Angus Paton , Tineke Grent- ’t-Jong , Ruchika Gajwani , Joachim Gross , Andrew I. Gumley , Stephen M. Lawrie , Matthias Schwannauer , Frauke Schultze-Lutter , Peter J. Uhlhaas
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In addition, correlations between dMRI and rsfMRI-data, clinical and neurocognitive variables as well as with clinical outcomes were investigated.</div><div>We observed hyper- and hypoconnectivity across occipital, parietal, temporal, and frontal cortices in both dMRI and rsfMRI-data in CHR-Ps. Moreover, dMRI- and rsfMRI-defined overlapping nodes that differed between CHR-Ps vs. HC overlapped with visual networks, right ventral attention network, and right default mode network. Correlational analyses indicated significant relationships between the severity of CHR-P symptoms, cognitive deficits, and dMRI/rsfMRI-defined hypo- and hyper-connectivity. Finally, CHR-P individuals with persistent attenuated psychotic symptoms (APS) were characterised by aberrant dMRI and rsfMRI connectivity compared to non-persistent APS.</div><div>Our study shows subtle but widespread disruptions in dMRI and rsfMRI connectivity in CHR-P participants. 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Overlapping structural and functional connectivity disruptions in clinical high-risk for psychosis participants: A network analysis study
Schizophrenia involves aberrant connectivity of anatomical and functional networks. However, it is currently unclear whether such disruptions are present in clinical high-risk for psychosis (CHR-P) participants and whether there may be an overlap between structural and functional connectivity alterations.
We obtained diffusion magnetic resonance imaging (dMRI) and resting-state, magnetic resonance imaging (rsfMRI) data from N = 110 CHR-P participants and N = 49 healthy controls (HC). A network analysis approach was employed to explore differences in dMRI and rsfMRI connectivity as well as potential overlap between both modalities. In addition, correlations between dMRI and rsfMRI-data, clinical and neurocognitive variables as well as with clinical outcomes were investigated.
We observed hyper- and hypoconnectivity across occipital, parietal, temporal, and frontal cortices in both dMRI and rsfMRI-data in CHR-Ps. Moreover, dMRI- and rsfMRI-defined overlapping nodes that differed between CHR-Ps vs. HC overlapped with visual networks, right ventral attention network, and right default mode network. Correlational analyses indicated significant relationships between the severity of CHR-P symptoms, cognitive deficits, and dMRI/rsfMRI-defined hypo- and hyper-connectivity. Finally, CHR-P individuals with persistent attenuated psychotic symptoms (APS) were characterised by aberrant dMRI and rsfMRI connectivity compared to non-persistent APS.
Our study shows subtle but widespread disruptions in dMRI and rsfMRI connectivity in CHR-P participants. Specifically, we identified several occipital, parietal, temporal, and frontal regions that were characterised by hyper and hypoconnectivity which correlated with the severity of clinical symptoms and cognitive impairments. Moreover, our findings suggest that dMRI and rsfMRI connectivity measures could serve as a potential biomarker for clinical outcomes in CHR-Ps.
期刊介绍:
NeuroImage: Clinical, a journal of diseases, disorders and syndromes involving the Nervous System, provides a vehicle for communicating important advances in the study of abnormal structure-function relationships of the human nervous system based on imaging.
The focus of NeuroImage: Clinical is on defining changes to the brain associated with primary neurologic and psychiatric diseases and disorders of the nervous system as well as behavioral syndromes and developmental conditions. The main criterion for judging papers is the extent of scientific advancement in the understanding of the pathophysiologic mechanisms of diseases and disorders, in identification of functional models that link clinical signs and symptoms with brain function and in the creation of image based tools applicable to a broad range of clinical needs including diagnosis, monitoring and tracking of illness, predicting therapeutic response and development of new treatments. Papers dealing with structure and function in animal models will also be considered if they reveal mechanisms that can be readily translated to human conditions.