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The Role of Quantitative EEG in the Diagnosis of Alzheimer’s Disease
Open accessAbstract
Alzheimer’s disease is the most prevalent neurodegenerative disorder leading to progressive cognitive decline and functional impairment. Although advanced neuroimaging and cerebrospinal fluid biomarkers have improved early detection, their high costs, invasiveness, and limited accessibility restrict universal screening. Quantitative electroencephalography (qEEG) offers a non-invasive and cost-effective alternative for assessing neurophysiological changes associated with AD. This review critically evaluates current evidence on EEG biomarkers, including spectral, connectivity, and complexity measures, discussing their pathophysiological basis, diagnostic accuracy, and clinical utility in AD. Limitations and future perspectives, especially in developing standardized protocols and integrating machine learning techniques, are also addressed.
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“Quantitative EEG serves as a viable solution, providing a scalable screening instrument for vulnerable groups through the detection of spectral slowing and connectivity disruptions when advanced neuroimaging is inaccessible”
From Multimodal neuroimaging and AI integration in cognitive disorders: advances, challenges, and future directions for precision medicine (2026) · cites this paper as Papaliagkas, 2025
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Neuropathological stageing of Alzheimer-related changes.
Braak, H., & Braak, E. (1991) · Acta Neuropathologica · doi:10.1007/bf00308809 · Cited by 16,123
Zhang, J., Zhang, Y., Wang, J., Xia, Y., Zhang, J., & Chen, L. (2024) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-024-01911-3 · Cited by 1,138 · cited 1×
“Research conducted over time demonstrates that spectral slowing with increased theta power and higher theta/alpha ratios appears in patients with MCI who develop AD [46,47].”
Neuroimaging advances regarding subjective cognitive decline in preclinical Alzheimer's disease
Wang, X., Huang, W., Su, L., Xing, Y., Jessen, F., Sun, Y., Shu, N., & Han, Y. (2020) · Molecular Neurodegeneration · doi:10.1186/s13024-020-00395-3 · Cited by 265
Research works printed but not linked: 64
- Brookmeyer, 2007, Forecasting the global burden of Alzheimer’s disease, Alzheimer’s Dement., 3, 186, 10.1016/j.jalz.2007.04.381 · DOI · Paper page
- Hardy, 2002, The amyloid hypothesis of Alzheimer’s disease: Progress and problems, Science, 297, 353, 10.1126/science.1072994 · DOI · Paper page
- Jack, 2010, ypothetical model of dynamic biomarkers of the Alzheimer’s disease pathological cascade, Lancet Neurol., 9, 119, 10.1016/S1474-4422(09)70299-6 · DOI · Paper page
- McKhann, 2011, The diagnosis of dementia due to Alzheimer’s disease: Recommendations from the National Institute on Aging-Alzheimer’s Association workgroups, Alzheimer’s Dement., 7, 263, 10.1016/j.jalz.2011.03.005 · DOI · Paper page
- Blennow, 2010, Cerebrospinal fluid and plasma biomarkers in Alzheimer disease, Nat. Rev. Neurol., 6, 131, 10.1038/nrneurol.2010.4 · DOI · Paper page
- Hansson, 2019, Biomarkers of Alzheimer’s disease: Current status and future perspectives, Alzheimer’s Res. Ther., 11, 86
- Varesi, A., Carrara, A., Pires, V.G., Floris, V., Pierella, E., Savioli, G., Prasad, S., Esposito, C., Ricevuti, G., and Chirumbolo, S. (2022). Blood-Based Biomarkers for Alzheimer’s Disease Diagnosis and Progression: An Overview. Cells, 11. · DOI
- Dasari, 2025, Blood-Based β-Amyloid and Phosphorylated Tau (p-Tau) Biomarkers in Alzheimer’s Disease: A Systematic Review of Their Diagnostic Potential, Cureus, 17, e79881
- Li, 2022, Prospective biomarkers of Alzheimer’s disease: A systematic review and meta-analysis, Ageing Res. Rev., 81, 101699, 10.1016/j.arr.2022.101699 · DOI
- Niedermeyer, E., and Lopes da Silva, F.H. (2004). Electroencephalography: Basic Principles, Clinical Applications, and Related Fields, Lippincott Williams & Wilkins.
