全部 标题 作者
关键词 摘要

OALib Journal期刊
ISSN: 2333-9721
费用:99美元

查看量下载量

相关文章

更多...

Brain Functional Connectivity Network (BFCN) Analysis Using Scalp-Recorded EEGs after Human Papilloma Virus Vaccination

DOI: 10.4236/jbise.2025.188023, PP. 317-327

Keywords: HANS (Human Papilloma Virus Vaccination Associated Neuro-Immunopathic Syndrome), EEGs (Electroencephalograms), Functional Connectivity, Network Properties

Full-Text   Cite this paper   Add to My Lib

Abstract:

Background/Objectives: HANS (human papillomavirus vaccination-associated neuroimmunopathic syndrome) is a type of adverse reaction to HPV vaccination that causes cognitive dysfunction. Human brain function can be represented by functional connectivity and the Brain Functional Connectivity Network (BFCN), which are constructed by scalp-recorded electroencephalograms (EEGs). Functional connectivity and BFCN are used to estimate functional efficiency. The effects of cognitive dysfunction on network properties have been reported. However, network properties in HANS patients are incompletely understood. In this study, we examined (1) identifiability between HANS patients and young controls and (2) the impact of cognitive dysfunction due to HANS on BFCN for five frequency bands. Methods: 16-ch EEGs were recorded in a resting state with eyes closed for 14 HANS patients and 12 young controls. We used Synchronization Likelihood (SL) as measured functional connectivity, which is used for classification by machine learning and for the construction of BFCN for five frequency bands. In (1), SL values were used as features for classification. Accuracies were calculated by leave-one-out cross-validation. Accuracies for five frequency bands were compared to that of random prediction. In (2), clustering coefficient, characteristic path length, and small-worldness of BFCN were compared between HANS patients and young controls. Results: Our study revealed (1) high accuracies were illustrated for lower alpha and theta bands and (2) a significant decrease compared to controls in small-worldness in HANS patients for the gamma band. Conclusion: Our study shows identifiability between HANS patients and young controls. In addition, changes in network characteristics based on functional connectivity are relevant to cognitive dysfunction in HANS.

