Department of Critical Care Medicine, Nanjing Zhong-Da Hospital, Southeast University School of Medicine, 87 Ding jia Qiao, Nanjing, China.
Respir Med. 2011 Oct;105(10):1485-90. doi: 10.1016/j.rmed.2011.06.009. Epub 2011 Jul 13.
Acute Lung Injury (ALI) with genetic predisposition is fatal. Relationship between angiotensin-converting enzyme insertion/deletion (ACE I/D) polymorphism and the prognosis of local Chinese patients with ALI was investigated; meanwhile, the mechanisms involved were explored.
101 ALI patients, 408 non-ALI patients and 236 healthy blood donors were enrolled. ACE I/D polymorphism was detected by polymerase chain reaction, then ACE genotype (II, ID, DD) and allele (I, D) frequencies were compared. Clinical data of ALI patients was calculated. Also, peripheral blood mononuclear cells (PBMC) were isolated from healthy volunteers with different ACE genotypes. Lipopolysaccharide (LPS)-induced ACE gene mRNA expression and ACE activity was measured.
There was no significant difference in the frequencies of the genotypes and alleles. Acute Physiology and Chronic Health Evaluation (APACHE) II score was higher in DD subgroup than in II subgroup (19.7 ± 8.7 and 15.6 ± 6.2; P < 0.05). The 28-day mortality was significantly different (17.4%, 26.8%, and 64.3% for II, ID, and DD; P = 0.013). DD genotype was the independent prognostic factor for 28-day outcome. Furthermore, LPS-induced ACE mRNA expression and ACE activity from PBMC in DD genotype subgroup were both significantly higher than those in the other two subgroups.
ACE I/D polymorphism is a prognostic factor for ALI. Patients with the DD genotype have higher mortality of ALI. Polymorphism influences the expression of ACE gene in LPS-stimulated PBMC, DD genotype leads to higher level of mRNA and enzyme activity. It may be one of the mechanisms involved.
具有遗传易感性的急性肺损伤(ALI)是致命的。本研究旨在探讨血管紧张素转换酶插入/缺失(ACE I/D)多态性与中国局部地区 ALI 患者预后的关系,并探讨其相关机制。
纳入 101 例 ALI 患者、408 例非 ALI 患者和 236 例健康献血者。采用聚合酶链反应检测 ACE I/D 多态性,比较 ACE 基因型(II、ID、DD)和等位基因(I、D)频率。计算 ALI 患者的临床数据。同时,从不同 ACE 基因型的健康志愿者中分离外周血单个核细胞(PBMC)。测量脂多糖(LPS)诱导的 ACE 基因 mRNA 表达和 ACE 活性。
基因型和等位基因频率无显著差异。DD 亚组的急性生理学和慢性健康评估(APACHE)II 评分高于 II 亚组(19.7±8.7 和 15.6±6.2;P<0.05)。28 天死亡率有显著差异(II、ID 和 DD 亚组分别为 17.4%、26.8%和 64.3%;P=0.013)。DD 基因型是 28 天预后的独立预测因素。此外,DD 基因型亚组 LPS 诱导的 PBMC 中 ACE mRNA 表达和 ACE 活性均明显高于其他两组。
ACE I/D 多态性是 ALI 的预后因素。DD 基因型患者的 ALI 死亡率更高。多态性影响 LPS 刺激的 PBMC 中 ACE 基因的表达,DD 基因型导致更高的 mRNA 和酶活性。这可能是其中的机制之一。