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Influence of variation in the catechol-O-methyltransferase gene on the clinical outcome after lumbar spine surgery for one-level symptomatic disc disease: a report on 176 cases
Background This study was aimed at the evaluation of the relationship between genetic polymorphisms of catechol- O -methyltransferase (COMT) (rs4680:A > G—Val158Met, rs6269:A > G, rs4633:C > T, rs4818:C > G) and pain sensitivity after lumbar discectomy. Methods All patients had one-level...
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Published in: | Acta neurochirurgica 2014-02, Vol.156 (2), p.245-252 |
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creator | Rut, Marcin Machoy-Mokrzyńska, Anna Ręcławowicz, Daniel Słoniewski, Paweł Kurzawski, Mateusz Droździk, Marek Safranow, Krzysztof Morawska, Michalina Białecka, Monika |
description | Background
This study was aimed at the evaluation of the relationship between genetic polymorphisms of catechol-
O
-methyltransferase (COMT) (rs4680:A > G—Val158Met, rs6269:A > G, rs4633:C > T, rs4818:C > G) and pain sensitivity after lumbar discectomy.
Methods
All patients had one-level symptomatic disc herniation from L3 to S1. The primary data recorded included visual analogue pain scales assessing back and leg pain, Oswestry Disability Questionnaire assessing quality of life and pain intensity, received/filled pre- and postoperatively. Each subject was genotyped for single-nucleotide polymorphism in the
COMT
gene. Clinical outcome was measured by difference between pre- and postoperative values and those results were analyzed with genetics findings.
Results
Pain intensity was associated with the
COMT
polymorphism. Carriers of rs6269
AA
, rs4633
TT
, rs4818
CC
, and rs4680
AA
genotypes were characterized by the lowest preoperative scores related to pain intensity and lower pain intensity at 1 year after the surgery. The rs4633
CC
, rs4680
GG
genotypes demonstrated significant clinical improvement in VAS
BACK
score at 1 year after the surgery. Patients with COMT haplotype associated with low metabolic activity of enzyme (A_C_C_G) showed better clinical outcome measured by ODI score and VAS
BACK
score 1 year after surgery. We did not observe any significant correlation between leg pain and single-nucleotide polymorphisms in the COMT gene.
Conclusions
The results of our study indicate that polymorphism in the
COMT
gene may play an important role in the mechanism of pain perception, which may have a potential implication for clinical decision-making in the future. |
doi_str_mv | 10.1007/s00701-013-1895-6 |
format | article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3898361</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>3187106401</sourcerecordid><originalsourceid>FETCH-LOGICAL-c503t-12a205759134977aa6e72e3f10dbf38d708d3be44bb03fee810f77f78d3f281e3</originalsourceid><addsrcrecordid>eNqNks9u1DAQxiMEoqXwAFyQJS5cDHacxA4HJFTxp1KlXuBsOcl415VjL7az0r4Vj8iku1QFCYnLxM785huP_VXVS87ecsbku4yBccq4oFz1Le0eVeesb2qKgT3GNcNsV3fqrHqW8y3uatmIp9VZ3XCpeM_Oq59XwfoFwggkWrI3yZniYiAukLIFMpoC4zZ6ekNnKNuDL8mEbCGZDGQDAatOoHfBjcaTuJQxzkCMLZCIX-bBJJJ3DtG8pA2kA7ExYRlQD3vwJB_mXYkzth3J5PJdAJR_TwxJsIuprD247PAwGfLz6ok1PsOL0_ei-v7507fLr_T65svV5cdrOrZMFMprU7NWtj0XTS-lMR3IGoTlbBqsUJNkahIDNM0wMGEBFGdWSivxr60VB3FRfTjq7pZhhmmEgKN7vUtuNumgo3H6z0xwW72Jey1Ur0THUeDNSSDFHwvkomecDrw3AeKSNW_6TvWsb_v_QfERObtTff0XehuXFPAmVooppZq2Q4ofqTHFnBPY-3Nzplfr6KN1NFpHr9bRa82rhwPfV_z2CgL1EciYCviSD1r_U_UXCSLR0g</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1490888456</pqid></control><display><type>article</type><title>Influence of variation in the catechol-O-methyltransferase gene on the clinical outcome