REM sleep theta changes in frequent nightmare recallers
Open accessAbstract
Study Objectives: To replicate and expand upon past research by evaluating sleep and wake electroencephalographic spectral activity in samples of frequent nightmare (NM) recallers and healthy controls. Methods: Computation of spectral activity for sleep (non-REM and REM) and wake electroencephalogram recordings from 18 frequent NM recallers and 15 control participants. Results: There was higher "slow-theta" (2-5 Hz) for NM recallers than for controls during wake, non-REM sleep and REM sleep. Differences were clearest for frontal and central derivations and for REM sleep cycles 2-4. There was also higher beta activity during NREM sleep for NM recallers. Findings partially replicate past research by demonstrating higher relative "slow-theta" (3-4Hz) for NM recallers than for controls. Conclusions: Findings are consistent with a neurocognitive model of nightmares that stipulates cross-state anomalies in emotion processing in NM-prone individuals.
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
Idiopathic nightmares originating in early childhood result from a dysfunctional hippocampal-amygdala-prefrontal circuit that controls fear memory formation and extinction.
“Moreover, also the idiopathic nightmares originating in early childhood results from dysfunctional hippocampal-amygdala-prefrontal circuit that controls fears memory formation and extinction (Nielsen and Levin, 2007; Marquis et al., 2017).”
From The Functional Role of Dreaming in Emotional Processes (2019) · cites this paper as Marquis et al., 2017
The Introduction and Conclusion describe a neurocognitive model in which idiopathic nightmares result from alterations in a hippocampal–amygdala–prefrontal circuit involved in fear memory formation and extinction. But the Introduction says a separate theory links them to early childhood adversity, not that the nightmares themselves originate in early childhood. The paper presents the circuit account as a model consistent with its findings, rather than an established cause. (LLM, conf=0.88)
Experimental — accuracy not yet measuredTheta activity and EEG characterized by high cortical activation appear crucial in the production and retrieval of DE.
“Once again, the theta activity (Marquis et al., 2017) and the EEG characterized by high cortical activation (Simor et al., 2013; D'Atri et al., 2019) appear to be crucial in the production and retrieval of DE.”
From The Functional Role of Dreaming in Emotional Processes (2019) · cites this paper as Marquis et al., 2017
The Results and Discussion report elevated slow-theta power in frequent nightmare recallers, especially during REM sleep, and discuss its possible role in nightmare pathology. They do not establish that theta activity is crucial to the production or retrieval of dream experiences generally. The high-cortical-activation part of the sentence is attributed to other citations, not Marquis et al. (LLM, conf=0.84)
Experimental — accuracy not yet measuredHigher slow theta (2-5 Hz) activity over frontal and central areas characterized the nightmares group especially during REM sleep compared to controls.
“Interestingly, a recent study investigated EEG activity in frequent nightmares recallers and controls, observing that higher slow theta (2–5 Hz) activity over frontal and central areas characterized the nightmares group especially during REM sleep compared to controls (Marquis et al., 2017).”
From The Functional Role of Dreaming in Emotional Processes (2019) · cites this paper as Marquis et al., 2017
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
Diagnostic and Statistical Manual of Mental Disorders
American Psychiatric Association (2013) · doi:10.1176/appi.books.9780890425596 · Cited by 116,369 · see citing works
Diagnostic and Statistical Manual of Mental Disorders
Williams, J. B. W., & First, M. B. (2013) · Oxford University Press eBooks · doi:10.1093/acrefore/9780199975839.013.104 · Cited by 109,841 · see citing works
The Pittsburgh Sleep Quality Index: a new instrument for psychiatric practice and research
Buysse, D. J., Reynolds, C. F., Monk, T. H., Berman, S. R., & Kupfer, D. J. (1989) · Psychiatry Research · doi:10.1016/0165-1781(89)90047-4 · Cited by 35,234 · see citing works
The ten-twenty electrode system of the international federation
Jasper, H. H. (1958) · Electroencephalography and Clinical Neurophysiology · Cited by 6,567 · see citing works
The International Classification of Sleep Disorders
Daroff, R. B. (1991) · Neurology · doi:10.1212/wnl.41.1.160 · Cited by 5,025 · see citing works
The International Classification of Sleep Disorders: Diagnostic and Coding Manual
(1991) · Annals of Internal Medicine · doi:10.7326/0003-4819-115-5-413_1 · Cited by 2,416 · see citing works
Klem, G. H., Lüders, H. O., Jasper, H. H., & Elger, C. E. (1999) · PubMed · Cited by 2,361 · see citing works
Psychometric evaluation of the pittsburgh sleep quality index
Carpenter, J. S., & Andrykowski, M. A. (1998) · Journal of Psychosomatic Research · doi:10.1016/s0022-3999(97)00298-5 · Cited by 1,618 · see citing works
A psychometric evaluation of the Beck Depression Inventory–II.
