Neurocognitive and functional heterogeneity in depressed youth

被引:16
作者
Baller, Erica B. [1 ]
Kaczkurkin, Antonia N. [1 ,2 ]
Sotiras, Aristeidis [3 ,4 ,5 ]
Adebimpe, Azeez [1 ]
Bassett, Danielle S. [1 ,6 ,7 ,8 ,9 ,10 ,11 ]
Calkins, Monica E. [1 ,12 ,13 ]
Chand, Ganesh B. [3 ,5 ]
Cui, Zaixu [1 ]
Gur, Raquel E. [1 ,3 ,9 ,12 ,13 ]
Gur, Ruben C. [1 ,3 ,12 ,13 ]
Linn, Kristin A. [14 ]
Moore, Tyler M. [1 ,12 ,13 ]
Roalf, David R. [1 ]
Varol, Erdem [3 ,5 ]
Wolf, Daniel H. [1 ,5 ,12 ,13 ]
Xia, Cedric H. [1 ]
Davatzikos, Christos [3 ,5 ]
Satterthwaite, Theodore D. [1 ,5 ,12 ,13 ]
机构
[1] Univ Penn, Perelman Sch Med, Dept Psychiat, Philadelphia, PA 19104 USA
[2] Vanderbilt Univ, Dept Psychol, Nashville, TN 37235 USA
[3] Univ Penn, Perelman Sch Med, Dept Radiol, Philadelphia, PA 19104 USA
[4] Washington Univ, Dept Radiol, St Louis, MO 63130 USA
[5] Univ Penn, Ctr Biomed Image Comp & Analyt, Philadelphia, PA 19104 USA
[6] Univ Penn, Dept Bioengn, Philadelphia, PA 19104 USA
[7] Univ Penn, Penn Ctr Neuroimaging & Therapeut, Philadelphia, PA 19104 USA
[8] Univ Penn, Dept Elect & Syst Engn, Philadelphia, PA 19104 USA
[9] Univ Penn, Dept Neurol, Philadelphia, PA 19104 USA
[10] Univ Penn, Dept Phys & Astron Epidemiol & Informat, Philadelphia, PA 19104 USA
[11] Santa Fe Inst, Santa Fe, NM 87501 USA
[12] Penn Med, Lifespan Brain Inst, Philadelphia, PA 19104 USA
[13] Childrens Hosp Philadelphia, Philadelphia, PA 19104 USA
[14] Univ Penn, Dept Biostat Epidemiol & Informat, Philadelphia, PA 19104 USA
关键词
STATE-TRAIT ANXIETY; WORKING-MEMORY; LIFETIME PREVALENCE; ANTERIOR CINGULATE; EXECUTIVE SYSTEM; ADOLESCENTS; DISORDERS; BRAIN; CHILDREN; VERSION;
D O I
10.1038/s41386-020-00871-w
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Depression is a common psychiatric illness that often begins in youth, and is sometimes associated with cognitive deficits. However, there is significant variability in cognitive dysfunction, likely reflecting biological heterogeneity. We sought to identify neurocognitive subtypes and their neurofunctional signatures in a large cross-sectional sample of depressed youth. Participants were drawn from the Philadelphia Neurodevelopmental Cohort, including 712 youth with a lifetime history of a major depressive episode and 712 typically developing (TD) youth matched on age and sex. A subset (MDDn = 368, TDn = 200) also completed neuroimaging. Cognition was assessed with the Penn Computerized Neurocognitive Battery. A recently developed semi-supervised machine learning algorithm was used to delineate neurocognitive subtypes. Subtypes were evaluated for differences in both clinical psychopathology and brain activation during ann-back working memory fMRI task. We identified three neurocognitive subtypes in the depressed group. Subtype 1 was high-performing (high accuracy, moderate speed), Subtype 2 was cognitively impaired (low accuracy, slow speed), and Subtype 3 was impulsive (low accuracy, fast speed). While subtypes did not differ in clinical psychopathology, they diverged in their activation profiles in regions critical for executive function, which mirrored differences in cognition. Taken together, these data suggest disparate mechanisms of cognitive vulnerability and resilience in depressed youth, which may inform the identification of biomarkers for prognosis and treatment response.
引用
收藏
页码:783 / 790
页数:8
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