2014)

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摘要
Objectives Mismatch negativity (MMN) and its magnetic counterpart (MMNm) are thought to reflect an automatic process that detects a difference between an incoming stimulus and the sensory memory trace of preceding stimuli. In patients with schizophrenia, an attenuation of the MMN/MMNm amplitude has been repeatedly reported. Heschl's gyrus (HG) is one of the major generators of MMN and the functional alteration of HG has been reported in patients with bipolar disorder. The present study investigated the pitch-MMNm in patients with bipolar disorder using whole-head 306-ch magnetoencephalography (MEG). Methods Twenty-two patients and 22 healthy controls participated in this study. Subjects were presented with two types of auditory stimulus sequences. One consisted of 1,000Hz standards (probability=90%) and 1,200Hz deviants (probability=10%), and the other consisted of 1,000Hz standards (90%) and 1,200Hz deviants (10%). These two tasks were each performed twice. Event-related brain responses to standard tones were subtracted from responses to deviant tones. Results Patients with bipolar disorder showed a significant bilateral reduction in magnetic global field power (mGFP) amplitudes (p=0.02) and dipole moments of the MMNm (p=0.04) compared with healthy controls. Patients with admission experience showed significantly reduced mGFP amplitudes of MMNm compared with patients without admission experience (p=0.004). Additionally, patients with more severe manic symptoms had smaller mGFP amplitudes of MMNm (=-0.50, p=0.05). Conclusions The results of this study suggest that patients with bipolar disorder may exhibit preattentive auditory dysfunction indexed by reduced pitch-MMNm responses. Pitch-MMNm could be a potential trait marker reflecting the global severity of bipolar disorder.
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关键词
bipolar disorder,magnetoencephalography,mismatch negativity,preattentive dysfunction
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