Brainstem depolarization-induced lethal apnea associated with gain-of-function <i>SCN1A</i>^L263V is prevented by sodium channel blockade.

Abstract

Apneic events are frightening but largely benign events that often occur in infants. Here, we report apparent life-threatening apneic events in an infant with the homozygous <i>SCN1A</i>^L263V missense mutation, which causes familial hemiplegic migraine type 3 in heterozygous family members, in the absence of epilepsy. Observations consistent with the events in the infant were made in an <i>Scn1a</i>^L263V knock-in mouse model, in which apnea was preceded by a large brainstem DC-shift, indicative of profound brainstem depolarization. The L263V mutation caused gain of Na_V1.1 function effects in transfected HEK293 cells. Sodium channel blockade mitigated the gain-of-function characteristics, rescued lethal apnea in <i>Scn1a</i>^L263V mice, and decreased the frequency of severe apneic events in the patient. Hence, this study shows that <i>SCN1A</i>^L263V can cause life-threatening apneic events, which in a mouse model were caused by profound brainstem depolarization. In addition to being potentially relevant to sudden infant death syndrome pathophysiology, these data indicate that sodium channel blockers may be considered therapeutic for apneic events in patients with these and other gain-of-function <i>SCN1A</i> mutations.