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COMT genotype and non-recovery after a whiplash injury in a Northern European population
BACKGROUND: The COMT (Catechol-O-Methyl Transferase) gene may influence a person’s vulnerability to develop long-term pain and some COMT single nucleotide polymorphisms (SNPs) may associate with patterns of acute or chronic pain. Many patients with whiplash-associated disorders (WADs) suffer from lo...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5709856/ https://www.ncbi.nlm.nih.gov/pubmed/29195501 http://dx.doi.org/10.1186/s12891-017-1810-z |
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author | Rydman, Eric Comasco, Erika Pettersson, H. Oreland, L. Ponzer, S. Ottosson, C. |
author_facet | Rydman, Eric Comasco, Erika Pettersson, H. Oreland, L. Ponzer, S. Ottosson, C. |
author_sort | Rydman, Eric |
collection | PubMed |
description | BACKGROUND: The COMT (Catechol-O-Methyl Transferase) gene may influence a person’s vulnerability to develop long-term pain and some COMT single nucleotide polymorphisms (SNPs) may associate with patterns of acute or chronic pain. Many patients with whiplash-associated disorders (WADs) suffer from long-term pain and other related symptoms, but it is less known if genetic factors play a role in the recovery process. The primary aim of this study was to evaluate whether self-reported non-recovery, including pain, was related to COMT genotype in patients with WAD. The secondary aim was to investigate whether or not background factors, including mental health, were related to genotype and non-recovery. METHODS: A total of 133 patients with neck pain after a whiplash trauma were included. Background factors were collected and blood samples were taken during the acute phase after the accident. DNA was isolated from blood and used to genotype the SNPs rs6269, rs4633, rs4818 and rs4680 in the COMT gene; additionally haplotypes were estimated and haplogenotypes inferred. The patients were followed up after 12 months and asked to rate their recovery including pain, mental health and quality of life. RESULTS: The overall reported non-recovery rate at 12 months was 44% with no significant differences in distribution of the COMT haplotypes. High levels of self-reported pain (OR 7.2) and anxiety (OR 4.4) after the accident were associated with non-recovery, but not related to the haplotypes. None of the other background factors were related to the haplotypes or non-recovery. CONCLUSION: No association between self-reported non-recovery or pain levels and COMT haplotypes in patients with acute whiplash injuries could be detected. Independent replications are necessary to discard the hypothesis that COMT haplotypes do not influence non-recovery or pain levels in patients with acute whiplash injuries. High levels of initial pain and anxiety were associated with non-recovery, thereby confirming previously published reports. |
format | Online Article Text |
id | pubmed-5709856 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-57098562017-12-06 COMT genotype and non-recovery after a whiplash injury in a Northern European population Rydman, Eric Comasco, Erika Pettersson, H. Oreland, L. Ponzer, S. Ottosson, C. BMC Musculoskelet Disord Research Article BACKGROUND: The COMT (Catechol-O-Methyl Transferase) gene may influence a person’s vulnerability to develop long-term pain and some COMT single nucleotide polymorphisms (SNPs) may associate with patterns of acute or chronic pain. Many patients with whiplash-associated disorders (WADs) suffer from long-term pain and other related symptoms, but it is less known if genetic factors play a role in the recovery process. The primary aim of this study was to evaluate whether self-reported non-recovery, including pain, was related to COMT genotype in patients with WAD. The secondary aim was to investigate whether or not background factors, including mental health, were related to genotype and non-recovery. METHODS: A total of 133 patients with neck pain after a whiplash trauma were included. Background factors were collected and blood samples were taken during the acute phase after the accident. DNA was isolated from blood and used to genotype the SNPs rs6269, rs4633, rs4818 and rs4680 in the COMT gene; additionally haplotypes were estimated and haplogenotypes inferred. The patients were followed up after 12 months and asked to rate their recovery including pain, mental health and quality of life. RESULTS: The overall reported non-recovery rate at 12 months was 44% with no significant differences in distribution of the COMT haplotypes. High levels of self-reported pain (OR 7.2) and anxiety (OR 4.4) after the accident were associated with non-recovery, but not related to the haplotypes. None of the other background factors were related to the haplotypes or non-recovery. CONCLUSION: No association between self-reported non-recovery or pain levels and COMT haplotypes in patients with acute whiplash injuries could be detected. Independent replications are necessary to discard the hypothesis that COMT haplotypes do not influence non-recovery or pain levels in patients with acute whiplash injuries. High levels of initial pain and anxiety were associated with non-recovery, thereby confirming previously published reports. BioMed Central 2017-12-01 /pmc/articles/PMC5709856/ /pubmed/29195501 http://dx.doi.org/10.1186/s12891-017-1810-z Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Rydman, Eric Comasco, Erika Pettersson, H. Oreland, L. Ponzer, S. Ottosson, C. COMT genotype and non-recovery after a whiplash injury in a Northern European population |
title | COMT genotype and non-recovery after a whiplash injury in a Northern European population |
title_full | COMT genotype and non-recovery after a whiplash injury in a Northern European population |
title_fullStr | COMT genotype and non-recovery after a whiplash injury in a Northern European population |
title_full_unstemmed | COMT genotype and non-recovery after a whiplash injury in a Northern European population |
title_short | COMT genotype and non-recovery after a whiplash injury in a Northern European population |
title_sort | comt genotype and non-recovery after a whiplash injury in a northern european population |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5709856/ https://www.ncbi.nlm.nih.gov/pubmed/29195501 http://dx.doi.org/10.1186/s12891-017-1810-z |
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