Growing Together and Growing Apart: Regional and Sex Differences in the Lifespan Developmental Trajectories of Functional Homotopy

被引:613
作者
Zuo, Xi-Nian [1 ,2 ]
Kelly, Clare [1 ]
Di Martino, Adriana [1 ,3 ]
Mennes, Maarten [1 ]
Margulies, Daniel S. [4 ]
Bangaru, Saroja [1 ]
Grzadzinski, Rebecca [1 ]
Evans, Alan C. [5 ]
Zang, Yu-Feng [2 ]
Castellanos, F. Xavier [1 ,6 ]
Milham, Michael P. [1 ,6 ]
机构
[1] NYU, Langone Med Ctr, Phyllis Green & Randolph Cowen Inst Pediat Neuros, New York, NY 10016 USA
[2] Beijing Normal Univ, State Key Lab Cognit Sci & Learning, Beijing 100875, Peoples R China
[3] Univ Cagliari, Dept Neurosci, Div Child & Adolescent Neuropsychiat, I-09126 Cagliari, Italy
[4] Max Planck Inst Human Cognit & Brain Sci, D-04103 Leipzig, Germany
[5] McGill Univ, Montreal Neurol Inst, McConnell Brain Imaging Ctr, Montreal, PQ H3A 2B4, Canada
[6] Nathan S Kline Inst Psychiat Res, Orangeburg, NY 10962 USA
关键词
ANTERIOR CINGULATE CORTEX; RESTING-STATE NETWORKS; HUMAN BRAIN; CORPUS-CALLOSUM; HEMISPHERIC-ASYMMETRY; DISCOVERY SCIENCE; NEURAL SYNCHRONY; WORKING-MEMORY; EEG COHERENCE; MOTOR CORTEX;
D O I
10.1523/JNEUROSCI.2612-10.2010
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Functional homotopy, the high degree of synchrony in spontaneous activity between geometrically corresponding interhemispheric (i.e., homotopic) regions, is a fundamental characteristic of the intrinsic functional architecture of the brain. However, despite its prominence, the lifespan development of the homotopic resting-state functional connectivity (RSFC) of the human brain is rarely directly examined in functional magnetic resonance imaging studies. Here, we systematically investigated age-related changes in homotopic RSFC in 214 healthy individuals ranging in age from 7 to 85 years. We observed marked age-related changes in homotopic RSFC with regionally specific developmental trajectories of varying levels of complexity. Sensorimotor regions tended to show increasing homotopic RSFC, whereas higher-order processing regions showed decreasing connectivity (i.e., increasing segregation) with age. More complex maturational curves were also detected, with regions such as the insula and lingual gyrus exhibiting quadratic trajectories and the superior frontal gyrus and putamen exhibiting cubic trajectories. Sex-related differences in the developmental trajectory of functional homotopy were detected within dorsolateral prefrontal cortex (Brodmann areas 9 and 46) and amygdala. Evidence of robust developmental effects in homotopic RSFC across the lifespan should serve to motivate studies of the physiological mechanisms underlying functional homotopy in neurodegenerative and psychiatric disorders.
引用
收藏
页码:15034 / 15043
页数:10
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