Potential clinical utility of MUC5B und TOLLIP single nucleotide polymorphisms (SNPs) in the management of patients with IPF

• Published in: Orphanet journal of rare diseases Vol. 16; no. 1; pp. 111 - 9
• Main Authors: Bonella, Francesco, Campo, Ilaria, Zorzetto, Michele, Boerner, Eda, Ohshimo, Shinichiro, Theegarten, Dirk, Taube, Christian, Costabel, Ulrich
• Format: Journal Article
• Language: English
• Published: England BioMed Central Ltd 27.02.2021; BioMed Central; BMC
• Subjects: Alleles; Binding proteins; Care and treatment; Chromosome 11; Comorbidity; Deoxyribonucleic acid; Disease; Disease progression; DNA; DNA methylation; Fibrosis; Genetic aspects; Genetic diversity; Genetic Predisposition to Disease; Genotype; Genotype & phenotype; Haplotypes; Health aspects; Humans; Idiopathic Pulmonary Fibrosis - genetics; Intracellular Signaling Peptides and Proteins - genetics; IPF; Lung diseases; Medical prognosis; Medical research; MUC5B; Mucin-5B - genetics; Mucins; Polymorphism; Polymorphism, Single Nucleotide; Prognosis; Pulmonary fibrosis; Rare diseases; Retrospective Studies; Single nucleotide polymorphisms; Single-nucleotide polymorphism; Survival; TOLLIP; Tumor necrosis factor-TNF; Germany; United States > US; MUC5B; TOLLIP; IPF; Disease progression
• ISSN: 1750-1172; 1750-1172
• DOI: 10.1186/s13023-021-01750-3

Genetic variants of TOLLIP and MUC5B, both on chromosome 11, have been reported to be associated with the development and/or prognosis of idiopathic pulmonary fibrosis (IPF). This retrospective study was conducted to investigate the association of MUC5B and TOLLIP SNPs with disease outcome in IPF. 62 IPF patients and 50 healthy controls (HC) from our Institution were genotyped for SNPs within MUC5B (rs35705950) and TOLLIP (rs3750920 and rs5743890). Correlation of SNPs genotypes with survival, acute exacerbation (AE) or disease progression (defined as a decline of ≥ 5% in FVC and or ≥ 10% in DLco in one year) was investigated. The MUC5B rs35705950 minor allele (T) was more frequent in IPF subjects than in HC (35% vs 9% p < 0.001). TOLLIP SNPs alleles and genotype distribution did not differ between IPF and HC and did not vary according to gender, age, BMI and lung functional impairment at baseline. The minor allele (C) in TOLLIP rs5743890 was associated with worse survival and with disease progression in all performed analyses. The MUC5B rs35705950 or the TOLLIP rs3750920 minor allele, were not associated with disease progression or AE. We confirm that the minor allele of MUC5B rs35705950 is associated with IPF. The minor allele of TOLLIP rs5743890 appears to be a predictor of worse survival and more rapid disease progression, therefore being of potential utility to stratify IPF patients at baseline.