No evidence for a role of the catechol-O-methyltransferase pain sensitivity haplotypes in chronic widespread pain

Barbara I. Nicholl, Kate L. Holliday, Gary J. Macfarlane, Wendy Thomson, Kelly A. Davies, Terence W. O'Neill, G. Bártfai, Steven Boonen, Felipe Casanueva, Joseph D. Finn, Gianni Forti, Aleksander Giwercman, Ilpo T. Huhtaniemi, Krzysztof Kula, Margus Punab, Alan J. Silman, Dirk Vanderschueren, Frederick C W Wu, John McBeth, Luisa Petrone & 14 others Antonio Cilotti, Herman Borghs, Jolanta Slowikowska-Hilczer, Renata Walczak-Jedrzejowska, Philip Steer, Abdelouahid Tajar, David Lee, Stephen Pye, Marta Ocampo, Mary Lage, I. Földesi, I. Fejes, Paul Korrovitz, Min Jiang

Research output: Contribution to journalArticle

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Abstract

Objectives: The aim of this study was to investigate the association between the catechol-O-methyltransferase (COMT) 'pain sensitivity' haplotypes and chronic widespread pain (CWP) in two distinct cohorts. Methods: Cases of CWP and controls free of pain were selected from two population-based studies: the Epidemiology of Functional Disorders study (EPIFUND) (UK) and the European Male Ageing Study (European). The number of cases and controls were 164 and 172, and 204 and 935, respectively. Identical American College of Rheumatology criteria were used in both studies to ascertain CWP status. The EPIFUND study had three time points and cases were classified as subjects with CWP at two or three time points and controls as those free of pain at all three time points. Four single nucleotide polymorphisms (SNP): rs6269, rs4633, rs4818 and rs4680 (V158M) were genotyped using Sequenom technology. Allele and genotype frequencies were compared and haplotype analysis was conducted using PLINK software. Results: No differences in allele or genotype frequencies for any of the four SNP were observed between cases and controls for either cohort. Haplotype analysis also showed no difference in the frequency of haplotypes between cases and controls. Conclusions: There was no evidence of association between the COMT 'pain sensitivity' haplotypes and CWP in two population-based cohorts.

Original languageEnglish
Pages (from-to)2009-2012
Number of pages4
JournalAnnals of the Rheumatic Diseases
Volume69
Issue number11
DOIs
Publication statusPublished - Nov 2010

Fingerprint

Catechol O-Methyltransferase
Chronic Pain
Haplotypes
Pain
Epidemiology
Polymorphism
Single Nucleotide Polymorphism
Nucleotides
Genotype
Gene Frequency
Population
Software
Aging of materials
Alleles
Technology

ASJC Scopus subject areas

  • Rheumatology
  • Immunology
  • Biochemistry, Genetics and Molecular Biology(all)
  • Immunology and Allergy

Cite this

Nicholl, B. I., Holliday, K. L., Macfarlane, G. J., Thomson, W., Davies, K. A., O'Neill, T. W., ... Jiang, M. (2010). No evidence for a role of the catechol-O-methyltransferase pain sensitivity haplotypes in chronic widespread pain. Annals of the Rheumatic Diseases, 69(11), 2009-2012. https://doi.org/10.1136/ard.2009.126086

No evidence for a role of the catechol-O-methyltransferase pain sensitivity haplotypes in chronic widespread pain. / Nicholl, Barbara I.; Holliday, Kate L.; Macfarlane, Gary J.; Thomson, Wendy; Davies, Kelly A.; O'Neill, Terence W.; Bártfai, G.; Boonen, Steven; Casanueva, Felipe; Finn, Joseph D.; Forti, Gianni; Giwercman, Aleksander; Huhtaniemi, Ilpo T.; Kula, Krzysztof; Punab, Margus; Silman, Alan J.; Vanderschueren, Dirk; Wu, Frederick C W; McBeth, John; Petrone, Luisa; Cilotti, Antonio; Borghs, Herman; Slowikowska-Hilczer, Jolanta; Walczak-Jedrzejowska, Renata; Steer, Philip; Tajar, Abdelouahid; Lee, David; Pye, Stephen; Ocampo, Marta; Lage, Mary; Földesi, I.; Fejes, I.; Korrovitz, Paul; Jiang, Min.

In: Annals of the Rheumatic Diseases, Vol. 69, No. 11, 11.2010, p. 2009-2012.

