Inter-individual heterogeneity of functional brain networks in children with autism spectrum disorder.
Inter-individual heterogeneity of functional brain networks in children with autism spectrum disorder.
复制标题
自闭症谱系障碍儿童大脑功能网络的个体间异质性
DOI:
10.1186/s13229-022-00535-0
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发表时间:
2022-12-26
期刊:
影响因子:
6.2
通讯作者:
中科院分区:
文献类型:
--
作者:
Autism spectrum disorder (ASD) is a neurodevelopmental disorder with considerable clinical heterogeneity. This study aimed to explore the heterogeneity of ASD based on inter-individual heterogeneity of functional brain networks. Resting-state functional magnetic resonance imaging data from the Autism Brain Imaging Data Exchange database were used in this study for 105 children with ASD and 102 demographically matched typical controls (TC) children. Functional connectivity (FC) networks were first obtained for ASD and TC groups, and inter-individual deviation of functional connectivity (IDFC) from the TC group was then calculated for each individual with ASD. A k-means clustering algorithm was used to obtain ASD subtypes based on IDFC patterns. The FC patterns were further compared between ASD subtypes and the TC group from the brain region, network, and whole-brain levels. The relationship between IDFC and the severity of clinical symptoms of ASD for ASD subtypes was also analyzed using a support vector regression model. Two ASD subtypes were identified based on the IDFC patterns. Compared with the TC group, the ASD subtype 1 group exhibited a hypoconnectivity pattern and the ASD subtype 2 group exhibited a hyperconnectivity pattern. IDFC for ASD subtype 1 and subtype 2 was found to predict the severity of social communication impairments and the severity of restricted and repetitive behaviors in ASD, respectively. Only male children were selected for this study, which limits the ability to study the effects of gender and development on ASD heterogeneity. These results suggest the existence of subtypes with different FC patterns in ASD and provide insight into the complex pathophysiological mechanism of clinical manifestations of ASD. The online version contains supplementary material available at 10.1186/s13229-022-00535-0.
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DOI:
10.1073/pnas.0504136102
发表时间:
2005-07-05
影响因子:
11.1
作者:
Fox, MD;Snyder, AZ;Raichle, ME
通讯作者:
Raichle, ME
影响因子:
4.8
作者:
Fan YS;Li L;Peng Y;Li H;Guo J;Li M;Yang S;Yao M;Zhao J;Liu H;Liao W;Guo X;Han S;Cui Q;Duan X;Xu Y;Zhang Y;Chen H
通讯作者:
Chen H
影响因子:
11
作者:
Di Martino, A.;Yan, C-G;Li, Q.;Denio, E.;Castellanos, F. X.;Alaerts, K.;Anderson, J. S.;Assaf, M.;Bookheimer, S. Y.;Dapretto, M.;Deen, B.;Delmonte, S.;Dinstein, I.;Ertl-Wagner, B.;Fair, D. A.;Gallagher, L.;Kennedy, D. P.;Keown, C. L.;Keysers, C.;Lainhart, J. E.;Lord, C.;Luna, B.;Menon, V.;Minshew, N. J.;Monk, C. S.;Mueller, S.;Mueller, R. A.;Nebel, M. B.;Nigg, J. T.;O'Hearn, K.;Pelphrey, K. A.;Peltier, S. J.;Rudie, J. D.;Sunaert, S.;Thioux, M.;Tyszka, J. M.;Uddin, L. Q.;Verhoeven, J. S.;Wenderoth, N.;Wiggins, J. L.;Mostofsky, S. H.;Milham, M. P.
通讯作者:
Milham, M. P.
影响因子:
14.5
作者:
Just, MA;Cherkassky, VL;Minshew, NJ
通讯作者:
Minshew, NJ
影响因子:
9.9
作者:
Aylward, EH;Minshew, NJ;Singh, N
通讯作者:
Singh, N