Graph theory analysis reveals how sickle cell disease impacts neural networks of patients with more severe disease.


Journal

NeuroImage. Clinical
ISSN: 2213-1582
Titre abrégé: Neuroimage Clin
Pays: Netherlands
ID NLM: 101597070

Informations de publication

Date de publication:
2019
Historique:
received: 21 03 2018
revised: 28 10 2018
accepted: 13 11 2018
pubmed: 28 11 2018
medline: 27 12 2019
entrez: 28 11 2018
Statut: ppublish

Résumé

Sickle cell disease (SCD) is a hereditary blood disorder associated with many life-threatening comorbidities including cerebral stroke and chronic pain. The long-term effects of this disease may therefore affect the global brain network which is not clearly understood. We performed graph theory analysis of functional networks using non-invasive fMRI and high resolution EEG on thirty-one SCD patients and sixteen healthy controls. Resting state data were analyzed to determine differences between controls and patients with less severe and more severe sickle cell related pain. fMRI results showed that patients with higher pain severity had lower clustering coefficients and local efficiency. The neural network of the more severe patient group behaved like a random network when performing a targeted attack network analysis. EEG results showed the beta1 band had similar results to fMRI resting state data. Our data show that SCD affects the brain on a global level and that graph theory analysis can differentiate between patients with different levels of pain severity.

Identifiants

pubmed: 30477765
pii: S2213-1582(18)30347-4
doi: 10.1016/j.nicl.2018.11.009
pmc: PMC6411610
pii:
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, U.S. Gov't, Non-P.H.S.

Langues

eng

Sous-ensembles de citation

IM

Pagination

101599

Subventions

Organisme : NIBIB NIH HHS
ID : T32 EB008389
Pays : United States
Organisme : NIBIB NIH HHS
ID : R01 EB021027
Pays : United States
Organisme : NIMH NIH HHS
ID : RF1 MH114233
Pays : United States
Organisme : NIH HHS
ID : S10 OD021721
Pays : United States
Organisme : NINDS NIH HHS
ID : R01 NS096761
Pays : United States
Organisme : NHLBI NIH HHS
ID : U01 HL117664
Pays : United States
Organisme : NCCIH NIH HHS
ID : R01 AT009263
Pays : United States

Informations de copyright

Copyright © 2018 The Authors. Published by Elsevier Inc. All rights reserved.

Auteurs

Michelle Case (M)

Department of Biomedical Engineering, University of Minnesota, MN, USA. Electronic address: casex112@umn.edu.

Sina Shirinpour (S)

Department of Biomedical Engineering, University of Minnesota, MN, USA.

Vishal Vijayakumar (V)

Department of Electrical and Computer Engineering, University of Minnesota, MN, USA.

Huishi Zhang (H)

Department of Biomedical Engineering, University of Minnesota, MN, USA.

Yvonne Datta (Y)

Department of Medicine, University of Minnesota, MN, USA.

Stephen Nelson (S)

Department of Hematology Oncology, Children's Hospitals and Clinics of Minnesota, MN, USA.

Paola Pergami (P)

Department of Neurology, Children's National Health System, Washington, DC, USA.

Deepika S Darbari (DS)

Division of Hematology, Children's National Health System, Washington, DC, USA.

Kalpna Gupta (K)

Department of Medicine, University of Minnesota, MN, USA.

Bin He (B)

Department of Biomedical Engineering, University of Minnesota, MN, USA; Department of Biomedical Engineering, Carnegie Mellon University, PA, USA. Electronic address: bhe1@andrew.cmu.edu.

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Classifications MeSH