Dozois, D. J. A., Dobson, K. S., & Ahnberg, J. L. (1998) · Psychological Assessment · doi:10.1037/1040-3590.10.2.83 · Cited by 1,517 · see citing works
Overnight therapy? The role of sleep in emotional brain processing
Walker, M. P., & van der Helm, E. (2009) · Psychological Bulletin · doi:10.1037/a0016570 · Cited by 1,087 · see citing works
The visual scoring of sleep in adults
Silber, M. H., Ancoli-Israel, S., Bonnet, M. H., Chokroverty, S., Grigg-Damberger, M. M., Hirshkowitz, M., Kapen, S., Keenan, S. A., Kryger, M. H., Penzel, T., et al. (2007) · Journal of Clinical Sleep Medicine · doi:10.5664/jcsm.26814 · Cited by 1,064 · see citing works
Larson, J., Wong, D., & Lynch, G. (1986) · Brain Research · doi:10.1016/0006-8993(86)90579-2 · Cited by 1,037 · see citing works
Mechanisms of Gamma Oscillations in the Hippocampus of the Behaving Rat
Csicsvari, J., Jamieson, B. G., Wise, K. D., & Buzsáki, G. (2003) · Neuron · doi:10.1016/s0896-6273(02)01169-8 · Cited by 990 · see citing works
Coherence of gamma-band EEG activity as a basis for associative learning
Miltner, W. H. R., Braun, C., Arnold, M., Witte, H., & Taub, E. (1999) · Nature · doi:10.1038/17126 · Cited by 798 · see citing works
Principles and Practice of Sleep Medicine
Kryger, M. H., Roth, T. G., & Dement, W. C. (2016) · Elsevier eBooks · doi:10.1016/c2012-0-03543-0 · Cited by 785 · see citing works
Amygdalar and Hippocampal Theta Rhythm Synchronization During Fear Memory Retrieval
Seidenbecher, T., Laxmi, T. R., Stork, O., & Pape, H.-C. (2003) · Science · doi:10.1126/science.1085818 · Cited by 728 · see citing works
The neural correlates of dreaming
Siclari, F., Baird, B., Perogamvros, L., Bernardi, G., LaRocque, J. J., Riedner, B., Boly, M., Postle, B. R., & Tononi, G. (2017) · Nature Neuroscience · doi:10.1038/nn.4545 · Cited by 712 · see citing works
Sleep disturbances as the hallmark of PTSD: where are we now?
Germain, A. (2013) · American Journal of Psychiatry · doi:10.1176/appi.ajp.2012.12040432 · Cited by 634 · see citing works
REM sleep, prefrontal theta, and the consolidation of human emotional memory
Nishida, M., Pearsall, J., Buckner, R. L., & Walker, M. P. (2009) · Cerebral Cortex · doi:10.1093/cercor/bhn155 · Cited by 603 · see citing works
Sleep disturbance as the hallmark of posttraumatic stress disorder
(1989) · American Journal of Psychiatry · doi:10.1176/ajp.146.6.697 · Cited by 566 · see citing works
REM, not incubation, improves creativity by priming associative networks
Cai, D. J., Mednick, S. A., Harrison, E. M., Kanady, J. C., & Mednick, S. C. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0900271106 · Cited by 556 · see citing works
Levin, R., & Nielsen, T. A. (2007) · Psychological Bulletin · doi:10.1037/0033-2909.133.3.482 · Cited by 554 · see citing works
Self-citationCarrier, J., Land, S., Buysse, D. J., Kupfer, D. J., & Monk, T. H. (2001) · Psychophysiology · doi:10.1111/1469-8986.3820232 · Cited by 494 · see citing works
Hippocampal network patterns of activity in the mouse
Buzsáki, G., Buhl, D. L., Harris, K. D., Csicsvari, J., Czéh, B., & Morozov, A. (2003) · Neuroscience · doi:10.1016/s0306-4522(02)00669-3 · Cited by 486 · see citing works
Human hippocampal theta oscillations and the formation of episodic memories
Lega, B. C., Jacobs, J., & Kahana, M. (2012) · Hippocampus · doi:10.1002/hipo.20937 · Cited by 485 · see citing works
EEG power, frequency, asymmetry and coherence in male depression
Knott, V., Mahoney, C., Kennedy, S. H., & Evans, K. (2001) · Psychiatry Research Neuroimaging · doi:10.1016/s0925-4927(00)00080-9 · Cited by 409 · see citing works
Adaptation canadienne-française de la forme révisée du State-Trait Anxiety Inventory de Spielberger
Gauthier, J., & Bouchard, S. (1993) · Canadian Journal of Behavioural Science/Revue canadienne des sciences du comportement · doi:10.1037/h0078881 · Cited by 407 · see citing works
Nightmares: A new neurocognitive model
Nielsen, T., & Levin, R. (2007) · Sleep Medicine Reviews · doi:10.1016/j.smrv.2007.03.004 · Cited by 378 · see citing works
Spectral characteristics of sleep EEG in chronic insomnia
Merica, H., Blois, R., & Jm, G. (1998) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.1998.00189.x · Cited by 345 · see citing works
Coherent amygdalocortical theta promotes fear memory consolidation during paradoxical sleep
Popa, D., Duvarci, S., Popescu, A. T., Léna, C., & Paré, D. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0913016107 · Cited by 338 · see citing works
Frequency-specific network connectivity increases underlie accurate spatiotemporal memory retrieval
Watrous, A. J., Tandon, N., Conner, C. R., Pieters, T., & Ekstrom, A. D. (2013) · Nature Neuroscience · doi:10.1038/nn.3315 · Cited by 296 · see citing works
Nightmare Prevalence, Nightmare Distress, and Self-Reported Psychological Disturbance
(2002) · Sleep · doi:10.1093/sleep/25.2.205 · Cited by 285 · see citing works
Lesting, J., Narayanan, R. T., Kluge, C., Sangha, S., Seidenbecher, T., & Pape, H.-C. (2011) · PLoS ONE · doi:10.1371/journal.pone.0021714 · Cited by 275 · see citing works
Impaired functional connectivity at EEG alpha and theta frequency bands in major depression
Fingelkurts, A. A., Fingelkurts, A. A., Rytsälä, H. J., Suominen, K. H., Isometsä, E. T., & Kähkönen, S. (2006) · Human Brain Mapping · doi:10.1002/hbm.20275 · Cited by 274 · see citing works
Pizzagalli, D. A., Oakes, T. R., & Davidson, R. J. (2003) · Psychophysiology · doi:10.1111/1469-8986.00112 · Cited by 273 · see citing works
Jacobs, J. (2013) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2013.0304 · Cited by 259 · see citing works
Sleep and REM sleep disturbance in the pathophysiology of PTSD: the role of extinction memory
Pace-Schott, E. F., Germain, A., & Milad, M. R. (2015) · Biology of Mood & Anxiety Disorders · doi:10.1186/s13587-015-0018-9 · Cited by 255 · cited 2× · see citing works
“Current models of PTSD—for which NMs are a hallmark symptom32,33—emphasize the role of REM sleep in fear memory consolidation and extinction (for review, see Pace-Schott et al.34).”
