| Literature DB >> 29206633 |
Cheilonda Johnson1, Paul Rosen2, Thomas Lloyd3, Maureen Horton1, Lisa Christopher-Stine4, Chester V Oddis5, Andrew L Mammen6, Sonye K Danoff7.
Abstract
Interstitial lung disease (ILD) is common in patients with autoimmune myositis but factors that determine susceptibility are unknown. Familial and sporadic idiopathic pulmonary fibrosis (IPF) are strongly associated with a single nucleotide polymorphism in the promoter region of MUC5B (rs35705950). We sought to determine the relationship between MUC5B polymorphism expression and myositis-ILD. The MUC5B minor allele frequency (MAF) was examined in 402 European American participants; 60 with idiopathic interstitial pneumonia (IIP), 208 with myositis-ILD, and 134 unaffected controls. The MUC5B minor allele frequency was 26%, 8%, and 7% in those with non-myositis ILD, myositis-ILD, and unaffected controls, respectively. The MUC5B variant was associated with IIP (OR 4.10; p < 0.001). The MUC5B polymorphism was not significantly associated with myositis-ILD (OR 1.08; p = 0.80)]. We found MUC5B MAFs in our IIP cohort similar to published frequencies for subjects with familial and sporadic IPF. Overall, the MUC5B promoter variant does not appear to contribute to ILD risk in myositis patients.Entities:
Keywords: Dermatomyositis; Interstitial lung diseases; Mucin-5B; Polymyositis; Single nucleotide polymorphism
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Year: 2017 PMID: 29206633 DOI: 10.1016/j.rmed.2017.07.010
Source DB: PubMed Journal: Respir Med ISSN: 0954-6111 Impact factor: 3.415