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

被引:13
|
作者
Case, Michelle [1 ]
Shirinpour, Sina [1 ]
Vijayakumar, Vishal [2 ]
Zhang, Huishi [1 ]
Datta, Yvonne [3 ]
Nelson, Stephen [4 ]
Pergami, Paola [5 ]
Darbari, Deepika S. [6 ]
Gupta, Kalpna [3 ]
He, Bin [1 ,7 ]
机构
[1] Univ Minnesota, Dept Biomed Engn, Minneapolis, MN 55455 USA
[2] Univ Minnesota, Dept Elect & Comp Engn, Minneapolis, MN 55455 USA
[3] Univ Minnesota, Dept Med, Minneapolis, MN 55455 USA
[4] Childrens Hosp & Clin Minnesota, Dept Hematol Oncol, Minneapolis, MN USA
[5] Childrens Natl Hlth Syst, Dept Neurol, Washington, DC USA
[6] Childrens Natl Hlth Syst, Div Hematol, Washington, DC USA
[7] Carnegie Mellon Univ, Dept Biomed Engn, Pittsburgh, PA 15213 USA
关键词
Sickle cell disease; Electroencephalography (EEG); Functional magnetic resonance imaging (fMRI); Graph theory; Resting state; RESTING-STATE EEG; FUNCTIONAL CONNECTIVITY; BRAIN ACTIVITY; PAIN; CHILDREN; ANEMIA; SENSITIZATION; LOCALIZATION; ACTIVATION; FREQUENCY;
D O I
10.1016/j.nicl.2018.11.009
中图分类号
R445 [影像诊断学];
学科分类号
100207 ;
摘要
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.
引用
收藏
页数:14
相关论文
共 50 条
  • [21] Impairment of Cerebrovascular Hemodynamics in Patients With Severe and Milder Forms of Sickle Cell Disease
    Afzali-Hashemi, Liza
    Baas, Koen P. A.
    Schrantee, Anouk
    Coolen, Bram F.
    van Osch, Matthias J. P.
    Spann, Stefan M.
    Nur, Erfan
    Wood, John C.
    Biemond, Bart J.
    Nederveen, Aart J.
    FRONTIERS IN PHYSIOLOGY, 2021, 12
  • [22] Craniofacial morphology in patients with sickle cell disease: a cephalometric analysis
    Licciardello, Valeria
    Bertuna, Gregoria
    Samperi, Piera
    EUROPEAN JOURNAL OF ORTHODONTICS, 2007, 29 (03) : 238 - 242
  • [23] Training Neural Networks as Experimental Models: Classifying Biomedical Datasets for Sickle Cell Disease
    Khalaf, Mohammed
    Hussain, Abir Jaafar
    Al-Jumeily, Dhiya
    Keight, Robert
    Keenan, Russell
    Fergus, Paul
    Al-Askar, Haya
    Shaw, Andy
    Idowu, Ibrahim Olatunji
    INTELLIGENT COMPUTING THEORIES AND APPLICATION, ICIC 2016, PT I, 2016, 9771 : 784 - 795
  • [24] Detection of sickle cell disease using deep neural networks and explainable artificial intelligence
    Goswami, Neelankit Gautam
    Goswami, Anushree
    Sampathila, Niranjana
    Bairy, Muralidhar G.
    Chadaga, Krishnaraj
    Belurkar, Sushma
    JOURNAL OF INTELLIGENT SYSTEMS, 2024, 33 (01)
  • [25] The use of rituximab to prevent severe delayed haemolytic transfusion reaction in immunized patients with sickle cell disease
    Noizat-Pirenne, F.
    Habibi, A.
    Mekontso-Dessap, A.
    Razazi, K.
    Chadebech, P.
    Mahevas, M.
    Vingert, B.
    Bierling, P.
    Galacteros, F.
    Bartolucci, P.
    Michel, M.
    VOX SANGUINIS, 2015, 108 (03) : 262 - 267
  • [26] Red Cell Transfusions for Patients With Sickle Cell Disease: Do We Have More to Learn?
    Nuss, Rachelle
    PEDIATRIC BLOOD & CANCER, 2010, 54 (04) : 499 - 500
  • [27] Chronic renal failure in sickle cell disease: A retrospective analysis of 100 adults sickle cell patients from black Africa
    Ackoundou-N'Guessan, Clement
    Guei, Cyr Monley
    Lagou, Delphine Amelie
    Gbekedi, Serges
    Tia, Melanie Weu
    Coulibaly, Pessa Albert
    Nzoue, Sita
    Konan, Serges
    Koffi, Gustave
    Gnionsahe, Daze Apollinaire
    NEPHROLOGIE & THERAPEUTIQUE, 2016, 12 (03): : 149 - 155
  • [28] Electrocardiographic abnormalities in patients with sickle cell disease: A systematic review and meta-analysis
    Taherifard, Erfan
    Movahed, Hamed
    Taherifard, Ehsan
    Sadeghi, Alireza
    Dehdari Ebrahimi, Niloofar
    Ahmadkhani, Alireza
    Kheshti, Fatemeh
    Movahed, Hossein
    PEDIATRIC BLOOD & CANCER, 2024, 71 (05)
  • [29] Cost of health care for paediatric patients with sickle cell disease: An analysis of resource use and costs in a European country
    Thielen, Frederick W.
    Houwing, Maite E.
    Cnossen, Marjon H.
    al Hadithy-Irgiztseva, Ilona A.
    Hazelzet, Jan A.
    Groot, Carin A. Uyl-de
    de Pagter, Anne P. J.
    Blommestein, Hedwig M.
    PEDIATRIC BLOOD & CANCER, 2020, 67 (09)
  • [30] LC-MS/MS analysis of plasma polyunsaturated fatty acids in patients with homozygous sickle cell disease
    Aslan, Mutay
    Celmeli, Gamze
    Ozcan, Filiz
    Kupesiz, Alphan
    CLINICAL AND EXPERIMENTAL MEDICINE, 2015, 15 (03) : 397 - 403