- Placidi, G., Cinque, L., and Polsinelli, M. (2021). A fast and scalable framework for automated artifact recognition from EEG signals represented in scalp topographies of Independent Components. Comput. Biol. Med., 132. · DOI
- Scheuer, 2021, Seizure Detection: Interreader Agreement and Detection Algorithm Assessments Using a Large Dataset, J. Clin. Neurophysiol., 38, 439, 10.1097/WNP.0000000000000709 · DOI
- Beniczky, 2013, Standardized computer-based organized reporting of EEG: SCORE, Epilepsia, 54, 1112, 10.1111/epi.12135 · DOI
- Jeong, 2004, EEG dynamics in patients with Alzheimer’s disease, Clin. Neurophysiol., 115, 1490, 10.1016/j.clinph.2004.01.001 · DOI
- Rossini, 2020, Early diagnosis of Alzheimer’s disease: The role of biomarkers including advanced EEG signal analysis. Report from the IFCN-sponsored panel of experts, Clin. Neurophysiol., 131, 1287, 10.1016/j.clinph.2020.03.003 · DOI
- Babiloni, 2011, Resting state cortical rhythms in mild cognitive impairment and Alzheimer’s disease: Electroencephalographic evidence, J. Alzheimer’s Dis., 26, 201, 10.3233/JAD-2011-0051 · DOI
- Saini, M., Rohilla, S., and Kumar, R. (Curr. Aging Sci., 2025). Revolutionizing Therapeutic Approaches Against Pathophysiology of Alzheimer’s Disease: A Therapeutic Review, Curr. Aging Sci., online ahead of print. · DOI
- Greicius, 2008, Resting-state functional connectivity in neuropsychiatric disorders, Curr. Opin. Neurol., 21, 424, 10.1097/WCO.0b013e328306f2c5 · DOI · Paper page
- Sheline, 2013, Resting state functional connectivity in preclinical Alzheimer’s disease, Biol. Psychiatry, 74, 340, 10.1016/j.biopsych.2012.11.028 · DOI · Paper page
- 2004, Analisis espectral de la coherencia cerebral en la enfermedad de Alzheimer [Spectral analysis of EEG coherence in Alzheimer’s disease], Rev. Neurol., 38, 422, 10.33588/rn.3805.2003535 · DOI
- Li, Q., Song, J.L., Li, S.H., Westover, M.B., and Zhang, R. (2020). Effects of Cholinergic Neuromodulation on Thalamocortical Rhythms During NREM Sleep: A Model Study. Front. Comput. Neurosci., 23. · DOI
- Fide, 2021, Resting-state EEG alpha/theta power ratio discriminates early-onset Alzheimer’s disease from healthy controls, Clin. Neurophysiol., 132, 2019, 10.1016/j.clinph.2021.05.012 · DOI
- Dauwels, 2010, Diagnosis of Alzheimer’s disease from EEG signals using graph-theoretic features, Ann. Biomed. Eng., 38, 2974
- Sakkalis, 2011, Review of advanced techniques for the estimation of brain connectivity measured with EEG/MEG, Comput. Biol. Med., 41, 1110, 10.1016/j.compbiomed.2011.06.020 · DOI · Paper page
- Babiloni, 2010, Reactivity of cortical alpha rhythms to eye opening in mild cognitive impairment and Alzheimer’s disease: An EEG study, J. Alzheimer’s Dis., 22, 1047, 10.3233/JAD-2010-100798 · DOI
- Yuan, Y., and Zhao, Y. (2025). The role of quantitative EEG biomarkers in Alzheimer’s disease and mild cognitive impairment: Applications and insights. Front. Aging Neurosci., 17. · DOI
- Ahmadlou, 2011, Fractality and a wavelet-chaos-methodology for EEG-based diagnosis of Alzheimer disease, Alzheimer Dis. Assoc. Disord., 25, 85, 10.1097/WAD.0b013e3181ed1160 · DOI
- Bugdol, 2024, Quantitative EEG Spectral and Connectivity Analysis for Cognitive Decline in Amnestic Mild Cognitive Impairment, J. Alzheimer’s Dis., 97, 1235, 10.3233/JAD-230485 · DOI
