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1.
Neuropsychologia ; 201: 108943, 2024 Aug 13.
Article de Anglais | MEDLINE | ID: mdl-38908476

RÉSUMÉ

Research has documented changes in autobiographical memory and episodic future thinking in mild cognitive impairment (MCI) and Alzheimer's disease (AD). However, cognitive decline occurs gradually and recent findings suggest that subtle alterations in autobiographical cognition may be evident earlier in the trajectory towards dementia, before AD-related symptoms emerge or a clinical diagnosis has been given. The current study used the Autobiographical Interview to examine the episodic and semantic content of autobiographical past and future events generated by older adults (N = 38) of varying cognitive functioning who were grouped into High (N = 20) and Low Cognition (N = 18) groups based on their Montreal Cognitive Assessment (MoCA) scores. Participants described 12 past and 12 future autobiographical events, and transcripts were scored to quantify the numbers of internal (episodic) or external (non-episodic, including semantic) details. Although the Low Cognition group exhibited a differential reduction for internal details comprising both past and future events, they did not show the expected overproduction of external details relative to the High Cognition group. Multilevel modelling demonstrated that on trials lower in episodic content, semantic content was significantly increased in both groups. Although suggestive of a compensatory mechanism, the magnitude of this inverse relationship did not differ across groups or interact with MoCA scores. This finding indicates that external detail production may be underpinned by mechanisms not affected by cognitive decline, such as narrative style and the ability to contextualize one's past and future events in relation to broader autobiographical knowledge.


Sujet(s)
Mémoire épisodique , Pensée (activité mentale) , Humains , Sujet âgé , Mâle , Femelle , Pensée (activité mentale)/physiologie , Sujet âgé de 80 ans ou plus , Dysfonctionnement cognitif/physiopathologie , Vieillissement/physiologie , Cognition/physiologie , Tests neuropsychologiques , Sémantique , Adulte d'âge moyen
2.
J Gerontol A Biol Sci Med Sci ; 74(12): 1861-1869, 2019 11 13.
Article de Anglais | MEDLINE | ID: mdl-30247510

RÉSUMÉ

Gait impairment during complex walking in older adults is thought to result from a progressive failure to compensate for deteriorating peripheral inputs by central neural processes. It is the primary hypothesis of this article that failure of higher cerebral adaptations may already be present in middle-aged adults who do not present observable gait impairments. We, therefore, compared metabolic brain activity during steering of gait (ie, complex locomotion) and straight walking (ie, simple locomotion) in young and middle-aged individuals. Cerebral distribution of [18F]-fluorodeoxyglucose, a marker of brain synaptic activity, was assessed during over ground straight walking and steering of gait using positron emission tomography in seven young adults (aged 24 ± 3) and seven middle-aged adults (aged 59 ± 3). Brain regions involved in steering of gait (posterior parietal cortex, superior frontal gyrus, and cerebellum) are retained in middle age. However, despite similar walking performance, there are age-related differences in the distribution of [18F]-fluorodeoxyglucose during steering: middle-aged adults have (i) increased activation of precentral and fusiform gyri, (ii) reduced deactivation of multisensory cortices (inferior frontal, postcentral, and fusiform gyri), and (iii) reduced activation of the middle frontal gyrus and cuneus. Our results suggest that preclinical decline in central sensorimotor processing in middle age is observable during complex walking.


Sujet(s)
Cartographie cérébrale/méthodes , Démarche/physiologie , Voies nerveuses/imagerie diagnostique , Voies nerveuses/métabolisme , Tomographie par émission de positons , Marche à pied/physiologie , Adulte , Femelle , Fluorodésoxyglucose F18/pharmacocinétique , Humains , Mâle , Adulte d'âge moyen , Radiopharmaceutiques/pharmacocinétique
3.
Sci Rep ; 8(1): 12601, 2018 08 22.
Article de Anglais | MEDLINE | ID: mdl-30135496

RÉSUMÉ

Neuroimaging-derived markers are used to model post-stroke impairment. Among these, lesion size, corticospinal-tract lesion-load (CST-LL) and resting-state functional-connectivity (rs-FC) have been correlated with impairment. It has been shown that the sensory cortex (S1) is associated with motor learning and is essential for post-stroke recovery; yet stroke-induced changes in S1 connectivity alone are yet to be investigated. We aim to determine whether interhemispheric rs-FC could be used to refine imaging models of stroke-related impairment. Subjects' post-stroke and age-matched controls underwent rs-fMRI. Stroke-related disability was correlated with lesion size, CST-LL and interhemispheric S1 and M1 rs-FC as independent seeds. Regression analyses were performed to assess the contribution of these markers in stroke-related deficits. Post-stroke subjects showed an asymmetrical pattern of rs-FC in which affected hemisphere S1 and M1 were mostly connected with ipsi-lesional regions. Correlations between rs-FC and stroke-severity were found. Adding rs-FC of S1 to the regression model of impairment decreased the variance 31% compared to lesion size only. After a stroke, S1 interhemispheric connectivity is decreased, with S1 only connected with ipsi-lesional regions. This asymmetry correlates with neurological and motor impairment. Furthermore, when combined with lesion anatomical measures, S1 connectivity might be an important marker in explaining stroke outcome.


Sujet(s)
Réseau nerveux/anatomopathologie , Cortex somatosensoriel/anatomopathologie , Accident vasculaire cérébral/anatomopathologie , Sujet âgé , Cartographie cérébrale/méthodes , Connectome/méthodes , Femelle , Humains , Imagerie par résonance magnétique/méthodes , Mâle , Adulte d'âge moyen , Activité motrice/physiologie , Cortex moteur/anatomopathologie , Troubles moteurs/anatomopathologie , Neuroimagerie/méthodes , Récupération fonctionnelle
4.
J Mot Behav ; 47(4): 319-27, 2015.
Article de Anglais | MEDLINE | ID: mdl-25584657

RÉSUMÉ

The completion of an antisaccade delays the reaction time (RT) of a subsequent prosaccade; however, the converse switch does not influence RT. In accounting for this result, the task-set inertia hypothesis contends that antisaccades engender a persistent nonstandard task-set that delays the planning of a subsequent prosaccade. In contrast, the coordinate system transformation hypothesis asserts that the transformation required to construct a mirror-symmetrical target representation persistently inhibits prosaccade planning. The authors tested the latter hypothesis by examining switch-costs for pro- and antisaccades directed to visual (i.e., the stimuli used in previous work) and auditory targets. Notably, auditory cues are specified in a head-centered frame of reference prior to their conversion into the retinocentric coordinates necessary for saccade output. Thus, if the coordinate system transformation hypothesis is correct then auditory pro- and antisaccades should elicit a bidirectional switch-cost because each requires a coordinate transformation. RTs for visual and auditory modalities showed a reliable--and equivalent magnitude--prosaccade switch-cost. Moreover, performance (e.g., movement time) and kinematic (e.g., velocity) variables indicated the switch-cost was restricted to response planning. As such, results are incompatible with the coordinate system transformation hypothesis and therefore provide convergent evidence that a task-set inertia contributes to the prosaccade switch-cost.


Sujet(s)
Perception auditive/physiologie , Saccades/physiologie , Perception visuelle/physiologie , Signaux , Femelle , Humains , Inhibition psychologique , Mâle , Temps de réaction/physiologie , Jeune adulte
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