after lumbar spine surgery for one-level symptomatic disc disease: a report on 176 cases</title><source>Springer Nature:Jisc Collections:Springer Nature Read and Publish 2023-2025: Springer Reading List</source><creator>Rut, Marcin ; Machoy-Mokrzyńska, Anna ; Ręcławowicz, Daniel ; Słoniewski, Paweł ; Kurzawski, Mateusz ; Droździk, Marek ; Safranow, Krzysztof ; Morawska, Michalina ; Białecka, Monika</creator><creatorcontrib>Rut, Marcin ; Machoy-Mokrzyńska, Anna ; Ręcławowicz, Daniel ; Słoniewski, Paweł ; Kurzawski, Mateusz ; Droździk, Marek ; Safranow, Krzysztof ; Morawska, Michalina ; Białecka, Monika</creatorcontrib><description>Background
This study was aimed at the evaluation of the relationship between genetic polymorphisms of catechol-
O
-methyltransferase (COMT) (rs4680:A > G—Val158Met, rs6269:A > G, rs4633:C > T, rs4818:C > G) and pain sensitivity after lumbar discectomy.
Methods
All patients had one-level symptomatic disc herniation from L3 to S1. The primary data recorded included visual analogue pain scales assessing back and leg pain, Oswestry Disability Questionnaire assessing quality of life and pain intensity, received/filled pre- and postoperatively. Each subject was genotyped for single-nucleotide polymorphism in the
COMT
gene. Clinical outcome was measured by difference between pre- and postoperative values and those results were analyzed with genetics findings.
Results
Pain intensity was associated with the
COMT
polymorphism. Carriers of rs6269
AA
, rs4633
TT
, rs4818
CC
, and rs4680
AA
genotypes were characterized by the lowest preoperative scores related to pain intensity and lower pain intensity at 1 year after the surgery. The rs4633
CC
, rs4680
GG
genotypes demonstrated significant clinical improvement in VAS
BACK
score at 1 year after the surgery. Patients with COMT haplotype associated with low metabolic activity of enzyme (A_C_C_G) showed better clinical outcome measured by ODI score and VAS
BACK
score 1 year after surgery. We did not observe any significant correlation between leg pain and single-nucleotide polymorphisms in the COMT gene.
Conclusions
The results of our study indicate that polymorphism in the
COMT
gene may play an important role in the mechanism of pain perception, which may have a potential implication for clinical decision-making in the future.</description><identifier>ISSN: 0001-6268</identifier><identifier>EISSN: 0942-0940</identifier><identifier>DOI: 10.1007/s00701-013-1895-6</identifier><identifier>PMID: 24178190</identifier><language>eng</language><publisher>Vienna: Springer Vienna</publisher><subject>Adult ; Aged ; Aged, 80 and over ; Catechol O-Methyltransferase - genetics ; Clinical - Spine ; Clinical Article - Spine ; Clinical outcomes ; Female ; Genetic Predisposition to Disease ; Genotype ; Haplotypes - genetics ; Humans ; Interventional Radiology ; Intervertebral Disc Displacement - genetics ; Intervertebral Disc Displacement - surgery ; Male ; Medicine ; Medicine & Public Health ; Middle Aged ; Minimally Invasive Surgery ; Neurology ; Neuroradiology ; Neurosurgery ; Pain - genetics ; Polymorphism, Single Nucleotide ; Surgical Orthopedics ; Treatment Outcome ; Young Adult</subject><ispartof>Acta neurochirurgica, 2014-02, Vol.156 (2), p.245-252</ispartof><rights>The Author(s) 2013</rights><rights>Springer-Verlag Wien 