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Dive into the research topics where Marcel Daamen is active.

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Featured researches published by Marcel Daamen.


Neurology | 2012

Glucose metabolism, gray matter structure, and memory decline in subjective memory impairment

Lukas Scheef; Annika Spottke; Moritz Daerr; Alexius Joe; Nadine Striepens; Heike Kölsch; Julius Popp; Marcel Daamen; Dominik Gorris; Michael T. Heneka; Henning Boecker; Hans J. Biersack; Wolfgang Maier; Hans H. Schild; Michael Wagner; Frank Jessen

Objective: To identify biological evidence for Alzheimer disease (AD) in individuals with subjective memory impairment (SMI) and unimpaired cognitive performance and to investigate the longitudinal cognitive course in these subjects. Method: [18F]fluoro-2-deoxyglucose PET (FDG-PET) and structural MRI were acquired in 31 subjects with SMI and 56 controls. Cognitive follow-up testing was performed (average follow-up time: 35 months). Differences in baseline brain imaging data and in memory decline were assessed between both groups. Associations of memory decline with brain imaging data were tested. Results: The SMI group showed hypometabolism in the right precuneus and hypermetabolism in the right medial temporal lobe. Gray matter volume was reduced in the right hippocampus in the SMI group. At follow-up, subjects with SMI showed a poorer performance than controls on measures of episodic memory. Longitudinal memory decline in the SMI group was associated with reduced glucose metabolism in the right precuneus at baseline. Conclusion: The cross-sectional difference in 2 independent neuroimaging modalities indicates early AD pathology in SMI. The poorer memory performance at follow-up and the association of reduced longitudinal memory performance with hypometabolism in the precuneus at baseline support the concept of SMI as the earliest manifestation of AD.


Radiology | 2010

Resting-State Perfusion in Nonmedicated Schizophrenic Patients: A Continuous Arterial Spin-labeling 3.0-T MR Study

Lukas Scheef; Christoph Manka; Marcel Daamen; Kai-Uwe Kühn; Wolfgang Maier; Hans H. Schild; Frank Jessen

PURPOSE To determine whether well-described patterns of altered perfusion in schizophrenia can be identified by using continuous arterial spin labeling (CASL) with a whole-brain imaging sequence. MATERIALS AND METHODS This study was approved by the ethics committee of the local institutional review board, and written informed consent was obtained from all subjects. CASL was used to compare cerebral perfusion between 11 nonmedicated patients with schizophrenia and 25 healthy control subjects. Since antipsychotic medication may affect perfusion, only drug-free subjects were examined. Resting-state perfusion, as measured in terms of regional cerebral blood flow, was compared voxel wise by using an analysis of variance design in a statistical parametric mapping program, with patient age and sex as covariates. RESULTS Compared with the healthy control subjects, the schizophrenic patients had extensive areas of hypoperfusion in the frontal lobes bilaterally, in the anterior and medial cingulate gyri, and in the parietal lobes bilaterally. Increased perfusion was observed in the cerebellum, brainstem, and thalamus of the schizophrenic patients as compared with the perfusion in these areas in the control subjects. CONCLUSION CASL in schizophrenia revealed patterns of hypo- and hyperperfusion similar to the perfusion patterns in previously published positron emission tomographic and single photon emission computed tomographic studies. The advantages of CASL, including independence from injected contrast agents, no irradiation, and fast acquisition time, may facilitate intensive perfusion studies of the early recognition of schizophrenia and other psychiatric disorders, as well as longitudinal disease-monitoring research of these conditions.


