Neutrophil-to-lymphocyte ratio and outcomes in patients with new-onset or worsening heart failure with reduced and preserved ejection fraction

被引:51
|
作者
Curran, Fraser M. [1 ]
Bhalraam, U. [1 ]
Mohan, Mohapradeep [2 ]
Singh, Jagdeep S. [2 ]
Anker, Stefan D. [3 ,4 ]
Dickstein, Kenneth [5 ]
Doney, Alexander S. [6 ]
Filippatos, Gerasimos [7 ]
George, Jacob [2 ]
Metra, Marco [8 ]
Ng, Leong L. [9 ,10 ]
Palmer, Colin N. [6 ]
Samani, Nilesh J. [9 ,10 ]
van Veldhuisen, Dirk J. [11 ]
Voors, Adriaan A. [11 ]
Lang, Chim C. [2 ]
Mordi, Ify R. [2 ]
机构
[1] Univ Dundee, Sch Med, Dundee, Scotland
[2] Univ Dundee, Div Mol & Clin Med, Dundee DD1 9SY, Scotland
[3] Charite Univ Med Berlin, Dept Cardiol CVK, Berlin, Germany
[4] Charite Univ Med Berlin, Berlin Inst Hlth Ctr Regenerat Therapies BCRT, German Ctr Cardiovasc Res DZHK, Partner Site Berlin, Berlin, Germany
[5] Univ Bergen, Stavanger Univ Hosp, Stavanger, Norway
[6] Univ Dundee, Div Populat Hlth & Genom, Dundee, Scotland
[7] Natl & Kopodistrian Univ Athens, Sch Med, Dept Cardiol, Athens Univ Hosp Attikon,Heart Failure Unit, Athens, Greece
[8] Univ Brescia, Inst Cardiol, Dept Med & Surg Specialties, Radiol Sci & Publ Hlth, Brescia, Italy
[9] Univ Leicester, Dept Cardiovasc Sci, Leicester, England
[10] NIHR Leicester Biomed Res Ctr, Leicester, England
[11] Univ Groningen, Univ Med Ctr Groningen, Dept Cardiol, Groningen, Netherlands
来源
ESC HEART FAILURE | 2021年 / 8卷 / 04期
基金
英国惠康基金;
关键词
Heart failure; Neutrophil-to-lymphocyte ratio; Inflammation; Biomarkers; Outcome; TUMOR-NECROSIS-FACTOR; PROGNOSTIC VALUE; MORTALITY; THERAPY; INFLAMMATION; CYTOKINES; TRIAL; RECEPTORS; DISEASE; UTILITY;
D O I
10.1002/ehf2.13424
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aims 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.
引用
收藏
页码:3168 / 3179
页数:12
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