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dc.contributor.authorCurran, Fraser M.
dc.contributor.authorBhalraam, U.
dc.contributor.authorMohan, Mohapradeep
dc.contributor.authorSingh, Jagdeep S.
dc.contributor.authorAnker, Stefan D.
dc.contributor.authorDickstein, Kenneth
dc.contributor.authorDoney, Alexander S.
dc.contributor.authorFilippatos, Gerasimos
dc.contributor.authorGeorge, Jacob
dc.contributor.authorMetra, Marco
dc.contributor.authorNg, Leong L.
dc.contributor.authorPalmer, Colin N.
dc.contributor.authorSamani, Nilesh J.
dc.contributor.authorvan Veldhuisen, Dirk J.
dc.contributor.authorVoors, Adriaan A.
dc.contributor.authorLang, Chim C.
dc.contributor.authorMordi, Ify R.
dc.date.accessioned2022-04-21T09:29:29Z
dc.date.available2022-04-21T09:29:29Z
dc.date.created2022-01-24T09:28:03Z
dc.date.issued2021
dc.identifier.issn2055-5822
dc.identifier.urihttps://hdl.handle.net/11250/2991891
dc.description.abstractAims Inflammation is thought to play a role in heart failure (HF) pathophysiology. Neutrophil-to-lymphocyte ratio (NLR) is a simple, routinely available measure of inflammation. Its relationship with other inflammatory biomarkers and its association with clinical outcomes in addition to other risk markers have not been comprehensively evaluated in HF patients. Methods We evaluated patients with worsening or new-onset HF from the BIOlogy Study to Tailored Treatment in Chronic Heart Failure (BIOSTAT-CHF) study who had available NLR at baseline. The primary outcome was time to all-cause mortality or HF hospitalization. Outcomes were validated in a separate HF population. Results 1622 patients were evaluated (including 523 ventricular ejection fraction [LVEF] < 40% and 662 LVEF ≥ 40%). NLR was significantly correlated with biomarkers related to inflammation as well as NT-proBNP. NLR was significantly associated with the primary outcome in patients irrespective of LVEF (hazard ratio [HR] 1.18 per standard deviation increase; 95% confidence interval [CI] 1.11–1.26, P < 0.001). Patients with NLR in the highest tertile had significantly worse outcome than those in the lowest independent of LVEF (<40%: HR 2.75; 95% CI 1.84–4.09, P < 0.001; LVEF ≥ 40%: HR 1.51; 95% CI 1.05–2.16, P = 0.026). When NLR was added to the BIOSTAT-CHF risk score, there were improvements in integrated discrimination index (IDI) and net reclassification index (NRI) for occurrence of the primary outcome (IDI + 0.009; 95% CI 0.00–0.019, P = 0.030; continuous NRI + 0.112, 95% CI 0.012–0.176, P = 0.040). Elevated NLR was similarly associated with adverse outcome in the validation cohort. Decrease in NLR at 6 months was associated with reduced incidence of the primary outcome (HR 0.75; 95% CI 0.57–0.98, P = 0.036). Conclusions Elevated NLR is significantly associated with elevated markers of inflammation in HF patients and is associated with worse outcome. Elevated NLR might potentially be useful in identifying high-risk HF patients and may represent a treatment target.en_US
dc.language.isoengen_US
dc.publisherWileyen_US
dc.rightsNavngivelse 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/deed.no*
dc.titleNeutrophil-to-lymphocyte ratio and outcomes in patients with new-onset or worsening heart failure with reduced and preserved ejection fractionen_US
dc.typeJournal articleen_US
dc.typePeer revieweden_US
dc.description.versionpublishedVersionen_US
dc.rights.holderCopyright 2021 The Author(s)en_US
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1
dc.identifier.doi10.1002/ehf2.13424
dc.identifier.cristin1988249
dc.source.journalESC Heart Failureen_US
dc.source.pagenumber3168-3179en_US
dc.identifier.citationESC Heart Failure. 2021, 8 (4), 3168-3179.en_US
dc.source.volume8en_US
dc.source.issue4en_US


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