Journal of Psychopharmacology | 2009

Reduced memory and attention performance in a population-based sample of young adults with a moderate lifetime use of cannabis, ecstasy and alcohol

Friedrich Indlekofer; Michaela Piechatzek; Marcel Daamen; C Glasmacher; Roselind Lieb; Hildegard Pfister; Oliver Tucha; Klaus W. Lange; Hans-Ulrich Wittchen; Christian G. Schütz

Abstract Regular use of illegal drugs is suspected to cause cognitive impairments. Two substances have received heightened attention: 3,4-methylenedioxymethamphetamine (MDMA or ‘ecstasy’) and δ-9-tetrahydrocannabinol (THC or ‘cannabis’). Preclinical evidence, as well as human studies examining regular ecstasy consumers, indicated that ecstasy use may have negative effects on learning, verbal memory and complex attentional functions. Cannabis has also been linked to symptoms of inattention and deficits in learning and memory. Most of the published studies in this field of research recruited participants by means of newspaper advertisements or by using word-of-mouth strategies. Because participants were usually aware that their drug use was critical to the research design, this awareness may have caused selection bias or created expectation effects. Focussing on attention and memory, this study aimed to assess cognitive functioning in a community-based representative sample that was derived from a large-scale epidemiological study. Available data concerning drug use history allowed sampling of subjects with varying degrees of lifetime drug experiences. Cognitive functioning was examined in 284 young participants, between 22 and 34 years. In general, their lifetime drug experience was moderate. Participants completed a neuropsychological test battery, including measures for verbal learning, memory and various attentional functions. Linear regression analysis was performed to investigate the relationship between cognitive functioning and lifetime experience of drug use. Ecstasy and cannabis use were significantly related to poorer episodic memory function in a dose-related manner. For attentional measures, decrements of small effect sizes were found. Error measures in tonic and phasic alertness tasks, selective attention task and vigilance showed small but significant effects, suggesting a stronger tendency to experience lapses of attention. No indication for differences in reaction time was found. The results are consistent with decrements of memory and attentional performance described in previous studies. These effects are relatively small; however, it must be kept in mind that this study focussed on assessing young adults with moderate drug use from a population-based study.


Pain | 2012

An fMRI study on the acute effects of exercise on pain processing in trained athletes.

Lukas Scheef; Jakob Jankowski; Marcel Daamen; Gunther Weyer; Markus Klingenberg; Julia Renner; Sara Mueckter; Britta Schürmann; Frank Musshoff; Michael Wagner; Hans H. Schild; Andreas Zimmer; Henning Boecker

Summary Endurance exercise modulates affective pain ratings and pain‐evoked responses in distinct areas of the human pain matrix, presumably via central opioidergic modulation. Abstract Endurance exercise is known to promote sustained antinociceptive effects, and there is evidence that the reduction of pain perception mediated by exercise is driven by central opioidergic neurotransmission. To directly investigate the involved brain areas and the underlying neural mechanisms in humans, thermal heat‐pain challenges were applied to 20 athletes during 4 separate functional magnetic resonance imaging (fMRI) scans, i.e., before and after 2 hours of running (exercise condition) and walking (control condition), respectively. Imaging revealed a reproducible pattern of distributed pain‐related activation in all 4 conditions, including the mesial and lateral pain systems, and the periaqueductal gray (PAG) as a key region of the descending antinociceptive pathway. At the behavioral level, running as compared with walking decreased affective pain ratings. The influence of exercise on pain‐related activation was reflected in a significant time × treatment interaction in the PAG, along with similar trends in the pregenual anterior cingulate cortex and the middle insular cortex, where pain‐induced activation levels were elevated after walking, but decreased or unchanged after running. Our findings indicate that enhanced reactive recruitment of endogenous antinociceptive mechanisms after aversive repeated pain exposure is attenuated by exercise. The fact that running, but not walking, reproducibly elevated β‐endorphin levels in plasma indicates involvement of the opioidergic system in exercise. This may argue for an elevated opioidergic tone in the brain of athletes, mediating antinociceptive mechanisms. Our findings provide the first evidence using functional imaging to support the role of endurance exercise in pain modulation.


Human Psychopharmacology-clinical and Experimental | 2009

Is moderate substance use associated with altered executive functioning in a population-based sample of young adults?

