Literature DB >> 33901498

Clinical and Prognostic Impact of Low Diffusing Capacity for Carbon Monoxide Values in Patients With Global Initiative for Obstructive Lung Disease I COPD.

Juan P de-Torres1, Denis E O'Donnell2, Jose M Marín3, Carlos Cabrera4, Ciro Casanova5, Marta Marín6, Ana Ezponda7, Borja G Cosio8, Cristina Martinez9, Ingrid Solanes10, Antonia Fuster11, J Alberto Neder2, Jessica Gonzalez-Gutierrez12, Bartolome R Celli13.   

Abstract

BACKGROUND: The Global Initiative for Obstructive Lung Disease (GOLD) does not promote diffusing capacity for carbon monoxide (Dlco) values in the evaluation of COPD. In GOLD spirometric stage I COPD patients, the clinical and prognostic impact of a low Dlco has not been explored. RESEARCH QUESTION: Could a Dlco threshold help define an increased risk of death and a different clinical presentation in these patients? STUDY DESIGN AND METHODS: GOLD stage I COPD patients (n = 360) were enrolled and followed over 109 ± 50 months. Age, sex, pack-years' history, BMI, dyspnea, lung function measurements, exercise capacity, BODE index, and history of exacerbations were recorded. A cutoff value for Dlco was identified for all-cause mortality and the clinical and physiological characteristics of patients above and below the threshold compared. Cox regression analysis explored the predictive power of that cutoff value for all-cause mortality.
RESULTS: A Dlco cutoff value of <60% predicted was associated with all-cause mortality (Dlco ≥ 60%: 9% vs Dlco < 60%: 23%, P = .01). At a same FEV1% predicted and Charlson score, patients with Dlco < 60% had lower BMI, more dyspnea, lower inspiratory capacity (IC)/total lung capacity (TLC) ratio, lower 6-min walk distance (6MWD), and higher BODE. Cox multiple regression analysis confirmed that after adjusting for age, sex, pack-years history, smoking status, and BMI, a Dlco < 60% is associated with all-cause mortality (hazard ratio [HR], 95% CI = 3.37, 1.35-8.39; P = .009)
INTERPRETATION: In GOLD I COPD patients, a Dlco < 60% predicted is associated with increased risk of death and worse clinical presentation. What the cause(s) of this association are and whether they can be treated need to be determined.
Copyright © 2021 American College of Chest Physicians. Published by Elsevier Inc. All rights reserved.

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Keywords:  COPD; Dlco; clinical; mortality

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Year:  2021        PMID: 33901498      PMCID: PMC8448999          DOI: 10.1016/j.chest.2021.04.033

Source DB:  PubMed          Journal:  Chest        ISSN: 0012-3692            Impact factor:   10.262


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10.  Outcomes for symptomatic non-obstructed individuals and individuals with mild (GOLD stage 1) COPD in a population based cohort.

Authors:  Rogelio Perez-Padilla; Fernando C Wehrmeister; Maria Montes de Oca; Maria Victorina Lopez; Jose R Jardim; Adriana Muiño; Gonzalo Valdivia; Ana Maria B Menezes
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  3 in total

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Authors:  Franziska C Trudzinski; Rudolf A Jörres; Peter Alter; Julia Walter; Henrik Watz; Andrea Koch; Matthias John; Marek Lommatzsch; Claus F Vogelmeier; Hans-Ulrich Kauczor; Tobias Welte; Jürgen Behr; Amanda Tufman; Robert Bals; Felix J F Herth; Kathrin Kahnert
Journal:  Sci Rep       Date:  2022-05-24       Impact factor: 4.996

2.  Predictive model of postoperative pneumonia after neoadjuvant immunochemotherapy for esophageal cancer.

Authors:  Wei Wang; Yongkui Yu; Haibo Sun; Zongfei Wang; Yan Zheng; Guanghui Liang; Peinan Chen; Jiwei Cheng; Xiaoxia Xu; Funa Yang; Qi Liu; Weiqun Xing
Journal:  J Gastrointest Oncol       Date:  2022-04

3.  CD19 and POU2AF1 are Potential Immune-Related Biomarkers Involved in the Emphysema of COPD: On Multiple Microarray Analysis.

Authors:  Da-Wei Zhang; Jing-Jing Ye; Ying Sun; Shuang Ji; Jia-Ying Kang; Yuan-Yuan Wei; Guang-He Fei
Journal:  J Inflamm Res       Date:  2022-04-20
  3 in total

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