Genetics of pain in women with fibromyalgia: the promising role of reducing sedentary behaviour

Fernando Estevez-Lopez, Diego Salazar-Tortosa, Virginia A. Aparicio, Daniel Camiletti-Moiron, Blanca Gavilan Carrera, Pedro Acosta-Manzano, Inmaculada C. Alvarez-Gallardo, Victor Segura-Jimenez, Alberto Soriano Maldonado, Patrick Finan, R. Geenen, Manuel Delgado-Fernandez, Luis J. Martinez-Gonzalez, Jonatan R. Ruiz, Maria J. Alvarez-Cubero

Research output: Contribution to journalMeeting AbstractOther research output

Abstract

Background:Fibromyalgia is characterised by chronic pain and a heterogene-ous presentation of other symptoms (e.g., fatigue and depression) [1]. It is widelyaccepted that pain is promoted by both genetic susceptibility and environmentalfactors such as people’s behaviours [2]. In addition to genotype individual associ-ations and gene-gene interactions, when considering complex phenotypes suchas pain, gene-environmental interactions are likely present and can help to betterunderstand the disease (i.e. by unravelling underlying mechanisms [3]).

Objectives:To test the individual association of 64 polymorphisms (34 candi-date-genes) and the gene-gene, gene-physical activity, and gene-sedentarybehaviour interactions with pain and pain-related cognitions in fibromyalgia.

Methods:In 274 women with fibromyalgia, saliva samples were collected forextracting DNA. We measured physical activity and sedentary behaviour byaccelerometers for a week, pain with algometry and questionnaires, and pain cog-nitions with questionnaires. Age, body fat, and analgesics and antidepressantsconsumption were included as covariates. Significance was set at P-values lowerthan the Bonferroni’s correction or P- and false discovery rate values lower than0.05.

Results:The rs6311 and rs6313 polymorphisms were individually related to algo-meter scores. The interaction of rs4818 and rs1799971 polymorphisms wasrelated to pain catastrophizing. Five gene-behaviour interactions were significant:the interactions of sedentary behaviour with rs1383914, rs6860, rs4680,rs165599, and rs12994338 polymorphisms were associated with the bodily painsubscale of the SF-36.

Conclusion:The HTR2A gene (individually), COMT and OPRM1 gene-geneinteraction, and the interactions of sedentary behaviour with ADRA1A, CHMP1A,COMT, and SCN9A genes were associated with pain-related outcomes in fibro-myalgia females. Besides indicating the relevance of genetic background for painand pain-catastrophizing, the observed genotype-behaviour interactions suggestthat the effects of sedentary behaviour on pain may depend on the genotype ofwomen with fibromyalgia. Future clinical experimental research should examinewhether reducing sedentary behaviour is particularly beneficial for reducing painin women with specific genotypes
Original languageEnglish
Article numberAB0003
Pages (from-to)1468-1469
Number of pages2
JournalAnnals of the Rheumatic Diseases
Volume78
Issue number2
DOIs
Publication statusPublished - Jun 2019
EventEULAR Annual European Congress of Rheumatology - Feria de Madrid, Madrid, Spain
Duration: 12 Jun 201915 Jun 2019
https://www.congress.eular.org/

Fingerprint

Dive into the research topics of 'Genetics of pain in women with fibromyalgia: the promising role of reducing sedentary behaviour'. Together they form a unique fingerprint.

Cite this