Dear Editor, the recent report on “Neutrophil-to-Lymphocyte Ratio (NLR),
Platelet-to-Lymphocyte Ratio (PLR) and Heart Failure” is very interesting.[1] Durmus et al.[1] reported that “NLR can be used to predict mortality during
the follow-up of HF patients.” Indeed, the use of a new parameter for predicting heart
failure is very interesting. However, as Durmus et al.[1] mentioned, both NLR and PLR “were not sufficient to establish a
diagnosis of HF.” In addition, although the present report[1] was well designed as a matched case-control study, the
problem on NLR and PLR should be discussed in view of laboratory medicine. Both parameters
are non - specific. Several factors can affect neutrophils, lymphocytes and platelets.
Other concomitant disorders such as immunological and malignant disorders can alter the NLR
and PLR values.[2-3] Also, metabolic syndrome, which is common among the patients with
cardiac disease, can also affect NLP and PLR values.[4] In addition, different automated hematological analyzers can also
give different results of neutrophil, lymphocyte and platelet measurements.[5]We recently published a trial named "Neutrophil-to-Lymphocyte Ratio (NLR) and
Platelet-to-Lymphocyte Ratio (PLR) are Predictors of Heart Failure (HF)".[1] In this study, we found that NLR can be
used to predict mortality during the follow-up of HF patients. However, NLR and PLR were
not sufficient to establish a diagnosis of HF. According to guidelines, HF diagnosis is
generally made based on clinical signs and symptoms of patients. Other examinations and
laboratory test are used to support or to rule out the HF diagnosis.[2] Although NLR and PLR were higher in HF
patients when compared to healthy controls, they are not sufficient, alone, to establish
the diagnosis of HF. Use of n-terminal pro brain natriuretic peptide, a commonly used
biomarker in congestive HF management, alone, is also not enough for diagnosis of HF, as
the use of NLR alone.[3] Another problem
regarding the use of NLR and PLR in HF patients is the lack of specificity. NLR and PLR
are ratios of different subgroups of blood cells. So, they should be affected in various
disease situations. Neutrophil count may be increased in patients with a bacterial
infection and platelets count may also be increased in patients with essential
thrombocythemia. In our study, to minimize this problem, we excluded patients who had
malignancies, connective tissue diseases, acute and chronic infections, renal disease
and acute coronary syndromes.As mentioned in the letter, NLR and PLR can be affected by metabolic syndrome. In our
study population, we did not assess the presence of metabolic syndrome. However, there
was no difference between the NLR and PLR values of patients with or without
hypertension (HT), hyperlipidemia (HL) and diabetes mellitus (DM).[4] In a previously reported study, NLR levels
tended to be high in patients with HT and DM. Finally, another criticism is that
"different automated hematological analyzers can also give different results of
neutrophil, lymphocyte and platelet measurements". This is true, because different
automated hematological analyzers use different techniques.[5] But, considering the basic blood cell count, there was a
good correlation between different automated hematological analyzers.[6] And also, NLR and PLR are ratios of blood
cells parameters, so they are not affected by the type of analyzers.
Authors: James L Januzzi; Roland van Kimmenade; John Lainchbury; Antoni Bayes-Genis; Jordi Ordonez-Llanos; Miguel Santalo-Bel; Yigal M Pinto; Mark Richards Journal: Eur Heart J Date: 2005-11-17 Impact factor: 29.983
Authors: John J V McMurray; Stamatis Adamopoulos; Stefan D Anker; Angelo Auricchio; Michael Böhm; Kenneth Dickstein; Volkmar Falk; Gerasimos Filippatos; Cândida Fonseca; Miguel Angel Gomez-Sanchez; Tiny Jaarsma; Lars Køber; Gregory Y H Lip; Aldo Pietro Maggioni; Alexander Parkhomenko; Burkert M Pieske; Bogdan A Popescu; Per K Rønnevik; Frans H Rutten; Juerg Schwitter; Petar Seferovic; Janina Stepinska; Pedro T Trindade; Adriaan A Voors; Faiez Zannad; Andreas Zeiher Journal: Eur Heart J Date: 2012-05-19 Impact factor: 29.983