- Knyazeva, 2013, Evolution of source EEG synchronization in early Alzheimer’s disease, Neurobiol. Aging, 34, 694, 10.1016/j.neurobiolaging.2012.07.012 · DOI
- Simfukwe, 2023, qEEG as Biomarker for Alzheimer’s Disease: Investigating Relative PSD Difference and Coherence Analysis, Neuropsychiatr Dis. Treat., 19, 2423, 10.2147/NDT.S433207 · DOI
- Baik, K., Jung, J.H., Jeong, S.H., Chung, S.J., Yoo, H.S., Lee, P.H., Sohn, Y.H., Kang, S.W., and Ye, B.S. (2022). Implication of EEG theta/alpha and theta/beta ratio in Alzheimer’s and Lewy body disease. Sci. Rep., 12. · DOI
- Yeo, 2011, The organization of the human cerebral cortex estimated by intrinsic functional connectivity, J. Neurophysiol., 106, 1125, 10.1152/jn.00338.2011 · DOI · Paper page
- Blinowska, 2017, Functional and effective brain connectivity for discrimination between Alzheimer’s patients and healthy individuals: A study on resting state EEG rhythms, Clin. Neurophysiol., 128, 667, 10.1016/j.clinph.2016.10.002 · DOI
- Babiloni, 2021, Measures of resting state EEG rhythms for clinical trials in Alzheimer’s disease: Recommendations of an expert panel, Alzheimers Dement., 17, 1528, 10.1002/alz.12311 · DOI
- 2018, Multimodal Neuroimaging in Alzheimer’s Disease: Early Diagnosis, Physiopathological Mechanisms, and Impact of Lifestyle, J. Alzheimer’s Dis., 64, S199, 10.3233/JAD-179920 · DOI
- Saleem, T.J., Zahra, S.R., Wu, F., Alwakeel, A., Alwakeel, M., Jeribi, F., and Hijji, M. (2022). Deep Learning-Based Diagnosis of Alzheimer’s Disease. J. Pers. Med., 12. · DOI
- Al-Nuaimi, A.H., Blūma, M., Al-Juboori, S.S., Eke, C.S., Jammeh, E., Sun, L., and Ifeachor, E. (2021). Robust EEG Based Biomarkers to Detect Alzheimer’s Disease. Brain Sci., 11. · DOI
- Malik, I., Iqbal, A., Gu, Y.H., and Al-antari, M.A. (2024). Deep Learning for Alzheimer’s Disease Prediction: A Comprehensive Review. Diagnostics, 14. · DOI
- Bairagi, 2018, EEG signal analysis for early diagnosis of alzheimer disease using spectral and wavelet based features, Int. J. Inf. Technol., 10, 403
- Basaia, 2019, Automated classification of Alzheimer’s disease and mild cognitive impairment using a single MRI and deep neural networks, NeuroImage Clin., 21, 101645, 10.1016/j.nicl.2018.101645 · DOI · Paper page
- Nayana, B.R., Pavithra, M.N., Chaitra, S., Bhuvana Mohini, T.N., Stephan, T., Mohan, V., and Agarwal, N. (2025). EEG-based neurodegenerative disease diagnosis: Comparative analysis of conventional methods and deep learning models. Sci. Rep., 15. · DOI
- Lee, M.W., Kim, H.W., Choe, Y.S., Yang, H.S., Lee, J., Lee, H., Yong, J.H., Kim, D., Lee, M., and Kang, D.W. (2024). A multimodal machine learning model for predicting dementia conversion in Alzheimer’s disease. Sci. Rep., 14. · DOI
- Ganapathi, 2022, Differentiation of Subjective Cognitive Decline, Mild Cognitive Impairment, and Dementia Using qEEG/ERP-Based Cognitive Testing and Volumetric MRI in an Outpatient Specialty Memory Clinic, J. Alzheimer’s Dis., 90, 1761, 10.3233/JAD-220616 · DOI
- Aviles, 2024, Machine and Deep Learning Trends in EEG-Based Detection and Diagnosis of Alzheimer’s Disease: A Systematic Review, Eng, 5, 1464, 10.3390/eng5030078 · DOI
