State Key Laboratory of Trauma, Burns and Combined Injury, Institute of Surgery Research, Daping Hospital, Third Military Medical University, Chongqing, China.
PLoS One. 2013 Aug 19;8(8):e71237. doi: 10.1371/journal.pone.0071237. eCollection 2013.
Recent studies on the association between CD14-159C/T polymorphism and sepsis showed inconclusive results. Accordingly, we conducted a comprehensive literature search and a meta-analysis to determine whether the CD14-159C/T polymorphism conferred susceptibility to sepsis or was associated with increased risk of death from sepsis.
Data were collected from the following electronic databases: PubMed, Embase, Medline, Web of Knowledge, and HuGE Navigator, with the last report up to June 15, 2012. The odds ratio (OR) and 95% confidence interval (CI) were used to assess the strength of association. We summarized the data on the association between CD14-159C/T polymorphism and sepsis in the overall population and subgroup by ethnicity and sepsis subtype.
A total of 16 studies on sepsis morbidity (1369 cases and 2382 controls) and 4 studies on sepsis mortality (731 sepsis patients) met the inclusion criteria for meta-analysis. Overall analysis showed no strong evidences of association with sepsis susceptibility under any genetic model. However, slight associations were found in Asian populations (dominant model: OR = 1.38, 95%CI = 0.96-1.98, P = 0.08) and septic shock patients (dominant model: OR = 1.72, 95%CI 1.05-2.83, P = 0.03; allelic model: OR = 1.52, 95%CI 1.09-2.12, P = 0.01) in the stratified analysis. Moreover, there was borderline association between CD14-159C/T and sepsis mortality under the dominant genetic model (OR = 1.44, 95%CI = 0.98-2.11, P = 0.06).
CONCLUSIONS/SIGNIFICANCE: This meta-analysis suggests that the CD14-159C/T polymorphism may not be a significant susceptibility factor in the risk of sepsis and mortality. Only weak associations were observed in Asian populations and septic shock patients. More studies based on larger sample sizes and homogeneous sepsis patients are needed to confirm these findings.
最近的研究表明 CD14-159C/T 多态性与败血症之间的关联尚无定论。因此,我们进行了全面的文献检索和荟萃分析,以确定 CD14-159C/T 多态性是否导致败血症易感性或是否与败血症死亡风险增加相关。
数据来自以下电子数据库:PubMed、Embase、Medline、Web of Knowledge 和 HuGE Navigator,最后报告截至 2012 年 6 月 15 日。使用优势比(OR)和 95%置信区间(CI)来评估关联的强度。我们根据种族和败血症亚型汇总了 CD14-159C/T 多态性与败血症之间的关联数据。
共有 16 项关于败血症发病率(1369 例和 2382 例对照)和 4 项关于败血症死亡率(731 例败血症患者)的研究符合荟萃分析的纳入标准。总体分析显示,在任何遗传模型下,与败血症易感性均无强烈关联。然而,在亚洲人群中发现了轻微的关联(显性模型:OR=1.38,95%CI=0.96-1.98,P=0.08)和败血症性休克患者(显性模型:OR=1.72,95%CI 1.05-2.83,P=0.03;等位基因模型:OR=1.52,95%CI 1.09-2.12,P=0.01)在分层分析中。此外,在显性遗传模型下,CD14-159C/T 与败血症死亡率之间存在边缘关联(OR=1.44,95%CI=0.98-2.11,P=0.06)。
结论/意义:这项荟萃分析表明,CD14-159C/T 多态性可能不是败血症风险和死亡率的重要易感因素。仅在亚洲人群和败血症性休克患者中观察到微弱关联。需要更多基于更大样本量和同质败血症患者的研究来证实这些发现。