The Genetics of Neuropathic Pain from Model Organisms to Clinical Application

Calvo M.; Davies A.J.; Hébert H.L.; Weir G.A.; Chesler E.J.; Finnerup N.B.; Levitt R.C.; Smith B.H.; Neely G.G.; Costigan M.; Bennett D.L.

Abstract

Neuropathic pain (NeuP) arises due to injury of the somatosensory nervous system and is both common and disabling, rendering an urgent need for non-addictive, effective new therapies. Given the high evolutionary conservation of pain, investigative approaches from Drosophila mutagenesis to human Mendelian genetics have aided our understanding of the maladaptive plasticity underlying NeuP. Successes include the identification of ion channel variants causing hyper-excitability and the importance of neuro-immune signaling. Recent developments encompass improved sensory phenotyping in animal models and patients, brain imaging, and electrophysiology-based pain biomarkers, the collection of large well-phenotyped population cohorts,neurons derived from patient stem cells, and high-precision CRISPR generated genetic editing. We will discuss how to harness these resources to understand the pathophysiological drivers of NeuP, define its relationship with comorbidities such as anxiety, depression, and sleep disorders, and explore how to apply these findings to the prediction, diagnosis, and treatment of NeuP in the clinic.

Más información

Título según WOS: The Genetics of Neuropathic Pain from Model Organisms to Clinical Application
Título según SCOPUS: The Genetics of Neuropathic Pain from Model Organisms to Clinical Application
Título de la Revista: NEURON
Volumen: 104
Número: 4
Editorial: Cell Press
Fecha de publicación: 2019
Página de inicio: 637
Página final: 653
Idioma: English
DOI:

10.1016/j.neuron.2019.09.018

Notas: ISI, SCOPUS