Abstract
Methamphetamine addiction is a brain disease that causes abnormalities in the structure and function of the brain. EEG, a common signal acquired based on the noninvasive brain-computer interface, can reflect the altered brain activity associated with methamphetamine addiction. EEG-based analysis methods provide a perspective to explore the neural mechanisms of methamphetamine addiction and the effects on brain activity. This paper reports the results of a review of EEG-based assessment and classification of methamphetamine addiction. Current methods commonly used in EEG-based methamphetamine addiction research include traditional resting-state EEG analysis, brain network analysis, and analysis of event-related potentials. A small number of studies have classified methamphetamine addiction and healthy individuals based on resting state EEG features or event-related potentials. EEG is one of the common tools used to examine the effects of methamphetamine on brain function. In follow-up studies, new methods for analyzing resting-state EEG and event-related potentials may help to investigate the neural mechanisms of methamphetamine addiction.
Similar content being viewed by others
Data Availability
Not applicable.
Code Availability
Not applicable.
References
Leshner AI. Addiction is a brain disease, and it matters. Science. 1997;278(5335):45–7.
Lindsey KP, Gatley SJ, Volkow ND. Neuroimaging in drug abuse. Curr Psychiatry Rep. 2003;5(5):355–61.
American Psychiatric Association. Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition, Text Revision. Washington, DC: American Psychiatric Association; 2022.
Rawson RA, Condon TP. Why do we need an Addiction supplement focused on methamphetamine? Addiction. 2007;1:1–4.
Sabrini S, Wang GY, Lin JC, Ian JK, Curley LE. Methamphetamine use and cognitive function: a systematic review of neuroimaging research. Drug Alcohol Depend. 2019;194:75–87.
Baker A, et al. Brief cognitive behavioural interventions for regular amphetamine users: a step in the right direction. Addiction. 2005;100(3):367–78.
Elkashef A, Vocci F, Hanson G, White J, Wickes W, Tiihonen J. Pharmacotherapy of methamphetamine addiction: an update. Subst Abus. 2008;29(3):31–49.
Rawson RA, Marinelli-Casey P, Anglin MD, Dickow A, et al. Amulti-site comparison of psychosocial approaches for the treatment ofmethamphetamine dependence. Addiction. 2004;99:708–17.
Shoptaw S, et al. Randomized, placebo-controlled trial of bupropion for the treatment of methamphetamine dependence. Drug Alcohol Depend. 2008;96(3):222–32.
Zorick T, Sugar CA, Hellemann G, Shoptaw S, London ED. Poor response to sertraline in methamphetamine dependence is associated with sustained craving for methamphetamine. Drug Alcohol Depend. 2011;118(2–3):500–3.
Darke S, Darke S, Kaye S, Darke S, et al. Major physical andpsychological harms of methamphetamine use. Drug and Alcohol Review. 2008;27(3):253–62.
Kaye S, McKetin R, Duflou J, Darke S. Methamphetamine and cardiovascular pathology: a review of the evidence. Addiction. 2007;102(8):1204–11.
Yeo KK, et al. The association of methamphetamine use and cardiomyopathy in young patients. Am J Med. 2007;120(2):165–71.
Varner KJ, Ogden BA, Delcarpio J, Meleg-Smith S. Cardiovascular responses elicited by the “binge” administration of methamphetamine. J Pharmacol Exp Ther. 2002;301(1):152–9.
Wijetunga M, Seto T, Lindsay J, Schatz I. Crystal methamphetamine〢associated cardiomyopathy: tip of the iceberg? Clin Toxicol. 2003;41(7):981–6.
McKetin R, Lubman DI, Najman JM, Dawe S, Butterworth P, Baker AL. Does methamphetamine use increase violent behaviour? Evidence from a prospective longitudinal study. Addiction. 2014;109(5):798–806.
