Cargando…

Multi-center evaluation of baseline neutrophil-to-lymphocyte (NLR) ratio as an independent predictor of mortality and clinical risk stratifier in idiopathic pulmonary fibrosis

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Mikolasch, Theresia A., George, Peter M., Sahota, Jagdeep, Nancarrow, Thomas, Barratt, Shaney L., Woodhead, Felix A., Kouranos, Vasilis, Cope, Victoria S.A., Creamer, Andrew W., Fidan, Silan, Ganeshan, Balaji, Hoy, Luke, Mackintosh, John A., Shortman, Robert, Duckworth, Anna, Fallon, Janet, Garthwaite, Helen, Heightman, Melissa, Adamali, Huzaifa I., Lines, Sarah, Win, Thida, Wollerton, Rebecca, Renzoni, Elisabetta A., Steward, Matthew, Wells, Athol U., Gibbons, Michael, Groves, Ashley M., Gooptu, Bibek, Scotton, Chris J., Porter, Joanna C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9722446/
https://www.ncbi.nlm.nih.gov/pubmed/36483266
http://dx.doi.org/10.1016/j.eclinm.2022.101758
_version_ 1784843977316368384
author Mikolasch, Theresia A.
George, Peter M.
Sahota, Jagdeep
Nancarrow, Thomas
Barratt, Shaney L.
Woodhead, Felix A.
Kouranos, Vasilis
Cope, Victoria S.A.
Creamer, Andrew W.
Fidan, Silan
Ganeshan, Balaji
Hoy, Luke
Mackintosh, John A.
Shortman, Robert
Duckworth, Anna
Fallon, Janet
Garthwaite, Helen
Heightman, Melissa
Adamali, Huzaifa I.
Lines, Sarah
Win, Thida
Wollerton, Rebecca
Renzoni, Elisabetta A.
Steward, Matthew
Wells, Athol U.
Gibbons, Michael
Groves, Ashley M.
Gooptu, Bibek
Scotton, Chris J.
Porter, Joanna C.
author_facet Mikolasch, Theresia A.
George, Peter M.
Sahota, Jagdeep
Nancarrow, Thomas
Barratt, Shaney L.
Woodhead, Felix A.
Kouranos, Vasilis
Cope, Victoria S.A.
Creamer, Andrew W.
Fidan, Silan
Ganeshan, Balaji
Hoy, Luke
Mackintosh, John A.
Shortman, Robert
Duckworth, Anna
Fallon, Janet
Garthwaite, Helen
Heightman, Melissa
Adamali, Huzaifa I.
Lines, Sarah
Win, Thida
Wollerton, Rebecca
Renzoni, Elisabetta A.
Steward, Matthew
Wells, Athol U.
Gibbons, Michael
Groves, Ashley M.
Gooptu, Bibek
Scotton, Chris J.
Porter, Joanna C.
author_sort Mikolasch, Theresia A.
collection PubMed
description 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 < 2.9) were associated with increased risk of mortality in IPF (HR 2.04, 95% CI 1.09–3.81, n = 71, p = 0.025). This was confirmed in the validation (HR 1.91, 95% CI 1.15–3.18, n = 134, p = 0.0114) and combined cohorts (HR 1.65, n = 999, 95% CI 1.39–1.95; p < 0·0001). NLR correlated with GAP stage and GAP index (p < 0.0001). Stratifying patients by NLR category (low/high) showed significant differences in survival for GAP stage 2 (p < 0.0001), however not for GAP stage 1 or 3. In a multivariate analysis, a high NLR was an independent predictor of mortality/progression after adjustment for individual GAP components and steroid/anti-fibrotic use (p < 0·03). Furthermore, incorporation of baseline NLR in a modified GAP-stage/index, GAP–index/stage-plus, refined prognostic ability as measured by concordance (C)-index. INTERPRETATION: We have identified NLR as a widely available test that significantly correlates with lung function, can predict outcomes in IPF and refines cohort staging with GAP. NLR may allow timely prioritisation of at-risk patients, even in the absence of lung function. FUNDING: Breathing Matters, 10.13039/100004330GSK, CF Trust, BLF-Asthma, 10.13039/501100000265MRC, NIHR Alpha-1 Foundation.
