MUC2MUC5B and TOLLIP variants: no association with disease progression and survival in an IPF cohort

C. Stock (London, United Kingdom), P. Molyneaux (London, United Kingdom), P. Saunders (London, United Kingdom), M. Kokosi (London, United Kingdom), P. George (London, United Kingdom), V. Kouranos (London, United Kingdom), F. Chua (London, United Kingdom), A. Wells (London, United Kingdom), T. Maher (London, United Kingdom), E. Renzoni (London, United Kingdom)

Source: Virtual Congress 2020 – Biomarkers and mechanistic aspects of idiopathic pulmonary fibrosis
Session: Biomarkers and mechanistic aspects of idiopathic pulmonary fibrosis
Session type: E-poster session
Number: 736
Disease area: Interstitial lung diseases

Congress or journal article abstractE-poster

Rating: 0
You must login to grade this presentation.

Share or cite this content

Citations should be made in the following way:
C. Stock (London, United Kingdom), P. Molyneaux (London, United Kingdom), P. Saunders (London, United Kingdom), M. Kokosi (London, United Kingdom), P. George (London, United Kingdom), V. Kouranos (London, United Kingdom), F. Chua (London, United Kingdom), A. Wells (London, United Kingdom), T. Maher (London, United Kingdom), E. Renzoni (London, United Kingdom). MUC2MUC5B and TOLLIP variants: no association with disease progression and survival in an IPF cohort. 736

You must login to share this Presentation/Article on Twitter, Facebook, LinkedIn or by email.

Member's Comments

No comment yet.
You must Login to comment this presentation.


Related content which might interest you:
Telomere length and genetic variant associations with interstitial lung disease progression and survival
Source: Eur Respir J, 53 (4) 1801641; 10.1183/13993003.01641-2018
Year: 2019



TERT expression in lung cancer associated with IPF: a case-control study
Source: Virtual Congress 2021 – Translational and other aspects of idiopathic interstitial pneumonia
Year: 2021


Collagen1a1 mRNA expression in BAL cells is associated with disease progression and poor survival in ILDs
Source: Virtual Congress 2020 – Biomarkers and mechanistic aspects of idiopathic pulmonary fibrosis
Year: 2020


IL8 as a marker of severity of disease progression in patients with idiopathic pulmonary fibrosis (IPF)
Source: Eur Respir J 2007; 30: Suppl. 51, 373s
Year: 2007

MUC5B genotype affects survival of patients with idiopathic pulmonary fibrosis (IPF) on antifibrotic treatment
Source: International Congress 2019 – Treatment and prognosis of idiopathic interstitial pneumonia
Year: 2019

Plasma microfibrillar-associated protein 4 is not prognostic of emphysema progression but is associated with cardiovascular disease history and mortality in COPD patients
Source: ERJ Open Res, 5 (2) 00021-2019; 10.1183/23120541.00021-2019
Year: 2019



Genome-wide association analysis reveals 12q13.3–q14.1 as new risk locus for sarcoidosis
Source: Eur Respir J 2013; 41: 888-900
Year: 2013



The functional MUC5B rs35705950 promoter polymorphism is associated with IPF but not with systemic sclerosis related interstitial lung disease
Source: Annual Congress 2012 - Idiopathic pulmonary fibrosis
Year: 2012


HLA-DRB1 allele frequencies in Finnish sarcoidosis patients and associations with disease prognosis
Source: Annual Congress 2010 - Lung cancer, idiopathic pulmonary fibrosis and sarcoidosis: the genetic approach
Year: 2010


A BTNL2 gene variant confers to sarcoidosis susceptibility by an increased risk towards the chronic form of the disease
Source: Eur Respir J 2006; 28: Suppl. 50, 148s
Year: 2006

Correlation of IL-1 alpha and IL-4 promotor region gene polymorphisms and clinical parameters in idiopathic pulmonary fibrosis
Source: Annual Congress 2006 - Systemic diseases, environmental and genetic factors in interstitial lung disease
Year: 2006


IL-6 and IL-8 in stable and exacerbated IPF patients and their association to outcome
Source: International Congress 2016 – ILD: from the bench to the bedside
Year: 2016


Investigating tensin1 expression and the presence of SNP identified in GWAS in COPD
Source: International Congress 2016 – Mechanisms of disease
Year: 2016

Effect of MUC5B gene polymorphism on survival in a Lebanese population of patients with idiopathic pulmonary fibrosis
Source: International Congress 2018 – Pitfalls in the diagnosis and management of rare diffuse parenchymal lung diseases (DPLDs)
Year: 2018

A genome-wide association study on the risk variations for susceptibility to early COPD
Source: International Congress 2019 – New molecular signatures in COPD, lung cancer and a1-antitrypsin deficiency
Year: 2019


Risk factors for lung disease progression in children with cystic fibrosis; a longitudinal cohort study
Source: International Congress 2017 – Cystic fibrosis: treatments and monitoring
Year: 2017

Baseline characteristics and survival of patients with idiopathic pulmonary fibrosis (IPF): analysis from the Swedish IPF registry
Source: Virtual Congress 2020 – Real life in the field of idiopathic pulmonary fibrosis: treatments and registries
Year: 2020


Potential clinical utility of MUC5B and TOLLIP single nucleotide polymorphisms (SNP) in in the management of patients with IPF.
Source: International Congress 2019 – Translational aspects of idiopathic pulmonary fibrosis
Year: 2019

Blood biomarkers predicting disease progression in patients with IPF: data from the INMARK trial
Source: International Congress 2019 – The evolving field of idiopathic interstitial pneumonia
Year: 2019




A family history of ILD is a significant risk factor for worse transplant-free survival in IPF patients
Source: Virtual Congress 2020 – Idiopathic pulmonary fibrosis and interstitial lung disease: progression, genes and more
Year: 2020