Changes in Neutrophil–Lymphocyte or Platelet–Lymphocyte Ratios and Their Associations with Clinical Outcomes in Idiopathic Pulmonary Fibrosis

Identification of prognostic and predictive biomarkers in idiopathic pulmonary fibrosis (IPF) could aid assessment of disease severity and prediction of progression and response to treatment. This analysis examined reference ranges for neutrophil–lymphocyte ratio (NLR) and platelet–lymphocyte ratio...

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Main Authors: Steven D. Nathan, Jayesh Mehta, John Stauffer, Elizabeth Morgenthien, Ming Yang, Susan L. Limb, Sangeeta Bhorade
Format: Article
Language:English
Published: MDPI AG 2021-04-01
Series:Journal of Clinical Medicine
Subjects:
Online Access:https://www.mdpi.com/2077-0383/10/7/1427
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author Steven D. Nathan
Jayesh Mehta
John Stauffer
Elizabeth Morgenthien
Ming Yang
Susan L. Limb
Sangeeta Bhorade
author_facet Steven D. Nathan
Jayesh Mehta
John Stauffer
Elizabeth Morgenthien
Ming Yang
Susan L. Limb
Sangeeta Bhorade
author_sort Steven D. Nathan
collection DOAJ
description Identification of prognostic and predictive biomarkers in idiopathic pulmonary fibrosis (IPF) could aid assessment of disease severity and prediction of progression and response to treatment. This analysis examined reference ranges for neutrophil–lymphocyte ratio (NLR) and platelet–lymphocyte ratio (PLR) in IPF, and the relationship between NLR or PLR changes and clinical outcomes over 12 months. This post hoc analysis included patients with IPF from the Phase III, double-blind trials of pirfenidone, ASCEND (NCT01366209) and CAPACITY (NCT00287716 and NCT00287729). The relationship between change from baseline to Month 12 in NLR or PLR (divided into quartiles (Q1–Q4)) and outcomes (mortality, respiratory hospitalization, declines in lung function, exercise capacity and quality of life) was assessed. Estimated reference ranges at baseline for all patients analyzed (<i>n</i> = 1334) were 1.1–6.4 for NLR and 56.8–250.5 for PLR. Significant trends were observed across NLR and PLR quartiles for all outcomes in placebo-treated patients, with patients manifesting the greatest NLR or PLR changes experiencing the worst outcomes. These results suggest that the greatest NLR or PLR changes over 12 months were associated with worse clinical outcomes. Further research is needed to determine the utility of NLR and PLR as prognostic biomarkers in IPF.
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spelling doaj.art-0fcef396202d4972bf736e665a76725a2023-11-21T13:49:39ZengMDPI AGJournal of Clinical Medicine2077-03832021-04-01107142710.3390/jcm10071427Changes in Neutrophil–Lymphocyte or Platelet–Lymphocyte Ratios and Their Associations with Clinical Outcomes in Idiopathic Pulmonary FibrosisSteven D. Nathan0Jayesh Mehta1John Stauffer2Elizabeth Morgenthien3Ming Yang4Susan L. Limb5Sangeeta Bhorade6Advanced Lung Disease and Transplant Program, Inova Fairfax Hospital, 3300 Gallows Rd, Falls Church, VA 22042, USAFeinberg School of Medicine, Northwestern University, 420 E Superior St, Chicago, IL 60611, USAGenentech, Inc., 1 DNA Way, South San Francisco, CA 94080, USAGenentech, Inc., 1 DNA Way, South San Francisco, CA 94080, USAGenentech, Inc., 1 DNA Way, South San Francisco, CA 94080, USAGenentech, Inc., 1 DNA Way, South San Francisco, CA 94080, USAFeinberg School of Medicine, Northwestern University, 420 E Superior St, Chicago, IL 60611, USAIdentification of prognostic and predictive biomarkers in idiopathic pulmonary fibrosis (IPF) could aid assessment of disease severity and prediction of progression and response to treatment. This analysis examined reference ranges for neutrophil–lymphocyte ratio (NLR) and platelet–lymphocyte ratio (PLR) in IPF, and the relationship between NLR or PLR changes and clinical outcomes over 12 months. This post hoc analysis included patients with IPF from the Phase III, double-blind trials of pirfenidone, ASCEND (NCT01366209) and CAPACITY (NCT00287716 and NCT00287729). The relationship between change from baseline to Month 12 in NLR or PLR (divided into quartiles (Q1–Q4)) and outcomes (mortality, respiratory hospitalization, declines in lung function, exercise capacity and quality of life) was assessed. Estimated reference ranges at baseline for all patients analyzed (<i>n</i> = 1334) were 1.1–6.4 for NLR and 56.8–250.5 for PLR. Significant trends were observed across NLR and PLR quartiles for all outcomes in placebo-treated patients, with patients manifesting the greatest NLR or PLR changes experiencing the worst outcomes. These results suggest that the greatest NLR or PLR changes over 12 months were associated with worse clinical outcomes. Further research is needed to determine the utility of NLR and PLR as prognostic biomarkers in IPF.https://www.mdpi.com/2077-0383/10/7/1427NLRPLRidiopathic pulmonary fibrosisclinical outcomesbiomarker
spellingShingle Steven D. Nathan
Jayesh Mehta
John Stauffer
Elizabeth Morgenthien
Ming Yang
Susan L. Limb
Sangeeta Bhorade
Changes in Neutrophil–Lymphocyte or Platelet–Lymphocyte Ratios and Their Associations with Clinical Outcomes in Idiopathic Pulmonary Fibrosis
Journal of Clinical Medicine
NLR
PLR
idiopathic pulmonary fibrosis
clinical outcomes
biomarker
title Changes in Neutrophil–Lymphocyte or Platelet–Lymphocyte Ratios and Their Associations with Clinical Outcomes in Idiopathic Pulmonary Fibrosis
title_full Changes in Neutrophil–Lymphocyte or Platelet–Lymphocyte Ratios and Their Associations with Clinical Outcomes in Idiopathic Pulmonary Fibrosis
title_fullStr Changes in Neutrophil–Lymphocyte or Platelet–Lymphocyte Ratios and Their Associations with Clinical Outcomes in Idiopathic Pulmonary Fibrosis
title_full_unstemmed Changes in Neutrophil–Lymphocyte or Platelet–Lymphocyte Ratios and Their Associations with Clinical Outcomes in Idiopathic Pulmonary Fibrosis
title_short Changes in Neutrophil–Lymphocyte or Platelet–Lymphocyte Ratios and Their Associations with Clinical Outcomes in Idiopathic Pulmonary Fibrosis
title_sort changes in neutrophil lymphocyte or platelet lymphocyte ratios and their associations with clinical outcomes in idiopathic pulmonary fibrosis
topic NLR
PLR
idiopathic pulmonary fibrosis
clinical outcomes
biomarker
url https://www.mdpi.com/2077-0383/10/7/1427
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