BackgroundThe role of REM sleep theta activity in emotional memory
Hutchison, I. C., & Rathore, S. (2015) · Frontiers in Psychology · doi:10.3389/fpsyg.2015.01439 · Cited by 245 · see citing works
Newell, J., Mairesse, O., Verbanck, P., & Neu, D. (2012) · Psychiatry Research · doi:10.1016/j.psychres.2012.07.045 · Cited by 235 · see citing works
Boundaries in the mind: a new psychology of personality
(1992) · Choice Reviews Online · doi:10.5860/choice.29-5970 · Cited by 229 · see citing works
Cornwell, B. R., Johnson, L. L., Holroyd, T., Carver, F. W., & Grillon, C. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.5001-07.2008 · Cited by 229 · see citing works
Ohayon, M. M., Morselli, P. L., & Guilleminault, C. (1997) · SLEEP · doi:10.1093/sleep/20.5.340 · Cited by 222 · see citing works
Nightmares as Predictors of Suicide
Tanskanen, A. J., Tuomilehto, J., Viinamäki, H. T., Vartiainen, E. A., Lehtonen, J., & Puska, P. (2001) · SLEEP · doi:10.1093/sleep/24.7.845 · Cited by 222 · see citing works
Lega, B. C., Burke, J., Jacobs, J., & Kahana, M. J. (2014) · Cerebral Cortex · doi:10.1093/cercor/bhu232 · Cited by 221 · see citing works
The relationship of nightmare frequency and nightmare distress to well‐being
Blagrove, M., Farmer, L., & Williams, E. (2004) · Journal of Sleep Research · doi:10.1111/j.1365-2869.2004.00394.x · Cited by 211 · see citing works
Sex Differences in the Sleep EEG of Young Adults: Visual Scoring and Spectral Analysis
Dijk, D., Beersma, D. G. M., & Bloem, G. M. (1989) · SLEEP · doi:10.1093/sleep/12.6.500 · Cited by 206 · see citing works
Comments on Posttraumatic Stress Disorder
ROSS, R. J., BALL, W. A., & MORRISON, A. R. (1989) · American Journal of Psychiatry · doi:10.1176/ajp.146.1.128-a · Cited by 198 · see citing works
Effects of state and trait factors on nightmare frequency
Schredl, M. (2003) · European Archives of Psychiatry and Clinical Neuroscience · doi:10.1007/s00406-003-0438-1 · Cited by 197 · see citing works
Prevalence and Correlates of Frequent Nightmares: A Community-Based 2-Phase Study
Li, S. X., Zhang, B., Li, A. M., & Wing, Y. K. (2010) · SLEEP · doi:10.1093/sleep/33.6.774 · Cited by 184 · see citing works
Knutson, K. L., Rathouz, P. J., Yan, L. L., Liu, K., & Lauderdale, D. S. (2006) · SLEEP · doi:10.1093/sleep/29.11.1503 · Cited by 180 · see citing works
The prevalence of nightmares and their independence from anxiety.
