Functional connectome fingerprinting and stability in multiple sclerosis

Author:

Mantwill Maron12ORCID,Asseyer Susanna3456ORCID,Chien Claudia3467ORCID,Kuchling Joseph1348,Schmitz-Hübsch Tanja3456,Brandt Alexander U3569ORCID,Haynes John-Dylan21011,Paul Friedemann13456,Finke Carsten12

Affiliation:

1. Department of Neurology, Charité-Universitätsmedizin Berlin, Berlin, Germany

2. Faculty of Philosophy, Berlin School of Mind and Brain, Humboldt-Universität zu Berlin, Berlin, Germany

3. A cooperation between the Max Delbrück Center for Molecular Medicine in the Helmholtz Association and Charité-Universitätsmedizin, Experimental and Clinical Research Center, Berlin, Germany

4. Neuroscience Clinical Research Center, Charité-Universitätsmedizin Berlin, Berlin, Germany

5. Experimental and Clinical Research Center, Charité-Universitätsmedizin Berlin, Berlin, Germany

6. Max Delbrück Center for Molecular Medicine in the Helmholtz Association (MDC), Berlin, Germany

7. Department of Psychiatry and Neurosciences, Charité-Universitätsmedizin Berlin, Charitéplatz, Berlin, Germany

8. Berlin Institute of Health, Berlin, Germany

9. Department of Neurology, University of California, Irvine, CA, USA

10. Berlin Center for Advanced Neuroimaging, Charité-Universitätsmedizin Berlin, Berlin, Germany

11. Bernstein Center for Computational Neuroscience, Charité-Universitätsmedizin Berlin, Berlin, Germany

Abstract

Background Functional connectome fingerprinting can identify individuals based on their functional connectome. Previous studies relied mostly on short intervals between fMRI acquisitions. Objective This cohort study aimed to determine the stability of connectome-based identification and their underlying signatures in patients with multiple sclerosis and healthy individuals with long follow-up intervals. Methods We acquired resting-state fMRI in 70 patients with multiple sclerosis and 273 healthy individuals with long follow-up times (up to 4 and 9 years, respectively). Using functional connectome fingerprinting, we examined the stability of the connectome and additionally investigated which regions, connections and networks supported individual identification. Finally, we predicted cognitive and behavioural outcome based on functional connectivity. Results Multiple sclerosis patients showed connectome stability and identification accuracies similar to healthy individuals, with longer time delays between imaging sessions being associated with accuracies dropping from 89% to 76%. Lesion load, brain atrophy or cognitive impairment did not affect identification accuracies within the range of disease severity studied. Connections from the fronto-parietal and default mode network were consistently most distinctive, i.e., informative of identity. The functional connectivity also allowed the prediction of individual cognitive performances. Conclusion Our results demonstrate that discriminatory signatures in the functional connectome are stable over extended periods of time in multiple sclerosis, resulting in similar identification accuracies and distinctive long-lasting functional connectome fingerprinting signatures in patients and healthy individuals.

Funder

Deutsche Forschungsgemeinschaft

Publisher

SAGE Publications

Subject

Cellular and Molecular Neuroscience,Neurology (clinical)

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