Transdiagnostic, Connectome-Based Prediction of Memory Constructs Across Psychiatric Disorders

被引:41
作者
Barron, Daniel S. [1 ,2 ]
Gao, Siyuan [3 ]
Dadashkarimi, Javid [4 ]
Greene, Abigail S. [5 ]
Spann, Marisa N. [6 ]
Noble, Stephanie [7 ]
Lake, Evelyn M. R. [8 ]
Krystal, John H. [1 ]
Constable, R. Todd [7 ,8 ]
Scheinost, Dustin [3 ,7 ,9 ,10 ]
机构
[1] Yale Sch Med, Dept Psychiat, New Haven, CT 06510 USA
[2] Univ Washington, Dept Anesthesiol & Pain Med, Seattle, WA 98112 USA
[3] Yale Sch Engn & Appl Sci, Dept Biomed Engn, New Haven, CT 06520 USA
[4] Yale Univ, Dept Comp Sci, POB 2158, New Haven, CT 06520 USA
[5] Yale Univ, Interdept Neurosci Program, New Haven, CT 06520 USA
[6] Columbia Univ, Irving Med Ctr, New York, NY 10032 USA
[7] Yale Sch Med, Dept Radiol & Biomed Imaging, New Haven, CT 06520 USA
[8] Yale Sch Med, Dept Neurosurg, New Haven, CT 06520 USA
[9] Yale Univ, Dept Stat & Data Sci, New Haven, CT 06520 USA
[10] Yale Sch Med, Child Study Ctr, New Haven, CT 06520 USA
基金
美国国家卫生研究院;
关键词
(< 5): prediction; functional connectivity; machine learning; psychiatry; transdiagnostic; FUNCTIONAL CONNECTOME; CONNECTIVITY; IDENTIFICATION; DYSFUNCTION; STATE;
D O I
10.1093/cercor/bhaa371
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Memory deficits are observed in a range of psychiatric disorders, but it is unclear whether memory deficits arise from a shared brain correlate across disorders or from various dysfunctions unique to each disorder. Connectome-based predictive modeling is a computational method that captures individual differences in functional connectomes associated with behavioral phenotypes such as memory. We used publicly available task-based functional MRI data from patients with schizophrenia (n = 33), bipolar disorder (n = 34), attention deficit hyper-activity disorder (n = 32), and healthy controls (n = 73) to model the macroscale brain networks associated with working, short- and long-term memory. First, we use 10-fold and leave-group-out analyses to demonstrate that the same macroscale brain networks subserve memory across diagnostic groups and that individual differences in memory performance are related to individual differences within networks distributed throughout the brain, including the subcortex, default mode network, limbic network, and cerebellum. Next, we show that diagnostic groups are associated with significant differences in whole-brain functional connectivity that are distinct from the predictive models of memory. Finally, we show that models trained on the transdiagnostic sample generalize to novel, healthy participants (n= 515) from the Human Connectome Project. These results suggest that despite significant differences in whole-brain patterns of functional connectivity between diagnostic groups, the core macroscale brain networks that subserve memory are shared.
引用
收藏
页码:2523 / 2533
页数:11
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