مقایسه طیف توان برگرفته از الکتروآنسفالوگرافی در حالت استراحت (چشم بسته) و توان برگرفته از پتانسیل وابسته به رویداد در بیماران افسرده و افراد سالم

نویسندگان
1 دانشگاه تهران
2 دانشگاه تربیت مدرس
چکیده
افسردگی شایعترین اختلال روانی است و باعث اختلال در روند زندگی بیمار و تحمیل هزینه بر جامعه می‌شود. اخیرا استفاده از زیست‌نشانگر‌ها در تشخیص و بررسی روند درمان در اختلالات روانی مورد توجه قرار گرفته‌است. یکی از این زیست‌نشانگر‌ها، توان برگرفته از الکتروآنسفالوگرافی برای تفکیک بیماران افسرده از سالم هستند. هدف این پژوهش، مقایسه توان در باندهای فرکانسی مختلف در افراد افسرده و سالم است. شرکت‌کنندگان این پژوهش علی-مقایسه‌ای با استفاده از ملاک‌های بالینی بر مبنای راهنمای تشخیصی و آماری اختلالات روانی (DSM-5) در کلینیک آتیه در سال97-1396 انتخاب شدند (۲۹ زن و ۲۱ مرد افسرده؛ ۱۹ زن و ۳۱ مرد سالم). الکتروآنسفالوگرام با استفاده از سیستم ۱۰-۲۰، در ۱۹ کانال و پنج باند فرکانسی (دلتا، تتا، آلفا، بتا و گاما) در دو حالت استراحت (چشم بسته) و فعالیت (حین انجام تکلیف عملکرد پیوسته هیجانی) ثبت شد. نتایج نشان داد که در حالت استراحت، میانگین توان، تنها در باند گاما (Fz, Cz) ، به شکلی معنی‌دار در گروه افسرده بالاتر بود (p<.05). همچنین در حالت فعالیت در باند تتا (P8، O1 و O2)، آلفا (P4، P8 و O1)، بتا (Fp1، P3، Pz و P4) و گاما (Fp1، Fp2، Fz و O1) تفاوت معناداری مشاهده‌شد و میانگین توان در گروه افسرده بالاتر بود .(p<.05) به نظر می‌رسد توان در حالت فعالیت توانایی تمیز بیشتری از توان در حالت استراحت دارد و بالقوه می‌توان از آن به عنوان زیست‌نشانگر در تشخیص افسردگی استفاده کرد.
کلیدواژه‌ها

عنوان مقاله English

A Comparison between Spectral Power of Electroencephalogram at Rest (Eyes Closed) and Evoked Related Potential among Depressed and Healthy Individuals

نویسندگان English

Seid Nezamoddin Rostamkalaee 1
Reza Rostami 1
Abbas Rahiminezhad 1
Hojjatollah Farahani 2
2 Tarbiat Modares University
چکیده English

Depression is the most common mental disorder that disrupts patients’ lives and imposes costs on society. Recently, the use of biomarkers in the diagnosis and treatment of psychiatric disorders has been considered. The question is whether biomarkers derived from EEG are capable of separating depressed patients from healthy people. The objective of this study was to compare the power of different frequency bands in depressed and healthy individuals. The participants of this non-experimental study were selected using clinical criteria based on DSM-5 at Atieh Clinic in Tehran in 2016-2017 (29 women and 21 men who were depressed and 19 women and 31 men who were healthy). EEG was recorded in 19 channels and five frequency bands (delta, theta, alpha, beta and gamma) at rest (eyes closed) and during the Emtional Contineous Performance Task (ECPT). The results showed that at rest, the mean power was significantly higher in the depressed group only in the gamma band (Fz and Cz). Significant differences were also observed in theta (P8, O1 and O2), alpha (P4, P8 and O1), beta (Fp1, P3, Pz, and P4) and gamma (Fp1, Fp2, Fz and O1) during activity. Furthermore, mean powers in the depressed group were higher. It seems that EEG power during activity is a better discriminator than power in resting state and it could potentially be used as a biomarker for the diagnosis of depression.


