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The MMP9 rs17576 A>G polymorphism is associated with increased lumbopelvic pain-intensity in pregnant women.
Mahmood, Aqsa Khalid; Moen, Aurora; Stafne, Signe Nilssen; Robinson, Hilde Stendal; Vøllestad, Nina Køpke; Salvesen, Kjell Åsmund; Mørkved, Siv; Gjerstad, Johannes.
Afiliación
  • Mahmood AK; National Institute of Occupational Health, Oslo, Norway.
  • Moen A; National Institute of Occupational Health, Oslo, Norway.
  • Stafne SN; Department of Public Health and General Practice, Norwegian University of Science and Technology, Trondheim, Norway.
  • Robinson HS; Clinical Service, St. Olavs Hospital, Trondheim University Hospital, Trondheim, Norway.
  • Vøllestad NK; Department of Health Science, Institute of Health and Society, University of Oslo, Oslo, Norway.
  • Salvesen KÅ; Department of Health Science, Institute of Health and Society, University of Oslo, Oslo, Norway.
  • Mørkved S; Department of Public Health and General Practice, Norwegian University of Science and Technology, Trondheim, Norway.
  • Gjerstad J; Clinical Service, St. Olavs Hospital, Trondheim University Hospital, Trondheim, Norway.
Scand J Pain ; 18(1): 93-98, 2018 01 26.
Article en En | MEDLINE | ID: mdl-29794283
BACKGROUND AND AIMS: Matrix metalloproteinase 9 (MMP9) is an enzyme that may affect degradation of several extracellular matrix (ECM) components in the pelvic ligaments during pregnancy. Previous studies indicate that genetic variations in the gene encoding MMP9 may affect the enzymatic activity. One such genetic variant is a single nucleotide polymorphism (SNP), rs17576 A>G. In this study we investigated whether the MMP9 SNP rs17576 A>G may be associated with increased lumbopelvic pain in 838 pregnant woman. The study was registered with ClinicalTrials.gov (NCT 00476567) on May 21, 2007. METHODS: Lumbopelvic pain-intensity was measured by visual analog scale (VAS) at two time points during pregnancy, T1 (18-22 weeks), T2 (32-36 weeks) and 3 months after delivery. Blood samples were collected at each point and SNP genotyping was carried out using predesigned TaqMan SNP genotyping assays. RESULTS: The results showed a significant association between the number of G alleles and pain-intensity in the evening at T2. The pain among G/G carriers was higher than among A/G carriers, which in turn was higher than among the A/A carriers. The most pronounced association between the G allele and pain-intensity was observed in primiparae. CONCLUSIONS: We conclude that the MMP9 rs17576 A>G polymorphism is associated with increased lumbopelvic pain-intensity during pregnancy. The present data support the hypothesis that lumbopelvic pain during pregnancy may be related to a relaxin - MMP9 - tissue remodeling mechanism. IMPLICATIONS: The present findings may be important for future mechanistic studies on how MMP9 rs17576 A>G may affect changes in the ECM components in pelvic ligaments and lumbopelvic pain-intensity during pregnancy.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Complicaciones del Embarazo / Dolor de la Región Lumbar / Dolor Pélvico / Predisposición Genética a la Enfermedad / Metaloproteinasa 9 de la Matriz / Polimorfismo de Nucleótido Simple Tipo de estudio: Clinical_trials / Prognostic_studies / Risk_factors_studies Límite: Adult / Female / Humans / Middle aged / Pregnancy Idioma: En Revista: Scand J Pain Año: 2018 Tipo del documento: Article País de afiliación: Noruega Pais de publicación: Alemania

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Complicaciones del Embarazo / Dolor de la Región Lumbar / Dolor Pélvico / Predisposición Genética a la Enfermedad / Metaloproteinasa 9 de la Matriz / Polimorfismo de Nucleótido Simple Tipo de estudio: Clinical_trials / Prognostic_studies / Risk_factors_studies Límite: Adult / Female / Humans / Middle aged / Pregnancy Idioma: En Revista: Scand J Pain Año: 2018 Tipo del documento: Article País de afiliación: Noruega Pais de publicación: Alemania