LGMR, EA7402 University of Montpellier, 34093 Montpellier, France.
CRCM, CHU Montpellier, 34090 Montpellier, France.
Genes (Basel). 2021 Mar 19;12(3):441. doi: 10.3390/genes12030441.
Cystic fibrosis (CF) is a chronic genetic disease that mainly affects the respiratory and gastrointestinal systems. No curative treatments are available, but the follow-up in specialized centers has greatly improved the patient life expectancy. Robust biomarkers are required to monitor the disease, guide treatments, stratify patients, and provide outcome measures in clinical trials. In the present study, we outline a strategy to select putative DNA methylation biomarkers of lung disease severity in cystic fibrosis patients. In the discovery step, we selected seven potential biomarkers using a genome-wide DNA methylation dataset that we generated in nasal epithelial samples from the MethylCF cohort. In the replication step, we assessed the same biomarkers using sputum cell samples from the MethylBiomark cohort. Of interest, DNA methylation at the cg11702988 site ( gene) positively correlated with lung function and BMI, and negatively correlated with lung disease severity, chronic infection, and the number of exacerbations. These results were replicated in prospective sputum samples collected at four time points within an 18-month period and longitudinally. To conclude, (i) we identified a DNA methylation biomarker that correlates with CF severity, (ii) we provided a method to easily assess this biomarker, and (iii) we carried out the first longitudinal analysis of DNA methylation in CF patients. This new epigenetic biomarker could be used to stratify CF patients in clinical trials.
囊性纤维化 (CF) 是一种慢性遗传疾病,主要影响呼吸系统和胃肠道系统。目前尚无治愈方法,但在专门中心的随访大大提高了患者的预期寿命。需要强有力的生物标志物来监测疾病、指导治疗、对患者进行分层,并提供临床试验的结果衡量标准。在本研究中,我们概述了一种选择囊性纤维化患者肺部疾病严重程度的潜在 DNA 甲基化生物标志物的策略。在发现步骤中,我们使用我们在 MethylCF 队列的鼻腔上皮样本中生成的全基因组 DNA 甲基化数据集选择了七个潜在的生物标志物。在复制步骤中,我们使用来自 MethylBiomark 队列的痰细胞样本评估了相同的生物标志物。有趣的是,cg11702988 位点 (基因) 的 DNA 甲基化与肺功能和 BMI 呈正相关,与肺部疾病严重程度、慢性感染和恶化次数呈负相关。这些结果在 18 个月内的四个时间点收集的前瞻性痰样本中得到了复制,并进行了纵向分析。总之,(i) 我们确定了一个与 CF 严重程度相关的 DNA 甲基化生物标志物,(ii) 我们提供了一种简单评估该生物标志物的方法,(iii) 我们进行了 CF 患者中 DNA 甲基化的首次纵向分析。这种新的表观遗传生物标志物可用于临床试验中对 CF 患者进行分层。