2014</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c503t-12a205759134977aa6e72e3f10dbf38d708d3be44bb03fee810f77f78d3f281e3</citedby><cites>FETCH-LOGICAL-c503t-12a205759134977aa6e72e3f10dbf38d708d3be44bb03fee810f77f78d3f281e3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24178190$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Rut, Marcin</creatorcontrib><creatorcontrib>Machoy-Mokrzyńska, Anna</creatorcontrib><creatorcontrib>Ręcławowicz, Daniel</creatorcontrib><creatorcontrib>Słoniewski, Paweł</creatorcontrib><creatorcontrib>Kurzawski, Mateusz</creatorcontrib><creatorcontrib>Droździk, Marek</creatorcontrib><creatorcontrib>Safranow, Krzysztof</creatorcontrib><creatorcontrib>Morawska, Michalina</creatorcontrib><creatorcontrib>Białecka, Monika</creatorcontrib><title>Influence of variation in the catechol-O-methyltransferase gene on the clinical outcome after lumbar spine surgery for one-level symptomatic disc disease: a report on 176 cases</title><title>Acta neurochirurgica</title><addtitle>Acta Neurochir</addtitle><addtitle>Acta Neurochir (Wien)</addtitle><description>Background
This study was aimed at the evaluation of the relationship between genetic polymorphisms of catechol-
O
-methyltransferase (COMT) (rs4680:A > G—Val158Met, rs6269:A > G, rs4633:C > T, rs4818:C > G) and pain sensitivity after lumbar discectomy.
Methods
All patients had one-level symptomatic disc herniation from L3 to S1. The primary data recorded included visual analogue pain scales assessing back and leg pain, Oswestry Disability Questionnaire assessing quality of life and pain intensity, received/filled pre- and postoperatively. Each subject was genotyped for single-nucleotide polymorphism in the
COMT
gene. Clinical outcome was measured by difference between pre- and postoperative values and those results were analyzed with genetics findings.
Results
Pain intensity was associated with the
COMT
polymorphism. Carriers of rs6269
AA
, rs4633
TT
, rs4818
CC
, and rs4680
AA
genotypes were characterized by the lowest preoperative scores related to pain intensity and lower pain intensity at 1 year after the surgery. The rs4633
CC
, rs4680
GG
genotypes demonstrated significant clinical improvement in VAS
BACK
score at 1 year after the surgery. Patients with COMT haplotype associated with low metabolic activity of enzyme (A_C_C_G) showed better clinical outcome measured by ODI score and VAS
BACK
score 1 year after surgery. We did not observe any significant correlation between leg pain and single-nucleotide polymorphisms in the COMT gene.
Conclusions
The results of our study indicate that polymorphism in the
COMT
gene may play an important role in the mechanism of pain perception, which may have a potential implication for clinical decision-making in the future.</description><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Catechol O-Methyltransferase - genetics</subject><subject>Clinical - Spine</subject><subject>Clinical Article - Spine</subject><subject>Clinical outcomes</subject><subject>Female</subject><subject>Genetic Predisposition to Disease</subject><subject>Genotype</subject><subject>Haplotypes - genetics</subject><subject>Humans</subject><subject>Interventional Radiology</subject><subject>Intervertebral Disc Displacement - genetics</subject><subject>Intervertebral Disc Displacement - surgery</subject><subject>Male</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Middle Aged</subject><subject>Minimally Invasive Surgery</subject><subject>Neurology</subject><subject>Neuroradiology</subject><subject>Neurosurgery</subject><subject>Pain - genetics</subject><subject>Polymorphism, Single Nucleotide</subject><subject>Surgical Orthopedics</subject><subject>Treatment Outcome</subject><subject>Young