Department of Pulmonary and Critical Care Medicine, the Affiliated Drum Tower Hospital of Nanjing University Medical School, Nanjing, Jiangsu, China.
Key Laboratory of Environmental Medicine Engineering, Ministry of Education, School of Public Health, Southeast University, Nanjing, Jiangsu, China.
Sci Rep. 2019 Oct 25;9(1):15307. doi: 10.1038/s41598-019-51902-6.
Genetic factors were identified to be associated with the development of idiopathic pulmonary fibrosis (IPF). We aimed to investigate associations between mucin 5B (MUC5B) and telomerase reverse transcriptase (TERT) polymorphisms and telomere length (TL) with honeycombing extent and survival in a Chinese IPF cohort. Seventy-nine patients diagnosed with IPF were enrolled. The honeycombing extents in high resolution CT scan (HRCT) were quantitatively scored and defined as mild (<10%), moderate (10-50%), and severe (>50%) upon the honeycombing extents involving the total lung. We tested five single-nucleotide polymorphisms [rs35705950, rs868903 in MUC5B, rs2736100, rs2853676 in TERT and rs1881984 in Telomerase RNA Gene (TERC) and TLs in peripheral blood leucocytes, and evaluated their associations with radiographic extent and survival in IPF. The minor allele frequencies (MAF) were significantly greater for MUC5B rs868903 (P = 0.042) and TERT rs2853676 (P = 0.041) in IPF than those in healthy controls. CT/CC genotype of MUC5B rs868903 (p = 0.045) and short TLs (p = 0.035) were correlated with the more extensive honeycombing opacities in HRCT. After adjustment for age, sex, and smoking status, MUC5B rs868903 polymorphism was the significant gene risk factors for reduced survival (p = 0.044) in IPF. MUC5B promoter rs868903 polymorphism and TLs were associated with radiographic extent and survival in a Chinese IPF cohort. These findings suggested a genetic clue for exploring the underlying molecular basis and pathogenesis of IPF.
遗传因素被认为与特发性肺纤维化 (IPF) 的发展有关。我们旨在研究黏蛋白 5B (MUC5B) 和端粒酶逆转录酶 (TERT) 多态性与端粒长度 (TL) 与中国 IPF 队列中蜂巢程度和生存的关联。共纳入 79 例 IPF 患者。通过高分辨率 CT 扫描 (HRCT) 对蜂巢程度进行定量评分,并根据总肺受累的蜂巢程度将其定义为轻度 (<10%)、中度 (10-50%) 和重度 (>50%)。我们测试了五个单核苷酸多态性 [rs35705950、rs868903 在 MUC5B 中,rs2736100、rs2853676 在 TERT 中,以及 Telomerase RNA Gene (TERC) 中的 rs1881984 和外周血白细胞中的 TLs,并评估了它们与 IPF 中放射学范围和生存的关系。与健康对照组相比,IPF 中 MUC5B rs868903 (P=0.042) 和 TERT rs2853676 (P=0.041) 的次要等位基因频率 (MAF) 显著更高。MUC5B rs868903 的 CT/CC 基因型 (p=0.045) 和较短的 TLs (p=0.035) 与 HRCT 中更广泛的蜂巢样混浊有关。在调整年龄、性别和吸烟状况后,MUC5B rs868903 多态性是 IPF 生存时间缩短的显著基因危险因素 (p=0.044)。MUC5B 启动子 rs868903 多态性和 TLs 与中国 IPF 队列的放射学范围和生存相关。这些发现为探索 IPF 的潜在分子基础和发病机制提供了遗传线索。