Abstract
Original language | English |
---|---|
Journal | Scientific Reports |
Volume | 4 |
DOIs | |
Publication status | Published - 2014 |
Externally published | Yes |
Keywords
- adolescent
- brain mapping
- case control study
- child
- female
- frontal lobe
- human
- male
- multivariate analysis
- nerve cell network
- pathophysiology
- reproducibility
- Schizophrenia, Childhood
- temporal lobe
- Adolescent
- Brain Mapping
- Case-Control Studies
- Child
- Female
- Frontal Lobe
- Humans
- Male
- Multivariate Analysis
- Nerve Net
- Reproducibility of Results
- Temporal Lobe
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In: Scientific Reports, Vol. 4, 2014.
Research output: Contribution to journal › Article › peer-review
}
TY - JOUR
T1 - Brain network informed subject community detection in early-onset schizophrenia
AU - Yang, Zhi
AU - Xu, Yong
AU - Xu, Ting
AU - Hoy, Colin Weir
AU - Handwerker, Daniel A.
AU - Chen, Gang
AU - Northoff, Georg Franz Josef
AU - Zuo, Xi Nian
AU - Bandettini, Peter A.
N1 - Cited By :5 Export Date: 11 May 2016 Correspondence Address: Xu, Y.; Key Laboratory of Behavioral Science and Magnetic Resonance Imaging Research Center, Institute of Psychology, Chinese Academy of Sciences, Beijing, China; email: [email protected] References: Vyas, N.S., Hadjulis, M., Vourdas, A., Byrne, P., Frangou, S., The maudsley early onset schizophrenia study. Predictors of psychosocial outcome at 4-year followup (2007) Eur. Child Adoles. 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PY - 2014
Y1 - 2014
N2 - Early-onset schizophrenia (EOS) offers a unique opportunity to study pathophysiological mechanisms and development of schizophrenia. Using 26 drug-naïve, first-episode EOS patients and 25 age-and gender-matched control subjects, we examined intrinsic connectivity network (ICN) deficits underlying EOS. Due to the emerging inconsistency between behavior-based psychiatric disease classification system and the underlying brain dysfunctions, we applied a fully data-driven approach to investigate whether the subjects can be grouped into highly homogeneous communities according to the characteristics of their ICNs. The resultant subject communities and the representative characteristics of ICNs were then associated with the clinical diagnosis and multivariate symptom patterns. A default mode ICN was statistically absent in EOS patients. Another frontotemporal ICN further distinguished EOS patients with predominantly negative symptoms. Connectivity patterns of this second network for the EOS patients with predominantly positive symptom were highly similar to typically developing controls. Our post-hoc functional connectivity modeling confirmed that connectivity strength in this frontotemporal circuit was significantly modulated by relative severity of positive and negative syndromes in EOS. This study presents a novel subtype discovery approach based on brain networks and proposes complex links between brain networks and symptom patterns in EOS.
AB - Early-onset schizophrenia (EOS) offers a unique opportunity to study pathophysiological mechanisms and development of schizophrenia. Using 26 drug-naïve, first-episode EOS patients and 25 age-and gender-matched control subjects, we examined intrinsic connectivity network (ICN) deficits underlying EOS. Due to the emerging inconsistency between behavior-based psychiatric disease classification system and the underlying brain dysfunctions, we applied a fully data-driven approach to investigate whether the subjects can be grouped into highly homogeneous communities according to the characteristics of their ICNs. The resultant subject communities and the representative characteristics of ICNs were then associated with the clinical diagnosis and multivariate symptom patterns. A default mode ICN was statistically absent in EOS patients. Another frontotemporal ICN further distinguished EOS patients with predominantly negative symptoms. Connectivity patterns of this second network for the EOS patients with predominantly positive symptom were highly similar to typically developing controls. Our post-hoc functional connectivity modeling confirmed that connectivity strength in this frontotemporal circuit was significantly modulated by relative severity of positive and negative syndromes in EOS. This study presents a novel subtype discovery approach based on brain networks and proposes complex links between brain networks and symptom patterns in EOS.
KW - adolescent
KW - brain mapping
KW - case control study
KW - child
KW - female
KW - frontal lobe
KW - human
KW - male
KW - multivariate analysis
KW - nerve cell network
KW - pathophysiology
KW - reproducibility
KW - Schizophrenia, Childhood
KW - temporal lobe
KW - Adolescent
KW - Brain Mapping
KW - Case-Control Studies
KW - Child
KW - Female
KW - Frontal Lobe
KW - Humans
KW - Male
KW - Multivariate Analysis
KW - Nerve Net
KW - Reproducibility of Results
KW - Temporal Lobe
U2 - 10.1038/srep05549
DO - 10.1038/srep05549
M3 - Article
C2 - 24989351
SN - 2045-2322
VL - 4
JO - Scientific Reports
JF - Scientific Reports
ER -