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ABSTRACT: Background
Idiopathic pulmonary fibrosis (IPF) is a progressive, fatal disorder with a variable disease trajectory. The aim of this study was to assess the potential of neutrophil-to-lymphocyte ratio (NLR) to predict outcomes in IPF.Methods
We adopted a two-stage discovery (n = 71) and validation (n = 134) design using patients from the UCL partners (UCLp) cohort. We then combined discovery and validation cohorts and included an additional 794 people with IPF, using real-life data from 5 other UK centers, to give a combined cohort of 999 patients. Data were collected from patients presenting over a 13-year period (2006-2019) with mean follow up of 3.7 years (censoring: 2018-2020).Findings
In the discovery analysis, we showed that high values of NLR (>/ = 2.9 vs < 2.
SUBMITTER: Mikolasch TA
PROVIDER: S-EPMC9722446 | biostudies-literature | 2023 Jan
REPOSITORIES: biostudies-literature