Adult</subject><issn>0001-6268</issn><issn>0942-0940</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><recordid>eNqNks9u1DAQxiMEoqXwAFyQJS5cDHacxA4HJFTxp1KlXuBsOcl415VjL7az0r4Vj8iku1QFCYnLxM785huP_VXVS87ecsbku4yBccq4oFz1Le0eVeesb2qKgT3GNcNsV3fqrHqW8y3uatmIp9VZ3XCpeM_Oq59XwfoFwggkWrI3yZniYiAukLIFMpoC4zZ6ekNnKNuDL8mEbCGZDGQDAatOoHfBjcaTuJQxzkCMLZCIX-bBJJJ3DtG8pA2kA7ExYRlQD3vwJB_mXYkzth3J5PJdAJR_TwxJsIuprD247PAwGfLz6ok1PsOL0_ei-v7507fLr_T65svV5cdrOrZMFMprU7NWtj0XTS-lMR3IGoTlbBqsUJNkahIDNM0wMGEBFGdWSivxr60VB3FRfTjq7pZhhmmEgKN7vUtuNumgo3H6z0xwW72Jey1Ur0THUeDNSSDFHwvkomecDrw3AeKSNW_6TvWsb_v_QfERObtTff0XehuXFPAmVooppZq2Q4ofqTHFnBPY-3Nzplfr6KN1NFpHr9bRa82rhwPfV_z2CgL1EciYCviSD1r_U_UXCSLR0g</recordid><startdate>20140201</startdate><enddate>20140201</enddate><creator>Rut, Marcin</creator><creator>Machoy-Mokrzyńska, Anna</creator><creator>Ręcławowicz, Daniel</creator><creator>Słoniewski, Paweł</creator><creator>Kurzawski, Mateusz</creator><creator>Droździk, Marek</creator><creator>Safranow, Krzysztof</creator><creator>Morawska, Michalina</creator><creator>Białecka, Monika</creator><general>Springer Vienna</general><general>Springer Nature B.V</general><scope>C6C</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7TK</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>H94</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>PHGZM</scope><scope>PHGZT</scope><scope>PJZUB</scope><scope>PKEHL</scope><scope>PPXIY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>7X8</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope><scope>5PM</scope></search><sort><creationdate>20140201</creationdate><title>Influence of variation in the catechol-O-methyltransferase gene on the clinical outcome after lumbar spine surgery for one-level symptomatic disc disease: a report on 176 cases</title><author>Rut, Marcin ; Machoy-Mokrzyńska, Anna ; Ręcławowicz, Daniel ; Słoniewski, Paweł ; Kurzawski, Mateusz ; Droździk, Marek ; Safranow, Krzysztof ; Morawska, Michalina ; Białecka, Monika</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c503t-12a205759134977aa6e72e3f10dbf38d708d3be44bb03fee810f77f78d3f281e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Catechol O-Methyltransferase - genetics</topic><topic>Clinical - Spine</topic><topic>Clinical Article - Spine</topic><topic>Clinical outcomes</topic><topic>Female</topic><topic>Genetic Predisposition to Disease</topic><topic>Genotype</topic><topic>Haplotypes - genetics</topic><topic>Humans</topic><topic>Interventional Radiology</topic><topic>Intervertebral Disc Displacement - genetics</topic><topic>Intervertebral Disc Displacement - surgery</topic><topic>Male</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Middle Aged</topic><topic>Minimally Invasive Surgery</topic><topic>Neurology</topic><topic>Neuroradiology</topic><topic>Neurosurgery</topic><topic>Pain - genetics</topic><topic>Polymorphism, Single Nucleotide</topic><topic>Surgical Orthopedics</topic><topic>Treatment Outcome</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Rut, Marcin</creatorcontrib><creatorcontrib>Machoy-Mokrzyńska, Anna</creatorcontrib><creatorcontrib>Ręcławowicz, Daniel</creatorcontrib><creatorcontrib>Słoniewski, Paweł</creatorcontrib><creatorcontrib>Kurzawski, Mateusz</creatorcontrib><creatorcontrib>Droździk, Marek</creatorcontrib><creatorcontrib>Safranow, Krzysztof</creatorcontrib><creatorcontrib>Morawska, Michalina</creatorcontrib><creatorcontrib>Białecka, Monika</creatorcontrib><collection>Springer Nature OA Free Journals</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Neurosciences Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>ProQuest Central (New)</collection><collection>ProQuest One Academic (New)</collection><collection>ProQuest Health & Medical Research Collection</collection><collection>ProQuest One Academic Middle East (New)</collection><collection>ProQuest One Health & Nursing</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>MEDLINE - Academic</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Acta