Ernst T, Chang L, Leonido-Yee M, Speck O. Evidence for long-term neurotoxicity associated with methamphetamine abuse: a 1H MRS study. Neurology. 2000;54(6):1344–9.
Lineberry TW, Bostwick JM. Methamphetamine Abuse: A Perfect Stormof Complications. Mayo Clinic Proceedings. 2006;81(1):77–84.
Mohamad B, Sangchooli A, Ebrahimpoor M, Najafi M, et al. Temporal dynamics of the neural response to drug cues: an fMRI study among methamphetamine users. Basic Clin Neurosci. 2021;1–31.
Nestor LJ, Ghahremani DG, Monterosso J, London ED. Prefrontal hypoactivation during cognitive control in early abstinent methamphetamine-dependent subjects. Psychiatry Res. 2011;194(3):287–95.
Chang L, Alicata D, Ernst T, Volkow N. Structural and metabolic brain changes in the striatum associated with methamphetamine abuse. Addiction. 2007;102(Suppl 1):16–32.
Cho AK, Melega WP. Patterns of methamphetamine abuse and their consequences. J Addict Dis. 2001;21(1):21–34.
Anderson AJ, Perone S. Developmental change in the resting state electroencephalogram: Insights into cognition and the brain. Brain Cogn. 2018;126:40–52.
Babiloni C, et al. Brain neural synchronization and functional coupling in Alzheimer’s disease as revealed by resting state EEG rhythms. Int J Psychophysiol. 2016;103:88–102.
Newton TF, et al. Quantitative EEG abnormalities in recently abstinent methamphetamine dependent individuals. Clin Neurophysiol. 2003;114(3):410–5.
Newton TF, Kalechstein AD, Hardy DJ, Cook IA, et al. Association betweenquantitative EEG and neurocognition in methamphetamine-dependent volunteers. Clin Neurophysiol. 2004;115(1):194–8.
Kalechstein AD, De la Garza R, Newton TF, Green MF, Cook IA, Leuchter AF. Quantitative EEG abnormalities are associated with memory impairment in recently abstinent methamphetamine-dependent individuals. J Neuropsych Clin Neurosci. 2009;21(3):254–8.
Zhao D, et al. Neurophysiological correlate of incubation of craving in individuals with methamphetamine use disorder. Mol Psychiatry. 2021;26(11):6198–208.
Sabesan S, Narayanan K, Prasad A, Iasemidis LD, et al. Information Flow in Coupled Nonlinear Systems: Application to the Epileptic Human Brain. In: Pardalos PM, Boginski VL, Vazacopoulos A, editors. Data Mining in Biomedicine. (Springer US); 2007. p. 483–503.
Yun K, Park HK, Kwon DH, Cho SN, Jeong J. Decreased complexity of the EEG in patients with methamphetamine dependence. World Cong Med Phys Biomed Eng. 2006;14(1–6):997.
Yun K, et al. Decreased cortical complexity in methamphetamine abusers. Psychiatry Res. 2012;201(3):226–32.
Ahmadlou M, Ahmadi K, Rezazade M, Azad-Marzabadi E. Global organization of functional brain connectivity in methamphetamine abusers. Clin Neurophysiol. 2013;124(6):1122–31.
Khajehpour H, et al. Computer-aided classifying and characterizing of methamphetamine use disorder using resting-state EEG. Cogn Neurodyn. 2019;13(6):519–30.
Khajehpour H, Makkiabadi B, Ekhtiari H, Bakht S, et al. Disrupted resting-state brainfunctional network in methamphetamine abusers: A brain source space study by EEG. PLOS ONE. 2019;14(12):e0226249.
Chen T, et al. Disrupted brain network dynamics and cognitive functions in methamphetamine use disorder: insights from EEG microstates. BMC Psychiatry. 2020;20(1):334.
Shafiee-Kandjani AR, Jahan A, Moghadam-Salimi M, Fakhari A, et al. Resting-state electroencephalographic coherence in recently abstinent methamphetamine users. Int J High Risk Behav Addict. 2020;9(4):1–6.