Wood, J. M., & Bootzin, R. R. (1990) · Journal of Abnormal Psychology · doi:10.1037/0021-843x.99.1.64 · Cited by 175 · see citing works
Dynamics of slow-wave activity during the NREM sleep of sleepwalkers and control subjects
Gaudreau, H., Joncas, S., Zadra, A., & Montplaisir, J. (2000) · Sleep · doi:10.1093/sleep/23.6.1d · Cited by 169 · see citing works
van Liempt, S., van Zuiden, M., Westenberg, H., Super, A., & Vermetten, E. (2013) · Depression and Anxiety · doi:10.1002/da.22054 · Cited by 163 · see citing works
Belicki, K. (1992) · Dreaming · doi:10.1037/h0094355 · Cited by 157 · see citing works
Selective REM sleep deprivation in humans: effects on sleep and sleep EEG
Endo, T., Roth, C., Landolt, H., Werth, E., Aeschbach, D., Achermann, P., & Borbély, A. A. (1998) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.1998.274.4.r1186 · Cited by 144 · see citing works
Marzano, C., Ferrara, M., Mauro, F., Moroni, F., Gorgoni, M., Tempesta, D., Cipolli, C., & De Gennaro, L. (2011) · The Journal of Neuroscience · doi:10.1523/jneurosci.0412-11.2011 · Cited by 137 · see citing works
Sleep, dreams, and sudden death: the case for sleep as an autonomic stress test for the heart
Verrier, R. L., Muller, J. E., & Hobson, J. A. (1996) · Cardiovascular Research · doi:10.1016/s0008-6363(95)00211-1 · Cited by 137 · see citing works
Ferrarelli, F., Smith, R., Dentico, D., Riedner, B. A., Zennig, C., Benca, R. M., Lutz, A., Davidson, R. J., & Tononi, G. (2013) · PLoS ONE · doi:10.1371/journal.pone.0073417 · Cited by 122 · see citing works
Rhythmic hippocampal slow oscillation characterizes REM sleep in humans
Bódizs, R., Kántor, S., Szabó, G., Szûcs, A., Erõss, L., & Halász, P. (2001) · Hippocampus · doi:10.1002/hipo.1090 · Cited by 113 · see citing works
Narayanan, R. T., Seidenbecher, T., Kluge, C., Bergado, J. A., Stork, O., & Pape, H. (2007) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2007.05437.x · Cited by 111 · see citing works
PTSD-related hyperarousal assessed during sleep
Woodward, S. H., Murburg, M. M., & Bliwise, D. L. (2000) · Physiology & Behavior · doi:10.1016/s0031-9384(00)00271-7 · Cited by 108 · see citing works
EEG theta activity and pain insensitivity in self-injurious borderline patients
Russ, M. J., Campbell, S. S., Kakuma, T., Harrison, K. M., & Zanine, E. (1999) · Psychiatry Research · doi:10.1016/s0165-1781(99)00113-4 · Cited by 107 · see citing works
Jokić‐Begić, N., & Begić, D. (2003) · Nordic Journal of Psychiatry · doi:10.1080/08039480310002688 · Cited by 107 · see citing works
Tendler, A., & Wagner, S. (2015) · eLife · doi:10.7554/elife.03614 · Cited by 106 · see citing works
Simor, P., Horváth, K., Gombos, F., Takács, K. P., & Bódizs, R. (2012) · European Archives of Psychiatry and Clinical Neuroscience · doi:10.1007/s00406-012-0318-7 · Cited by 100 · see citing works
Prevalence of nightmare disorder in psychiatric outpatients
Swart, M. L., van Schagen, A. M., Lancee, J., & van den Bout, J. (2013) · Psychotherapy and Psychosomatics · doi:10.1159/000343590 · Cited by 99 · see citing works
Confirmatory Factor Analysis of the Pittsburgh Sleep Quality Index in Rheumatoid Arthritis Patients
Nicassio, P., Ormseth, S. R., Custodio, M. K., Olmstead, R., Weisman, M., & Irwin, M. R. (2013) · Behavioural Sleep Medicine · doi:10.1080/15402002.2012.720315 · Cited by 98 · see citing works
Characteristics of the frequent nightmare sufferer.
Berquier, A., & Ashton, R. (1992) · Journal of Abnormal Psychology · doi:10.1037//0021-843x.101.2.246 · Cited by 95 · see citing works
Cowdin, N., Kobayashi, I., & Mellman, T. A. (2014) · Experimental Brain Research · doi:10.1007/s00221-014-3857-5 · Cited by 92 · cited 3× · see citing works
“seem to have used a more selective sampling procedure that resulted in their cohort leaning more toward the “high distress” type of idiopathic NM recaller.(39) Nevertheless, the reduced psychopathology of our NM recaller sample also increases our confidence that the results are not simply due to differences in trait a…”
BackgroundInfluentialChanges in Cardiac Variability after REM Sleep Deprivation in Recurrent Nightmares
Nielsen, T., Paquette, T., Solomonova, E., Lara-Carrasco, J., Colombo, R., & Lanfranchi, P. A. (2010) · SLEEP · doi:10.1093/sleep/33.1.113 · Cited by 89 · see citing works
Prefrontal oscillations during recall of conditioned and extinguished fear in humans
Mueller, E. M., Panitz, C., Hermann, C., & Pizzagalli, D. A. (2014) · The Journal of Neuroscience · doi:10.1523/jneurosci.3427-13.2014 · Cited by 89 · see citing works
Do slow and fast gamma rhythms correspond to distinct functional states in the hippocampal network?
Colgin, L. L. (2015) · Brain Research · doi:10.1016/j.brainres.2015.01.005 · Cited by 89 · see citing works
Reduced alpha power associated with the recall of mentation from Stage 2 and Stage REM sleep
Esposito, M. J., Nielsen, T. A., & Paquette, T. (2004) · Psychophysiology · doi:10.1111/j.1469-8986.00143.x · Cited by 86 · see citing works
Slow‐wave sleep and delta power in rapid eye movement sleep behavior disorder
Massicotte-Marquez, J., Carrier, J., Décary, A., Mathieu, A., Vendette, M., Petit, D., & Montplaisir, J. Y. (2005) · Annals of Neurology · doi:10.1002/ana.20373 · Cited by 83 · see citing works
Morrison, P. D., Nottage, J. F., Stone, J. M., Bhattacharyya, S., Tunstall, N., Brenneisen, R., Holt, D., Wilson, D., Sumich, A. L., McGuire, P. K., et al. (2010) · Neuropsychopharmacology · doi:10.1038/npp.2010.222 · Cited by 82 · see citing works
Schema-conformant memories are preferentially consolidated during REM sleep
Durrant, S. J., Cairney, S. A., McDermott, C., & Lewis, P. A. (2015) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2015.02.011 · Cited by 75 · see citing works
Cortical activation patterns herald successful dream recall after NREM and REM sleep
Chellappa, S. L., Frey, S., Knoblauch, V., & Cajochen, C. (2011) · Biological Psychology · doi:10.1016/j.biopsycho.2011.03.004 · Cited by 75 · see citing works
Sheaves, B., Onwumere, J., Keen, N., Stahl, D., & Kuipers, E. (2015) · The Canadian Journal of Psychiatry · doi:10.1177/070674371506000804 · Cited by 74 · see citing works
Distinct contributions of human hippocampal theta to spatial cognition and anxiety
Cornwell, B. R., Arkin, N., Overstreet, C., Carver, F. W., & Grillon, C. (2012) · Hippocampus · doi:10.1002/hipo.22019 · Cited by 73 · see citing works
Sleep in the Human Hippocampus: A Stereo-EEG Study
Moroni, F., Nobili, L., Curcio, G., Carli, F. D., Fratello, F., Marzano, C., Gennaro, L. D., Ferrillo, F., Cossu, M., Francione, S., et al. (2007) · PLoS ONE · doi:10.1371/journal.pone.0000867 · Cited by 72 · see citing works
Predicting dream recall: EEG activation during NREM sleep or shared mechanisms with wakefulness?
