Global incidence and prevalence of idiopathic pulmonary fibrosis

TM Maher, E Bendstrup, L Dron, J Langley, G Smith… - Respiratory …, 2021 - Springer
Background Idiopathic pulmonary fibrosis (IPF) is a progressive debilitating lung disease
with considerable morbidity. Heterogeneity in epidemiologic studies means the full impact of …

Idiopathic pulmonary fibrosis

FJ Martinez, HR Collard, A Pardo, G Raghu… - Nature reviews Disease …, 2017 - nature.com
Idiopathic pulmonary fibrosis (IPF) is a chronic, progressive lung disease characterized by
progressive lung scarring and the histological picture of usual interstitial pneumonia (UIP). It …

The European IPF registry (eurIPFreg): baseline characteristics and survival of patients with idiopathic pulmonary fibrosis

A Guenther, E Krauss, S Tello, J Wagner, B Paul… - Respiratory …, 2018 - Springer
Background Since 2009, IPF patients across Europe are recruited into the eurIPFreg,
providing epidemiological data and biomaterials for translational research. Methods The …

Pulmonary involvement in antineutrophil cytoplasmic antibodies (ANCA)-associated vasculitis: the influence of ANCA subtype

AJ Mohammad, KH Mortensen, J Babar… - The Journal of …, 2017 - jrheum.org
Objective. To describe pulmonary involvement at time of diagnosis in antineutrophil
cytoplasmic antibodies (ANCA)-associated vasculitis (AAV), as defined by computed …

Incidence and prevalence of interstitial lung diseases worldwide: a systematic literature review

RS Gupta, A Koteci, A Morgan… - BMJ Open …, 2023 - bmjopenrespres.bmj.com
Interstitial lung disease (ILD) is a collective term representing a diverse group of pulmonary
fibrotic and inflammatory conditions. Due to the diversity of ILD conditions, paucity of …

Comorbidity burden and survival in patients with idiopathic pulmonary fibrosis: the EMPIRE registry study

DM Jovanovic, M Šterclová, N Mogulkoc… - Respiratory …, 2022 - Springer
Background Patients with idiopathic pulmonary fibrosis (IPF) frequently have multiple
comorbidities, which may influence survival but go under-recognised in clinical practice. We …

The histone methyltransferase DOT1L is a new epigenetic regulator of pulmonary fibrosis

D Yang, P Xu, H Su, W Zhong, J Xu, Z Su, X Liu - Cell Death & Disease, 2022 - nature.com
Idiopathic pulmonary fibrosis (IPF) is a progressive interstitial lung disease with increasing
occurrence, high death rates, and unfavorable treatment regimens. The pathogenesis …

A systematic review of the research progress of traditional Chinese medicine against pulmonary fibrosis: from a pharmacological perspective

S Qin, P Tan, J Xie, Y Zhou, J Zhao - Chinese Medicine, 2023 - Springer
Pulmonary fibrosis is a chronic progressive interstitial lung disease caused by a variety of
etiologies. The disease can eventually lead to irreversible damage to the lung tissue …

New therapeutic approaches against pulmonary fibrosis

D Yu, Y Xiang, T Gou, R Tong, C Xu, L Chen… - Bioorganic …, 2023 - Elsevier
Pulmonary fibrosis is the end-stage change of a large class of lung diseases characterized
by the proliferation of fibroblasts and the accumulation of a large amount of extracellular …

Low-level ambient sulfur dioxide exposure and genetic susceptibility associated with incidence of idiopathic pulmonary fibrosis: A national prospective cohort study

X Wang, X Deng, Y Wu, Z Qian, M Cai, H Li, H Lin - Chemosphere, 2023 - Elsevier
Background The association between long-term air pollution exposure and the development
of idiopathic pulmonary fibrosis (IPF) has been established, but the evidence regarding the …