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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...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2006
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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 |
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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 |
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