Scarpelli, S., D’Atri, A., Mangiaruga, A., Marzano, C., Gorgoni, M., Schiappa, C., Ferrara, M., & De Gennaro, L. (2017) · Brain Topography · doi:10.1007/s10548-017-0563-1 · Cited by 63 · see citing works
The Stress Acceleration Hypothesis of Nightmares
Nielsen, T. (2017) · Frontiers in Neurology · doi:10.3389/fneur.2017.00201 · Cited by 63 · see citing works
Covert Waking Brain Activity Reveals Instantaneous Sleep Depth
McKinney, S. M., Dang‐Vu, T. T., Buxton, O. M., Solet, J. M., & Ellenbogen, J. M. (2011) · PLoS ONE · doi:10.1371/journal.pone.0017351 · Cited by 60 · see citing works
Spectral analysis of all‐night human sleep EEG in narcoleptic patients and normal subjects
Mukai, J., Uchida, S., Miyazaki, S., Nishihara, K., & Honda, Y. (2003) · Journal of Sleep Research · doi:10.1046/j.1365-2869.2003.00331.x · Cited by 59 · see citing works
Characteristics of the frequent nightmare sufferer.
Berquier, A., & Ashton, R. (1992) · Journal of Abnormal Psychology · doi:10.1037/0021-843x.101.2.246 · Cited by 57 · see citing works
REM sleep characteristics of nightmare sufferers before and after REM sleep deprivation
Nielsen, T., Paquette, T., Solomonova, E., Lara-Carrasco, J., Popova, A. A., & Levrier, K. (2009) · Sleep Medicine · doi:10.1016/j.sleep.2008.12.018 · Cited by 54 · see citing works
Paul, F., Schredl, M., & Alpers, G. W. (2015) · Borderline Personality Disorder and Emotion Dysregulation · doi:10.1186/s40479-014-0023-4 · Cited by 54 · see citing works
Simor, P., Bódizs, R., Horváth, K., & Ferri, R. (2013) · SLEEP · doi:10.5665/sleep.2462 · Cited by 52 · see citing works
Miró, E., & Martínez, M. P. (2005) · Dreaming · doi:10.1037/1053-0797.15.2.89 · Cited by 51 · see citing works
Simor, P., Horváth, K., Ujma, P. P., Gombos, F., & Bódizs, R. (2013) · Biological Psychology · doi:10.1016/j.biopsycho.2013.05.022 · Cited by 48 · see citing works
Nielsen, T., Stenstrom, P., Takeuchi, T., Saucier, S., Lara-Carrasco, J., Solomonova, E., & Martel, E. (2005) · SLEEP · doi:10.1093/sleep/28.9.1083 · Cited by 48 · see citing works
Quantitative EEG correlates of panic disorder
Knott, V., Bakish, D., Lusk, S., Barkely, J., & Perugini, M. (1996) · Psychiatry Research Neuroimaging · doi:10.1016/s0925-4927(96)02962-9 · Cited by 46 · see citing works
Alpha activity in the human REM sleep EEG: topography and effect of REM sleep deprivation
Roth, C., Achermann, P., & Borbély, A. A. (1999) · Clinical Neurophysiology · doi:10.1016/s1388-2457(98)00060-1 · Cited by 45 · see citing works
Nightmare Disorder, Psychopathology Levels, and Coping in a Diverse Psychiatric Sample
van Schagen, A. M., Lancee, J., Swart, M. L., Spoormaker, V. I., & van den Bout, J. (2016) · Journal of Clinical Psychology · doi:10.1002/jclp.22315 · Cited by 41 · see citing works
Morning REM Sleep Naps Facilitate Broad Access to Emotional Semantic Networks
Carr, M., & Nielsen, T. (2015) · SLEEP · doi:10.5665/sleep.4504 · Cited by 39 · see citing works
Trait–state interactions in the etiology of nightmares.
