Biological Function of Dreaming in Dreaming and Non-Dreaming Patients With PCA Infarction

NCT ID: NCT04749992

Last Updated: 2024-03-12

Basic Information

• Recruitment Status: TERMINATED
• Total Enrollment: 142 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2018-08-01
• Study Completion Date: 2024-03-08

Brief Summary

This study is a quasi-experimental between-group design. Using a prospective two-arm controlled exploratory study, data will be collected on an initial assessment of the effects of a specific neurological sample after thrombotic infarction (PCA infarction) who lost the ability to dream due to the infarction (experimental group) compared to a specific neurological sample after thrombotic infarction (PCA infarction) without loss of the ability to dream (comparison group) in terms of subjective and objective sleep quality and memory consolidation. Besides the importance to further elucidate the role of dreaming for sleep architecture and memory consolidation, the results of the evaluation are of great clinical relevance in a further scientific investigation regarding the treatment of a specifically neurological sample with acute thrombotic infarction.

Detailed Description

The aim of the study is to investigate the biological function of dreams, which differs from that of REM (rapid eye-movement) sleep. People spend almost a third of every day asleep. About a fifth of this time they dream.

Why do dreams occupy such a significant part of human life? What is the biological function of dreams? The physiological function of dreaming for humans has been investigated in extensive studies. However, these are predominantly in the area of memory research and address the question of whether dreaming is conducive to memory consolidation. However, other biological functions of dreaming, such as their influence on the restorative effects of sleep, remain virtually unexplored to date. Therefore, the planned DFG (Deutsche Forschungsgemeinschaft) study will investigate the effect of dream activity on the objective and subjective quality of sleep.

Solms was able to show that damage to the parieto-occipital brain region leads to a complete loss of dream recall in a large number of clinical cases (in 44 of 361 cases). This discovery holds the possibility of relating the biological function of dreaming to neuroanatomical structures. Obviously, the loss of dream memory must be related to the specific damage of the brain, or its biological functions.

Further studies also show that acute thrombotic infarction of the occipital lobe in the current area of the posterior cerebral artery can lead to complete loss of dream activity with simultaneous maintenance of REM sleep. The authors Bischof & Bassetti noticed, seemingly by chance and without grasping the theoretical implications of the discovery, that their patient was suffering from insomnia with difficulty falling asleep and staying asleep.

Based on these observations, Solms conducted a pilot study comparing the sleep patterns of five dreaming and five nondreaming patients with thrombotic infarcts in the same arterial territory-as observed by Bischof & Bassetti . Solms and his research group observed that within the non-dreaming group there was a striking decrease in absolute sleep duration, as well as a more frequent number of nocturnal awakenings, more arousals, as well as microarousals (previously unpublished data).

The study of populations that have forfeited the ability to dream with preserved REM sleep makes it possible to test not only the classical theory on the function of dreams, but also such theories that deal with the role of dreams in memory consolidation during sleep. In recent years, there has been increased interest in the hypothesis that sleep contributes to and significantly influences memory processing.

In this context, dreaming is postulated to play a specific role in memory processing during sleep.

There are several hypotheses regarding the role of dreaming in memory consolidation. For example, Stickgold et al. found that during REM sleep, limbic forebrain structures are activated along with the amygdala, while there is concomitant inhibition of hippocampal signalling, which presumably prevents re-activation of episodic memory content. Accordingly, dreams would mainly occur via weak neocortical associations available during REM sleep. The authors hypothesize that this feature reflects the brain's attempts to recognize and evaluate new cortical associations in the context of emotions mediated by limbic structures. They concluded that one function of REM sleep was to enhance or attenuate specifically activated associations with regression to pictorial imaginings to compensate for the relative loss of motor activity during sleep.

Similarly, it has been postulated that the occurrence of memories in dreams promotes learning by, first, reactivating memory elements in their original perceptual state and, second, that linking a wide variety of memory elements strengthens and consolidates them and, third, that dreaming newly learned material facilitates later recall.

Relevance and research questions of the study:

Through a specific choice of sample of neurological patients with posterior cortical lesions who are at risk of losing the ability to dream due to the lesion, the proposed project is particularly aimed at understanding the biological function of dreaming as distinct from REM sleep. Based on the neuropsychoanalytic theory of Solms, as well as neuropsychological findings that REM sleep and dreaming are doubly dissociable phenomena, the central hypothesis that dreams serve to maintain sleep (Sigmund Freud's hypothesis) will be investigated. By this, Freud meant that dreams serve to respond to sometimes highly affect-laden impulses to action with hallucinatory wish fulfillment, so that they do not lead to premature awakening. Secondly, it will be investigated whether dreams influence affective memory consolidation. This will be investigated using two groups of neurological patients with thrombotic infarction in the posterior stream area, i.e., the posterior cerebral artery (PCA infarction) during preserved REM sleep (i) who have lost the ability to recall dreams, and (ii) in whom the ability to recall dreams has been preserved. This has far-reaching implications not only for sleep medicine and neuroscience, but also for clinical neurology. Sleep pathologies have not yet been considered clinically-scientifically as a consequence of PCA infarction and, accordingly, have not yet been studied, but could provide significant clues for the clinical management of such patients. Similarly, findings on memory consolidation after PCA infarction during preserved REM sleep are significant because an important aspect of memory processing during sleep is examined with the distinction between preserved and nonsustained dreaming, which also has not been considered in scientific studies to date but is of clinical relevance.

Hypotheses Our hypotheses are that patients who have lost the ability to dream during preserved REM sleep will have (i) poorer sleep quality and (ii) poorer emotional declarative memory and non-declarative motor memory consolidation.

