Björnsdotter Malin, Wang Nancy, Pelphrey Kevin, Kaiser Martha D
Center for Social and Affective Neuroscience, Department of Clinical and Experimental Medicine, Linköping University, Linköping, Sweden2Institute of Neuroscience and Physiology, University of Gothenburg, Gothenburg, Sweden.
Center for Translational Developmental Neuroscience, Child Study Center, Yale School of Medicine, New Haven, Connecticut.
JAMA Psychiatry. 2016 Jun 1;73(6):614-21. doi: 10.1001/jamapsychiatry.2016.0219.
Autism spectrum disorder (ASD) is marked by social disability and is associated with dysfunction in brain circuits supporting social cue perception. The degree to which neural functioning reflects individual-level behavioral phenotype is unclear, slowing the search for functional neuroimaging biomarkers of ASD.
To examine whether quantified neural function in social perception circuits may serve as an individual-level marker of ASD in children and adolescents.
DESIGN, SETTING, AND PARTICIPANTS: The cohort study was conducted at the Yale Child Study Center and involved children and adolescents diagnosed as having ASD and typically developing participants. Participants included a discovery cohort and a larger replication cohort. Individual-level social perception circuit functioning was assessed as functional magnetic resonance imaging brain responses to point-light displays of coherent vs scrambled human motion.
Outcome measures included performance of quantified brain responses in affected male and female participants in terms of area under the receiver operating characteristic curve (AUC), sensitivity and specificity, and correlations between brain responses and social behavior.
Of the 39 participants in the discovery cohort aged 4 to 17 years, 22 had ASD and 30 were boys. Of the 75 participants in the replication cohort aged 7 to 20 years, 37 had ASD and 52 were boys. A relative reduction in social perception circuit responses was identified in discovery cohort boys with ASD at an AUC of 0.75 (95% CI, 0.52-0.89; P = .01); however, typically developing girls and girls with ASD could not be distinguished (P = .54). The results were confirmed in the replication cohort, where brain responses were identified in boys with ASD at an AUC of 0.79 (95% CI, 0.64-0.91; P < .001) and failed to distinguish affected and unaffected girls (P = .82). Across both cohorts, boys were identified at an AUC of 0.77 (95% CI, 0.64-0.86) with corresponding sensitivity and specificity of 76% each. Additionally, brain responses were associated with social behavior in boys but not in girls.
Quantified social perception circuit activity is a promising individual-level candidate neural marker of the male ASD behavioral phenotype. Our findings highlight the need to better understand effects of sex on social perception processing in relation to ASD phenotype manifestations.
自闭症谱系障碍(ASD)以社交障碍为特征,与支持社交线索感知的脑回路功能障碍有关。神经功能反映个体水平行为表型的程度尚不清楚,这减缓了对ASD功能性神经影像生物标志物的寻找。
研究社交感知回路中量化的神经功能是否可作为儿童和青少年ASD的个体水平标志物。
设计、地点和参与者:这项队列研究在耶鲁儿童研究中心进行,纳入了被诊断为患有ASD的儿童和青少年以及发育正常的参与者。参与者包括一个发现队列和一个更大的重复队列。个体水平的社交感知回路功能通过功能性磁共振成像对连贯与混乱人体运动的点光显示的脑反应来评估。
结局指标包括受影响的男性和女性参与者中量化脑反应在接受者操作特征曲线下面积(AUC)、敏感性和特异性方面的表现,以及脑反应与社交行为之间的相关性。
在发现队列的39名4至17岁参与者中,22名患有ASD,30名是男孩。在重复队列的75名7至20岁参与者中,37名患有ASD,52名是男孩。在发现队列中,患有ASD的男孩社交感知回路反应相对降低,AUC为0.75(95%CI,0.52 - 0.89;P = 0.01);然而,无法区分发育正常的女孩和患有ASD的女孩(P = 0.54)。这些结果在重复队列中得到证实,在该队列中,患有ASD的男孩脑反应的AUC为0.79(95%CI,0.64 - 0.91;P < 0.001),且无法区分受影响和未受影响的女孩(P = 0.82)。在两个队列中,男孩的AUC为0.77(95%CI,0.64 - 0.86),相应的敏感性和特异性均为76%。此外,脑反应与男孩的社交行为相关,但与女孩无关。
量化的社交感知回路活动是男性ASD行为表型一个有前景的个体水平候选神经标志物。我们的研究结果强调需要更好地理解性别对与ASD表型表现相关的社交感知处理的影响。