Rationale and design of the prognostic transcriptomic signature in fibrotic hypersensitivity pneumonitis (PREDICT) study

Author:

Fernández Pérez Evans R.ORCID,Leach Sonia M.ORCID,Vestal BrianORCID,Fernández Pérez Evans R.,Leach Sonia M.,Vestal Brian,Maier Lisa,Fier Kaitlin,Del Real Elizabeth,Arthofer Adrea,Lynch David,Groshong Steve,Moua Teng,Daley Shannon,Sood Namita,Foster Elena,Sergill Anastasia,Adams Traci,Gordon Rhoda,Morfin Brian,Chaudhary Sachin,Erickson Heidi,Scholand Mary Beth,Chloe Kirkpatrick,Ayodeji Adegunsoye,Spring Maleckar,Karina Mak,

Abstract

Hypersensitivity pneumonitis is an immunologically mediated form of lung disease, resulting from inhalational exposure to a large variety of antigens. A subgroup of patients with fibrotic hypersensitivity pneumonitis (FHP) develop symptomatic, functional and radiographic disease progression. Mortality occurs primarily from respiratory failure as a result of progressive and self-sustaining lung injury that often occurs despite immunosuppression and removal of the inciting antigen. The development and validation of a prognostic transcriptomic signature for FHP (PREDICT-HP) is an observational multicentre cohort study designed to explore a transcriptomic signature from peripheral blood mononuclear cells in patients with FHP that is predictive of disease progression. This article describes the design and rationale of the PREDICT-HP study. This study will enrol ∼135 patients with FHP at approximately seven academic medical sites. Participants with a confirmed diagnosis of FHP are followed over 24 months and undergo physical examinations, self-administered questionnaires, chest computed tomography, pulmonary function tests, a 6-min walk test and blood testing for transcriptomic analyses. At each 6-month follow-up visit the study will assess the participants' clinical course and clinical events including hospitalisations and respiratory exacerbations. The PREDICT study has the potential to enhance our ability to predict disease progression and fundamentally advance our understanding of the pathobiology of FHP disease progression.

Funder

National Heart, Lung, and Blood Institute

Publisher

European Respiratory Society (ERS)

Subject

Pulmonary and Respiratory Medicine

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