Blagrove, M., & Fisher, S. (2009) · Dreaming · doi:10.1037/a0016294 · Cited by 32 · see citing works
NREM sleep spindles are associated with dream recall
Nielsen, T., Carr, M., Blanchette-Carrière, C., Marquis, L.-P., Dumel, G., Solomonova, E., Julien, S.-H., Picard-Deland, C., & Paquette, T. (2017) · Sleep Spindles & Cortical Up States · doi:10.1556/2053.1.2016.003 · Cited by 30 · see citing works
Self-citationNightmares and Nightmare Function
Nielsen, T., & Carr, M. (2016) · Elsevier eBooks · doi:10.1016/b978-0-323-24288-2.00053-2 · Cited by 25 · see citing works
Kis, A., Szakadát, S., Simor, P., Gombos, F., Horváth, K., & Bódizs, R. (2013) · Behavioral Sleep Medicine · doi:10.1080/15402002.2013.829062 · Cited by 23 · see citing works
Evening and morning EEG differences between young men and women adults
Brière, M.-È., Forest, G., Chouinard, S., & Godbout, R. (2003) · Brain and Cognition · doi:10.1016/s0278-2626(03)00097-6 · Cited by 23 · see citing works
Dumel, G., Carr, M., Marquis, L., Blanchette‐Carrière, C., Paquette, T., & Nielsen, T. (2015) · Journal of Sleep Research · doi:10.1111/jsr.12286 · Cited by 20 · see citing works
Carr, M., Blanchette-Carrière, C., Marquis, L.-P., Ting, C. T., & Nielsen, T. (2016) · Sleep Medicine · doi:10.1016/j.sleep.2015.11.013 · Cited by 17 · cited 2× · see citing works
“Another possibility would be to investigate EEG activity in NM-prone individuals during phases of high-REM propensity using a morning nap paradigm.(68)”
MethodResultChen, H., Li, Y., Chen, F., Yan, J., Yang, N., Wang, Y.-J., Zhu, Z.-R., Hu, Z., Sui, J.-F., & Hu, B. (2013) · Behavioural Brain Research · doi:10.1016/j.bbr.2013.05.009 · Cited by 15 · see citing works
Cornwell, B., Overstreet, C., & Grillon, C. (2013) · Behavioural Brain Research · doi:10.1016/j.bbr.2013.12.031 · Cited by 14 · see citing works
Contribution to the Definition of the Power Bands Limits of Sleep EEG by Linear Prediction
Lanquart, J. ‐. (1998) · Computers and Biomedical Research · doi:10.1006/cbmr.1998.1474 · Cited by 3 · see citing works
Flagged first, then by citations
Research works printed but not linked: 7
- [11]11. Tanskanen A, Tuomilehto J, Viinamaki H, Vartiainen E, Lehtonen J, Puska P. Nightmares as predictors of suicide. Sleep. 2001; 24: 845–848. [PubMed] [Google Scholar]
- [40]40. Levin R, Nielsen T. Disturbed dreaming, posttraumatic stress disorder, and affect distress: a review and neurocognitive model. Psychol Bull. 2007; 133(3): 482–528. [DOI] [PubMed] [Google Scholar]
- [44]44. Spielberger CD, Gorsuch R.. State-Trait Anxiety Inventory for Adults: Manual and Sample: Manual, Instrument and Scoring Guide. Palo Alto, CA: Consulting Psychologists Press; 1983. [Google Scholar]
- [46]46. Beck A, Steer R, Brown G.. Manual for the BDI-II. San Antonio, TX: The Psychological Corporation; 1996. [Google Scholar]
- [56]56. Izard CE. The Differential Emotions Scale: DES IV-A; A Method of Measuring the Meaning of Subjective Experience of Discrete Emotions. Newark, DE: University of Delaware; 1993. [Google Scholar]
- [58]58. Stellate Systems Inc. Harmonie v6.2b Montréal, Québec, Canada:Stellate Systems Inc 2007. [Google Scholar]
- [75]75. Lega B, Burke J, Jacobs J, Kahana MJ. Slow-theta-to-gamma phase-amplitude coupling in human hippocampus supports the formation of new episodic memories. Cereb Cortex. 2016; 26(1): 268–278. [DOI] [PMC free article] [PubMed] [Google Scholar]
Cited by
Sorted by citations
The Functional Role of Dreaming in Emotional Processes
Scarpelli, S., Bartolacci, C., D'Atri, A., Gorgoni, M., & De Gennaro, L. (2019) · Frontiers in Psychology · doi:10.3389/fpsyg.2019.00459 · Cited by 190 · see citing works
“Interestingly, a recent study investigated EEG activity in frequent nightmares recallers and controls, observing that higher slow theta (2–5Hz) activity over frontal and central areas characterized the nightmares group especially during REM sleep compared to controls (Marquis et al., 2017).”
BackgroundWhat about dreams ? State of the art and open questions
Scarpelli, S., Alfonsi, V., Gorgoni, M., & Gennaro, L. D. (2022) · Journal of Sleep Research · doi:10.1111/jsr.13609 · Cited by 68 · see citing works
“In other words, nightmares could be related to the dysfunction in the hippocampal–amygdala prefrontal system that controls fear memory formation and extinction (Marquis et al., 2017; Nielsen & Levin, 2007).”
BackgroundIncreased heartbeat-evoked potential during REM sleep in nightmare disorder
Perogamvros, L., Park, H.-D., Bayer, L., Perrault, A. A., Blanke, O., & Schwartz, S. (2019) · NeuroImage Clinical · doi:10.1016/j.nicl.2019.101701 · Cited by 66 · see citing works
“In addition, higher theta activity in a frontal region which roughly corresponds to ACC was found in REM sleep of nightmare patients compared to controls (Marquis et al., 2017).”
Eichenlaub, J.-B., van Rijn, E., Gaskell, M. G., Lewis, P. A., Maby, E., Malinowski, J. E., Walker, M. P., Boy, F., & Blagrove, M. (2018) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nsy041 · Cited by 53 · see citing works
“, 2014), and suggests frontal theta activity as a brain mechanism underlying such processing (Nishida et al., 2009; PrehnKristensen et al., 2013; Cowdin et al., 2014; Durrant et al., 2015; Seeley et al., 2016; Marquis et al., 2017).”