Research output: Contribution to journalArticle

Nicholl, BI, Holliday, KL, Macfarlane, GJ, Thomson, W, Davies, KA, O'Neill, TW, Bártfai, G, Boonen, S, Casanueva, F, Finn, JD, Forti, G, Giwercman, A, Huhtaniemi, IT, Kula, K, Punab, M, Silman, AJ, Vanderschueren, D, Wu, FCW, McBeth, J, Petrone, L, Cilotti, A, Borghs, H, Slowikowska-Hilczer, J, Walczak-Jedrzejowska, R, Steer, P, Tajar, A, Lee, D, Pye, S, Ocampo, M, Lage, M, Földesi, I, Fejes, I, Korrovitz, P & Jiang, M 2010, 'No evidence for a role of the catechol-O-methyltransferase pain sensitivity haplotypes in chronic widespread pain', Annals of the Rheumatic Diseases, vol. 69, no. 11, pp. 2009-2012. https://doi.org/10.1136/ard.2009.126086
Nicholl, Barbara I. ; Holliday, Kate L. ; Macfarlane, Gary J. ; Thomson, Wendy ; Davies, Kelly A. ; O'Neill, Terence W. ; Bártfai, G. ; Boonen, Steven ; Casanueva, Felipe ; Finn, Joseph D. ; Forti, Gianni ; Giwercman, Aleksander ; Huhtaniemi, Ilpo T. ; Kula, Krzysztof ; Punab, Margus ; Silman, Alan J. ; Vanderschueren, Dirk ; Wu, Frederick C W ; McBeth, John ; Petrone, Luisa ; Cilotti, Antonio ; Borghs, Herman ; Slowikowska-Hilczer, Jolanta ; Walczak-Jedrzejowska, Renata ; Steer, Philip ; Tajar, Abdelouahid ; Lee, David ; Pye, Stephen ; Ocampo, Marta ; Lage, Mary ; Földesi, I. ; Fejes, I. ; Korrovitz, Paul ; Jiang, Min. / No evidence for a role of the catechol-O-methyltransferase pain sensitivity haplotypes in chronic widespread pain. In: Annals of the Rheumatic Diseases. 2010 ; Vol. 69, No. 11. pp. 2009-2012.
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abstract = "Objectives: The aim of this study was to investigate the association between the catechol-O-methyltransferase (COMT) 'pain sensitivity' haplotypes and chronic widespread pain (CWP) in two distinct cohorts. Methods: Cases of CWP and controls free of pain were selected from two population-based studies: the Epidemiology of Functional Disorders study (EPIFUND) (UK) and the European Male Ageing Study (European). The number of cases and controls were 164 and 172, and 204 and 935, respectively. Identical American College of Rheumatology criteria were used in both studies to ascertain CWP status. The EPIFUND study had three time points and cases were classified as subjects with CWP at two or three time points and controls as those free of pain at all three time points. Four single nucleotide polymorphisms (SNP): rs6269, rs4633, rs4818 and rs4680 (V158M) were genotyped using Sequenom technology. Allele and genotype frequencies were compared and haplotype analysis was conducted using PLINK software. Results: No differences in allele or genotype frequencies for any of the four SNP were observed between cases and controls for either cohort. Haplotype analysis also showed no difference in the frequency of haplotypes between cases and controls. Conclusions: There was no evidence of association between the COMT 'pain sensitivity' haplotypes and CWP in two population-based cohorts.",
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T1 - No evidence for a role of the catechol-O-methyltransferase pain sensitivity haplotypes in chronic widespread pain

AU - Nicholl, Barbara I.

AU - Holliday, Kate L.

AU - Macfarlane, Gary J.

AU - Thomson, Wendy

AU - Davies, Kelly A.

AU - O'Neill, Terence W.

AU - Bártfai, G.

AU - Boonen, Steven

AU - Casanueva, Felipe

AU - Finn, Joseph D.

AU - Forti, Gianni

AU - Giwercman, Aleksander

AU - Huhtaniemi, Ilpo T.

AU - Kula, Krzysztof

AU - Punab, Margus

AU - Silman, Alan J.

AU - Vanderschueren, Dirk

AU - Wu, Frederick C W

AU - McBeth, John

AU - Petrone, Luisa

AU - Cilotti, Antonio

AU - Borghs, Herman

AU - Slowikowska-Hilczer, Jolanta

AU - Walczak-Jedrzejowska, Renata

AU - Steer, Philip

AU - Tajar, Abdelouahid

AU - Lee, David

AU - Pye, Stephen

AU - Ocampo, Marta

AU - Lage, Mary

AU - Földesi, I.

AU - Fejes, I.

AU - Korrovitz, Paul

AU - Jiang, Min

PY - 2010/11

Y1 - 2010/11

N2 - Objectives: The aim of this study was to investigate the association between the catechol-O-methyltransferase (COMT) 'pain sensitivity' haplotypes and chronic widespread pain (CWP) in two distinct cohorts. Methods: Cases of CWP and controls free of pain were selected from two population-based studies: the Epidemiology of Functional Disorders study (EPIFUND) (UK) and the European Male Ageing Study (European). The number of cases and controls were 164 and 172, and 204 and 935, respectively. Identical American College of Rheumatology criteria were used in both studies to ascertain CWP status. The EPIFUND study had three time points and cases were classified as subjects with CWP at two or three time points and controls as those free of pain at all three time points. Four single nucleotide polymorphisms (SNP): rs6269, rs4633, rs4818 and rs4680 (V158M) were genotyped using Sequenom technology. Allele and genotype frequencies were compared and haplotype analysis was conducted using PLINK software. Results: No differences in allele or genotype frequencies for any of the four SNP were observed between cases and controls for either cohort. Haplotype analysis also showed no difference in the frequency of haplotypes between cases and controls. Conclusions: There was no evidence of association between the COMT 'pain sensitivity' haplotypes and CWP in two population-based cohorts.

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