The ratio of neutrophil-to-lymphocyte and platelet-to-lymphocyte and association with mortality in community-acquired pneumonia: a derivation-validation cohort study

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The ratio of neutrophil-to-lymphocyte and platelet-to-lymphocyte and association with mortality in community-acquired pneumonia : a derivation-validation cohort study. / Enersen, Christian Cosmus; Egelund, Gertrud Baunbæk; Petersen, Pelle Trier; Andersen, Stine; Ravn, Pernille; Rohde, Gernot; Lindegaard, Birgitte; Jensen, Andreas Vestergaard.

In: Infection, Vol. 51, No. 5, 2023, p. 1339-1347.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Enersen, CC, Egelund, GB, Petersen, PT, Andersen, S, Ravn, P, Rohde, G, Lindegaard, B & Jensen, AV 2023, 'The ratio of neutrophil-to-lymphocyte and platelet-to-lymphocyte and association with mortality in community-acquired pneumonia: a derivation-validation cohort study', Infection, vol. 51, no. 5, pp. 1339-1347. https://doi.org/10.1007/s15010-023-01992-2

APA

Enersen, C. C., Egelund, G. B., Petersen, P. T., Andersen, S., Ravn, P., Rohde, G., Lindegaard, B., & Jensen, A. V. (2023). The ratio of neutrophil-to-lymphocyte and platelet-to-lymphocyte and association with mortality in community-acquired pneumonia: a derivation-validation cohort study. Infection, 51(5), 1339-1347. https://doi.org/10.1007/s15010-023-01992-2

Vancouver

Enersen CC, Egelund GB, Petersen PT, Andersen S, Ravn P, Rohde G et al. The ratio of neutrophil-to-lymphocyte and platelet-to-lymphocyte and association with mortality in community-acquired pneumonia: a derivation-validation cohort study. Infection. 2023;51(5):1339-1347. https://doi.org/10.1007/s15010-023-01992-2

Author

Enersen, Christian Cosmus ; Egelund, Gertrud Baunbæk ; Petersen, Pelle Trier ; Andersen, Stine ; Ravn, Pernille ; Rohde, Gernot ; Lindegaard, Birgitte ; Jensen, Andreas Vestergaard. / The ratio of neutrophil-to-lymphocyte and platelet-to-lymphocyte and association with mortality in community-acquired pneumonia : a derivation-validation cohort study. In: Infection. 2023 ; Vol. 51, No. 5. pp. 1339-1347.

Bibtex

@article{a5c50f4ac3324002817c83646c9c62a6,
title = "The ratio of neutrophil-to-lymphocyte and platelet-to-lymphocyte and association with mortality in community-acquired pneumonia: a derivation-validation cohort study",
abstract = "Rationale: The ratio of neutrophil-to-lymphocyte (NLR), monocyte-to-lymphocyte (MLR) and platelet-to-lymphocyte (PLR) are biomarkers that have shown potential for predicting mortality in several diseases. For patients hospitalized with community-acquired pneumonia (CAP), the prognostic capabilities of these biomarkers are unknown. Objective: Investigate whether NLR, MLR or PLR were associated with 90-day mortality in CAP. Further, investigate whether the prediction rule CURB-65 could be improved by adding these biomarkers. Methods: A derivation-validation study using a Danish multicentre retrospective cohort as the derivation cohort (N = 831) and a European multicentre prospective cohort as the validation cohort (N = 2463). Associations between biomarkers and mortality were assessed using Cox proportional hazard models with adjustments for sex, CURB-65 and comorbidities. A cut-off value for biomarkers was determined using Youden{\textquoteright}s J Statistics. The performance of CURB-65 with added biomarkers was evaluated using receiver-operating characteristics. Results: In both cohorts increasing NLR and PLR were associated with 90-day mortality. In the derivation cohort, the hazard ratios for NLR and PLR were 1.016 (95% confidence interval (CI) 1.001–1.032, P = 0.038) and 1.001 (95% CI 1.000–1.001, P = 0.035), respectively. Adding these biomarkers to CURB-65 did not improve its performance. Conclusions: NLR and PLR were associated with 90-day mortality in CAP, but did not improve CURB-65.",
keywords = "Community-acquired pneumonia, Mortality, Neutrophil-to-lymphocyte ratio",
author = "Enersen, {Christian Cosmus} and Egelund, {Gertrud Baunb{\ae}k} and Petersen, {Pelle Trier} and Stine Andersen and Pernille Ravn and Gernot Rohde and Birgitte Lindegaard and Jensen, {Andreas Vestergaard}",
note = "Publisher Copyright: {\textcopyright} 2023, The Author(s), under exclusive licence to Springer-Verlag GmbH Germany.",
year = "2023",
doi = "10.1007/s15010-023-01992-2",
language = "English",
volume = "51",
pages = "1339--1347",
journal = "Therapies",
issn = "0300-8126",
publisher = "Springer Medizin",
number = "5",

