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Connectome-based individualized prediction of loneliness
Feng, C., Wang, L., Li, T. & Xu, P., Apr-2019, In : Social Cognitive and Affective Neuroscience. 14, 4, p. 353-365 13 p.Research output: Contribution to journal › Article › Academic › peer-review
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Connectome-based individualized prediction of loneliness. / Feng, Chunliang; Wang, Li; Li, Ting; Xu, Pengfei.
In: Social Cognitive and Affective Neuroscience, Vol. 14, No. 4, 04.2019, p. 353-365.Research output: Contribution to journal › Article › Academic › peer-review
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TY - JOUR
T1 - Connectome-based individualized prediction of loneliness
AU - Feng, Chunliang
AU - Wang, Li
AU - Li, Ting
AU - Xu, Pengfei
PY - 2019/4
Y1 - 2019/4
N2 - Loneliness is an increasingly prevalent condition linking with enhanced morbidity and premature mortality. Despite recent proposal on medicalization of loneliness, so far no effort has been made to establish a model capable of predicting loneliness at the individual level. Here, we applied a machine-learning approach to decode loneliness from whole-brain resting-state functional connectivity (RSFC). The relationship between whole-brain RSFC and loneliness was examined in a linear predictive model. The results revealed that individual loneliness could be predicted by within- and between-network connectivity of prefrontal, limbic and temporal systems, which are involved in cognitive control, emotional processing and social perceptions and communications, respectively. Key nodes that contributed to the prediction model comprised regions previously implicated in loneliness, including the dorsolateral prefrontal cortex, lateral orbital frontal cortex, ventromedial prefrontal cortex, caudate, amygdala and temporal regions. Our findings also demonstrated that both loneliness and associated neural substrates are modulated by levels of neuroticism and extraversion. The current data-driven approach provides the first evidence on the predictive brain features of loneliness based on organizations of intrinsic brain networks. Our work represents initial efforts in the direction of making individualized prediction of loneliness that could be useful for diagnosis, prognosis and treatment.
AB - Loneliness is an increasingly prevalent condition linking with enhanced morbidity and premature mortality. Despite recent proposal on medicalization of loneliness, so far no effort has been made to establish a model capable of predicting loneliness at the individual level. Here, we applied a machine-learning approach to decode loneliness from whole-brain resting-state functional connectivity (RSFC). The relationship between whole-brain RSFC and loneliness was examined in a linear predictive model. The results revealed that individual loneliness could be predicted by within- and between-network connectivity of prefrontal, limbic and temporal systems, which are involved in cognitive control, emotional processing and social perceptions and communications, respectively. Key nodes that contributed to the prediction model comprised regions previously implicated in loneliness, including the dorsolateral prefrontal cortex, lateral orbital frontal cortex, ventromedial prefrontal cortex, caudate, amygdala and temporal regions. Our findings also demonstrated that both loneliness and associated neural substrates are modulated by levels of neuroticism and extraversion. The current data-driven approach provides the first evidence on the predictive brain features of loneliness based on organizations of intrinsic brain networks. Our work represents initial efforts in the direction of making individualized prediction of loneliness that could be useful for diagnosis, prognosis and treatment.
KW - loneliness
KW - connectome-based predictive modeling
KW - resting-state functional connectivity
KW - PERCEIVED SOCIAL-ISOLATION
KW - CROSS-LAGGED ANALYSES
KW - RESTING-STATE
KW - FUNCTIONAL CONNECTIVITY
KW - ENVIRONMENTAL CONTRIBUTIONS
KW - HUMAN BRAIN
KW - NETWORK
KW - SELF
KW - ATTENTION
KW - CORTEX
U2 - 10.1093/scan/nsz020
DO - 10.1093/scan/nsz020
M3 - Article
VL - 14
SP - 353
EP - 365
JO - Social Cognitive and Affective Neuroscience
JF - Social Cognitive and Affective Neuroscience
SN - 1749-5016
IS - 4
ER -
ID: 92901619