Non-dreamers vs. dreamers.

Null hypothesis (H0):

There is no difference in terms of loss of ability to dream during preserved REM sleep, related to poorer sleep quality, as well as poorer emotional declarative and non-declarative motor memory consolidation between the experimental group and the comparison group

Alternative hypothesis (H1):

There is a difference in loss of ability to dream with preserved REM sleep related to worse sleep quality and worse emotional declarative and non-declarative motor memory consolidation between experimental group and comparison group

Design

Prospective two-arm controlled observational study (quasi-experimental between-group design).

Conditions

Dream Disorder; Thrombotic Infarction; PCA Infarct

Study Design

• Observational Model Type: CASE_CONTROL
• Study Time Perspective: PROSPECTIVE

Study Groups

Non-Dreamers

Experimental Group

Polysomnographic examination in sleep laboratory (PSG measurement)

Intervention Type: PROCEDURE

Recording of sleep quality and quantity by sleep parameters, such as total sleep time - TST; duration of sleep stages - S1t, S2t, S3t, rapid eye movement - REMt; sleep onset latency - SL; wake after sleep onset - WASO, sleep efficiency - SE.

Dreamers

Comparison Group

Polysomnographic examination in sleep laboratory (PSG measurement)

Intervention Type: PROCEDURE

Recording of sleep quality and quantity by sleep parameters, such as total sleep time - TST; duration of sleep stages - S1t, S2t, S3t, rapid eye movement - REMt; sleep onset latency - SL; wake after sleep onset - WASO, sleep efficiency - SE.

Interventions

Polysomnographic examination in sleep laboratory (PSG measurement)

Recording of sleep quality and quantity by sleep parameters, such as total sleep time - TST; duration of sleep stages - S1t, S2t, S3t, rapid eye movement - REMt; sleep onset latency - SL; wake after sleep onset - WASO, sleep efficiency - SE.

Intervention Type: PROCEDURE

Eligibility Criteria

Inclusion Criteria

• Acute thrombotic infarction in the posterior stream area of the cerebral artery (parieto-temporo-occipital (PTO) lesions)
• Dream recall before infarction more than 1 dream/week
• REM sleep present
• Willingness of the patient to participate in the sleep laboratory examinations within the scope of the study or to fill in questionnaires/diaries.
• Patient is cognitively and linguistically able to comprehend the meaning of the study
• Existence of a written declaration of consent

Exclusion Criteria

• Extension of the lesion to the brainstem.
• Diagnosis of any previously known sleep disorder confounding with the study results, recorded on 1st screening night (sleep laboratory)

1. severe insomnia

2. Restless Leg Syndrome (RLS)

3. periodic movements of the extremities during sleep (PLMS), and

4. obstructive sleep apnea syndrome (OSAS)

• Diagnosis of any neurological or psychiatric disorders or other conditions that may conflict with the study results
• Cerebral insults in areas outside the posterior cerebral artery (excluding small vessel disease)
• Medication use affecting sleep architecture, such as benzodiazepines, anticonvulsants, SSRIs.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 90 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Charite University, Berlin, Germany

OTHER

Sponsor Role: collaborator

International Psychoanalytic University Berlin

OTHER

Sponsor Role: lead

Responsible Party

Tamara Fischmann

Professor for clinical psychology and psychoanalysis

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Tamara Fischmann, Prof.

Role: PRINCIPAL_INVESTIGATOR

International Psychoanalytic University

Michael Koslowski, Dr.

Role: PRINCIPAL_INVESTIGATOR

Charite university medicine

Locations

Charite university medicine

Berlin, , Germany

International Psychoanalytic University

Berlin, , Germany

Countries

Germany

References

Wamsley EJ, Tucker M, Payne JD, Benavides JA, Stickgold R. Dreaming of a learning task is associated with enhanced sleep-dependent memory consolidation. Curr Biol. 2010 May 11;20(9):850-5. doi: 10.1016/j.cub.2010.03.027. Epub 2010 Apr 22.

Reference Type: BACKGROUND

PMID: 20417102 (View on PubMed)

Pace-Schott EF, Hobson JA. The neuropsychology of dreams: a clinico-anatomical study. Trends Cogn Sci. 1998 May 1;2(5):199-200. doi: 10.1016/s1364-6613(98)01166-8.

Reference Type: BACKGROUND

PMID: 21227155 (View on PubMed)

Bischof M, Bassetti CL. Total dream loss: a distinct neuropsychological dysfunction after bilateral PCA stroke. Ann Neurol. 2004 Oct;56(4):583-6. doi: 10.1002/ana.20246.

Reference Type: BACKGROUND

PMID: 15389890 (View on PubMed)

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Reference Type: BACKGROUND

PMID: 23589831 (View on PubMed)

Stickgold R, Hobson JA, Fosse R, Fosse M. Sleep, learning, and dreams: off-line memory reprocessing. Science. 2001 Nov 2;294(5544):1052-7. doi: 10.1126/science.1063530.

Reference Type: BACKGROUND

PMID: 11691983 (View on PubMed)

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PMID: 16251954 (View on PubMed)

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Solms M. Neurobiology and the neurological basis of dreaming. Handb Clin Neurol. 2011;98:519-44. doi: 10.1016/B978-0-444-52006-7.00034-4. No abstract available.

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Reference Type: BACKGROUND

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Freud, S. (1948). Die Traumdeutung.[Erstausgabe 1900]. Freud, Sigmund Gesammelte Werke. Chronologisch geordnet. London: Imago, Bde, 2.

Reference Type: BACKGROUND

Other Identifiers

InternationalPUB

Identifier Type: -

Identifier Source: org_study_id