Minnerly C, Shokry IM, To W, Callanan JJ, Tao R. Characteristic changes in EEG spectral powers of patients with opioid-use disorder as compared with those with methamphetamine- and alcohol-use disorders. PLoS ONE. 2021;16(9):e0248794.
Chen CC, et al. Neuronal abnormalities induced by an intelligent virtual reality system for methamphetamine use disorder. IEEE J Biomed Health Inform. 2022;26(7):3458–65.
Khajehpour H, et al. Effects of transcranial direct current stimulation on attentional bias to methamphetamine cues and its association with EEG-derived functional brain network topology. Int J Neuropsychopharmacol. 2022;25(8):631–44.
Lin Q, Li D, Hu C, Shen Z, Wang Y. Altered EEG microstates dynamics during cue-induced methamphetamine craving in virtual reality environments. Front Psychiatry. 2022;13:891719.
Wang D, Zhou C, Chang YK. Acute exercise ameliorates craving and inhibitory deficits in methamphetamine: An ERP study. Physiol Behav. 2015;147:38–46.
Haifeng J, et al. P300 event-related potential in abstinent methamphetamine-dependent patients. Physiol Behav. 2015;149:142–8.
Wang D, Zhou C, Zhao M, Wu X, Chang YK. Dose-response relationships between exercise intensity, cravings, and inhibitory control in methamphetamine dependence: an ERPs study. Drug Alcohol Depend. 2016;161:331–9.
Wang DS, Zhu T, Zhou CL, Chang YK. Aerobic exercise training ameliorates craving and inhibitory control in methamphetamine dependencies: a randomized controlled trial and event-related potential study. Psychol Sport Exerc. 2017;30:82–90.
Wei S, et al. Enhanced neural responses to monetary rewards in methamphetamine use disordered individuals compared to healthy controls. Physiol Behav. 2018;195:118–27.
Stock A-K, Rädle M, Beste C. Methamphetamine-associateddifficulties in cognitive control allocation may normalize after prolongedabstinence. Progress in Neuro-Psychopharmacology and Biological Psychiatry. 2019;88:41–52.
Xiong Y, Gao J, Zhang J. Detection methamphetamine patients using ERP features. In: 2019 6th International Conference on Information Science and Control Engineering (ICISCE). Shanghai, China; 2019. p. 259–62.
Zhong N, et al. Smaller Feedback-related negativity (FRN) reflects the risky decision-making deficits of methamphetamine dependent individuals. Front Psychiatry. 2020;11:320.
Chen T, et al. Modulation of methamphetamine-related attention bias by intermittent theta-burst stimulation on left dorsolateral prefrontal cortex. Front Cell Dev Biol. 2021;9:667476.
Zhao Q, Lu YZ, Zhou CL, Wang XC. Effects of chronic exercise on attentional bias among individuals with methamphetamine use disorder. Psychol Sport Exerc. 2021;52:101842.
Li X, Zhou Y, Zhang G, Lu Y, Zhou C, Wang H. Behavioral and brain reactivity associated with drug-related and non-drug-related emotional stimuli in methamphetamine addicts. Front Hum Neurosci. 2022;16:894911.
Franken IH. Drug craving and addiction: integrating psychological and neuropsychopharmacological approaches. Prog Neuropsychopharmacol Biol Psychiatry. 2003;27(4):563–79.
Wang Y, Ruhe G. The cognitive process of decision making. Int J Cogn Inf Nat Intell. 2007;1(2):73–85.
Verdejo-Garcia A, Chong TT, Stout JC, Yucel M, London ED. Stages of dysfunctional decision-making in addiction. Pharmacol Biochem Behav. 2018;164:99–105.
Bechara A. Risky business: emotion, decision-making, and addiction. J Gambl Stud. 2003;19(1):23–51.
Droutman V, et al. Neurocognitive decision-making processes of casual methamphetamine users. Neuroimage Clin. 2019;21:101643.