- Wang, 2021, Multi-modal neuroimaging and EEG biomarkers for early Alzheimer’s diagnosis: Progress and perspectives, J. Neuroimaging, 31, 626
- Briels, 2020, Reproducibility of EEG functional connectivity in Alzheimer’s disease, Alzheimer’s Res. Ther., 12, 68, 10.1186/s13195-020-00632-3 · DOI
- Schmidt, M.T., Kanda, P.A.M., Basile, L.F.H., da Silva Lopes, H.F., Baratho, R., Demario, J.L.C., Jorge, M.S., Nardi, A.E., Machado, S., and Ianof, J.N. (2013). Index of alpha/theta ratio of the electroencephalogram: A new marker for Alzheimer’s disease. Front. Aging Neurosci., 5. · DOI
- Siuly, 2020, A new framework for automatic detection of patients with mild cognitive impairment using resting-state EEG signals, IEEE Trans. Neural Syst. Rehabil. Eng., 28, 1966, 10.1109/TNSRE.2020.3013429 · DOI
- Babiloni, 2018, Abnormalities of resting state cortical EEG rhythms in subjects with mild cognitive impairment due to alzheimer’s and lewy body diseases, J. Alzheimer’s Dis., 62, 247, 10.3233/JAD-170703 · DOI
- Dottori, M., Sedeño, L., Caro, M.M., Alifano, F., Hesse, E., Mikulan, E., García, A.M., Ruiz-Tagle, A., Lillo, P., and Slachevsky, A. (2017). Towards affordable biomarkers of frontotemporal dementia: A classification study via network’s information sharing. Sci. Rep., 7. · DOI · Paper page
- Ieracitano, 2019, A convolutional neural network approach for classification of dementia stages based on 2D-spectral representation of EEG recordings, Neurocomputing, 323, 96, 10.1016/j.neucom.2018.09.071 · DOI
- Klepl, 2022, EEG-based graph neural network classification of Alzheimer’s disease: An empirical evaluation of functional connectivity methods, IEEE Trans. Neural Syst. Rehabil. Eng., 30, 2651, 10.1109/TNSRE.2022.3204913 · DOI
- Gkenios, G., Latsiou, K., Diamantaras, K., Chouvarda, I., and Tsolaki, M. (2022, January 11–15). Diagnosis of Alzheimer’s disease and mild cognitive impairment using EEG and recurrent neural networks. Proceedings of the 2022 44th Annual International Conference of the IEEE Engineering in Medicine & Biology Society (EMBC), Glasgow, UK. · DOI
- Klepl, 2023, Adaptive gated graph convolutional network for explainable diagnosis of Alzheimer’s disease using EEG data, IEEE Trans. Neural Syst. Rehabil. Eng., 31, 3978, 10.1109/TNSRE.2023.3321634 · DOI
- Jiao, 2023, Neural biomarker diagnosis and prediction to mild cognitive impairment and Alzheimer’s disease using EEG technology, Alzheimer’s Res. Ther., 15, 32, 10.1186/s13195-023-01181-1 · DOI
- Hasan Saif, F., Al-Andoli, M.N., and Bejuri, W.M.Y.W. (2024). Explainable AI for Alzheimer Detection: A Review of Current Methods and Applications. Appl. Sci., 14. · DOI
- Ehteshamzad, 2024, Assessing the Potential of EEG in Early Detection of Alzheimer’s Disease: A Systematic Comprehensive Review (2000–2023), J. Alzheimer’s Dis. Rep., 8, 1153, 10.3233/ADR-230159 · DOI
- Akbar, 2025, Unlocking the potential of EEG in Alzheimer’s disease research: Current status and pathways to precision detection, Brain Res. Bull., 223, 111281, 10.1016/j.brainresbull.2025.111281 · DOI
- Zhang, T. (2022). Efficient deep learning approaches for EEG-based early Alzheimer’s detection: A review of recent progress. Front. Aging Neurosci., 14.