format Online
Article
Text
id pubmed-9722446
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Elsevier
record_format MEDLINE/PubMed
spelling pubmed-97224462022-12-07 Multi-center evaluation of baseline neutrophil-to-lymphocyte (NLR) ratio as an independent predictor of mortality and clinical risk stratifier in idiopathic pulmonary fibrosis Mikolasch, Theresia A. George, Peter M. Sahota, Jagdeep Nancarrow, Thomas Barratt, Shaney L. Woodhead, Felix A. Kouranos, Vasilis Cope, Victoria S.A. Creamer, Andrew W. Fidan, Silan Ganeshan, Balaji Hoy, Luke Mackintosh, John A. Shortman, Robert Duckworth, Anna Fallon, Janet Garthwaite, Helen Heightman, Melissa Adamali, Huzaifa I. Lines, Sarah Win, Thida Wollerton, Rebecca Renzoni, Elisabetta A. Steward, Matthew Wells, Athol U. Gibbons, Michael Groves, Ashley M. Gooptu, Bibek Scotton, Chris J. Porter, Joanna C. eClinicalMedicine Articles 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 < 2.9) were associated with increased risk of mortality in IPF (HR 2.04, 95% CI 1.09–3.81, n = 71, p = 0.025). This was confirmed in the validation (HR 1.91, 95% CI 1.15–3.18, n = 134, p = 0.0114) and combined cohorts (HR 1.65, n = 999, 95% CI 1.39–1.95; p < 0·0001). NLR correlated with GAP stage and GAP index (p < 0.0001). Stratifying patients by NLR category (low/high) showed significant differences in survival for GAP stage 2 (p < 0.0001), however not for GAP stage 1 or 3. In a multivariate analysis, a high NLR was an independent predictor of mortality/progression after adjustment for individual GAP components and steroid/anti-fibrotic use (p < 0·03). Furthermore, incorporation of baseline NLR in a modified GAP-stage/index, GAP–index/stage-plus, refined prognostic ability as measured by concordance (C)-index. INTERPRETATION: We have identified NLR as a widely available test that significantly correlates with lung function, can predict outcomes in IPF and refines cohort staging with GAP. NLR may allow timely prioritisation of at-risk patients, even in the absence of lung function. FUNDING: Breathing Matters, 10.13039/100004330GSK, CF Trust, BLF-Asthma, 10.13039/501100000265MRC, NIHR Alpha-1 Foundation. Elsevier 2022-12-01 /pmc/articles/PMC9722446/ /pubmed/36483266 http://dx.doi.org/10.1016/j.eclinm.2022.101758 Text en © 2022 The Authors https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Articles
Mikolasch, Theresia A.
George, Peter M.
Sahota, Jagdeep
Nancarrow, Thomas
Barratt, Shaney L.
Woodhead, Felix A.
Kouranos, Vasilis
Cope, Victoria S.A.
Creamer, Andrew W.
Fidan, Silan
Ganeshan, Balaji
Hoy, Luke
Mackintosh, John A.
Shortman, Robert
Duckworth, Anna
Fallon, Janet
Garthwaite, Helen
Heightman, Melissa
Adamali, Huzaifa I.
Lines, Sarah
Win, Thida
Wollerton, Rebecca
Renzoni, Elisabetta A.
Steward, Matthew
Wells, Athol U.
Gibbons, Michael
Groves, Ashley M.
Gooptu, Bibek
Scotton, Chris J.
Porter, Joanna C.
Multi-center evaluation of baseline neutrophil-to-lymphocyte (NLR) ratio as an independent predictor of mortality and clinical risk stratifier in idiopathic pulmonary fibrosis
title Multi-center evaluation of baseline neutrophil-to-lymphocyte (NLR) ratio as an independent predictor of mortality and clinical risk stratifier in idiopathic pulmonary fibrosis
title_full Multi-center evaluation of baseline neutrophil-to-lymphocyte (NLR) ratio as an independent predictor of mortality and clinical risk stratifier in idiopathic pulmonary fibrosis
title_fullStr Multi-center evaluation of baseline neutrophil-to-lymphocyte (NLR) ratio as an independent predictor of mortality and clinical risk stratifier in idiopathic pulmonary fibrosis
title_full_unstemmed Multi-center evaluation of baseline neutrophil-to-lymphocyte (NLR) ratio as an independent predictor of mortality and clinical risk stratifier in idiopathic pulmonary fibrosis
title_short Multi-center evaluation of baseline neutrophil-to-lymphocyte (NLR) ratio as an independent predictor of mortality and clinical risk stratifier in idiopathic pulmonary fibrosis
title_sort multi-center evaluation of baseline neutrophil-to-lymphocyte (nlr) ratio as an independent predictor of mortality and clinical risk stratifier in idiopathic pulmonary fibrosis
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9722446/
https://www.ncbi.nlm.nih.gov/pubmed/36483266
http://dx.doi.org/10.1016/j.eclinm.2022.101758
work_keys_str_mv AT mikolaschtheresiaa multicenterevaluationofbaselineneutrophiltolymphocytenlrratioasanindependentpredictorofmortalityandclinicalriskstratifierinidiopathicpulmonaryfibrosis
AT georgepeterm multicenterevaluationofbaselineneutrophiltolymphocytenlrratioasanindependentpredictorofmortalityandclinicalriskstratifierinidiopathicpulmonaryfibrosis
