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   <subfield code="a">The IL - 1 β (+3953 T/C) gene polymorphism associates to symptomatic lumbar disc herniation</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[J. Paz Aparicio, I. Fernández Bances, E. López-Anglada Fernández, A. Montes, A. Paz Aparicio, J. Pena Vázquez, S. Ramos García, S. Antón García, P. López Fernández, E. Valle-Garay, V. Asensi]</subfield>
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   <subfield code="a">Purpose: To determine whether polymorphisms (SNPs) in the genes encoding cytokines and nitric oxide synthase (NOS) might play some role in lumbar disc herniation (LDH). Patients and methods: Case-control study in which 179 patients were retrospectively reviewed. The case group was made of 50 patients with symptomatic LDH diagnosed by MRI while the control group was made of 129 individuals undergoing routine hip or knee arthroplasty with a lifetime lack of low back pain. SNPs in the cytokine genes of IL-1 [IL-1α (−889 C/T), IL-1β (+3953 T/C)], TNF-α (−308 G/A and −238 G/A) and NOS genes [eNOS (r 27bp, intron 4 and −786 T/C) and iNOS (22G/A)]. Results: The CC genotype and C allele of the IL-1β (+3953 T/C) SNP were significantly more frequent among LDH patients compared to controls. On the other hand, eNOS (−768 T/C) and iNOS (22G/A) SNPs were significantly more common in the control group. Conclusions: Carriers of the CC genotype of the IL-1β (+3953 T/C) SNP were more frequent among LDH patients suggesting some potential role of the IL-1β SNP on LDH pathogenesis. The eNOS (−786 T/C) and iNOS (22 G/A) SNPs were more frequent among the control subjects, suggesting their possible protective role against LDH. Genotyping these SNPs could be useful to identify persons with an increased lifetime risk of disc herniation in whom measures to avoid LDH could be implemented.</subfield>
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   <subfield code="a">Springer-Verlag, 2011</subfield>
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   <subfield code="a">Lumbar disc herniation</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">Polymorphism</subfield>
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   <subfield code="a">Cytokine</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">Nitric oxide synthase</subfield>
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   <subfield code="a">Paz Aparicio</subfield>
   <subfield code="D">J.</subfield>
   <subfield code="u">Servicio de Cirugía Ortopédica y Traumatología, Hospital Universitario Central de Asturias, Celestino Villamil s/n, 33006, Oviedo, Spain</subfield>
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   <subfield code="a">Fernández Bances</subfield>
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   <subfield code="a">López-Anglada Fernández</subfield>
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   <subfield code="u">Servicio de Cirugía Ortopédica y Traumatología, Hospital Universitario Central de Asturias, Celestino Villamil s/n, 33006, Oviedo, Spain</subfield>
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   <subfield code="u">Biochemistry and Molecular Biology, Oviedo University Medical School, Oviedo, Spain</subfield>
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   <subfield code="a">Paz Aparicio</subfield>
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   <subfield code="t">European Spine Journal</subfield>
   <subfield code="d">Springer-Verlag</subfield>
   <subfield code="g">20(2011-08-01), 383-389</subfield>
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