Magnetoencephalography was used to investigate the effect of directed attention on changes in sensorimotor mu (8-12Hz) response (mu reactivity) to non-painful electrical stimulation of the median nerve in healthy adults. Results indicated attention-related sex differences in mu reactivity, with females showing i) prolonged mu suppression when attending to somatosensory stimuli indicating active processing of the sensory stimuli; ii) task-dependent attentional modulation of the mu response, which was absent in males, and iii) a trend for greater neuronal excitability of the primary somatosensory region suggesting greater physiological responsiveness to stimulation overall. Sex-related differences in attentional modulation of sensorimotor rhythms suggest that females and males use different top-down control strategies when processing somatosensory information. These sex differences in attention may underlie well-documented sex-related biases in pain processing wherein females typically report greater sensitivity to experimental and clinical pain.

Magnetoencephalography was used to investigate the effect of directed attention on changes in sensorimotor mu (8-12Hz) response (mu reactivity) to non-painful electrical stimulation of the median nerve in healthy adults. Results indicated attention-related sex differences in mu reactivity, with females showing i) prolonged mu suppression when attending to somatosensory stimuli indicating active processing of the sensory stimuli; ii) task-dependent attentional modulation of the mu response, which was absent in males, and iii) a trend for greater neuronal excitability of the primary somatosensory region suggesting greater physiological responsiveness to stimulation overall. Sex-related differences in attentional modulation of sensorimotor rhythms suggest that females and males use different top-down control strategies when processing somatosensory information. These sex differences in attention may underlie well-documented sex-related biases in pain processing wherein females typically report greater sensitivity to experimental and clinical pain.