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Association of an Interleukin-16 Gene Polymorphism with the Risk and Pain Phenotype of Endometriosis

机译:白介素16基因多态性与子宫内膜异位症的风险和疼痛表型的关联。

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Interleukin-16 (IL-16), a proinflammatory cytokine, plays a pivotal role in inflammatory diseases as well as in the pathogenesis of endometriosis. The aim of this study was to evaluate the association of IL-16 gene polymorphisms with the risk and clinical phenotypes of endometriosis in Chinese women. We analyzed rs4778889 T/C, rs11556218 T/G polymorphisms of the IL-16 gene in 230 patients with endometriosis and 203 controls in a Chinese population, using a polymerase chain reaction-high resolution melting analysis strategy and DNA sequencing methods. There was no significant difference in the genotype and allele frequencies of the rs11556218 T/G polymorphism between patients with endometriosis and controls (p>0.05). In contrast, the genotype and allele frequencies of the rs4778889 T/C polymorphism were statistically different between patients with endometriosis and controls, which resulted from a significantly increased proportion of TC heterozygote and CC homozygote carriers among patients with endometriosis (p=0.001 and 0.012, respectively); moreover, further subgroup analysis found that the genotype difference was more evident in patients with endometriosis who also experienced pain symptoms (p<0.001) than in patients without pain symptoms (p=0.625) when compared with controls. Our results suggest that the rs4778889 T/C polymorphism of the IL-16 gene may be associated with risk of endometriosis in the Chinese population, especially in patients with pain phenotype.
机译:白细胞介素16(IL-16)是一种促炎性细胞因子,在炎症性疾病以及子宫内膜异位症的发病机理中起着关键作用。这项研究的目的是评估中国女性子宫内膜异位症的风险和临床表型与IL-16基因多态性的关系。我们使用聚合酶链反应-高分辨率熔解分析策略和DNA测序方法,分析了230例子宫内膜异位患者和203例对照中IL-16基因的rs4778889 T / C,rs11556218 T / G多态性。子宫内膜异位症患者与对照组之间的rs11556218 T / G多态性的基因型和等位基因频率无显着差异(p> 0.05)。相比之下,子宫内膜异位症患者和对照组之间rs4778889 T / C多态性的基因型和等位基因频率在统计学上是不同的,这是由于子宫内膜异位症患者中TC杂合子和CC纯合子携带者的比例显着增加(p = 0.001和0.012,分别);此外,进一步的亚组分析发现,与对照组相比,子宫内膜异位症患者也经历疼痛症状(p <0.001)的基因型差异比无疼痛症状的患者(p = 0.625)更明显。我们的研究结果表明,IL-16基因的rs4778889 T / C多态性可能与中国人群子宫内膜异位症的风险有关,尤其是在具有疼痛表型的患者中。

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