Parsing brain structural heterogeneity in males with autism spectrum disorder reveals distinct clinical subtypes

被引:53
作者
Chen, Heng [1 ,2 ,3 ]
Uddin, Lucina Q. [4 ]
Guo, Xiaonan [1 ,2 ]
Wang, Jia [5 ]
Wang, Runshi [1 ,2 ]
Wang, Xiaomin [5 ]
Duan, Xujun [1 ,2 ]
Chen, Huafu [1 ,2 ]
机构
[1] Univ Elect Sci & Technol China, Chengdu Brain Sci Inst, MOE Key Lab Neuroinformat, Clin Hosp, Chengdu, Sichuan, Peoples R China
[2] Univ Elect Sci & Technol China, Ctr Informat Med, Sch Life Sci & Technol, Chengdu, Sichuan, Peoples R China
[3] Guizhou Univ, Sch Med, Guiyang, Guizhou, Peoples R China
[4] Univ Miami, Dept Psychol, POB 248185, Coral Gables, FL 33124 USA
[5] Harbin Med Univ, Publ Hlth Coll, Dept Childrens & Adolescent Hlth, Harbin, Heilongjiang, Peoples R China
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
autism spectrum disorder; data-driven; neuroanatomical heterogeneity; searchlight classification; PHENOTYPIC HETEROGENEITY; ORBITOFRONTAL CORTEX; PATTERNS; CHILDREN; AGE; ARCHITECTURE; SEVERITY; VOLUME;
D O I
10.1002/hbm.24400
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Autism spectrum disorder (ASD) is a neurodevelopmental disorder with considerable neuroanatomical heterogeneity. Thus, how and to what extent the brains of individuals with ASD differ from each other is still unclear. In this study, brain structural MRI data from 356 right-handed, male subjects with ASD and 403 right-handed male healthy controls were selected from the Autism Brain Image Data Exchange database (age range 5-35years old). Voxel-based morphometry preprocessing steps were conducted to compute the gray matter volume maps for each subject. Individual neuroanatomical difference patterns for each ASD individual were calculated. A data-driven clustering method was next utilized to stratify individuals with ASD into several subtypes. Whole-brain functional connectivity and clinical severity were compared among individuals within the ASD subtypes identified. A searchlight analysis was applied to determine whether subtyping ASD could improve the classification accuracy between ASD and healthy controls. Three ASD subtypes with distinct neuroanatomical difference patterns were revealed. Different degrees of clinical severity and atypical brain functional connectivity patterns were observed among these three subtypes. By dividing ASD into three subtypes, the classification accuracy between subjects of two out of the three subtypes and healthy controls was improved. The current study confirms that ASD is not a disorder with a uniform neuroanatomical signature. Understanding neuroanatomical heterogeneity in ASD could help to explain divergent patterns of clinical severity and outcomes.
引用
收藏
页码:628 / 637
页数:10
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