Cargando…

Genetic polymorphisms in monoamine neurotransmitter systems show only weak association with acute post-surgical pain in humans

BACKGROUND: Candidate gene studies on the basis of biological hypotheses have been a practical approach to identify relevant genetic variation in complex traits. Based on previous reports and the roles in pain pathways, we have examined the effects of variations of loci in the genes of monoamine neu...

Descripción completa

Detalles Bibliográficos
Autores principales: Kim, Hyungsuk, Lee, Hyewon, Rowan, Janet, Brahim, Jaime, Dionne, Raymond A
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1543620/
https://www.ncbi.nlm.nih.gov/pubmed/16848906
http://dx.doi.org/10.1186/1744-8069-2-24
_version_ 1782129183410880512
author Kim, Hyungsuk
Lee, Hyewon
Rowan, Janet
Brahim, Jaime
Dionne, Raymond A
author_facet Kim, Hyungsuk
Lee, Hyewon
Rowan, Janet
Brahim, Jaime
Dionne, Raymond A
author_sort Kim, Hyungsuk
collection PubMed
description BACKGROUND: Candidate gene studies on the basis of biological hypotheses have been a practical approach to identify relevant genetic variation in complex traits. Based on previous reports and the roles in pain pathways, we have examined the effects of variations of loci in the genes of monoamine neurotransmitter systems including metabolizing enzymes, receptors and transporters on acute clinical pain responses in humans. RESULTS: Variations in the catecholamine metabolizing enzyme genes (MAOA and COMT) showed significant associations with the maximum post-operative pain rating while the serotonin transporter gene (SLC6A4) showed association with the onset time of post-operative pain. Analgesic onset time after medication was significantly associated with the norepinephrine transporter gene (SLC6A2). However, the association between COMT genetic variation and pain sensitivity in our study differ from previous studies with small sample sizes, population stratification and pain phenotype derived from combining different types of pain stimuli. Correcting for multiple comparisons did not sustain these genetic associations between monoamine neurotransmitter systems and pain sensitivity even in this large and homogeneous sample. CONCLUSION: These results suggest that the previously reported associations between genetic polymorphisms in the monoamine neurotransmitter systems and the interindividual variability in pain responses cannot be replicated in a clinically relevant pain phenotype.
format Text
id pubmed-1543620
institution National Center for Biotechnology Information
language English
publishDate 2006
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-15436202006-08-15 Genetic polymorphisms in monoamine neurotransmitter systems show only weak association with acute post-surgical pain in humans Kim, Hyungsuk Lee, Hyewon Rowan, Janet Brahim, Jaime Dionne, Raymond A Mol Pain Research BACKGROUND: Candidate gene studies on the basis of biological hypotheses have been a practical approach to identify relevant genetic variation in complex traits. Based on previous reports and the roles in pain pathways, we have examined the effects of variations of loci in the genes of monoamine neurotransmitter systems including metabolizing enzymes, receptors and transporters on acute clinical pain responses in humans. RESULTS: Variations in the catecholamine metabolizing enzyme genes (MAOA and COMT) showed significant associations with the maximum post-operative pain rating while the serotonin transporter gene (SLC6A4) showed association with the onset time of post-operative pain. Analgesic onset time after medication was significantly associated with the norepinephrine transporter gene (SLC6A2). However, the association between COMT genetic variation and pain sensitivity in our study differ from previous studies with small sample sizes, population stratification and pain phenotype derived from combining different types of pain stimuli. Correcting for multiple comparisons did not sustain these genetic associations between monoamine neurotransmitter systems and pain sensitivity even in this large and homogeneous sample. CONCLUSION: These results suggest that the previously reported associations between genetic polymorphisms in the monoamine neurotransmitter systems and the interindividual variability in pain responses cannot be replicated in a clinically relevant pain phenotype. BioMed Central 2006-07-18 /pmc/articles/PMC1543620/ /pubmed/16848906 http://dx.doi.org/10.1186/1744-8069-2-24 Text en Copyright © 2006 Kim et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Kim, Hyungsuk
Lee, Hyewon
Rowan, Janet
Brahim, Jaime
Dionne, Raymond A
Genetic polymorphisms in monoamine neurotransmitter systems show only weak association with acute post-surgical pain in humans
title Genetic polymorphisms in monoamine neurotransmitter systems show only weak association with acute post-surgical pain in humans
title_full Genetic polymorphisms in monoamine neurotransmitter systems show only weak association with acute post-surgical pain in humans
title_fullStr Genetic polymorphisms in monoamine neurotransmitter systems show only weak association with acute post-surgical pain in humans
title_full_unstemmed Genetic polymorphisms in monoamine neurotransmitter systems show only weak association with acute post-surgical pain in humans
title_short Genetic polymorphisms in monoamine neurotransmitter systems show only weak association with acute post-surgical pain in humans
title_sort genetic polymorphisms in monoamine neurotransmitter systems show only weak association with acute post-surgical pain in humans
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1543620/
https://www.ncbi.nlm.nih.gov/pubmed/16848906
http://dx.doi.org/10.1186/1744-8069-2-24
work_keys_str_mv AT kimhyungsuk geneticpolymorphismsinmonoamineneurotransmittersystemsshowonlyweakassociationwithacutepostsurgicalpaininhumans
AT leehyewon geneticpolymorphismsinmonoamineneurotransmittersystemsshowonlyweakassociationwithacutepostsurgicalpaininhumans
AT rowanjanet geneticpolymorphismsinmonoamineneurotransmittersystemsshowonlyweakassociationwithacutepostsurgicalpaininhumans
AT brahimjaime geneticpolymorphismsinmonoamineneurotransmittersystemsshowonlyweakassociationwithacutepostsurgicalpaininhumans
AT dionneraymonda geneticpolymorphismsinmonoamineneurotransmittersystemsshowonlyweakassociationwithacutepostsurgicalpaininhumans