References

[1]  Nishioka, K., Yokota, S. and Matsumoto, Y. (2014) Clinical Features and Preliminary Diagnostic Criteria of Hu-man Papillomavirus Vaccination Associated with Neuroimmunopathic Syndrome (HANS). International Journal of Rheumatic Diseases, 17, 29.
[2]  Kuroiwa, Y., Yokota, S., Nakamura, I., Nakajima, T. and Nishioka, K. (2018) Human Papilloma Virus Vaccination (HPVV)-Associated Neuro-Immunopathic Syndrome (HANS): A Comparative Study of the Symptomatic Com-plex Occurring in Japanese and Danish Young Females after HPVV. Autonomic Nervous System, 55, 21-30.
[3]  Hirai, T., Kuroiwa, Y., Hayashi, T., Uchiyama, M., Nakamura, I., Yokota, S., et al. (2016) Adverse Effects of Human Papilloma Virus Vaccination on Central Nervous System: Neuro-Endocrinological Disorders of Hypothalamo-Pituitary Axis. Autonomic Neuroscience, 201, 74.
https://doi.org/10.1016/j.autneu.2016.09.011
[4]  Matsudaira, T., Terada, T., Obi, T., Yokokura, M., Takahashi, Y. and Ouchi, Y. (2020) Coexistence of Cerebral Hypometabolism and Neuroinflammation in the Thalamo-Limbic-Brainstem Region in Young Women with Functional Somatic Syndrome. EJNMMI Research, 10, Article No. 29.
https://doi.org/10.1186/s13550-020-00617-1
[5]  Hineno, A., Ikeda, S., Scheibenbogen, C., Heidecke, H., Schulze-Forster, K., Junker, J., Riemekasten, G., Dechend, R., Dragun, D. and Shoenfeld, Y. (2019) Autoantibodies against Autonomic Nerve Receptors in Adolescent Japanese Girls after Immunization with Human Papillomavirus Vaccine. Annals of Arthritis and Clinical Rheumatology, 2, 1014.
[6]  Sporns, O. (2016) Network of the Brain. MIT Press.
[7]  Chiarion, G., Sparacino, L., Antonacci, Y., Faes, L. and Mesin, L. (2023) Connectivity Analysis in EEG Data: A Tutorial Review of the State of the Art and Emerging Trends. Bioengineering, 10, Article No. 372.
https://doi.org/10.3390/bioengineering10030372
[8]  Raveendran, S., et al. (2025) Functional Connectivity in EEG: A Multiclass Classification Approach for Disorders of Consciousness. Frontiers in Neuroscience, 19, Article ID: 1550581.
https://doi.org/10.3389/fnins.2025.1550581
[9]  Antonacci, Y., Toppi, J., Pietrabissa, A., Anzolin, A. and Astolfi, L. (2024) Measuring Connectivity in Linear Multivariate Processes with Penalized Regression Techniques. IEEE Access, 12, 30638-30652.
https://doi.org/10.1109/access.2024.3368637
[10]  Stam, C.J. and van Dijk, B.W. (2002) Synchronization Likelihood: An Unbiased Measure of Generalized Synchronization in Multivariate Data Sets. Physica D: Nonlinear Phenomena, 163, 236-251.
https://doi.org/10.1016/s0167-2789(01)00386-4
[11]  Montez, T., Linkenkaer-Hansen, K., van Dijk, B.W. and Stam, C.J. (2006) Synchronization Likelihood with Explicit Time-Frequency Priors. NeuroImage, 33, 1117-1125.
https://doi.org/10.1016/j.neuroimage.2006.06.066
[12]  Mumtaz, W., Ali, S.S.A., Yasin, M.A.M. and Malik, A.S. (2017) A Machine Learning Framework Involving EEG-Based Functional Connectivity to Diagnose Major Depressive Disorder (MDD). Medical & Biological Engineering & Computing, 56, 233-246.
https://doi.org/10.1007/s11517-017-1685-z
[13]  Takeoka, C., Yamazaki, T., Kuroiwa, Y., Fujino, K., Hirai, T. and Mizusawa, H. (2023) Functional Connectivity and Small-World Networks in Prion Disease. IEICE Transactions on Information and Systems, 106, 427-430.
https://doi.org/10.1587/transinf.2022edl8049
[14]  Stam, C., Jones, B., Nolte, G., Breakspear, M. and Scheltens, P. (2006) Small-World Networks and Functional Connectivity in Alzheimer’s Disease. Cerebral Cortex, 17, 92-99.
https://doi.org/10.1093/cercor/bhj127
[15]  Stam, C.J., Van Der Made, Y., Pijnenburg, Y.A.L. and Scheltens, P. (2003) EEG Synchronization in Mild Cognitive Impairment and Alzheimer’s Disease. Acta Neurologica Scandinavica, 108, 90-96.
https://doi.org/10.1034/j.1600-0404.2003.02067.x
[16]  Sanz-Arigita, E.J., Schoonheim, M.M., Damoiseaux, J.S., Rombouts, S.A.R.B., Maris, E., Barkhof, F., et al. (2010) Loss of “Small-World” Networks in Alzheimer’s Disease: Graph Analysis of fMRI Resting-State Functional Connectivity. PLOS ONE, 5, e13788.
https://doi.org/10.1371/journal.pone.0013788
[17]  Gaál, Z.A., Boha, R., Stam, C.J. and Molnár, M. (2010) Age-Dependent Features of EEG-Reactivity—Spectral, Complexity, and Network Characteristics. Neuroscience Letters, 479, 79-84.
https://doi.org/10.1016/j.neulet.2010.05.037
[18]  Teng, C., Cheng, Y., Wang, C., Ren, Y., Xu, W. and Xu, J. (2018) Aging-Related Changes of EEG Synchronization during a Visual Working Memory Task. Cognitive Neurodynamics, 12, 561-568.
https://doi.org/10.1007/s11571-018-9500-6
[19]  Aratani, S., Fujita, H., Kuroiwa, Y., Usui, C., Yokota, S., Nakamura, I., et al. (2016) Murine Hypothalamic Destruction with Vascular Cell Apoptosis Subsequent to Combined Administration of Human Papilloma Virus Vaccine and Pertussis Toxin. Scientific Reports, 6, Article No. 36943.
https://doi.org/10.1038/srep36943
[20]  Ozawa, K., Hineno, A., Kinoshita, T., Ishihara, S. and Ikeda, S. (2017) Suspected Adverse Effects after Human Papillomavirus Vaccination: A Temporal Relationship between Vaccine Administration and the Appearance of Symptoms in Japan. Drug Safety, 40, 1219-1229.
https://doi.org/10.1007/s40264-017-0574-6
[21]  Stam, C.J. and Reijneveld, J.C. (2007) Graph Theoretical Analysis of Complex Networks in the Brain. Nonlinear Biomedical Physics, 1, Article No. 3.
https://doi.org/10.1186/1753-4631-1-3
[22]  Latora, V. and Marchiori, M. (2001) Efficient Behavior of Small-World Networks. Physical Review Letters, 87, Article ID: 198701.
https://doi.org/10.1103/physrevlett.87.198701
[23]  Chen, Y., Bressler, S.L. and Ding, M. (2006) Frequency Decomposition of Conditional Granger Causality and Application to Multivariate Neural Field Potential Data. Journal of Neuroscience Methods, 150, 228-237.
https://doi.org/10.1016/j.jneumeth.2005.06.011
[24]  Pereda, E., Quiroga, R.Q. and Bhattacharya, J. (2005) Nonlinear Multivariate Analysis of Neurophysiological Signals. Progress in Neurobiology, 77, 1-37.
https://doi.org/10.1016/j.pneurobio.2005.10.003
[25]  Gong, G., He, Y. and Evans, A.C. (2011) Brain Connectivity: Gender Makes a Difference. The Neuroscientist, 17, 575-591.
https://doi.org/10.1177/1073858410386492

Full-Text

Contact Us

service@oalib.com

QQ:3279437679

WhatsApp +8615387084133