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首页> 外文期刊>Tissue antigens. >The 32-base pair deletion of the chemokine receptor 5 gene (CCR5-Delta32) is not associated with primary sclerosing cholangitis in 363 Scandinavian patients.
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The 32-base pair deletion of the chemokine receptor 5 gene (CCR5-Delta32) is not associated with primary sclerosing cholangitis in 363 Scandinavian patients.

机译:在363名斯堪的纳维亚患者中,趋化因子受体5基因(CCR5-Delta32)的32个碱基对的缺失与原发性硬化性胆管炎无关。

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摘要

CCR5 is a chemokine receptor expressed on T-cells and macrophages. A 32-base pair deletion in the chemokine receptor 5 gene (CCR5-Delta32) leads to a non-functional receptor. Conflicting evidence exists whether this deletion is associated with primary sclerosing cholangitis (PSC). We genotyped the CCR5-Delta32 variant in 363 PSC patients and 366 controls. No significant increase in the Delta32 allele frequency was detected in the PSC patients compared to controls (12.7% vs 10.7% OR = 1.22, 95% CI [0.88, 1.68], P = 0.23). Survival analysis did not reveal any significant effects from CCR5-Delta32 genotypes on disease progression. Thus, in this study (power > 90%, given OR = 2, alpha = 0.05), we were unable to replicate previous findings and our results do not support an involvement of CCR5-Delta32 in either PSC susceptibility or progression.
机译:CCR5是在T细胞和巨噬细胞上表达的趋化因子受体。趋化因子受体5基因(CCR5-Delta32)中的一个32个碱基对的删除导致一个无功能的受体。有证据表明这种缺失是否与原发性硬化性胆管炎(PSC)有关。我们对363名PSC患者和366名对照的CCR5-Delta32变异进行了基因分型。与对照组相比,PSC患者中未检测到Delta32等位基因频率的显着增加(12.7%vs. 10.7%OR = 1.22,95%CI [0.88,1.68],P = 0.23)。生存分析未显示CCR5-Delta32基因型对疾病进展有任何重大影响。因此,在这项研究中(功效> 90%,给定OR = 2,α= 0.05),我们无法复制以前的发现,我们的结果不支持CCR5-Delta32参与PSC易感性或进展。

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