کلیدواژه‌ها English

depression
Power
EEG
ERP
Biomarker
Alhaj, H., Wisniewski, G., & Mcallister-Williams, R. H. (2010). The use of the EEG in measuring therapeutic drug action: focus on depression and antidepressants. Journal of Psychopharmacology, 25(9), 1175–1191. doi: 10.1177/0269881110388323.
Baskaran, A., Milev, R., & Mcintyre, R. S. (2012). The neurobiology of the EEG biomarker as a predictor of treatment response in depression. Neuropharmacology, 63(4), 507–513. doi: 10.1016/j.neuropharm.2012.04.021.
Biomarkers and surrogate endpoints: Preferred definitions and conceptual framework. (2001). Clinical Pharmacology & Therapeutics, 69(3), 89–95. doi: 10.1067/mcp.2001.113989.
Brunner, J. F., Hansen, T. I., Olsen, A., Skandsen, T., Håberg, A., & Kropotov, J. (2013). Long-term test-retest reliability of the P3 NoGo wave and two independent components decomposed from the P3 NoGo wave in a visual Go/NoGo task. International Journal of Psychophysiology, 89(1), 106–114. doi: 10.1016/j.ijpsycho.2013.06.005.
Cai, H., Sha, X., Han, X., Wei, S., & Hu, B. (2016). Pervasive EEG diagnosis of depression using Deep Belief Network with three-electrodes EEG collector. 2016 IEEE International Conference on Bioinformatics and Biomedicine (BIBM). doi: 10.1109/bibm.2016.7822696.
Castrén, E., & Rantamäki, T. (2010). The role of BDNF and its receptors in depression and antidepressant drug action: Reactivation of developmental plasticity. Developmental Neurobiology, 70(5), 289–297. doi: 10.1002/dneu.20758.
Chapotot, F. (1998). Cortisol Secretion Is Related to Electroencephalographic Alertness in Human Subjects during Daytime Wakefulness. Journal of Clinical Endocrinology & Metabolism, 83(12), 4263–4268. doi: 10.1210/jc.83.12.4263.
Das, J., & Yadav, S. (2020). Resting state quantitative electroencephalogram power spectra in patients with depressive disorder as compared to normal controls: An observational study. Indian Journal of Psychological Medicine, 42(1), 30. doi: 10.4103/ijpsym.ijpsym_568_17.
Diagnostic and statistical manual of mental disorders: DSM-5. (2013). Arlington, VA: American Psychiatric Association.
Dolsen, M. R., Cheng, P., Arnedt, J. T., Swanson, L., Casement, M. D., Kim, H. S., … Deldin, P. J. (2017). Neurophysiological correlates of suicidal ideation in major depressive disorder: Hyperarousal during sleep. Journal of Affective Disorders, 212, 160–166. doi: 10.1016/j.jad.2017.01.025.
Fitzgerald, P. J., & Watson, B. O. (2018). Gamma oscillations as a biomarker for major depression: an emerging topic. Translational Psychiatry, 8(1). doi: 10.1038/s41398-018-0239-y.
Freeman, W. J., & Quiroga, R. Q. (2013). Imaging brain function with Eeg: advanced temporal and spatial analysis of electroencephalographic signals. New York, N.Y.: Springer.
Gennaro, L. D., Marzano, C., Fratello, F., Moroni, F., Pellicciari, M. C., Ferlazzo, F., … Rossini, P. M. (2008). The electroencephalographic fingerprint of sleep is genetically determined: A twin study. Annals of Neurology, 64(4), 455–460. doi: 10.1002/ana.21434.
Grin-Yatsenko, V. A., Baas, I., Ponomarev, V. A., & Kropotov, J. D. (2010). Independent component approach to the analysis of EEG recordings at early stages of depressive disorders. Clinical Neurophysiology, 121(3), 281–289. doi: 10.1016/j.clinph.2009.11.015.
