Gyrification abnormalities in presymptomatic c9orf72 expansion carriers

被引:24
|
作者
Caverzasi, Eduardo [1 ]
Battistella, Giovanni [1 ]
Chu, Stephanie A. [2 ]
Rosen, Howie [2 ]
Zanto, Theodore P. [1 ]
Karydas, Anna [1 ]
Shwe, Wendy [2 ]
Coppola, Giovanni [3 ]
Geschwind, Daniel H. [4 ]
Rademakers, Rosa [5 ]
Miller, Bruce L. [2 ,6 ]
Gorno-Tempini, Maria Luisa [2 ]
Lee, Suzee E. [1 ]
机构
[1] Univ Calif San Francisco, Neurol, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Neurol Memory & Aging Ctr, San Francisco, CA 94143 USA
[3] Univ Calif Los Angeles, Neurol, Los Angeles, CA USA
[4] Univ Calif Los Angeles, Semel Inst Neurosci & Human Behav, Psychiat & Neurol, Los Angeles, CA 90024 USA
[5] Mayo Clin, Coll Med, Neurosci, Jacksonville, FL 32224 USA
[6] Univ Calif San Francisco, San Francisco, CA 94143 USA
来源
基金
美国国家卫生研究院;
关键词
HEXANUCLEOTIDE REPEAT EXPANSION; SURFACE-BASED ANALYSIS; FRONTOTEMPORAL DEMENTIA; CORTICAL GYRIFICATION; CONNECTIVITY; ADOLESCENTS; DISORDER; CHILDREN; ATROPHY; AREA;
D O I
10.1136/jnnp-2018-320265
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective To investigate in-vivo cortical gyrification patterns measured by the local gyrification index (lGI) in presymptomatic c9orf72 expansion carriers compared with healthy controls, and investigate relationships between lGI and cortical thickness, an established morphometric measure of neurodegeneration. Methods We assessed cortical gyrification and thickness patterns in a cohort of 15 presymptomatic c9orf72 expansion carriers (age 43.7 +/- 10.2 years, 9 females) compared with 67 (age 42.4 +/- 12.4 years, 36 females) age and sex matched healthy controls using the dedicated Freesurfer pipeline. Results Compared with controls, presymptomatic carriers showed significantly lower lGI in left frontal and right parieto-occipital regions. Interestingly, those areas with abnormal gyrification in presymptomatic carriers showed no concomitant cortical thickness abnormality. Overall, for both presymptomatic carriers and healthy controls, gyrification and cortical thickness measures were not correlated, suggesting that gyrification captures a feature distinct from cortical thickness. Conclusions Presymptomatic c9orf72 expansion carriers show regions of abnormally low gyrification as early as their 30s, decades before expected symptom onset. Cortical gyrification represents a novel grey matter metric distinctive from grey matter thickness or volume and detects differences in presymptomatic carriers at an early age.
引用
收藏
页码:1005 / 1010
页数:6
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