Evidence map›Paper›PMID 42323163›Full record

Observational studyThe American journal of clinical nutrition2026

Nutritional anemia is associated with increased risk of severe COPD exacerbations: a prospective cohort study.

Valerie Dehondt, Nicolas Kint, Lowie Egw Vanfleteren, Lies Lahousse

Abstract readObservational Study
In one paragraph

Observational study in The American journal of clinical nutrition, 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

4 authors.

Valerie DehondtDepartment of Bioanalysis, Ghent University, Ghent, Belgium.
Nicolas KintDepartment of Hematology, Ghent University Hospital, Ghent, Belgium.
Lowie Egw VanfleterenDepartment of Respiratory Medicine, Ghent University Hospital, Ghent, Belgium; Department of Internal Medicine and Clinical Nutrition, Institute of Medicine, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden; Department of Specialist Medicine, COPD Center, Sahlgrenska University Hospital, Gothenburg, Region Västra Götaland, Sweden.
Lies LahousseDepartment of Bioanalysis, Ghent University, Ghent, Belgium; Department of Epidemiology, Erasmus Medical Center, Rotterdam, The Netherlands. Electronic address: Lies.Lahousse@UGent.be.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAnemia prevalence in chronic obstructive pulmonary disease (COPD) varies widely across studies, and data on anemia subtypes and their association with mortality or COPD exacerbation readmission are limited.

objectivesWe aimed to investigate anemia subtypes and their association with mortality and readmission for acute exacerbation of COPD (AECOPD) in patients hospitalized for AECOPD.

methodsIn this prospective observational cohort study, patients with COPD aged ≥45 y hospitalized for severe exacerbations in a Belgian nationwide database were included. Cox regression models investigated associations between anemia (or its subtypes) and (postdischarge) mortality and AECOPD readmission, adjusted for age, sex, socioeconomic status, smoking, weight, and age-adjusted Charlson Comorbidity Index. Inverse probability of treatment weighting examined the association between anemia treatment and mortality across anemia subtypes.

resultsAmong 32,152 patients with COPD discharged from the hospital, 5956 (18.5%) had anemia. Nutritional anemia was most frequent (49.3%), followed by anemia of chronic disease (ACD; 31.3%). Anemia was associated with a 30% higher postdischarge mortality risk [adjusted hazard ratio (aHR): 1.30, 95% confidence interval (CI): 1.23, 1.37], and 8% higher readmission risk (aHR:1.08, 95% CI: 1.03, 1.14). Patients with hematologic anemia had the highest postdischarge mortality risk (aHR: 1.75, 95% CI: 1.54, 1.99), followed by nutritional anemia (aHR: 1.29, 95% CI: 1.20, 1.39). Only nutritional anemia was associated with increased readmission risk (aHR: 1.18, 95% CI: 1.10, 1.25). Treatment effects differed by anemia subtype, with iron, vitamin B12, and erythroid-stimulating agent (ESA) associated with lower postdischarge mortality in nutritional anemia; folic acid and iron in hematologic anemia; and ESA and iron in ACD.

conclusionsNutritional anemia is the predominant subtype in hospitalized patients with AECOPD, and its increased readmission risk calls closer attention to iron deficiency in patients with COPD. All subtypes of anemia are associated with higher postdischarge mortality risk, but targeted treatment may reduce mortality risk and represents a potential strategy to improve outcomes.

Indexed as

AnemiaPulmonary Disease, Chronic ObstructiveAgedAged, 80 and overBelgiumCohort StudiesFemaleHospitalizationHumansMaleMiddle AgedPatient ReadmissionProspective StudiesRisk Factorsanemiachronic obstructive pulmonary diseaseexacerbationshospitalizationinflammationiron deficiencymortalitynutrition

Identifiers

PMID42323163
PMCPMC13494100

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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.