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. 2014 Feb;156(2):245-52.
doi: 10.1007/s00701-013-1895-6. Epub 2013 Nov 1.

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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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

Marcin Rut et al. Acta Neurochir (Wien). 2014 Feb.

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 VASBACK 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 VASBACK 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.

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Figures

Fig. 1
Fig. 1
Illustration of incidence of different SNPs, depicted on the right are minor allele frequencies
Fig. 2
Fig. 2
ad Plots of changes in different pain scales after surgery and 1-year follow-up, grouped by distinct genotypes. Asterisk (*) depicts differences with p < 0,05. (A)—denotes minor allele, (B)—major allele

References

    1. Ameyaw MM, Syvänen AC, Ulmanen I, Ofori-Adjei D, McLeod HL. Pharmacogenetics of catechol-O-methyltransferase: frequency of low activity allele in a Ghanaian population. Hum Mutat. 2000;16(5):445–446. doi: 10.1002/1098-1004(200011)16:5<445::AID-HUMU13>3.0.CO;2-3. - DOI - PubMed
    1. An H, Thomas A. Spinal Stenosis. Princ. Tech. Spine Surg. Baltimore: Williams & Wilkins; 1997. pp. 443–460.
    1. Asch HL, Lewis PJ, Moreland DB, Egnatchik JG, Yu YJ, Clabeaux DE, Hyland AH. Prospective multiple outcomes study of outpatient lumbar microdiscectomy: should 75 to 80% success rates be the norm? J Neurosurg. 2002;96(1 Suppl):34–44. - PubMed
    1. Atlas SJ, Keller RB, Chang Y, Deyo RA, Singer DE. Surgical and nonsurgical management of sciatica secondary to a lumbar disc herniation: five-year outcomes from the Maine Lumbar Spine Study. Spine. 2001;26(10):1179–1187. doi: 10.1097/00007632-200105150-00017. - DOI - PubMed
    1. Campbell CM, Edwards RR, Fillingim RB. Ethnic differences in responses to multiple experimental pain stimuli. Pain. 2005;113(1–2):20–26. doi: 10.1016/j.pain.2004.08.013. - DOI - PubMed

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