Difference between revisions of "Breathing inhibited when seizures spread to the amygdala and upon amygdala stimulation"

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(Created page with "''Dlouhy BJ, Gehlbach BK, Kreple CJ, et al. (2015) Breathing inhibited when seizures spread to the amygdala and upon amygdala stimulation. J Neurosci. 2015 Jul 15;35(28):10281...")
 
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In a patient with severe epilepsy undergoing monitoring, seizure involvement of amygdala led to apnea, and stimulation of the amygdala had the same effect, which was also seen in two other patients.  Curiously there was no dyspnea.  For further discussion of amygdala in SUDEP see the Context section at [[Respiratory modulation of neuronal discharge in the central nucleus of the amygdala during sleep and waking states|Zhang et al., 1986]].
  
 
==Comments==
 
==Comments==

Revision as of 21:25, 25 August 2018

Dlouhy BJ, Gehlbach BK, Kreple CJ, et al. (2015) Breathing inhibited when seizures spread to the amygdala and upon amygdala stimulation. J Neurosci. 2015 Jul 15;35(28):10281-9.

Link to Article

Abstract: Sudden unexpected death in epilepsy (SUDEP) is increasingly recognized as a common and devastating problem. Because impaired breathing is thought to play a critical role in these deaths, we sought to identify forebrain sites underlying seizure-evoked hypoventilation in humans. We took advantage of an extraordinary clinical opportunity to study a research participant with medically intractable epilepsy who had extensive bilateral frontotemporal electrode coverage while breathing was monitored during seizures recorded by intracranial electrodes and mapped by high-resolution brain imaging. We found that central apnea and O2 desaturation occurred when seizures spread to the amygdala. In the same patient, localized electrical stimulation of the amygdala reproduced the apnea and O2 desaturation. Similar effects of amygdala stimulation were observed in two additional subjects, including one without a seizure disorder. The participants were completely unaware of the apnea evoked by stimulation and expressed no dyspnea, despite being awake and vigilant. In contrast, voluntary breath holding of similar duration caused severe dyspnea. These findings suggest a functional connection between the amygdala and medullary respiratory network in humans. Moreover, they suggest that seizure spread to the amygdala may cause loss of spontaneous breathing of which patients are unaware, and thus has potential to contribute to SUDEP. SIGNIFICANCE STATEMENT: Sudden unexpected death in epilepsy (SUDEP) is the most common cause of death in patients with chronic refractory epilepsy. Impaired breathing during and after seizures is common and suspected to play a role in SUDEP. Understanding the cause of this peri-ictal hypoventilation may lead to preventative strategies. In epilepsy patients, we found that seizure invasion of the amygdala co-occurred with apnea and oxygen desaturation, and electrical stimulation of the amygdala reproduced these respiratory findings. Strikingly, the subjects were unaware of the apnea. These findings indicate a functional connection between the amygdala and brainstem respiratory network in humans and suggest that amygdala seizures may cause loss of spontaneous breathing of which patients are unaware-a combination that could be deadly.

Keywords: amygdala; brainstem; breathing; epilepsy; sudden death; SUDEP

Context

In a patient with severe epilepsy undergoing monitoring, seizure involvement of amygdala led to apnea, and stimulation of the amygdala had the same effect, which was also seen in two other patients. Curiously there was no dyspnea. For further discussion of amygdala in SUDEP see the Context section at Zhang et al., 1986.

Comments