ICU Departments, First Affiliated Hospital of Bengbu Medical College, Bengbu 233004, China.
Lipids Health Dis. 2014 May 13;13:79. doi: 10.1186/1476-511X-13-79.
Apolipoprotein A1 (ApoA1) is the major apoprotein constituent of high density lipoprotein (HDL) which exerts innate protective effects in systemic inflammation. However, its role in the acute lung injury (ALI) has not been well studied. In the present study we investigated the association between polymorphisms of ApoA1 gene and ALI in a Chinese population.
Three polymorphisms of the ApoA1 gene (rs11216153, rs2070665, and rs632153) were genotyped by TaqMan method in 290 patients with sepsis-associated ALI, 285 patients sepsis alone and 330 age- and sex-matched healthy controls.
We found rs11216153 polymorphism of ApoA1 was associated with ALI, the GG genotype and G allele was common in the ALI patients (76.9%, 88.1%, respectively) than both in the control subjects (55.8%, 75.8%, respectively) and in the sepsis alone patients (58.2%, 78.4%, respectively). Haplotype consisting of these three SNPs strengthened the association with ALI susceptibility. The frequency of haplotype GTG in the ALI samples was significantly higher than that in the healthy control group (OR = 2.261, 95% CI: 1.735 ~ 2.946, P <0.001) and the sepsis alone group (OR = 1.789, 95% CI: 1.373 ~ 2.331.P < 0.001). Carriers of the haplotype TTG had a lower risk for ALI compared with healthy control group (OR = 0.422, 95% CI: 0.310 ~ 0.574, P < 0.001) and sepsis alone group (OR = 0.491, 95% CI: 0.356 ~ 0.676, P <0.001).
These results indicated that genetic variants in the ApoA1 gene might be associated with susceptibility to sepsis-associated ALI in Han Chinese population.
载脂蛋白 A1(ApoA1)是高密度脂蛋白(HDL)的主要载脂蛋白成分,在全身炎症中发挥先天的保护作用。然而,其在急性肺损伤(ALI)中的作用尚未得到很好的研究。在本研究中,我们调查了载脂蛋白 A1 基因多态性与中国人群 ALI 的关系。
采用 TaqMan 法检测 290 例脓毒症相关性 ALI 患者、285 例脓毒症患者和 330 例年龄和性别匹配的健康对照者的载脂蛋白 A1 基因(rs11216153、rs2070665 和 rs632153)三个多态性。
我们发现载脂蛋白 A1 的 rs11216153 多态性与 ALI 相关,GG 基因型和 G 等位基因在 ALI 患者(分别为 76.9%、88.1%)中比健康对照组(分别为 55.8%、75.8%)和单纯脓毒症患者(分别为 58.2%、78.4%)更为常见。由这三个 SNP 组成的单体型与 ALI 易感性的相关性增强。在 ALI 样本中,GTG 单体型的频率明显高于健康对照组(OR=2.261,95%CI:1.7352.946,P<0.001)和单纯脓毒症组(OR=1.789,95%CI:1.3732.331,P<0.001)。与健康对照组相比,携带 TTG 单体型的患者发生 ALI 的风险较低(OR=0.422,95%CI:0.3100.574,P<0.001)和单纯脓毒症组(OR=0.491,95%CI:0.3560.676,P<0.001)。
这些结果表明,载脂蛋白 A1 基因的遗传变异可能与汉族人群脓毒症相关性 ALI 的易感性有关。