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Toxins (Basel) ; 12(3)2020 03 09.
Artículo en Inglés | MEDLINE | ID: mdl-32182879

RESUMEN

The purpose of this study is to evaluate the effects of botulinum toxin type A (BoNT-A) for managing sleep bruxism (SB) in a randomized, placebo-controlled trial. Thirty SB subjects were randomly assigned into two groups evenly. The placebo group received saline injections into each masseter muscle, and the treatment group received BoNT-A injections into each masseter muscle. Audio-video-polysomnographic recordings in the sleep laboratory were made before, at four weeks after, and at 12 weeks after injection. Sleep and SB parameters were scored according to the diagnostic and coding manual of American Academy of Sleep Medicine. The change of sleep and SB parameters were investigated using repeated measures analysis of variance (RM-ANOVA). Twenty-three subjects completed the study (placebo group 10, treatment group 13). None of the SB episode variables showed a significant time and group interaction (p > 0.05) except for electromyography (EMG) variables. The peak amplitude of EMG bursts during SB showed a significant time and group interaction (p = 0.001). The injection decreased the peak amplitude of EMG bursts during SB only in the treatment group for 12 weeks (p < 0.0001). A single BoNT-A injection cannot reduce the genesis of SB. However, it can be an effective management option for SB by reducing the intensity of the masseter muscle.


Asunto(s)
Toxinas Botulínicas Tipo A/uso terapéutico , Músculo Masetero/efectos de los fármacos , Bruxismo del Sueño/tratamiento farmacológico , Adulto , Método Doble Ciego , Electromiografía , Femenino , Humanos , Inyecciones Intramusculares , Masculino , Músculo Masetero/fisiología , Persona de Mediana Edad , Bruxismo del Sueño/fisiopatología , Resultado del Tratamiento , Adulto Joven
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