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Functional connectome fingerprinting and stability in multiple sclerosis.
Mantwill, Maron; Asseyer, Susanna; Chien, Claudia; Kuchling, Joseph; Schmitz-Hübsch, Tanja; Brandt, Alexander U; Haynes, John-Dylan; Paul, Friedemann; Finke, Carsten.
Afiliação
  • Mantwill M; Department of Neurology, Charité-Universitätsmedizin Berlin, Berlin, Germany.
  • Asseyer S; Faculty of Philosophy, Berlin School of Mind and Brain, Humboldt-Universität zu Berlin, Berlin, Germany.
  • Chien C; A cooperation between the Max Delbrück Center for Molecular Medicine in the Helmholtz Association and Charité-Universitätsmedizin, Experimental and Clinical Research Center, Berlin, Germany.
  • Kuchling J; Neuroscience Clinical Research Center, Charité-Universitätsmedizin Berlin, Berlin, Germany.
  • Schmitz-Hübsch T; Experimental and Clinical Research Center, Charité-Universitätsmedizin Berlin, Berlin, Germany.
  • Brandt AU; Max Delbrück Center for Molecular Medicine in the Helmholtz Association (MDC), Berlin, Germany.
  • Haynes JD; A cooperation between the Max Delbrück Center for Molecular Medicine in the Helmholtz Association and Charité-Universitätsmedizin, Experimental and Clinical Research Center, Berlin, Germany.
  • Paul F; Neuroscience Clinical Research Center, Charité-Universitätsmedizin Berlin, Berlin, Germany.
  • Finke C; Max Delbrück Center for Molecular Medicine in the Helmholtz Association (MDC), Berlin, Germany.
Mult Scler J Exp Transl Clin ; 9(3): 20552173231195879, 2023.
Article em En | MEDLINE | ID: mdl-37641618
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.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Idioma: En Revista: Mult Scler J Exp Transl Clin Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Idioma: En Revista: Mult Scler J Exp Transl Clin Ano de publicação: 2023 Tipo de documento: Article