Dominguez-Salas S, Diaz-Batanero C, Lozano-Rojas OM, Verdejo-Garcia A. Impact of general cognition and executive function deficits on addiction treatment outcomes: systematic review and discussion of neurocognitive pathways. Neurosci Biobehav Rev. 2016;71:772–801.
Sulzer D, Sonders MS, Poulsen NW, Galli A. Mechanisms of neurotransmitter release by amphetamines: a review. Prog Neurobiol. 2005;75(6):406–33.
Tanovic E, Joormann J. Anticipating the unknown: the stimulus-preceding negativity is enhanced by uncertain threat. Int J Psychophysiol. 2019;139:68–73.
Hackley SA, Valle-Inclán F, Masaki H, Hebert K. Chapter 17 - Stimulus-Preceding Negativity (SPN) and Attention to Rewards. In: Mangun GR, editor. Cognitive Electrophysiology of Attention (Academic Press). 2014. p. 216–25.
Ilieva IP, Hook CJ, Farah MJ. Prescription stimulants’ effects on healthy inhibitory control, working memory, and episodic memory: a meta-analysis. J Cogn Neurosci. 2015;27(6):1069–89.
Tolliver BK, et al. Impaired cognitive performance in subjects with methamphetamine dependence during exposure to neutral versus methamphetamine-related cues. Am J Drug Alcohol Abuse. 2012;38(3):251–9.
Folstein JR, Van Petten C. Influence of cognitive control and mismatch on the N2 component of the ERP: a review. Psychophysiology. 2008;45(1):152–70.
Sokhadze E, Stewart C, Hollifield M, Tasman A. Event-related potential study of executive dysfunctions in a speeded reaction task in cocaine addiction. J Neurother. 2008;12(4):185–204.
Torres A, et al. Emotional and non-emotional pathways to impulsive behavior and addiction. Front Hum Neurosci Original Res. 2013;7:43.
Funding
This work was supported in part by the National Natural Science Foundation of China, grant no. 61904038 and no. U1913216; National Key R&D Program of China, grant no. 2021YFC0122702 and no. 2018YFC2002300; Shanghai Sailing Program, grant no. 19YF1403600 and no. 22YF1404200; Shanghai Municipal Science and Technology Commission, grant no. 19441907600, no.19441908200, and no. 19511132000; Opening Project of Zhejiang Lab, grant no. 2021MC0AB01; Fudan University-CIOMP Joint Fund, grant no.FC2019-002; Opening Project of Shanghai Robot R&D and Transformation Functional Platform, grant no. KEH2310024; Ji Hua Laboratory, grant no. X190021TB190 and no. X190021TB193; National Natural Integration Project, grant no. 91948302; Shanghai Municipal Science and Technology Major Project, grant no. 2021SHZDZX0103 and no. 2018SHZDZX01.
Author information
Authors and Affiliations
Contributions
HJ, LZ, and XK contributed to the study conception and design. GZ, HS, PW, and JW collaborated on literature research and collation. The first draft of the manuscript was written by GZ. All authors commented on previous versions of the manuscript. All authors read and approved the final manuscript.
Corresponding author
Ethics declarations
Ethics Approval
Not applicable.
Consent to Participate
Not applicable.
Consent for Publication
Not applicable.
Conflict of Interest
The authors declare no competing interests.
Additional information
Publisher's Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Supplementary Information
Below is the link to the electronic supplementary material.
Rights and permissions
Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.
About this article
Cite this article
Zhan, G., Su, H., Wang, P. et al. Non-Invasive Brain-Computer Interfaces: a New Perspective on the Assessment and Classification of Individuals with Methamphetamine Addiction. SN Compr. Clin. Med. 5, 240 (2023). https://doi.org/10.1007/s42399-023-01585-y
Accepted:
Published:
DOI: https://doi.org/10.1007/s42399-023-01585-y