Title
Genetic components of human pain sensitivity: A protocol for a genome-wide association study of experimental pain in healthy volunteers
Date Issued
01 April 2019
Access level
open access
Resource Type
journal article
Author(s)
Schmid A.B.
Adhikari K.
Ramirez-Aristeguieta L.M.
Chacón-Duque J.C.
Rothhammer F.
Bedoya G.
Ruiz-Linares A.
Bennett D.L.
Publisher(s)
BMJ Publishing Group
Abstract
Introduction Pain constitutes a major component of the global burden of diseases. Recent studies suggest a strong genetic contribution to pain susceptibility and severity. Whereas most of the available evidence relies on candidate gene association or linkage studies, research on the genetic basis of pain sensitivity using genome-wide association studies (GWAS) is still in its infancy. This protocol describes a proposed GWAS on genetic contributions to baseline pain sensitivity and nociceptive sensitisation in a sample of unrelated healthy individuals of mixed Latin American ancestry. Methods and analysis A GWAS on genetic contributions to pain sensitivity in the naïve state and following nociceptive sensitisation will be conducted in unrelated healthy individuals of mixed ancestry. Mechanical and thermal pain sensitivity will be evaluated with a battery of quantitative sensory tests evaluating pain thresholds. In addition, variation in mechanical and thermal sensitisation following topical application of mustard oil to the skin will be evaluated. Ethics and dissemination This study received ethical approval from the University College London research ethics committee (3352/001) and from the bioethics committee of the Odontology Faculty at the University of Antioquia (CONCEPTO 01-2013). Findings will be disseminated to commissioners, clinicians and service users via papers and presentations at international conferences.
Volume
9
Issue
4
Language
English
OCDE Knowledge area
Genética humana Otras ciencias médicas
Scopus EID
2-s2.0-85064994960
PubMed ID
Source
BMJ Open
ISSN of the container
20446055
Sponsor(s)
Funding Work leading to this publication was funded by grants from: the Newton Fund Institutional Links Grant from the British Research Council (grant number 216398412), the Excellence Initiative of Aix-Marseille University— A*MIDEX (a French 'Investissements d’Avenir' programme) and from a Wellcome Trust Senior Scientist Fellowship to DLB (ref. no. 095698z/11/z and 202747/Z/16/Z). KA was supported by a Wellcome Investigator Award WT107055AIA (to C.D. Stern). ABS was supported by the National Institute for Health Research (NIHR) Biomedical Research Centre (BRC) Oxford.
Sources of information: Directorio de Producción Científica Scopus