Hosseinifard, B., Moradi, M. H., & Rostami, R. (2013). Classifying depression patients and normal subjects using machine learning techniques and nonlinear features from EEG signal. Computer Methods and Programs in Biomedicine, 109(3), 339–345. doi: 10.1016/j.cmpb.2012.10.008.
Iversen, L. (n.d.). The Monoamine Hypothesis of Depression. Biology of Depression, 71–86. doi: 10.1002/9783527619672.ch5.
Jaworska, N., Blier, P., Fusee, W., & Knott, V. (2012). Alpha power, alpha asymmetry and anterior cingulate cortex activity in depressed males and females. Journal of Psychiatric Research, 46(11), 1483–1491. doi: 10.1016/j.jpsychires.2012.08.003.
Jaworska, N., & Protzner, A. (2013). Electrocortical Features of Depression and Their Clinical Utility in Assessing Antidepressant Treatment Outcome. The Canadian Journal of Psychiatry, 58(9), 509–514. doi: 10.1177/070674371305800905.
Jentsch, M. C., Buel, E. M. V., Bosker, F. J., Gladkevich, A. V., Klein, H. C., Voshaar, R. C. O., … Schoevers, R. A. (2015). Biomarker approaches in major depressive disorder evaluated in the context of current hypotheses. Biomarkers in Medicine, 9(3), 277–297. doi: 10.2217/bmm.14.114.
Kalev, K., & Bachmann, M. (2015). Selection of EEG Frequency Bands for Detection of Depression. IFMBE Proceedings 16th Nordic-Baltic Conference on Biomedical Engineering, 55–58. doi: 10.1007/978-3-319-12967-9_15.
Koo, P. C., Berger, C., Kronenberg, G., Bartz, J., Wybitul, P., Reis, O., & Hoeppner, J. (2018). Combined cognitive, psychomotor and electrophysiological biomarkers in major depressive disorder. European Archives of Psychiatry and Clinical Neuroscience, 269(7), 823–832. doi: 10.1007/s00406-018-0952-9.
Kropotov, J. D. (2016). Functional neuromarkers for psychiatry: applications for diagnosis and treatment. Amsterdam: Elsevier/Academic Press.
Laufs, H., Kleinschmidt, A., Beyerle, A., Eger, E., Salek-Haddadi, A., Preibisch, C., & Krakow, K. (2003). EEG-correlated fMRI of human alpha activity. NeuroImage, 19(4), 1463–1476. doi: 10.1016/s1053-8119(03)00286-6.
Li, Q., Zhao, Y., Chen, Z., Long, J., Dai, J., Huang, X., … Gong, Q. (2019). Correction: Meta-analysis of cortical thickness abnormalities in medication-free patients with major depressive disorder. Neuropsychopharmacology. doi: 10.1038/s41386-019-0587-1.
Liu, M., Zhou, L., Wang, X., Jiang, Y., & Liu, Q. (2017). Deficient manipulation of working memory in remitted depressed individuals: Behavioral and electrophysiological evidence. Clinical Neurophysiology, 128(7), 1206–1213. doi: 10.1016/j.clinph.2017.04.011.
Mahato, S., & Paul, S. (2018). Electroencephalogram (EEG) Signal Analysis for Diagnosis of Major Depressive Disorder (MDD): A Review. Nanoelectronics, Circuits and Communication Systems Lecture Notes in Electrical Engineering, 323–335. doi: 10.1007/978-981-13-0776-8_30.
Mantri, S., Patil, D., Agrawal, P., & Wadhai, V. (2015). Non invasive EEG signal processing framework for real time depression analysis. 2015 SAI Intelligent Systems Conference (IntelliSys). doi: 10.1109/intellisys.2015.7361188.
Mohammadi, M., Al-Azab, F., Raahemi, B., Richards, G., Jaworska, N., Smith, D., … Knott, V. (2015). Data mining EEG signals in depression for their diagnostic value. BMC Medical Informatics and Decision Making, 15(1). doi: 10.1186/s12911-015-0227-6.
Neto, F. S., & Rosa, J. L. (2019). Depression biomarkers using non-invasive EEG: A review. Neuroscience & Biobehavioral Reviews,105, 83-93. doi: 10.1016/j.neubiorev.2019.07.021.
