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The Pro12Ala Polymorphism of PPAR-γ Gene Is Associated with Sepsis Disease Severity and Outcome in Chinese Han Population

机译:PPAR-γ基因的Pro12Ala多态性与中国汉族人群的败血症疾病严重程度和结果相关

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摘要

Peroxisome proliferator-activated receptor-γ (PPAR-γ) is a ligand-binding nuclear receptor, and its activation plays a prominent role in regulating the inflammatory response. Therefore, PPAR-γ has been suggested as a candidate gene for sepsis. In the present study, we investigated the association between the Pro12Ala polymorphism of PPAR-γ and sepsis in a Han Chinese population. A total of 308 patients with sepsis and 345 healthy controls were enrolled in this study. Genotyping was performed using the polymerase chain reaction-ligation detection reaction (PCR-LDR) method. No significant differences were detected in the allele and genotype distributions of the PPAR-γ Pro12Ala SNP between septic patients and controls (P = 0.622 for genotype; P = 0.629 for allele). However, stratification by subtypes (sepsis, septic shock, and severe sepsis) revealed a statistically significant difference in the frequency of the Ala allele and Ala-carrier genotype between the patients with the sepsis subtype and the healthy controls (P = 0.014 for allele and P = 0.012, for genotype). Moreover, significant differences were found in the frequency of the Ala allele and genotype between the sepsis survivors and nonsurvivors (all P = 0.002). In the survivors, the PPAR-γ Pro12Ala genotype was significantly associated with decreased disease severity and recovery time (all P < 0.001). Thus, genetic polymorphism is thought to play a role in the development and outcome of sepsis.
机译:过氧化物酶体增殖物激活受体-γ(PPAR-γ)是一种配体结合核受体,其激活在调节炎症反应中起着重要作用。因此,已提出PPAR-γ作为败血症的候选基因。在本研究中,我们调查了汉族人群中PPAR-γ的Pro12Ala多态性与败血症之间的关系。本研究共纳入308名败血症患者和345名健康对照者。使用聚合酶链反应-连接检测反应(PCR-LDR)方法进行基因分型。在败血病患者和对照组之间,PPAR-γPro12Ala SNP的等位基因和基因型分布没有发现显着差异(基因型P = 0.622;等位基因P = 0.629)。然而,按亚型(败血症,败血性休克和严重脓毒症)分层显示,脓毒症亚型患者和健康对照者之间的Ala等位基因频率和Ala携带者基因型频率存在统计学差异(P = 0.014,等位基因和对于基因型,P = 0.012)。此外,发现败血症幸存者和非幸存者之间的Ala等位基因频率和基因型存在显着差异(所有P = 0.002)。在幸存者中,PPAR-γPro12Ala基因型与疾病严重程度降低和恢复时间显着相关(所有P <0.001)。因此,遗传多态性被认为在败血症的发生和结果中起作用。

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