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Increased resting state functional connectivity in the default mode network in recovered anorexia nervosa
Felicity A Cowdrey1, Nicola Filippini, Rebecca J Park
1University of Oxford Department of Psychiatry, Warneford Hospital, Oxford, United Kingdom.
Human Brain Mapping
|October 4, 2012
Summary
Recovered anorexia nervosa (AN) patients show altered brain connectivity during rest. This resting-state brain network dysfunction may indicate a vulnerability marker for developing AN.
Area of Science:
- Neuroscience
- Psychiatry
- Medical Imaging
Background:
- Previous studies show abnormal brain activity in recovered anorexia nervosa (AN) patients during tasks.
- This persistent abnormal activity may represent the neurobiology of AN and serve as a neural biomarker.
- No prior research examined resting-state functional connectivity changes in recovered AN without task-induced activity.
Purpose of the Study:
- To investigate whole-brain resting-state functional connectivity in nonmedicated women recovered from AN.
- To identify potential neural markers of AN vulnerability in resting brain networks.
Main Methods:
- Functional magnetic resonance imaging (fMRI) was used to scan 16 recovered AN participants and 15 healthy controls.
- Independent component analysis (ICA) identified resting-state functional networks.
- Dual regression analysis assessed temporal correlations within these networks.
Main Results:
- Recovered AN participants exhibited increased temporal coherence (connectivity) in the default mode network (DMN).
- This increased DMN connectivity was observed between the DMN and the precuneus and dorsolateral prefrontal cortex/inferior frontal gyrus.
- These findings were significant compared to healthy control participants.
Conclusions:
- Dysfunction in resting-state functional connectivity, particularly in self-referential processing and cognitive control regions, may be a vulnerability marker for AN.
- Altered DMN connectivity during rest could play a role in the neurobiology of AN.
- Resting-state fMRI may offer insights into the neural underpinnings of AN susceptibility.