AT sahotajagdeep multicenterevaluationofbaselineneutrophiltolymphocytenlrratioasanindependentpredictorofmortalityandclinicalriskstratifierinidiopathicpulmonaryfibrosis
AT nancarrowthomas multicenterevaluationofbaselineneutrophiltolymphocytenlrratioasanindependentpredictorofmortalityandclinicalriskstratifierinidiopathicpulmonaryfibrosis
AT barrattshaneyl multicenterevaluationofbaselineneutrophiltolymphocytenlrratioasanindependentpredictorofmortalityandclinicalriskstratifierinidiopathicpulmonaryfibrosis
AT woodheadfelixa multicenterevaluationofbaselineneutrophiltolymphocytenlrratioasanindependentpredictorofmortalityandclinicalriskstratifierinidiopathicpulmonaryfibrosis
AT kouranosvasilis multicenterevaluationofbaselineneutrophiltolymphocytenlrratioasanindependentpredictorofmortalityandclinicalriskstratifierinidiopathicpulmonaryfibrosis
AT copevictoriasa multicenterevaluationofbaselineneutrophiltolymphocytenlrratioasanindependentpredictorofmortalityandclinicalriskstratifierinidiopathicpulmonaryfibrosis
AT creamerandreww multicenterevaluationofbaselineneutrophiltolymphocytenlrratioasanindependentpredictorofmortalityandclinicalriskstratifierinidiopathicpulmonaryfibrosis
AT fidansilan multicenterevaluationofbaselineneutrophiltolymphocytenlrratioasanindependentpredictorofmortalityandclinicalriskstratifierinidiopathicpulmonaryfibrosis
AT ganeshanbalaji multicenterevaluationofbaselineneutrophiltolymphocytenlrratioasanindependentpredictorofmortalityandclinicalriskstratifierinidiopathicpulmonaryfibrosis
AT hoyluke multicenterevaluationofbaselineneutrophiltolymphocytenlrratioasanindependentpredictorofmortalityandclinicalriskstratifierinidiopathicpulmonaryfibrosis
AT mackintoshjohna multicenterevaluationofbaselineneutrophiltolymphocytenlrratioasanindependentpredictorofmortalityandclinicalriskstratifierinidiopathicpulmonaryfibrosis
AT shortmanrobert multicenterevaluationofbaselineneutrophiltolymphocytenlrratioasanindependentpredictorofmortalityandclinicalriskstratifierinidiopathicpulmonaryfibrosis
AT duckworthanna multicenterevaluationofbaselineneutrophiltolymphocytenlrratioasanindependentpredictorofmortalityandclinicalriskstratifierinidiopathicpulmonaryfibrosis
AT fallonjanet multicenterevaluationofbaselineneutrophiltolymphocytenlrratioasanindependentpredictorofmortalityandclinicalriskstratifierinidiopathicpulmonaryfibrosis
AT garthwaitehelen multicenterevaluationofbaselineneutrophiltolymphocytenlrratioasanindependentpredictorofmortalityandclinicalriskstratifierinidiopathicpulmonaryfibrosis
AT heightmanmelissa multicenterevaluationofbaselineneutrophiltolymphocytenlrratioasanindependentpredictorofmortalityandclinicalriskstratifierinidiopathicpulmonaryfibrosis
AT adamalihuzaifai multicenterevaluationofbaselineneutrophiltolymphocytenlrratioasanindependentpredictorofmortalityandclinicalriskstratifierinidiopathicpulmonaryfibrosis
AT linessarah multicenterevaluationofbaselineneutrophiltolymphocytenlrratioasanindependentpredictorofmortalityandclinicalriskstratifierinidiopathicpulmonaryfibrosis
AT winthida multicenterevaluationofbaselineneutrophiltolymphocytenlrratioasanindependentpredictorofmortalityandclinicalriskstratifierinidiopathicpulmonaryfibrosis
AT wollertonrebecca multicenterevaluationofbaselineneutrophiltolymphocytenlrratioasanindependentpredictorofmortalityandclinicalriskstratifierinidiopathicpulmonaryfibrosis
AT renzonielisabettaa multicenterevaluationofbaselineneutrophiltolymphocytenlrratioasanindependentpredictorofmortalityandclinicalriskstratifierinidiopathicpulmonaryfibrosis
AT stewardmatthew multicenterevaluationofbaselineneutrophiltolymphocytenlrratioasanindependentpredictorofmortalityandclinicalriskstratifierinidiopathicpulmonaryfibrosis
AT wellsatholu multicenterevaluationofbaselineneutrophiltolymphocytenlrratioasanindependentpredictorofmortalityandclinicalriskstratifierinidiopathicpulmonaryfibrosis
AT gibbonsmichael multicenterevaluationofbaselineneutrophiltolymphocytenlrratioasanindependentpredictorofmortalityandclinicalriskstratifierinidiopathicpulmonaryfibrosis
AT grovesashleym multicenterevaluationofbaselineneutrophiltolymphocytenlrratioasanindependentpredictorofmortalityandclinicalriskstratifierinidiopathicpulmonaryfibrosis
AT gooptubibek multicenterevaluationofbaselineneutrophiltolymphocytenlrratioasanindependentpredictorofmortalityandclinicalriskstratifierinidiopathicpulmonaryfibrosis
AT scottonchrisj multicenterevaluationofbaselineneutrophiltolymphocytenlrratioasanindependentpredictorofmortalityandclinicalriskstratifierinidiopathicpulmonaryfibrosis
AT porterjoannac multicenterevaluationofbaselineneutrophiltolymphocytenlrratioasanindependentpredictorofmortalityandclinicalriskstratifierinidiopathicpulmonaryfibrosis