Michaela Piechatzek; Friedrich Indlekofer; Marcel Daamen; Christoph Glasmacher; Roselind Lieb; Hildegard Pfister; Oliver Tucha; Klaus W. Lange; Hans-Ulrich Wittchen; Christian G. Schütz

Substance use (SU) has been linked with impaired cognitive functioning. Evidence comes mainly from clinical studies or studies examining heavy users. Though, the majority of users are not involved in heavy use. This study investigates the association between moderate use and cognition in a population‐based sample.


Open access journal of sports medicine | 2010

Advocating neuroimaging studies of transmitter release in human physical exercise challenges studies.

Henning Boecker; Ahmed Othman; Sarah Mueckter; Lukas Scheef; Max Pensel; Marcel Daamen; Jakob Jankowski; H. H. Schild; Thomas R. Tölle; M Schreckenberger

This perspective attempts to outline the emerging role of positron emission tomography (PET) ligand activation studies in human exercise research. By focusing on the endorphinergic system and its acclaimed role for exercise-induced antinociception and mood enhancement, we like to emphasize the unique potential of ligand PET applied to human athletes for uncovering the neurochemistry of exercise-induced psychophysiological phenomena. Compared with conventional approaches, in particular quantification of plasma beta-endorphin levels under exercise challenges, which are reviewed in this article, studying opioidergic effects directly in the central nervous system (CNS) with PET and relating opioidergic binding changes to neuropsychological assessments, provides a more refined and promising experimental strategy. Although a vast literature dating back to the 1980s of the last century has been able to reproducibly demonstrate peripheral increases of beta-endorphin levels after various exercise challenges, so far, these studies have failed to establish robust links between peripheral beta-endorphin levels and centrally mediated behavioral effects, ie, modulation of mood and/or pain perception. As the quantitative relation between endorphins in the peripheral blood and the CNS remains unknown, the question arises, to what extent conventional blood-based methods can inform researchers about central neurotransmitter effects. As previous studies using receptor blocking approaches have also revealed equivocal results regarding exercise effects on pain and mood processing, it is expected that PET and other functional neuroimaging applications in athletes may in future help uncover some of the hitherto unknown links between neurotransmission and psychophysiological effects related to physical exercise.


Archive | 2012

Psychological Assessments in Physical Exercise

Marcel Daamen; Markus Raab

This chapter will present a short review of psychological assessment techniques which are frequently used to measure cognitive and affective functions. If available, these measurement approaches are illustrated with examples from recent sports- and exercise-related studies. In addition, the chapter will discuss important caveats and methodological perspectives and that may be relevant for future studies in this research field, especially in the context of neuroimaging applications.


Suchttherapie | 2005

Deutsche Übersetzung des WHO ASSIST Screening-Fragebogens

Christian G. Schütz; Marcel Daamen; Corinna van Niekerk

Fragestellung: Bisher gibt es fur den deutschsprachigen Raum noch kein etabliertes Instrument, das ein umfassendes Screening des Substanzkonsums in allen verbreiteten Substanzkategorien erla...


Brain Research | 2009

Multimodal motion processing in area V5/MT: Evidence from an artificial class of audio-visual events

Lukas Scheef; Henning Boecker; Marcel Daamen; Ursula Fehse; Martin W. Landsberg; Dirk-Oliver Granath; Heinz Mechling; Alfred O. Effenberg


Journal of Psychiatric Research | 2011

Influence of 5-HTTLPR polymorphism on resting state perfusion in patients with major depression

Holger Brockmann; Astrid Zobel; Anna Schuhmacher; Marcel Daamen; Alexius Joe; Kim Biermann; Sibylle G. Schwab; Hans-Juergen Biersack; Wolfgang Maier; Henning Boecker

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Henning Boecker

German Center for Neurodegenerative Diseases

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Christian G. Schütz

University of British Columbia

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Hans-Ulrich Wittchen

Dresden University of Technology

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