Home > Riviste > Minerva Anestesiologica > Fascicoli precedenti > Minerva Anestesiologica 2016 Ottobre;82(10) > Minerva Anestesiologica 2016 Ottobre;82(10):1089-97





Rivista di Anestesia, Rianimazione, Terapia Antalgica e Terapia Intensiva

Official Journal of the Italian Society of Anesthesiology, Analgesia, Resuscitation and Intensive Care
Indexed/Abstracted in: Current Contents/Clinical Medicine, EMBASE, PubMed/MEDLINE, Science Citation Index Expanded (SciSearch), Scopus
Impact Factor 2,036




Minerva Anestesiologica 2016 Ottobre;82(10):1089-97

lingua: Inglese

Whole-exome sequencing of a family with local anesthetic resistance

Nathan CLENDENEN 1, Ashley D. CANNON 2, Steven PORTER 3, Christopher B. ROBARDS 3, Alexander S. PARKER 4, Steven R. CLENDENEN 3

1 Yale University School of Medicine, New Haven, CT, USA; 2 Department of Genetics at the University of Alabama, Birmingham, AL, USA; 3 Department of Anesthesiology, Mayo Clinic, Jacksonville, FL, USA; 4 Department of Health Sciences Research, Mayo Clinic, Jacksonville, FL, USA


BACKGROUND: Local anesthetics (LA) work by blocking sodium conductance through voltage-gated sodium channels. Complete local anesthetic resistance is infrequent, and the cause is unknown. Genetic variation in sodium channels is a potential mechanism for local anesthetic resistance. A patient with a history of inadequate loss of sensation following LA administration underwent an ultrasound-guided brachial plexus nerve block with a complete failure of the block. We hypothesized that LA resistance is due to a variant form of voltage-gated sodium channel.
METHODS: Whole-Exome Sequencing. The patient and her immediate family provided consent for exome sequencing, and they were screened with a questionnaire to identify family members with a history of LA resistance. Exome sequencing results for four individuals were referenced to the 1000 Genomes Project and the NHLBI ESP to identify variants associated with local anesthetic resistance present in less than 1% of the general population and located in functional regions of the genome.
RESULTS: Exome sequencing of the four family members identified one genetic variant in the voltage-gated sodium channel shared by the three individuals with LA resistance but not present in the unaffected family member. Specifically, we noted the A572D mutation in the SCN5A gene encoding for Nav1.5.
CONCLUSIONS: We identified a genetic variant that is associated with LA resistance in the gene encoding for Nav1.5. We also demonstrate that Nav1.5 is present in human peripheral nerves to support the plausibility that an abnormal form of the Nav1.5 protein could be responsible for the observed local anesthetic resistance.

inizio pagina

Publication History

Per citare questo articolo

Corresponding author e-mail