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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
Main Authors: Rut, Marcin, Machoy-Mokrzyńska, Anna, Ręcławowicz, Daniel, Słoniewski, Paweł, Kurzawski, Mateusz, Droździk, Marek, Safranow, Krzysztof, Morawska, Michalina, Białecka, Monika
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container_title Acta neurochirurgica
container_volume 156
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
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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 &amp; 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 &gt; G—Val158Met, rs6269:A &gt; G, rs4633:C &gt; T, rs4818:C &gt; 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 &amp; 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 ; 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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 &amp; 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G—Val158Met, rs6269:A &gt; G, rs4633:C &gt; T, rs4818:C &gt; 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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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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