4.6 Article

MUC5B promoter polymorphism in Japanese patients with idiopathic pulmonary fibrosis

期刊

RESPIROLOGY
卷 20, 期 3, 页码 439-444

出版社

WILEY
DOI: 10.1111/resp.12466

关键词

genetic; interstitial lung disease; lung fibrosis; single nucleotide polymorphism

资金

  1. Ministry of Education, Culture, Sports, Science and Technology of Japan
  2. Arbeitsgemeinschaft zur Forderung der Pneumologie an der Ruhrlandklinik (AFPR)
  3. Grants-in-Aid for Scientific Research [25860646] Funding Source: KAKEN

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Background and objectiveA single nucleotide polymorphism (SNP) rs35705950 in the promoter of Mucin 5B (MUC5B) has been reported to be associated with idiopathic pulmonary fibrosis (IPF) mainly in Caucasian populations. This study was conducted to confirm the association between rs35705950 and IPF in a Japanese population. MethodsGenomic DNA was extracted from blood samples in 384 Japanese and 137 German subjects, and rs35705950 was detected by commercially available genotyping assay. ResultsThe genotype distributions of rs35705950 in Japanese patients with IPF, nonspecific interstitial pneumonia (NSIP) and healthy subjects (HS) were significantly different from those in the German counterparts (P<0.001, P<0.001 and P=0.010, respectively). The rs35705950 T allele frequencies in patients with IPF, NSIP and HS were 3.4%, 1.7% and 0.8%, respectively in the Japanese, while they were 33.1%, 27.4% and 4.3%, respectively in the German cohort. The T allele frequencies in patients with IPF were significantly higher than those in HS both in the Japanese (P=0.031) and German (P<0.001) cohorts. ConclusionsThe association between rs35705950 and IPF was also present in this Japanese cohort, but was not as strong as the German counterpart. To our knowledge, this is the first study to successfully validate the association between rs35705950 and IPF in a Japanese ethnicity.

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