Matthieu Casteran

Dr. Matthieu Casteran

Development, Adaptation and Handicap, University of Lorraine, Nancy, Grand Est, France
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Research Focus & Metrics

Academic Career Length

15Years (2012-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 November 2016 in Clinical Neurophysiology
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Matthieu CasteranMatthieu Casteran
Matthieu Casteran
APAlain Putot
Alain Putot
FPFrançois Pfitzenmeyer
François Pfitzenmeyer
ETElizabeth Thomas
Elizabeth Thomas
Patrick ManckoundiaPatrick Manckoundia
Patrick Manckoundia

1 October 2012 in Neuroscience
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Journal Article
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ABAmbra Bisio
Ambra Bisio
Matthieu CasteranMatthieu Casteran
Matthieu Casteran
YBY. Ballay
Y. Ballay
Patrick ManckoundiaPatrick Manckoundia
Patrick Manckoundia
FMF. Mourey
F. Mourey
TPThierry Pozzo
Thierry Pozzo

7 March 2016 in Frontiers in Aging Neuroscience
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Journal Article
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ABAmbra Bisio
Ambra Bisio
Matthieu CasteranMatthieu Casteran
Matthieu Casteran
YBYves Ballay
Yves Ballay
Patrick ManckoundiaPatrick Manckoundia
Patrick Manckoundia
FMFrance Mourey
France Mourey
TPThierry Pozzo
Thierry Pozzo
Although Alzheimer's disease (AD) primarily manifests as cognitive deficits, the implicit sensorimotor processes that underlie social interactions, such as automatic imitation, seem to be preserved in mild and moderate stages of the disease, as is the ability to communicate with other persons. Nevertheless, when AD patients face more challenging tasks, which do not rely on automatic processes but on explicit voluntary mechanisms and require the patient to pay attention to external events, the cognitive deficits resulting from the disease might negatively affect patients’ behaviour. The aim of the present study was to investigate whether voluntary motor imitation, i.e. a volitional mechanism that involves observing another person’s action and translating this perception into one’s own action, was affected in patients with Alzheimer’s disease. Further, we tested whether this ability was modulated by the nature of the observed stimulus by comparing the ability to reproduce the kinematic features of a human demonstrator with that of a computerized-stimulus. AD patients showed an intact ability to reproduce the velocity of the observed movements, particularly when the stimulus was a human agent. This result suggests that high-level cognitive processes involved in voluntary imitation might be preserved in mild and moderate stages of AD and that voluntary imitation abilities might benefit from the implicit interpersonal communication established between the patient and the human demonstrator.

4 November 2024 in Audiology Research
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Enrico ArmatoEnrico Armato
Enrico Armato
Georges DUMASGeorges DUMAS
Georges DUMAS
FPFlavio Perottino
Flavio Perottino
Matthieu CasteranMatthieu Casteran
Matthieu Casteran
Philippe PerrinPhilippe Perrin
Philippe Perrin
Background: Vestibular Neuritis (VN) can induce unilateral acute vestibular syndrome (AVS). This study aimed to identify predictive factors of recovery from vestibular neuritis considering total restitution and/or compensation. Methods: In this longitudinal study, 40 patients were included. The initial assessment, performed within 36 to 72 h from the onset (T0), included medical history taking (general and specific), including screening for cardiovascular risk factors (CVRFs), and a battery of diagnostic vestibular tests, comprising the bithermal caloric test (BCT), video head impulse test (VHIT), and skull vibration-induced nystagmus (SVIN) test. All patients also completed a Dizziness Handicap Inventory (DHI). All assessments were repeated 90 ± 15 days later (T3). Subjective compensation criteria were based on the DHI total score, and objective compensation criteria were based on laboratory test results. Four groups of patients (A, B, C, D) were delineated by combining patients with normal vs. abnormal vestibular tests and patients with normal vs. abnormal DHI. Results: CVRFs (but not age or body mass index (BMI)) were associated with a poorer recovery of symptoms. The BCT (lateral semicircular canal paresis %), VHIT (lateral semicircular canal gain), and SVINT (nystagmus slow phase velocity) recovered to normal values in 20%, 20%, and 27% of patients, respectively, at T3. Conclusions: Vascular risk factors (hypercholesterolemia) are correlated with patients who do not recover their symptoms via either total restitution or compensation. There was no significant difference between high- and low-frequency vestibular tests in patients recovering from their symptoms. Some patients with objective recovery may continue to have persistent subjective symptoms.

5 May 2018 in The Journals of Gerontology, Series A: Biological Sciences and Medical Sciences
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Matthieu CasteranMatthieu Casteran
Matthieu Casteran
PHPauline HILT
Pauline HILT
FMFrance Mourey
France Mourey
PMPatrick Manckoundia
Patrick Manckoundia
RFRobert French
Robert French
ETElizabeth Thomas
Elizabeth Thomas
In this study, we compared key temporal points in the whole body pointing movement of healthy aging and young subjects. During this movement, subject leans forward from a standing position to reach a target. As it involves forward inclination of the trunk, the movement creates a risk for falling. We examined two strategic time points during the task—first, the crossover point where the velocity of the center of mass (CoM) in the vertical dimension outstripped the velocity in the anteroposterior dimension and secondly, the time to peak of the CoM velocity profile. Transitions to stabilizing postures occur at these time points. They both occurred earlier in aging subjects. The crossover point also showed adjustments with target distance in aging subjects, while this was not observed in younger subjects. The shifts in these key time points could not be attributed to differences in movement duration between the two groups. Investigation with an optimal control model showed that the temporal adjustment as a function of target distance in the healthy aging subjects fits into a strategy that emphasized equilibrium maintenance rather than absolute work as a control strategy.

14 January 2013 in PLOS ONE
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Matthieu CasteranMatthieu Casteran
Matthieu Casteran
Patrick ManckoundiaPatrick Manckoundia
Patrick Manckoundia
TPThierry Pozzo
Thierry Pozzo
ETElizabeth Thomas
Elizabeth Thomas
Our aim was to investigate how the organization of a whole body movement is altered when movement duration (MD) is varied. Subjects performed the same whole body pointing movement over long, normal and short MDs. The kinematic trajectories were then analyzed on a normalized time base. A principal components analysis (PCA) revealed that the degree of coordination between the elevation angles of the body did not change with MD. This lack of significant differences in the coordination was interesting given that small spatial and temporal differences were observed in the individual kinematic trajectories. They were revealed by studying the trajectories of the elevation angles, joint markers and center of mass. The elevation angle excursions displayed modifications primarily in their spatial characteristics. These alterations were more marked for the short rather than long duration movements. The temporal characteristics of the elevation angles as measured by the time to peak of angular velocity were not modified in the same fashion hence displaying a dissociation in the tuning of the spatial and temporal aspects of the elevation angles. Modifications in the temporal characteristics of the movement were also studied by examining the velocity profiles of the joint markers. Interestingly, unlike the disordered nature of this variable for the elevation angles, the time to peak velocity was neatly ordered as a function of MD for the joint markers – It arrived first for the short duration movements, followed by those of the normal and finally long duration movements. Despite the modifications observed in the kinematic trajectories, a PCA with the elevation angle excursions at different MDs revealed that two principal components were sufficient to account for nearly all the variance in the data. Our results suggest that although similar, the kinematic trajectories at different MDs are not achieved by a simple time scaling.