Suppr超能文献

细胞因子基因启动子多态性与急性肾衰竭患者的死亡率

Cytokine gene promoter polymorphisms and mortality in acute renal failure.

作者信息

Jaber Bertrand L, Rao Madhumathi, Guo Daqing, Balakrishnan Vaidyanathapuram S, Perianayagam Mary C, Freeman Richard B, Pereira Brian J G

机构信息

Division of Nephrology, Tufts-New England Medical Center, Boston, MA 02111, USA.

出版信息

Cytokine. 2004 Mar 7;25(5):212-9. doi: 10.1016/j.cyto.2003.11.004.

Abstract

BACKGROUND

Although cytokines play a pivotal role in the inflammatory responses that mediate the severity of acute renal failure (ARF), the importance of pro- and anti-inflammatory cytokine gene promoter polymorphisms has been unexplored.

METHODS

We prospectively evaluated the relationship of single nucleotide polymorphism in the promoter region of tumor necrosis factor alpha (TNF-alpha) and interleukin-10 (IL-10) to mortality in 61 patients with ARF requiring intermittent hemodialysis. Cytokine genotyping was performed on leukocytes using PCR techniques. Cox proportional-hazards regression analysis was used to explore these relationships.

RESULTS

The mean (+/-SD) APACHE II score was 24 +/- 7, MOF score 2 +/- 1, and 64% had sepsis. The TNF-alpha high producer genotype (-308 A-allele carrier) was associated with a higher risk of death after adjustment for the APACHE II score (HR=2.5; P=0.04), and the IL-10 intermediate/high producer genotype (-1082 G-allele carrier) was associated with a lower risk of death after adjustment for the MOF score (HR=0.36; P=0.03). Considering combinations of genotypes, the TNF-alpha high and IL-10 low producer genotype combination was associated with a approximately 6-fold increased risk of death compared to the TNF-alpha-low and IL-10 intermediate/high producer genotype combination, after adjustment for either APACHE II (P=0.004), MOF score (P=0.004) or sepsis (P=0.006).

CONCLUSIONS

TNF-alpha and IL-10 gene polymorphisms are related to the risk of death among patients with ARF who require dialysis. Larger studies are needed to confirm these relationships.

摘要

背景

尽管细胞因子在介导急性肾衰竭(ARF)严重程度的炎症反应中起关键作用,但促炎和抗炎细胞因子基因启动子多态性的重要性尚未得到探索。

方法

我们前瞻性评估了61例需要间歇性血液透析的ARF患者中肿瘤坏死因子α(TNF-α)和白细胞介素-10(IL-10)启动子区域单核苷酸多态性与死亡率的关系。使用PCR技术对白细胞进行细胞因子基因分型。采用Cox比例风险回归分析来探索这些关系。

结果

平均(±标准差)急性生理与慢性健康状况评分系统(APACHE II)评分为24±7,多器官功能障碍评分(MOF)为2±1,64%的患者患有脓毒症。调整APACHE II评分后,TNF-α高产生基因型(-308 A等位基因携带者)与较高的死亡风险相关(风险比[HR]=2.5;P=0.04),调整MOF评分后,IL-10中等/高产生基因型(-1082 G等位基因携带者)与较低的死亡风险相关(HR=0.36;P=0.03)。考虑基因型组合,调整APACHE II(P=0.004)、MOF评分(P=0.004)或脓毒症(P=0.006)后,与TNF-α低和IL-10中等/高产生基因型组合相比,TNF-α高和IL-10低产生基因型组合的死亡风险增加约6倍。

结论

TNF-α和IL-10基因多态性与需要透析的ARF患者的死亡风险相关。需要更大规模的研究来证实这些关系。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验