BackgroundMental Sleep Activity and Disturbing Dreams in the Lifespan
Scarpelli, S., Bartolacci, C., D’Atri, A., Gorgoni, M., & De Gennaro, L. (2019) · International Journal of Environmental Research and Public Health · doi:10.3390/ijerph16193658 · Cited by 41 · see citing works
Blaskovich, B., Reichardt, R., Gombos, F., Spoormaker, V. I., & Simor, P. (2019) · SLEEP · doi:10.1093/sleep/zsz201 · Cited by 30 · see citing works
Sleep spindle and psychopathology characteristics of frequent nightmare recallers
Picard‐Deland, C., Carr, M., Paquette, T., Saint‐Onge, K., & Nielsen, T. (2017) · Sleep Medicine · doi:10.1016/j.sleep.2017.10.003 · Cited by 27 · see citing works
Marquis, L.-P., Julien, S.-H., Baril, A.-A., Blanchette-Carrière, C., Paquette, T., Carr, M., Soucy, J.-P., Montplaisir, J., & Nielsen, T. (2019) · Journal of Clinical Sleep Medicine · doi:10.5664/jcsm.7628 · Cited by 25 · see citing works
“22 Chronic hypoactivity of mPFC among individuals who were nightmare recallers may thus reflect chronic fear overgeneral - ization or a fear-extinction deficit.”
Pereira, S. I. R., Tsimpanouli, M.-E., Hutchison, I. C., Schneider, J., Anderson, I. M., McFarquhar, M., Elliott, R., & Lewis, P. A. (2022) · NeuroImage · doi:10.1016/j.neuroimage.2022.119120 · Cited by 21 · see citing works
“For the second-level models, we used the MRM toolbox ( McFarquhar et al., 2016 ) to specify a repeated measures model with within-subject factors of cueing (cued and non-cued levels) and emotion (negative and neutral levels).”
MethodScarpelli, S., D’Atri, A., Bartolacci, C., Mangiaruga, A., Gorgoni, M., & Gennaro, L. D. (2019) · Frontiers in Neurology · doi:10.3389/fneur.2019.00985 · Cited by 20 · see citing works
“Albeit our results confirm previous findings on young adults for what concerns the theta activity (2, 4, 7, 53), we have to”
ResultTwo Tell-tale Perspectives of PTSD
Shahid, F., Rahman, W., Islam, A., Paul, N., Khan, N. S., Rahman, M. S., Haque, M. M., & Islam, A. B. M. A. A. (2019) · Proceedings of the ACM on Interactive Mobile Wearable and Ubiquitous Technologies · doi:10.1145/3351259 · Cited by 13 · see citing works
“Earlier study reported that higher beta power was observed in waking state at C3, C4, F3, F4, and O1 regions of scalp among PTSD patients and nightmare recallers [100].”
BackgroundResultSlow-wave sleep and REM sleep differentially contribute to memory representational transformation
Liu, J., Chen, D., Xia, T., Zeng, S., Xue, G., & Hu, X. (2025) · Communications Biology · doi:10.1038/s42003-025-08812-3 · Cited by 15 · see citing works
“Thescoring resultswerethendouble-checkedandcorrectedbyanexperiencedsleep researchertoensureaccuracyandreliability.”
Bogdány, T., Perakakis, P., Bódizs, R., & Simor, P. (2021) · NeuroImage Clinical · doi:10.1016/j.nicl.2021.102933 · Cited by 11 · see citing works
Tomacsek, V., Blaskovich, B., Király, A., Reichardt, R., & Simor, P. (2023) · European Archives of Psychiatry and Clinical Neuroscience · doi:10.1007/s00406-023-01573-2 · Cited by 11 · see citing works
“…of participants with chronic nightmares is fragmented due to awakenings and microarousals, and is characterized by a decrease in low frequency and an increase in high-frequency electroencephalographic (EEG) spectral power indicating disrupted sleep regulation, especially during NREM sleep [15–17].”
BackgroundCortical hyperarousal in individuals with frequent nightmares
Sayk, C., Saftien, S., Koch, N., Ngo, H.-V. V., Junghanns, K., & Wilhelm, I. (2023) · Journal of Sleep Research · doi:10.1111/jsr.14003 · Cited by 10 · see citing works
“Broadening the view from the role of cortical hyperarousal as a transdiagnostic factor, this process might be related to difficulties in memory consolidation during sleep (Puetz et al., 2011) but also with increased dream (Moyne et al., 2022) and nightmare recall (Marquis et al., 2017).”
