首发精神分裂症患者的音高和持续时间错配负性与不同的听觉皮层和额叶下皮层体积相关。

Schizophrenia Bulletin Open Pub Date : 2021-02-23 eCollection Date: 2021-01-01 DOI:10.1093/schizbullopen/sgab005
Mark T Curtis, Brian A Coffman, Dean F Salisbury
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引用次数: 10

摘要

背景:首发精神分裂症(FESz)患者的音高和持续时间错配负性(pMMN/dMMN)与左海马回灰质体积有关。以前的方法无法描绘Heschl回内外的功能亚区。人类连接组计划多模态分割(HCP-MMP)图谱通过分割这些功能子区域克服了这一限制。此外,MMN在额叶下皮层产生,因此可能与额叶下皮层病理有关。利用新颖的HCP-MMP精确分割听觉和下额叶皮层,我们研究了FESz中灰质与pMMN和dMMN之间的关系。方法:测定27名FESz和27名健康对照者Fz处的pMMN和dMMN。进行t1加权MRI扫描。HCP-MMP图谱应用于个体,并计算双侧听觉和额叶下皮层包裹的灰质体积,并与MMN相关。多重比较采用FDR校正。结果:仅在FESz中,pMMN与听觉皮层左内侧带和下额叶皮层47L区呈负相关。MMN持续时间与以下听觉包块呈负相关:左侧内侧带、外侧带、旁带、TA2和右侧A5。此外,dMMN与下额叶皮层左侧47L区、右侧44区和右侧47L区相关。结论:新方法揭示了FESz的听觉和额叶下皮层pMMN和dMMN的重叠和不同的灰质关联。因此,pMMN和dMMN可以作为相似和略有不同的皮层区域潜在病理缺陷的生物标志物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Pitch and Duration Mismatch Negativity are Associated With Distinct Auditory Cortex and Inferior Frontal Cortex Volumes in the First-Episode Schizophrenia Spectrum.

Pitch and Duration Mismatch Negativity are Associated With Distinct Auditory Cortex and Inferior Frontal Cortex Volumes in the First-Episode Schizophrenia Spectrum.

Pitch and Duration Mismatch Negativity are Associated With Distinct Auditory Cortex and Inferior Frontal Cortex Volumes in the First-Episode Schizophrenia Spectrum.

Pitch and Duration Mismatch Negativity are Associated With Distinct Auditory Cortex and Inferior Frontal Cortex Volumes in the First-Episode Schizophrenia Spectrum.

Background: Pitch and duration mismatch negativity (pMMN/dMMN) are related to left Heschl's gyrus gray matter volumes in first-episode schizophrenia (FESz). Previous methods were unable to delineate functional subregions within and outside Heschl's gyrus. The Human Connectome Project multimodal parcellation (HCP-MMP) atlas overcomes this limitation by parcellating these functional subregions. Further, MMN has generators in inferior frontal cortex, and therefore, may be associated with inferior frontal cortex pathology. With the novel use of the HCP-MMP to precisely parcellate auditory and inferior frontal cortex, we investigated relationships between gray matter and pMMN and dMMN in FESz.

Methods: pMMN and dMMN were measured at Fz from 27 FESz and 27 matched healthy controls. T1-weighted MRI scans were acquired. The HCP-MMP atlas was applied to individuals, and gray matter volumes were calculated for bilateral auditory and inferior frontal cortex parcels and correlated with MMN. FDR correction was used for multiple comparisons.

Results: In FESz only, pMMN was negatively correlated with left medial belt in auditory cortex and area 47L in inferior frontal cortex. Duration MMN negatively correlated with the following auditory parcels: left medial belt, lateral belt, parabelt, TA2, and right A5. Further, dMMN was associated with left area 47L, right area 44, and right area 47L in inferior frontal cortex.

Conclusions: The novel approach revealed overlapping and distinct gray matter associations for pMMN and dMMN in auditory and inferior frontal cortex in FESz. Thus, pMMN and dMMN may serve as biomarkers of underlying pathological deficits in both similar and slightly different cortical areas.

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