TY - JOUR
T1 - Variable global dysconnectivity and individual differences in schizophrenia
AU - Cole, Michael W.
AU - Anticevic, Alan
AU - Repovs, Grega
AU - Barch, Deanna
N1 - Funding Information:
This study was supported by the McDonnell Center for Systems Neuroscience. We would like to thank staff at the Conte Center for Neuroscience of Mental Disorders for their help in recruiting participants and collecting data as well as Todd Braver and Phil Corlett for insightful comments and suggestions.
PY - 2011/7/1
Y1 - 2011/7/1
N2 - Background: A fundamental challenge for understanding neuropsychiatric disease is identifying sources of individual differences in psychopathology, especially when there is substantial heterogeneity of symptom expression, such as is found in schizophrenia (SCZ). We hypothesized that such heterogeneity might arise in part from consistently widespread yet variably patterned alterations in the connectivity of focal brain regions. Methods: We used resting state functional connectivity magnetic resonance imaging to identify variable global dysconnectivity in 23 patients with DSM-IV SCZ relative to 22 age-, gender-, and parental socioeconomic status-matched control subjects with a novel global brain connectivity method that is robust to high variability across individuals. We examined cognitive functioning with a modified Sternberg task and subtests from the Wechsler Adult Intelligence ScaleThird Edition. We measured symptom severity with the Scale for Assessment of Positive and Negative Symptoms. Results: We identified a dorsolateral prefrontal cortex (PFC) region with global and highly variable dysconnectivity involving within-PFC underconnectivity and non-PFC overconnectivity in patients. Variability in this "under/over" pattern of dysconnectivity strongly predicted the severity of cognitive deficits (matrix reasoning IQ, verbal IQ, and working memory performance) as well as individual differences in every cardinal symptom domain of SCZ (poverty, reality distortion, and disorganization). Conclusions: These results suggest that global dysconnectivity underlies dorsolateral PFC involvement in the neuropathology of SCZ. Furthermore, these results demonstrate the possibility that specific patterns of dysconnectivity with a given network hub region might explain individual differences in symptom presentation in SCZ. Critically, such findings might extend to other neuropathologies with diverse presentation.
AB - Background: A fundamental challenge for understanding neuropsychiatric disease is identifying sources of individual differences in psychopathology, especially when there is substantial heterogeneity of symptom expression, such as is found in schizophrenia (SCZ). We hypothesized that such heterogeneity might arise in part from consistently widespread yet variably patterned alterations in the connectivity of focal brain regions. Methods: We used resting state functional connectivity magnetic resonance imaging to identify variable global dysconnectivity in 23 patients with DSM-IV SCZ relative to 22 age-, gender-, and parental socioeconomic status-matched control subjects with a novel global brain connectivity method that is robust to high variability across individuals. We examined cognitive functioning with a modified Sternberg task and subtests from the Wechsler Adult Intelligence ScaleThird Edition. We measured symptom severity with the Scale for Assessment of Positive and Negative Symptoms. Results: We identified a dorsolateral prefrontal cortex (PFC) region with global and highly variable dysconnectivity involving within-PFC underconnectivity and non-PFC overconnectivity in patients. Variability in this "under/over" pattern of dysconnectivity strongly predicted the severity of cognitive deficits (matrix reasoning IQ, verbal IQ, and working memory performance) as well as individual differences in every cardinal symptom domain of SCZ (poverty, reality distortion, and disorganization). Conclusions: These results suggest that global dysconnectivity underlies dorsolateral PFC involvement in the neuropathology of SCZ. Furthermore, these results demonstrate the possibility that specific patterns of dysconnectivity with a given network hub region might explain individual differences in symptom presentation in SCZ. Critically, such findings might extend to other neuropathologies with diverse presentation.
KW - fMRI
KW - functional connectivity
KW - global brain connectivity
KW - prefrontal cortex
KW - psychopathology
KW - schizophrenia
UR - http://www.scopus.com/inward/record.url?scp=79958808956&partnerID=8YFLogxK
U2 - 10.1016/j.biopsych.2011.02.010
DO - 10.1016/j.biopsych.2011.02.010
M3 - Article
C2 - 21496789
AN - SCOPUS:79958808956
SN - 0006-3223
VL - 70
SP - 43
EP - 50
JO - Biological Psychiatry
JF - Biological Psychiatry
IS - 1
ER -