Literature DB >> 32843183

The association between white blood cell count and outcomes in patients with idiopathic pulmonary fibrosis.

Steven D Nathan1, A Whitney Brown2, Nesrin Mogulkoc3, Flavia Soares4, Ashley C Collins2, Joyce Cheng2, Jake Peterson2, Brenna Cannon2, Christopher S King2, Scott D Barnett2.   

Abstract

BACKGROUND: The course of idiopathic pulmonary fibrosis (IPF) is uncertain with variable patterns of disease progression. We sought to evaluate the prognostic utility of the WBC, a routinely performed lab test, in a well-defined cohort of outpatient IPF subjects.
METHODS: We reviewed IPF patient records from two independent ILD centers (Inova Fairfax in Falls Church, VA, USA and Ege University Hospital in Izmir, Turkey) between 2007 and 2018. Demographics, CBC data, and patient outcomes were obtained. Survival differences were analyzed.
RESULTS: There were 436 IPF outpatients in the cohort with a median WBC of 8.9 × 109 cells per liter. For pragmatic purposes, patients were categorized into two groups, WBC ≥9 or WBC <9. Patients with WBC <9 had a median transplant-free survival of 50.5 months from the time of the CBC, compared to 32.4 months for those with WBC ≥9 (p < 0.0001). The association between WBC and attenuated survival remained significant after adjusting for GAP stage, steroid use, and antifibrotic use when WBC was analyzed both as a continuous (HR: 1.11; 95% CI: 1.05-1.17) and a dichotomized variable (high (WBC ≥9) vs. low (WBC <9), (HR: 1.53; 95% CI:1.09-2.15). WBC and absolute neutrophil count (ANC) were highly correlated suggesting that PMNs account for most of this association (r = 0.92).
CONCLUSIONS: Baseline WBC may impart important and readily available prognostic information in outpatients with IPF. Further studies are warranted to validate this as a potential biomarker for IPF, as well as to define the biologic basis for the association.
Copyright © 2020 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Biomarkers; Idiopathic pulmonary fibrosis; Interstitial; Leukocyte count; Lung diseases; Neutrophils

Mesh:

Substances:

Year:  2020        PMID: 32843183     DOI: 10.1016/j.rmed.2020.106068

Source DB:  PubMed          Journal:  Respir Med        ISSN: 0954-6111            Impact factor:   3.415


  6 in total

1.  Neutrophil lymphocyte ratio as an indicator for disease progression in Idiopathic Pulmonary Fibrosis.

Authors:  Andrew Achaiah; Amila Rathnapala; Andrea Pereira; Harriet Bothwell; Kritica Dwivedi; Rosie Barker; Valentina Iotchkova; Rachel Benamore; Rachel K Hoyles; Ling-Pei Ho
Journal:  BMJ Open Respir Res       Date:  2022-06

Review 2.  Neutrophils Modulate Fibrogenesis in Chronic Pulmonary Diseases.

Authors:  Lili Ding; Juan Yang; Chunmei Zhang; Xiuna Zhang; Pujun Gao
Journal:  Front Med (Lausanne)       Date:  2021-04-27

3.  Use of peripheral neutrophil to lymphocyte ratio and peripheral monocyte levels to predict survival in fibrotic hypersensitivity pneumonitis (fHP): a multicentre retrospective cohort study.

Authors:  Shaney L Barratt; Andrew W Creamer; Huzaifa I Adamali; Anna Duckworth; Janet Fallon; Silan Fidan; Tom Nancarrow; Rebecca Wollerton; Matthew Steward; Bibek Gooptu; Michael Gibbons; Felix Alexander Woodhead; Chris Scotton
Journal:  BMJ Open Respir Res       Date:  2021-11

Review 4.  Neutrophil Extracellular Traps in ANCA-Associated Vasculitis and Interstitial Lung Disease: A Scoping Review.

Authors:  Miriana d'Alessandro; Edoardo Conticini; Laura Bergantini; Paolo Cameli; Luca Cantarini; Bruno Frediani; Elena Bargagli
Journal:  Life (Basel)       Date:  2022-02-20

Review 5.  Mortality and survival in idiopathic pulmonary fibrosis: a systematic review and meta-analysis.

Authors:  Qiang Zheng; Ingrid A Cox; Julie A Campbell; Qing Xia; Petr Otahal; Barbara de Graaff; Tamera J Corte; Alan K Y Teoh; E Haydn Walters; Andrew J Palmer
Journal:  ERJ Open Res       Date:  2022-03-14

6.  Fibrotic lung disease inhibits immune responses to staphylococcal pneumonia via impaired neutrophil and macrophage function.

Authors:  Helen I Warheit-Niemi; Summer J Edwards; Shuvasree SenGupta; Carole A Parent; Xiaofeng Zhou; David N O'Dwyer; Bethany B Moore
Journal:  JCI Insight       Date:  2022-02-22
  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.