Finnish Institute of Occupational Health, Helsinki, Finland.
Eur Spine J. 2009 Dec;18(12):1963-70. doi: 10.1007/s00586-009-1139-x. Epub 2009 Aug 22.
According to recent systematic reviews, Modic changes are associated with low-back pain. However, their pathophysiology remains largely unknown. A previous study of Northern Finnish males implicated that IL1A and MMP3 polymorphisms play a role in type II Modic changes. The purpose of the current study was to examine the association of IL1 cluster polymorphisms with Modic changes amongst middle-aged men in Southern Finland. The final study sample consisted of 108 men from three different occupations, who underwent magnetic resonance imaging (MRI) with a 0.1 T-scanner. Six single nucleotide polymorphisms (SNP) in the IL1 gene cluster (IL1A c.1-889C>T; IL1B c.3954C>T; IL1RN c.1812G>A; IL1RN c.1887G>C; IL1RN c.11100T>C; IL1RN c.1506G>A) were genotyped with the SNP-TRAP method or by allele-specific primer extension on modified microarray. In all, 45 subjects had Modic changes at one or more disc levels. The presence of the minor allele of IL1A (c.1-889C>T) was associated with these changes (any Modic change p = 0.031, type II changes p = 0.036). The carriers of the T-allele had a 2.5-fold risk of Modic change and the association was independent of the other IL1 gene cluster loci studied. In addition, a minor haplotype, with a frequency of 7.5% in the study population, including the minor alleles of IL1A c.1-889C>T, IL1RN c.1812G>A, and IL1RN c.1506G>A, was significantly associated with Modic changes. This observation is in accordance with the previous finding from a different geographical area, and thus confirms the importance of the IL1A gene in the pathophysiology of Modic changes.
根据最近的系统评价,Modic 改变与下腰痛有关。然而,其病理生理学仍知之甚少。先前对芬兰北部男性的研究表明,IL1A 和 MMP3 多态性在 II 型 Modic 改变中起作用。本研究旨在研究白细胞介素 1 簇多态性与芬兰南部中年男性 Modic 改变之间的关系。最终的研究样本包括来自三种不同职业的 108 名男性,他们使用 0.1 T 扫描仪进行了磁共振成像(MRI)。在白细胞介素 1 基因簇(IL1A c.1-889C>T;IL1B c.3954C>T;IL1RN c.1812G>A;IL1RN c.1887G>C;IL1RN c.11100T>C;IL1RN c.1506G>A)中,共检测到 6 个单核苷酸多态性(SNP),采用 SNP-TRAP 方法或在改良微阵列上用等位基因特异性引物延伸进行基因分型。共有 45 名受试者在一个或多个椎间盘水平发生 Modic 改变。IL1A(c.1-889C>T)的次要等位基因的存在与这些改变相关(任何 Modic 改变 p=0.031,II 型改变 p=0.036)。携带 T 等位基因的个体发生 Modic 改变的风险增加了 2.5 倍,且这种关联独立于其他研究的白细胞介素 1 基因簇位点。此外,在研究人群中频率为 7.5%的一个小单倍型,包括 IL1A c.1-889C>T、IL1RN c.1812G>A 和 IL1RN c.1506G>A 的次要等位基因,与 Modic 改变显著相关。这一观察结果与来自不同地理区域的先前发现一致,从而证实了白细胞介素 1A 基因在 Modic 改变的病理生理学中的重要性。