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作 者:刘慧琳[1] 田勍[2] 洪天配[2] 刘桂花[1] 潘欢[3] 王海宁[2] 高洪伟[2]
机构地区:[1]北京大学第三医院急诊科,北京100191 [2]北京大学第三医院内分泌科,北京100191 [3]北京大学人类疾病基因研究中心,北京100191
出 处:《北京大学学报(医学版)》2013年第2期238-241,共4页Journal of Peking University:Health Sciences
摘 要:目的:探讨血清程序化细胞死亡因子5(programmed cell death 5 protein,PDCD5)水平在全身炎症反应综合征(systemic inflammatory response syndrome,SIRS)、脓毒症及重症脓毒症患者中的变化。方法:78例患者纳入本研究,其中SIRS(脓毒症除外)患者28例、脓毒症(重症脓毒症除外)患者23例、重症脓毒症患者27例,并选取健康对照22例,分别收集其静脉血清,采用酶联免疫吸附法检测PDCD5水平,比较PDCD5水平的差异。采用Spearman相关分析评价血清PDCD5水平与急性生理和慢性健康状况评分Ⅱ(acute physiology and chronic health evaluationⅡ,APACHEⅡ)积分、超敏C反应蛋白(high-sensitivity C-reactive protein,hs-CRP)、白细胞计数、中性粒细胞计数和年龄等因素的相关性。结果:在SIRS组、脓毒症组及重症脓毒症组中,血清PDCD5水平分别为(19.07±8.91)、(29.03±13.27)及(42.83±17.32)μg/L,显著高于健康对照组的(0.32±0.02)μg/L(P<0.05);血清PDCD5水平在SIRS组、脓毒症组及重症脓毒症组中呈现依次升高的变化规律,组间差异具有统计学意义(P<0.05)。此外,血清PDCD5水平与APACHEⅡ积分呈正相关(r=0.572,P<0.05)。结论:脓毒症患者血清PDCD5水平随着病情加重呈升高趋势,提示PDCD5表达上调在脓毒症发生、发展中可能起到一定作用。Objective: To investigate the changes of serum programmed cell death 5 ( PDCD5 ) levels in patients with critical illnesses including systemic inflammatory response syndrome (SIRS, except sep-sis), sepsis (except severe sepsis) and severe sepsis. Methods: A total of 78 patients were enrolled in this study, of whom, 28 were with SIRS, 23 with sepsis and 27 with severe sepsis. Twenty-two healthy individuals were included as controls. The levels of serum PDCD5 were evaluated by enzyme-linked im-mune sorbent assay. And the correlation analyses were made in the levels of sreum PDCD5 and acute physiology and chronic health evaluation Ⅱ ( APACHE Ⅱ ) , high-sensitivity C-reactive protein ( hs- CRP), white blood cell count, neutrophil count and age factors. Results: Serum PDCD5 levels in the SIRS, sepsis and severe sepsis groups were (19.07 ±8.91 ), (29.03 ± 13.27) and (42.83 ± 17.32) μg/L respectively, which were significantly higher than that in the healthy control group (0.32 _± 0.02) μg/L. Serum PDCD5 levels in SIRS, sepsis and severe sepsis groups were gradually increased with significant difference at any in-between comparison ( P 〈 0.05 ). Moreover, serum PDCD5 levels were positively correlated with the acute physiology and chronic health evaluation Ⅱ (APACHE Ⅱ ) score ( r = 0.572, P 〈 0.05 ). Conclusion: The serum PDCD5 levels in the critically ill patients with sepsis were progressively increased with the worsened condition. The up-regulated expression of PDCD5 may play an important role in the development and progression of sepsis.
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