Research Unit, Hospital Universitario Nuestra Señora de Candelaria, Santa Cruz de Tenerife, Spain.
BMC Med Genet. 2011 Oct 10;12:132. doi: 10.1186/1471-2350-12-132.
TNF-α mediated inflammation is thought to play a key role in the respiratory and systemic features of Chronic Obstructive Pulmonary Disease. The aim of the present study was to replicate and extend recent findings in Taiwanese and Caucasian populations of associations between COPD susceptibility and variants of the TNFA gene in a Spanish cohort.
The 3 reported SNPs were complemented with nine tag single nucleotide polymorphisms (SNP) of the TNFA and LTA genes and genotyped in 724 individuals (202 COPD patients, 90 smokers without COPD and 432 healthy controls). Pulmonary function parameters and serum inflammatory markers were also measured in COPD patients.
The TNFA rs1800630 (-863C/A) SNP was associated with a lower COPD susceptibility (ORadj = 0.50, 95% CI = 0.33-0.77, p = 0.001). The -863A allele was also associated with less severe forms of the disease (GOLD stages I and II) (ORadj = 0.303, 95%CI = 0.14-0.65, p = 0.014) and with lower scores of the BODE index (< 2) (ORadj = 0.40, 95%CI = 0.17-0.94, p = 0.037). Moreover, the -863A carrier genotype was associated with a better FEV1 percent predicted (p = 0.004) and a lower BODE index (p = 0.003) over a 2 yrs follow-up period. None of the TNFA or LTA gene variants correlated with the serum inflammatory markers in COPD patients (p > 0.05).
We replicated the previously reported association between the TNFA -863 SNP and COPD. TNFA -863A allele may confer a protective effect to the susceptibility to the disease in the Spanish population.
TNF-α 介导的炎症被认为在慢性阻塞性肺疾病的呼吸系统和全身特征中起关键作用。本研究的目的是在西班牙队列中复制并扩展先前在台湾和高加索人群中 COPD 易感性与 TNFA 基因变异之间关联的发现。
补充了 TNFA 和 LTA 基因的 3 个报告 SNP 与 9 个标签单核苷酸多态性(SNP),并在 724 名个体(202 名 COPD 患者、90 名无 COPD 的吸烟者和 432 名健康对照者)中进行了基因分型。还测量了 COPD 患者的肺功能参数和血清炎症标志物。
TNFA rs1800630(-863C/A)SNP 与较低的 COPD 易感性相关(ORadj = 0.50,95%CI = 0.33-0.77,p = 0.001)。-863A 等位基因也与疾病的较轻形式(GOLD 阶段 I 和 II)相关(ORadj = 0.303,95%CI = 0.14-0.65,p = 0.014),并且 BODE 指数评分较低(<2)(ORadj = 0.40,95%CI = 0.17-0.94,p = 0.037)。此外,-863A 携带者基因型与更好的 FEV1 预计百分比(p = 0.004)和较低的 BODE 指数(p = 0.003)相关,随访时间为 2 年。在 COPD 患者中,TNFA 或 LTA 基因变异均与血清炎症标志物无相关性(p>0.05)。
我们复制了先前报道的 TNFA-863SNP 与 COPD 之间的关联。TNFA-863A 等位基因可能在西班牙人群中对疾病的易感性具有保护作用。