Neuner, I., Arrubla, J., Werner, C. J., Hitz, K., Boers, F., Kawohl, W., & Shah, N. J. (2014). The Default Mode Network and EEG Regional Spectral Power: A Simultaneous fMRI-EEG Study. PLoS ONE, 9(2). doi: 10.1371/journal.pone.0088214.
Nolan, B. (2009). The Electroencephalographic Fingerprint of Sleep Is Genetically Determined: A Twin Study. Yearbook of Neurology and Neurosurgery, 2009, 175–176. doi: 10.1016/s0513-5117(09)79238-5.
Olbrich, S., & Arns, M. (2013). EEG biomarkers in major depressive disorder: Discriminative power and prediction of treatment response. International Review of Psychiatry, 25(5), 604–618. doi: 10.3109/09540261.2013.816269.
Palazidou, E. (2012). The neurobiology of depression. British Medical Bulletin, 101(1), 127–145. doi: 10.1093/bmb/lds004.
Pizzagalli, D. A., Oakes, T. R., & Davidson, R. J. (2003). Coupling of theta activity and glucose metabolism in the human rostral anterior cingulate cortex: An EEG/PET study of normal and depressed subjects. Psychophysiology, 40(6), 939–949. doi: 10.1111/1469-8986.00112.
Pizzagalli, D. A. (2010). Frontocingulate Dysfunction in Depression: Toward Biomarkers of Treatment Response. Neuropsychopharmacology, 36 (1), 183–206. doi: 10.1038/npp.2010.166.
Pizzagalli, D. A., Webb, C. A., Dillon, D. G., Tenke, C. E., Kayser, J., Goer, F., … Trivedi, M. H. (2018). Pretreatment Rostral Anterior Cingulate Cortex Theta Activity in Relation to Symptom Improvement in Depression. JAMA Psychiatry, 75(6), 547. doi: 10.1001/jamapsychiatry.2018.0252.
Price, G., Lee, J., Garvey, C., & Gibson, N. (2008). Appraisal of Sessional EEG Features as a Correlate of Clinical Changes in an rTMS Treatment of Depression. Clinical EEG and Neuroscience, 39(3), 131–138. doi: 10.1177/155005940803900307.
Rao, R. P. N. (2019). Brain-computer interfacing: an introduction. Cambridge, United Kingdom: Cambridge University Press.
Ricardo-Garcell, J. (2008). EEG sources in major depressive disorder. Clinical Neurophysiology, 119. doi: 10.1016/s1388-2457(08)60546-5.
Sadock, B. J., Sadock, V. A., & Ruiz, P. (2017). Kaplan & Sadocks comprehensive textbook of psychiatry. Philadelphia: Wolters Kluwer.
Saletu, B., Anderer, P., & Saletu-Zyhlarz, G. (2010). EEG Topography and Tomography (LORETA) in Diagnosis and Pharmacotherapy of Depression. Clinical EEG and Neuroscience, 41(4), 203–210. doi: 10.1177/155005941004100407.
Schiller, M. J. (2019). Quantitative Electroencephalography in Guiding Treatment of Major Depression. Frontiers in Psychiatry, 9. doi: 10.3389/fpsyt.2018.00779.
Shen, J., Zhao, S., Yao, Y., Wang, Y., & Feng, L. (2017). A novel depression detection method based on pervasive EEG and EEG splitting criterion. 2017 IEEE International Conference on Bioinformatics and Biomedicine (BIBM). doi: 10.1109/bibm.2017.8217946.
Vinne, N. V. D., Vollebregt, M. A., Putten, M. J. V., & Arns, M. (2017). Frontal alpha asymmetry as a diagnostic marker in depression: Fact or fiction? A meta-analysis. NeuroImage: Clinical, 16, 79–87. doi: 10.1016/j.nicl.2017.07.006.
Wolff, A., Salle, S. D. L., Sorgini, A., Lynn, E., Blier, P., Knott, V., & Northoff, G. (2019). Atypical Temporal Dynamics of Resting State Shapes Stimulus-Evoked Activity in Depression—An EEG Study on Rest–Stimulus Interaction. Frontiers in Psychiatry, 10. doi: 10.3389/fpsyt.2019.00719.
Zhang, F.-F., Peng, W., Sweeney, J. A., Jia, Z.-Y., & Gong, Q.-Y. (2018). Brain structure alterations in depression: Psychoradiological evidence. CNS Neuroscience & Therapeutics, 24(11), 994–1003. doi: 10.1111/cns.12835.