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Reduced higher dimensional temporal dynamism in neurofibromatosis type 1
Eva Mennigen1, Peter Schuette1, Ariana Vajdi1
1Department of Psychiatry and Biobehavioral Sciences, University of California, Los Angeles, CA, USA.
Neurofibromatosis type 1 (NF1) alters brain functional network connectivity (FNC), particularly in cognitive control networks. NF1 patients show different static and dynamic FNC patterns compared to controls, indicating potential global brain dysfunction.
Area of Science:
- Neuroscience
- Genetics
- Psychiatry
Background:
- Neurofibromatosis type 1 (NF1) is a common genetic disorder with multi-organ effects.
- NF1 is linked to cognitive impairments like learning disabilities and attention deficits.
- While structural brain anomalies in NF1 are known, functional connectivity patterns remain understudied.
Purpose of the Study:
- To investigate static and dynamic functional network connectivity (FNC) in individuals with NF1.
- To compare FNC patterns in NF1 patients with age- and sex-matched healthy controls.
- To explore novel meta-state analysis for higher-dimensional temporal dynamism of brain connectivity.
Main Methods:
- Recruited 30 NF1 participants and 30 healthy controls.
- Conducted comprehensive static and dynamic functional network connectivity (FNC) analysis.
- Utilized meta-state analysis to examine temporal dynamism of whole-brain connectivity.
Main Results:
- NF1 participants showed altered static FNC in cognitive control networks, with decreased anterior-cerebellar connectivity and increased within-network connectivity.
- These alterations were independent of IQ.
- Dynamic FNC analysis revealed NF1 patients spent more time in hypoconnected states and exhibited reduced temporal dynamism of FNC.
Conclusions:
- NF1 is associated with significant alterations in both static and dynamic functional network connectivity.
- Reduced temporal dynamism and increased hypoconnected states in NF1 may indicate broader brain dysfunction.
- Findings suggest potential shared neural mechanisms underlying brain dysfunction in NF1 and other disorders like schizophrenia.
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