Evidence map›Paper›PMID 41742158›Full record

ArticleBMC pulmonary medicine2026

Persistently low blood eosinophils identify a high-risk phenotype in COPD.

Wen Zhang, Si Yuan Chew, Xiaoli He, Yanlin Wu, Mariko Siyue Koh, Guansong Wang, Zhi Xu, Pei Yee Tiew

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Article in BMC pulmonary medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Wen ZhangDepartment of Respiratory and Critical Care Medicine, Singapore General Hospital, Singapore, Singapore. zhangwen1564@tmmu.edu.cn.
Si Yuan ChewDepartment of Respiratory and Critical Care Medicine, Singapore General Hospital, Singapore, Singapore.
Xiaoli HeDepartment of Pulmonary and Critical Care Medicine, Institute of Respiratory Diseases, Xinqiao Hospital, Army Medical University, Chongqing, China.
Yanlin WuDepartment of Pulmonary and Critical Care Medicine, Institute of Respiratory Diseases, Xinqiao Hospital, Army Medical University, Chongqing, China.
Mariko Siyue KohDepartment of Respiratory and Critical Care Medicine, Singapore General Hospital, Singapore, Singapore.
Guansong WangDepartment of Pulmonary and Critical Care Medicine, Institute of Respiratory Diseases, Xinqiao Hospital, Army Medical University, Chongqing, China.
Zhi XuDepartment of Pulmonary and Critical Care Medicine, Institute of Respiratory Diseases, Xinqiao Hospital, Army Medical University, Chongqing, China. xuzhihxk@tmmu.edu.cn.
Pei Yee TiewDepartment of Respiratory and Critical Care Medicine, Singapore General Hospital, Singapore, Singapore.

Funding

Chongqing Natural Science Foundation General Program CSTB2024NSCQ-MSX1114Chongqing Science and Health Joint Medical Research Project 2023QNXM045Chongqing Science and Health Joint Medical Research Project 2024GGXM001Chongqing Young and Middle-aged Key Talents in Public Health GWZQN202508Singapore Ministry of Health's National Medical Research Council under its under its Transition Award MOH-001275-00the Clinical Research Special Project of the Second Affiliated Hospital of Army Medical University 2024F030the National Research Foundation Singapore under its Open Fund-Large Collaborative Grant MOH-001636
6 · The paper itself

Abstract

backgroundBlood eosinophil count (BEC) is used to guide COPD therapy, yet its longitudinal stability and prognostic relevance remain debated. We investigated BEC variability and the clinical implications of eosinophil trajectories.

methodsStable COPD patients (n = 471) were prospectively recruited in Singapore from 2013 to 2025. BEC stability was assessed using paired baseline and 1-year measurements. Patients were classified as persistently low (LL), persistently high (HH), or variable (VAR) based on a 0.15 × 10⁹/L threshold across 1 year period. Associations with exacerbations and mortality were examined using multivariable regression, with findings validated in an independent cohort from China (n = 66).

resultsAmong 471 patients, low baseline BEC (< 0.15 × 10⁹/L) was associated with worse lung function, higher symptom burden, and increased unadjusted mortality (p < 0.05). Paired BEC measurements (n = 176) showed moderate reproducibility (intraclass correlation coefficient = 0.423), indicating within-individual variability. Trajectory analysis revealed that compared to the LL group, both HH and VAR groups had significantly lower historical exacerbation rates. During one-year follow-up, the LL group experienced higher rates of hospitalized exacerbations. Kaplan-Meier analysis demonstrated a trend toward increased mortality in the LL group (log-rank p = 0.066). In multivariable Cox models, the VAR group had a significantly lower mortality risk compared with LL (HR = 0.465, p = 0.031), while the HH group showed a non-significant trend toward reduced mortality (HR = 0.637, p = 0.171). These patterns of higher exacerbation risk and trend toward higher mortality in the LL phenotype were consistent in the validation cohort.

conclusionsPersistently low BEC identifies a high-risk phenotype associated with increased exacerbations and trend toward poor prognosis, a finding corroborated in an independent cohort, supporting the value of repeated assessment.

Indexed as

EosinophilsPulmonary Disease, Chronic ObstructiveAgedDisease ProgressionFemaleHumansKaplan-Meier EstimateLeukocyte CountMaleMiddle AgedPhenotypePrognosisProspective StudiesSingaporeBlood eosinophil countCOPDLongitudinal stabilityMortalityPhenotype

Identifiers

PMID41742158
PMCPMC13041083

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.