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偏头痛患者细胞因子多态性:一些提示偏头痛和炎症的线索。

Cytokine polymorphism in patients with migraine: some suggestive clues of migraine and inflammation.

机构信息

Department of Neurology, Mersin University School of Medicine, Mersin, Turkey.

出版信息

Pain Med. 2010 Apr;11(4):492-7. doi: 10.1111/j.1526-4637.2009.00791.x. Epub 2010 Jan 22.

DOI:10.1111/j.1526-4637.2009.00791.x
PMID:20113413
Abstract

OBJECTIVE

There are contrasting results obtained in migraineurs concerning the levels and the role of both pro-inflammatory and anti-inflammatory cytokines. In this study, the association of the occurrence and clinical characteristics of migraine with the polymorphisms of tumor necrosis factor alpha (TNF-alpha) -308 G/A (rs1800629), interleukin-1alpha (IL-1alpha) +4845 G/T (rs17561), IL-1beta+3953 C/T (rs1143634) and interleukin-1 receptor antagonist variable number tandem repeat (IL-1RA VNTR) genes were studied. We also investigated the genetic linkage between these genes.

DESIGN, SETTING, PATIENTS: Sixty-seven patients with migraine without aura (MwoA) and 96 unrelated, age- and sex-matched migraine-free, healthy control subjects from the same geographic area were investigated.

RESULTS

We observed significant differences in the genotypic distribution of the TNF-alpha-308 G/A and IL-1beta+3953 C/T polymorphism for migraineurs compared with controls (P = 0.004). Frequency of the TNF-alpha-308 GG genotype was higher in the control group than MwoA group (82.1% vs 55.2%). Differences in the distribution of the allele frequencies were also observed, being the TNF-alpha-308 G allele overrepresented in control group and TNF-alpha-308 A allele in MwoA group. In addition, there was a significant increase of the IL-1beta+3953 T allele in MwoA cases compared with controls (P = 0.004).

CONCLUSIONS

In conclusion, the present results indicate the possible contribution of TNF-alpha and IL-1beta gene polymorphisms to migraine headache generation in MwoA patients.

摘要

目的

在偏头痛患者中,促炎细胞因子和抗炎细胞因子的水平和作用存在相互矛盾的结果。在这项研究中,研究了肿瘤坏死因子-α(TNF-α)-308 G/A(rs1800629)、白细胞介素-1α(IL-1α)+4845 G/T(rs17561)、IL-1β+3953 C/T(rs1143634)和白细胞介素-1受体拮抗剂可变数串联重复(IL-1RA VNTR)基因的多态性与偏头痛的发生和临床特征的关联。我们还研究了这些基因之间的遗传连锁关系。

设计、地点、患者:来自同一地理区域的 67 例无先兆偏头痛(MwoA)患者和 96 例年龄和性别匹配的无偏头痛、健康对照者。

结果

与对照组相比,我们观察到 TNF-α-308 G/A 和 IL-1β+3953 C/T 多态性在偏头痛患者中的基因型分布存在显著差异(P = 0.004)。TNF-α-308 GG 基因型在对照组中的频率高于 MwoA 组(82.1%比 55.2%)。等位基因频率的分布也存在差异,TNF-α-308 G 等位基因在对照组中较多,TNF-α-308 A 等位基因在 MwoA 组中较多。此外,MwoA 病例中 IL-1β+3953 T 等位基因的分布显著增加,与对照组相比差异有统计学意义(P = 0.004)。

结论

总之,本研究结果表明 TNF-α 和 IL-1β 基因多态性可能导致 MwoA 患者偏头痛发作。

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