}

RIS

TY - JOUR

T1 - The ratio of neutrophil-to-lymphocyte and platelet-to-lymphocyte and association with mortality in community-acquired pneumonia

T2 - a derivation-validation cohort study

AU - Enersen, Christian Cosmus

AU - Egelund, Gertrud Baunbæk

AU - Petersen, Pelle Trier

AU - Andersen, Stine

AU - Ravn, Pernille

AU - Rohde, Gernot

AU - Lindegaard, Birgitte

AU - Jensen, Andreas Vestergaard

N1 - Publisher Copyright: © 2023, The Author(s), under exclusive licence to Springer-Verlag GmbH Germany.

PY - 2023

Y1 - 2023

N2 - Rationale: The ratio of neutrophil-to-lymphocyte (NLR), monocyte-to-lymphocyte (MLR) and platelet-to-lymphocyte (PLR) are biomarkers that have shown potential for predicting mortality in several diseases. For patients hospitalized with community-acquired pneumonia (CAP), the prognostic capabilities of these biomarkers are unknown. Objective: Investigate whether NLR, MLR or PLR were associated with 90-day mortality in CAP. Further, investigate whether the prediction rule CURB-65 could be improved by adding these biomarkers. Methods: A derivation-validation study using a Danish multicentre retrospective cohort as the derivation cohort (N = 831) and a European multicentre prospective cohort as the validation cohort (N = 2463). Associations between biomarkers and mortality were assessed using Cox proportional hazard models with adjustments for sex, CURB-65 and comorbidities. A cut-off value for biomarkers was determined using Youden’s J Statistics. The performance of CURB-65 with added biomarkers was evaluated using receiver-operating characteristics. Results: In both cohorts increasing NLR and PLR were associated with 90-day mortality. In the derivation cohort, the hazard ratios for NLR and PLR were 1.016 (95% confidence interval (CI) 1.001–1.032, P = 0.038) and 1.001 (95% CI 1.000–1.001, P = 0.035), respectively. Adding these biomarkers to CURB-65 did not improve its performance. Conclusions: NLR and PLR were associated with 90-day mortality in CAP, but did not improve CURB-65.

AB - Rationale: The ratio of neutrophil-to-lymphocyte (NLR), monocyte-to-lymphocyte (MLR) and platelet-to-lymphocyte (PLR) are biomarkers that have shown potential for predicting mortality in several diseases. For patients hospitalized with community-acquired pneumonia (CAP), the prognostic capabilities of these biomarkers are unknown. Objective: Investigate whether NLR, MLR or PLR were associated with 90-day mortality in CAP. Further, investigate whether the prediction rule CURB-65 could be improved by adding these biomarkers. Methods: A derivation-validation study using a Danish multicentre retrospective cohort as the derivation cohort (N = 831) and a European multicentre prospective cohort as the validation cohort (N = 2463). Associations between biomarkers and mortality were assessed using Cox proportional hazard models with adjustments for sex, CURB-65 and comorbidities. A cut-off value for biomarkers was determined using Youden’s J Statistics. The performance of CURB-65 with added biomarkers was evaluated using receiver-operating characteristics. Results: In both cohorts increasing NLR and PLR were associated with 90-day mortality. In the derivation cohort, the hazard ratios for NLR and PLR were 1.016 (95% confidence interval (CI) 1.001–1.032, P = 0.038) and 1.001 (95% CI 1.000–1.001, P = 0.035), respectively. Adding these biomarkers to CURB-65 did not improve its performance. Conclusions: NLR and PLR were associated with 90-day mortality in CAP, but did not improve CURB-65.

KW - Community-acquired pneumonia

KW - Mortality

KW - Neutrophil-to-lymphocyte ratio

U2 - 10.1007/s15010-023-01992-2

DO - 10.1007/s15010-023-01992-2

M3 - Journal article

C2 - 36763284

AN - SCOPUS:85147747788

VL - 51

SP - 1339

EP - 1347

JO - Therapies

JF - Therapies

SN - 0300-8126

IS - 5

ER -

ID: 367352520