neurochirurgica</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Rut, Marcin</au><au>Machoy-Mokrzyńska, Anna</au><au>Ręcławowicz, Daniel</au><au>Słoniewski, Paweł</au><au>Kurzawski, Mateusz</au><au>Droździk, Marek</au><au>Safranow, Krzysztof</au><au>Morawska, Michalina</au><au>Białecka, Monika</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Influence of variation in the catechol-O-methyltransferase gene on the clinical outcome after lumbar spine surgery for one-level symptomatic disc disease: a report on 176 cases</atitle><jtitle>Acta neurochirurgica</jtitle><stitle>Acta Neurochir</stitle><addtitle>Acta Neurochir (Wien)</addtitle><date>2014-02-01</date><risdate>2014</risdate><volume>156</volume><issue>2</issue><spage>245</spage><epage>252</epage><pages>245-252</pages><issn>0001-6268</issn><eissn>0942-0940</eissn><abstract>Background
This study was aimed at the evaluation of the relationship between genetic polymorphisms of catechol-
O
-methyltransferase (COMT) (rs4680:A > G—Val158Met, rs6269:A > G, rs4633:C > T, rs4818:C > G) and pain sensitivity after lumbar discectomy.
Methods
All patients had one-level symptomatic disc herniation from L3 to S1. The primary data recorded included visual analogue pain scales assessing back and leg pain, Oswestry Disability Questionnaire assessing quality of life and pain intensity, received/filled pre- and postoperatively. Each subject was genotyped for single-nucleotide polymorphism in the
COMT
gene. Clinical outcome was measured by difference between pre- and postoperative values and those results were analyzed with genetics findings.
Results
Pain intensity was associated with the
COMT
polymorphism. Carriers of rs6269
AA
, rs4633
TT
, rs4818
CC
, and rs4680
AA
genotypes were characterized by the lowest preoperative scores related to pain intensity and lower pain intensity at 1 year after the surgery. The rs4633
CC
, rs4680
GG
genotypes demonstrated significant clinical improvement in VAS
BACK
score at 1 year after the surgery. Patients with COMT haplotype associated with low metabolic activity of enzyme (A_C_C_G) showed better clinical outcome measured by ODI score and VAS
BACK
score 1 year after surgery. We did not observe any significant correlation between leg pain and single-nucleotide polymorphisms in the COMT gene.
Conclusions
The results of our study indicate that polymorphism in the
COMT
gene may play an important role in the mechanism of pain perception, which may have a potential implication for clinical decision-making in the future.</abstract><cop>Vienna</cop><pub>Springer Vienna</pub><pmid>24178190</pmid><doi>10.1007/s00701-013-1895-6</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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language | eng |
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source | Springer Nature:Jisc Collections:Springer Nature Read and Publish 2023-2025: Springer Reading List |
subjects | Adult Aged Aged, 80 and over Catechol O-Methyltransferase - genetics Clinical - Spine Clinical Article - Spine Clinical outcomes Female Genetic Predisposition to Disease Genotype Haplotypes - genetics Humans Interventional Radiology Intervertebral Disc Displacement - genetics Intervertebral Disc Displacement - surgery Male Medicine Medicine & Public Health Middle Aged Minimally Invasive Surgery Neurology Neuroradiology Neurosurgery Pain - genetics Polymorphism, Single Nucleotide Surgical Orthopedics Treatment Outcome Young Adult |
title | Influence of variation in the catechol-O-methyltransferase gene on the clinical outcome after lumbar spine surgery for one-level symptomatic disc disease: a report on 176 cases |
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