Backgroundvan der Wijk, G., Blaskovich, B., Farahzadi, Y., & Simor, P. (2020) · Sleep Medicine · doi:10.1016/j.sleep.2020.07.014 · Cited by 9 · see citing works
Marquis, L., Julien, S.-H., Daneault, V., Blanchette‐Carrière, C., Paquette, T., Carr, M., Soucy, J., Montplaisir, J. Y., & Nielsen, T. (2021) · Frontiers in Neuroscience · doi:10.3389/fnins.2021.645255 · Cited by 6 · see citing works
Vivid dreams are associated with a high percentage of REM sleep: a prospective study in veterans
Fattal, D., Platti, N., Hester, S., & Wendt, L. H. (2023) · Journal of Clinical Sleep Medicine · doi:10.5664/jcsm.10642 · Cited by 4 · see citing works
Zhong, B., Xu, Y., Xie, W., & Lü, J. (2019) · Neuropsychiatric Disease and Treatment · doi:10.2147/ndt.s202813 · Cited by 4 · see citing works
“Evidence from polysomnography studies has shown that REM rebound, the lengthening and increasing frequency and depth of REM, plays an important role in the occurrence of dreaminess and nightmares.(58,59) Because of the suppression effect of opioid administration on REM sleep, REM rebound happens after heroin withdrawa…”
BackgroundHolzinger, B., & Stefani, A. (2020) · Handbuch Schlafmedizin · doi:10.1016/b978-3-437-21321-2.00040-5 · Cited by 3 · see citing works
Domhoff, G. W. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108580298.041 · Cited by 3 · see citing works
EEG Based Artistic Visualization of Dreams
Chen, Y., Shen, K., Yu, G., Qiao, Y., Yan, X., Zhang, W., & Xu, Y. (2021) · International Symposium of Chinese CHI (Chinese CHI) · doi:10.1145/3490355.3490376 · Cited by 2 · see citing works
“The results of this study support the role of theta waves in emotional processing during REM sleep.[8] In 2019, Pilleriin et al.”
ResultAll-night spectral and microstate EEG analysis in patients with recurrent isolated sleep paralysis
Černý, F., Piorecká, V., Kliková, M., Kopřivová, J., Bušková, J., & Piorecký, M. (2024) · Frontiers in Neuroscience · doi:10.3389/fnins.2024.1321001 · Cited by 2 · see citing works
“Changes in EEG NREM sleep oscillations were also found during nightmares (Marquis et al., 2017; Blaskovich et al., 2020), which may be a decisive predictive factor for the frequency of RISP episodes (Liškovà et al., 2016).”
BackgroundScarpelli, S., Alfonsi, V., & Gennaro, L. D. (2025) · Oxford University Press eBooks · doi:10.1093/oxfordhb/9780197602751.013.21 · Cited by 1 · see citing works
Dream Activity Analysis in Low-number Electrode EEG: A Methodology Proposal
Piorecký, M., Miletínová, E., Schaabová, H., Sebek, J., & Bušková, J. (2019) · E-Health and Bioengineering Conference (EHB) · doi:10.1109/ehb47216.2019.8969949
“The dream recall was studied also for different issues such as frequent nightmare recall [5] or lucid dreaming [6].”
BackgroundDécoder l’émotion des rêves à l’aide des parasomnies et du sommeil paradoxal lucide
Maranci, J. (2022) · theses.fr (ABES) · doi:10.70675/2aa250b1zf8eez480dzae56z635743e1532a
Nightmare disorder shows reduced slow oscillation-dominant spindle coupling in NREM sleep
Papp, I., Cvetković, Z., Biabani, N., Rosenzweig, J., Speicher, C., Delogu, A., Nesbitt, A. D., Drakatos, P., Violante, I. R., Vilić, D., et al. (2026) · npj Biological Timing and Sleep · doi:10.1038/s44323-026-00094-0
“These fi ndings extend prior PSG studies that have described NREM sleep instability, altered CAP expression, increased arousals and spindle abnormalities in frequent nightmares 4 – 7 , while complementing REM sleep-focused work on autonomic, interoceptive and theta-related alterations 2,9,29 .”
Rêves et cauchemars : physiopathologie et neurobiologie
Maranci, J. (2025) · Elsevier eBooks · doi:10.1016/b978-2-294-78711-9.00008-6
Sayk, C., Probst, A., Lange, F., Eickemeier, S., Amores, J., Ngo, H.-V. V., Ehsanifard, M., Junghanns, K., & Wilhelm, I. (2026) · Journal of Sleep Research · doi:10.1111/jsr.70443
- Authors
- Marquis, L.-P., Paquette, T., Blanchette-Carrière, C., Dumel, G., & Nielsen, T.
- Affiliations
- Hôpital du Sacré-Cœur de Montréal (CA)
- Center for Advanced Research in Sleep Medicine, CIUSSS-NÎM – Hôpital du Sacré-Coeur de Montréal, Québec, Canada;
- Venue
- SLEEP
- Publisher
- Oxford University Press (OUP)
- Published
- 2017-06-23
- Volume
- 40
- Issue
- 9
- ISSN
- 0161-8105 (ISSN-L)
- 1550-9109
- PMC
- PMC5806577
- OpenAlex
- W2664764853
- Cited by
- 29
- References
- 105
- Citations by year
- 2026: 2 · 2025: 3 · 2024: 1 · 2023: 3 · 2022: 3 · 2021: 3 · 2020: 3 · 2019: 9 · 2018: 1 · 2017: 1
- FWCI
- 2.20
- Type
- journal article
- Language
- en
- Open access
- green
- europepmc.org
- Locations
- SLEEP (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Canadian Institutes of Health Research (MOP-115125)
- Natural Sciences and Engineering Research Council of Canada (312277)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Sleep and Wakefulness Research
- Social Sciences › Psychology › Experimental and Cognitive Psychology › Sleep and related disorders
- Social Sciences › Psychology › Clinical Psychology › Psychoanalysis and Psychopathology Research
- Keywords
- nightmares, REM sleep, beta activity, NREM sleep, emotional processing
- MeSH terms
- Adolescent, Adult, Dreams, Emotions, Female, Humans, Male, Mental Recall, Sleep, REM, Theta Rhythm, Case-Control Studies, Young Adult
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review