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1.
Neuroimage ; 210: 116562, 2020 04 15.
Artículo en Inglés | MEDLINE | ID: mdl-31972278

RESUMEN

It has been suggested that resting-state functional connectivity (rs-FC) between the primary motor area (M1) region of the brain and other brain regions may be a predictor of motor learning, although this suggestion is still controversial. In the work reported here, we investigated the relationship between M1 seed-based rs-FC and motor learning. Fifty-three healthy volunteers undertook random button-press and sequential motor learning tasks. Five-minute resting-state data acquisition was performed between the two tasks. Oscillatory neural activities during the random task and the rest period were measured using magnetoencephalography. M1 seed-based rs-FC was calculated for the alpha and beta bands using amplitude envelope correlation, in which the seed location was defined as an M1 position with peak event-related desynchronization value. The relationship between rs-FC and the performance of motor learning was examined using whole brain correlation analysis. The results showed that beta-band resting-state cross-network connectivity between the sensorimotor network and the core network, particularly the theory of mind network, affected the performance of subsequent motor learning tasks. Good learners could be distinguished from poor learners by the strength of rs-FC between the M1 and the left superior temporal gyrus, a part of the theory of mind network. These results suggest that cross-network connectivity between the sensorimotor network and the theory of mind network can be used as a predictor of motor learning performance.


Asunto(s)
Ritmo beta/fisiología , Conectoma , Aprendizaje/fisiología , Magnetoencefalografía , Actividad Motora/fisiología , Corteza Motora/fisiología , Red Nerviosa/fisiología , Desempeño Psicomotor/fisiología , Lóbulo Temporal/fisiología , Adulto , Conectoma/métodos , Femenino , Humanos , Magnetoencefalografía/métodos , Masculino , Descanso , Teoría de la Mente/fisiología
2.
Neuroscience ; 391: 131-139, 2018 11 01.
Artículo en Inglés | MEDLINE | ID: mdl-30244032

RESUMEN

Motor function can be modulated by transcranial alternating current stimulation (tACS) in alpha, beta, and high-gamma frequencies. However, few studies have investigated tACS-induced behavioral changes in combination with endogenous oscillatory neural activity in detail. Herein, we investigated the effect of tACS on motor learning capacity and endogenous oscillatory neural activity. Fifty-two healthy volunteers were randomly assigned to four stimulation groups (10 Hz, 20 Hz, 70 Hz, or sham) and performed a visually cued button press motor learning task before and after tACS, which was delivered at the left primary motor area. Oscillatory neural activities during the motor learning task were measured using magnetoencephalography (MEG). Following tACS, the capacity for motor learning was significantly increased for 70 Hz tACS compared to sham stimulation. Oscillation analysis revealed a significant increase in beta-band power after 70-Hz tACS but not in the other stimulation groups. Our finding that capacity for motor learning and endogenous oscillatory beta activity were modulated in parallel after 70-Hz tACS suggests that 70-Hz tACS may increase the motor learning capacity by cross-modulating beta oscillatory activity. Because high gamma and beta oscillatory activity have been shown to reflect the activity of excitatory and inhibitory interneuron, our results may derive from the modulation of excitatory and inhibitory interneurons in M1 by 70-Hz tACS.


Asunto(s)
Aprendizaje/fisiología , Corteza Motora/fisiología , Desempeño Psicomotor , Estimulación Transcraneal de Corriente Directa/métodos , Adulto , Ondas Encefálicas , Femenino , Humanos , Magnetoencefalografía , Masculino , Actividad Motora
3.
Semin Ophthalmol ; 33(4): 560-565, 2018.
Artículo en Inglés | MEDLINE | ID: mdl-28678594

RESUMEN

PURPOSE: EYS and USH2A are the most common causative genes for retinitis pigmentosa (RP) in Japan. We determined the clinical outcomes for USH2A-related non-syndromic RP or Usher syndrome type II (USH2). METHODS: Two non-syndromic RP and 11 USH2 patients with previously identified USH2A mutations were included. Their complete history and medical records were collected using standard procedures. Visual fields and acuity were compared with those of patients with EYS mutations. Clinical analyses were based on ophthalmic and otolaryngologic examinations. RESULTS: In all patients, the fundus displayed changes typical of RP. Most patients showed relatively well-preserved visual acuity in their thirties or forties, with rapid deterioration in their fifties. Concentric constriction started in the twenties or thirties, and no effective residual visual field was observed after the fifties. CONCLUSIONS: The visual outcome for non-syndromic RP or USH2 patients with USH2A mutations is consistent with that for RP patients with EYS mutations.


Asunto(s)
ADN/genética , Proteínas de la Matriz Extracelular/genética , Mutación , Retinitis Pigmentosa/genética , Síndromes de Usher/genética , Agudeza Visual , Campos Visuales/fisiología , Adolescente , Adulto , Niño , Análisis Mutacional de ADN , Exones , Proteínas de la Matriz Extracelular/metabolismo , Femenino , Genotipo , Humanos , Incidencia , Japón/epidemiología , Masculino , Persona de Mediana Edad , Linaje , Pronóstico , Retinitis Pigmentosa/epidemiología , Retinitis Pigmentosa/metabolismo , Síndromes de Usher/epidemiología , Síndromes de Usher/metabolismo , Adulto Joven
4.
Ophthalmic Genet ; 35(1): 25-34, 2014 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-23421333

RESUMEN

BACKGROUND: To characterize the clinical phenotypes associated with previously-reported mutations of the eyes shut homolog (EYS) gene, including a truncating mutation, c.4957_4958insA, which is a major causative mutation for retinitis pigmentosa (RP) in Japan. MATERIALS AND METHODS: The study population comprised ten unrelated RP subjects with very likely pathogenic mutations in both alleles, four of them with a homozygous c.4957_4958insA mutation. The phenotype analysis was based on ophthalmic examination, Goldmann perimetry, and digital fundus photography. RESULTS: The study population included six men and four women aged 34-74 years. The average age at first visit was 31 years (range, 14-44 years), and the patients typically presented with night blindness as the initial symptom and subsequently developed progressive constriction of the visual field. Myopia was noted in 9/20 affected eyes. For most patients, central visual acuity was preserved relatively well up to their thirties, after which it deteriorated rapidly over the next two decades. The visual acuity of patients homozygous for the c.4957_4958insA mutation was uniform. Visual fields were constricted symmetrically, and the extent of constriction seemed to be better correlated with age than visual acuity. The fundus displayed bone spicules, which increased in density with age, and attenuated retinal vessels. CONCLUSIONS: Although additional studies with more patients with mutations of the EYS gene are required, it appears that patients share a relatively uniform phenotype with near-normal central visual function up to their twenties. The patients homozygous for the c.4957_4958insA mutation showed a uniform course of visual acuity changes.


Asunto(s)
Proteínas del Ojo/genética , Mutación , Retinitis Pigmentosa/genética , Adulto , Anciano , Pueblo Asiatico/genética , Análisis Mutacional de ADN , Electrorretinografía , Femenino , Efecto Fundador , Humanos , Japón , Masculino , Persona de Mediana Edad , Fenotipo , Reacción en Cadena de la Polimerasa , Retinitis Pigmentosa/fisiopatología , Tomografía de Coherencia Óptica , Agudeza Visual/fisiología , Campos Visuales/fisiología
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