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Response to the Letter to the Editor: “Neutrophil-lymphocyte ratio: Can clinicians really trust it as an inflammatory indicator?”

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Response to the Letter to the Editor:

“Neutrophil-lymphocyte ratio: Can clinicians really trust it as an inflammatory indicator?”

We thank Balta et al. [1] for their comments.

As stated in our article, neutrophil to lympho- cyte ratio (NLR) was found to be an independent predictor for both short (30-day) and long-term (2-year) mortality after adjusting for biomarkers and hematological markers [2]. Additionally, a cut-off value of NLR ≥ 7.4 × 109/L significantly improved the predictive power in combination with standard- ized Thrombolysis in Myocardial Infarction (TIMI) risk score for ST elevation myocardial infarction (STEMI) [3]. Also NLR ≥ 7.4 × 109/L was found to be associated with higher TIMI [3], Global Reg- istry of Acute Coronary Events (GRACE) [4] and Mayo Clinic Risk Score (MCRS) [5] suggestive of overall poor prognosis. This highlights the clinical value of NLR as a risk predictor, which can easily be obtained at point of care in the emergency room even prior to revascularization. Thus, NLR can help guide health care providers to make appropriate patient care and management decisions. Subse- quent to our publication, other researchers have also confirmed NLR to be an excellent predictor of coronary blood flow and mortality after STEMI [6].

As described in our article, NLR represents both the innate neutrophil mediated reactive response and subsequent lymphocyte mediated adaptive immune responses. Since the pathophysi- ology of atherosclerosis is primarily mediated by inflammation, biomarkers like C-reactive protein have been studied and shown to be associated with mortality after STEMI as well [7]. However, these biomarkers are not routinely obtained and may re- quire longer processing time which may preclude their use as risk predictors during STEMI with

limited door-to-balloon time. In contrast, NLR is routinely obtained and can be serially monitored during hospitalization. Certainly, future studies are needed evaluating the role of NLR as a risk- predictor in patients with inflammatory diseases presenting with STEMI.

Conflict of interest: None declared

References

1. Balta S, Demırkol S, Unlu M, Ozturk C, Arslan Z, Celık T. Neu- trophil-lymphocyte ratio: Can clinicians really trust it as an in- flammatory indicator? Cardiol J, 2015; 22: 475.

2. Sawant AC, Adhikari P, Narra SR, Srivatsa SS, Mills PK, Srivatsa SS. Neutrophil to lymphocyte ratio predicts short- and long-term mortality following revascularization therapy for ST elevation myocardial infarction. Cardiol J, 2014; 21: 500–508.

3. Morrow DA, Antman EM, Charlesworth A et al. TIMI risk score for ST-elevation myocardial infarction: A convenient, bedside, clinical score for risk assessment at presentation: An intrave- nous nPA for treatment of infarcting myocardium early II trial substudy. Circulation, 2000; 102: 2031–2037.

4. Granger CB, Goldberg RJ, Dabbous O et al. Predictors of hospital mortality in the global registry of acute coronary events. Arch Intern Med, 2003; 163: 2345–2353.

5. Singh M, Gersh BJ, Li S et al. Mayo Clinic Risk Score for per- cutaneous coronary intervention predicts in-hospital mortality in patients undergoing coronary artery bypass graft surgery.

Circulation, 2008; 117: 356–362.

6. Arbel Y, Shacham Y, Ziv-Baran T et al. Higher neutrophil/lympho- cyte ratio is related to lower ejection fraction and higher long- term all-cause mortality in ST-elevation myocardial infarction patients. Can J Cardiol, 2014, 30: 1177–1182.

7. Marcucci R, Valente S, Gori AM et al. Global platelet hyperreac- tivity and elevated C-reactive protein levels predict long term mortality in STEMI patients. Thromb Res, 2014; 134: 884–888.

Abhishek C. Sawant1, Sanjay S. Srivatsa2

1Johns Hopkins Hospital, Baltimore, Maryland, USA

2Community Regional Medical Center, 7215 North Fresno Street, Suite 103, Fresno, California, 93720, USA, tel: (559) 438 1111 e-mail: sanjaysrivatsa@hotmail.com letter to the editor

Cardiology Journal 2015, Vol. 22, No. 4, 476 DOI: 10.5603/CJ.2015.0051 Copyright © 2015 Via Medica ISSN 1897–5593

476 www.cardiologyjournal.org

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