- Arya, 2023, A systematic review on machine learning and deep learning techniques in the effective diagnosis of Alzheimer’s disease, Brain Inform., 10, 17, 10.1186/s40708-023-00195-7 · DOI
- Del Percio, C., Lizio, R., Lopez, S., Noce, G., Carpi, M., Jakhar, D., Soricelli, A., Salvatore, M., Yener, G., and Güntekin, B. (2025). Resting-State EEG Alpha Rhythms Are Related to CSF Tau Biomarkers in Prodromal Alzheimer’s Disease. Int. J. Mol. Sci., 26. · DOI
- Jiang, X., Bian, G.-B., and Tian, Z. (2019). Removal of Artifacts from EEG Signals: A Review. Sensors, 19. · DOI
- Mostile, G., Terranova, R., Carlentini, G., Contrafatto, F., Terravecchia, C., Donzuso, G., Sciacca, G., Cicero, C.E., Luca, A., and Nicoletti, A. (2024). Differentiating neurodegenerative diseases based on EEG complexity. Sci. Rep., 14. · DOI
- Prichep, 2005, Use of normative databases and statistical methods in demonstrating clinical utility of QEEG: Importance and cautions, Clin. EEG Neurosci., 36, 82, 10.1177/155005940503600207 · DOI
Cited by
Dang, M., Liu, B., Chen, Y., & Zhang, Z. (2026) · Psychoradiology · doi:10.1093/psyrad/kkag007 · Cited by 10
Heterogeneous whole-brain neural network constructed by SW-SW architecture and PLV matrix
Ma, M.-L., Yuan, Z.-Y., & Zhao, X. (2026) · Nonlinear dynamics · doi:10.1007/s11071-025-12152-6 · Cited by 6
“Papaliagkas et al. also pointed out that as synaptic density decreases, phase synchronization indicators, such as PLV in the alpha band, decrease significantly, which can serve as an electrophysiological marker of network degradation [48].”
EEG spectral power differences in Alzheimer’s disease and frontotemporal dementia
Pan, Y., Zhu, L., & Wang, Z.-L. (2025) · International Journal of Neuroscience · doi:10.1080/00207454.2025.2591129 · Cited by 3
“Distinct electrophysiological signatures were observed: aD patients showed the classic ‘eeG slowing,’ characterized by posterior alpha reduction and frontal theta enhancement, consistent with thalamocortical dysregulation and impaired neural synchronization [15,21,22].”
Benussi, A., Cantoni, V., Palacino, F., Altomare, D., Moretti, D. V., Manganotti, P., & Borroni, B. (2026) · Alzheimer's & Dementia · doi:10.1002/dad2.70275 · Cited by 2
“17 23 The posterior topography of alpha and beta attenuation mirrors patterns of hypometabolism and atrophy on FDG-PET and MRI and provides an electrophysiological correlate of episodic memory and visuospatial deficits.”
Guyo, G. A., Trofimov, A. O., Volkova, E., Pavlova, O. N., Павлов, А. Н., & Semyachkina-Glushkovskaya, O. V. (2025) · Chaos An Interdisciplinary Journal of Nonlinear Science · doi:10.1063/5.0301587 · Cited by 2
Metadata
- Authors
- Papaliagkas, V.
- Affiliations
- International Hellenic University (GR)
- Corresponding author
- Papaliagkas, Vasileios
- Venue
- Diagnostics
- Publisher
- MDPI AG
- Published
- 2025-08-05
- Volume
- 15
- Issue
- 15
- Pages
- 1965
- ISSN
- 2075-4418 (ISSN-L)
- PMC
- PMC12346855
- OpenAlex
- W4412974787
- Cited by
- 14
- References
- 64
- Citations by year
- 2026: 9 · 2025: 5
- FWCI
- 2.50
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- Locations
- Diagnostics (publishedVersion, cc-by)
- Europe PMC (PubMed Central) (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Topics
- Health Sciences › Medicine › Psychiatry and Mental health › Dementia and Cognitive Impairment Research
- Life Sciences › Neuroscience › Cognitive Neuroscience › EEG and Brain-Computer Interfaces
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Alzheimer's disease research and treatments
- Keywords
- Alzheimer's disease, quantitative EEG, EEG biomarkers, spectral analysis, EEG connectivity, non-invasive diagnosis, neurodegeneration, machine learning, diagnostic accuracy
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![Figure 1 Power Spectral Density Map for (a) AD patients and (b) Controls. Figure adapted by Simfukwe C et al. [32], CC License 3.0.](/paper-figures/3f50991cfcba43f8aec5bbbdeabfb399/the-role-of-quantitative-eeg-in-the-diagnosis-of-alzheimers-disease-figure-1.jpg)