Join Us | Latest Articles | Contact

Journal Home


Editorial Board


Recent Articles


Submit to this journal


Special Issues


Current issue

International Journal of Respiratory and Pulmonary Medicine





DOI: 10.23937/2378-3516/1410043



Platelet to Lymphocyte Ratio as a Novel Prognostic Marker in Male Patients with Chronic Obstructive Pulmonary Disease

Sezgi Sahin Duyar1*, Yalcin Solak2, Dilek Tekis3, Jale Karakaya4, Ferit Kuscu5 and Asuman Erarslan6


1Karaman State Hospital, Department of Pulmonology, Turkey
2Karaman State Hospital, Department of Internal Medicine, Division of Nephrology, Turkey
3Karaman State Hospital, Department of Internal Medicine, Division of Gastroenterology, Turkey
4Hacettepe University, Faculty of Medicine, Department of Biostatistics, Turkey
5Beypazarı State Hospital, Department of Infectious Diseases, Turkey
6Karaman State Hospital, Department of Clinical Biochemistry, Turkey


*Corresponding author: Sezgi Sahin Duyar, Karaman State Hospital, Department of Pulmonology, Alacaatlı Mahallesi 3373/2 Sokak Gezgin 1 Sitesi Yasamkent, Ankara, Turkey, Tel: 05052975327, E-mail: drsezgisahin@gmail.com
Int J Respir Pulm Med, IJRPM-3-043, (Volume 3, Issue 1), Original Article; ISSN: 2378-3516
Received: February 25, 2016 | Accepted: March 28, 2016 | Published: March 31, 2016
Citation: Duyar SS, Solak Y, Tekis D, Karakaya J, Kuscu F, et al. (2016) Platelet to Lymphocyte Ratio as a Novel Prognostic Marker in Male Patients with Chronic Obstructive Pulmonary Disease. Int J Respir Pulm Med 3:043. 10.23937/2378-3516/1410043
Copyright: © 2016 Duyar SS, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.



Abstract

Background and aim: Neutrophil to lymphocyte ratio(NLR) and platalet to lymphocyte ratio (PLR) are recently defined novel inflammatory markers which are readily available. Their prognostic signifigance has been shown for a number of inflammatory diseases. A recent study evaluated the role of NLR in patients with chronic obstructive pulmonary disease(COPD). Thus, we aimed to investigate the relations between NLR, PLR and severity of COPD in male patients who had stable disease.

Patients and methods: The clinical and dermographical charecteristics of 39 patients were reviewed retrospectively. Complete blood cell counts and differential values were recorded from electronic database of the hospital. NLR and PLR were calculated from absolute neutrophil and lymphocyte counts from CBC, respectively.

Results: PLR was higher in high risk group of patients with severe airflow limitation (p = 0.011).

Conclusion: The results of this study showed that PLR could be a candidate as a prognostic marker in showing the severity of stable COPD.


Introduction

The pathogenesis of chronic obstructive pulmonary disease (COPD) is traditionally based on airflow limitation. During the last few decades, local and systemic inflammation which are associated with comorbidities, exacerbations and morbidity and mortality of COPD have also been described as significant components in pathogenesis.

Neutrophil to lymphocyte ratio (NLR) and platalet to lymphocyte ratio (PLR) are novel inflammatory markers which have been investigated for a variety of chronic diseases such as cardiovascular disease, metobolic syndrome, Alzheimer's disease, diabetes mellitus, and cancers such as Hodgkin lymphoma, colorectal, cervical and lung carcinomas [1-10]. On the other hand, there are limited data regarding the role of NLR in COPD. To our knowledge, PLR has not been investigated in context of COPD yet.

The main goal of this study was to investigate the relationship between NLR, PLR and the severity of stable COPD in terms of the stage of the disease, modified Medical Research Council (mMRC) dyspnea scale, airflow limitation (described as FEV1) and rate of exacerbations [11].


Patients and Methods

We retrospectively reviewed the clinical data of the patients who visited one of the pulmonology outpatient clinics in Karaman State Hospital between January 2012 and April 2013, using ICD codes J44.9. We recorded gender, age, history of smoking, cardiovascular (hypertension, atherosclerotic heart disease and valvular diseases) and other comorbidities, FEV1 % during the stable stage of COPD, the number of exacerbations causing ER admission and/or hospitalization or increase in symptoms causing prescription of additional medications during the last year, severity of dyspnea (according to mMRC scale), stage of the disease (according to GOLD guideline revised in 2014) and the results of complete blood count (including number of white blood cells, neutrophils, lymphocytes, plateletes) during stable stage and exacerbations [11]. Data extraction was carried out using computer based patient records of our hospital, and for the missing data we interviewed face to face with patients during their admission to our clinic or emergency room. Out of 220 patients, sufficient data were available for only 40 patients. Three patients were excluded due to long term steroid treatment for rheumatologic diseases and 27 patients were excluded because we could not reach an appropriate pulmonary function test result meeting GOLD criteria. CBC records of 40 patients that was obtained at least two weaks after the last exacerbation were found retrospectively. There was only one female patient with sufficient data so we excluded it and 39 male patients were analyzed.

Neutrophil and lymphocyte counts were taken from complete blood count and differentials which were studied by Fluorescence Flow Cytometry method. Platelet counts were studied with Direct Current-Sheath-Flow Detection method by Roche Sysmex XT2000İ (Roche Diagnostic GmbH, Mannheim, Germany) analyzers.


Statistical Analysis

The normality for continuous variables was checked by using Kolmogorov-Smirnov test. Mann Whitney U test was performed to compare the distribution of two groups for numerical data. Wilcoxon test was applied for the dependent two group comparisons. Chi-square test was used to examine difference between groups for categorical variables. Descriptive statistics were presented as Median (interquartile range) for quantitative data and frequency (percentages) for qualitative data. A p < 0.05 was accepted as statistically significant. Data analysis was performed by IBM SPSS Statistics 21.0 software package.


Results

The dermographic characteristics and median NLR and PLR values of 39 patients were summarized in Table 1. The median age of the study group was 67 and all patients were male. 44% of the patients have cardiovascular comorbidities (hypertension, atherosclerotic heart disease and valvular diseases). Other comorbidities were obstructive sleep apnea (2 patients), lung cancer (1 patients), diabetes mellitus (4 patients) and Alzheimer disease (1 patient). The frequent exacerbations (≥ 2/year) were seen in 20.5% of the patients and 74.4% of the patients were more symptomatic in terms of severity of dyspnea (mmrc ≥ 2). 63.1% of the patients was grouped in GOLD stage C and D.

The median values of NLR and PLR, in stable stage were depicted according to the demographic and clinic characteristics of the patients in Table 1. We could not showany statistically significant relation between NLR values and the clinical parameters including smoking history, cardiovascular comorbidities, rate of exacerbations, airflow limtation and GOLD stage (p > 0.05). On the other hand, PLR was nearly 1.6 fold higher in patients with severe airway limitation (FEV1 < 50%)andhigh risk group (GOLD class C and D) than in patients with mild and moderate airway limitation and low risk group (GOLD class A and B), (p = 0.011).



Table 1: The relationship between mean value of N/L, P/L ratio, CRP and clinical characteristics in stable COPD. View Table 1


Discussion

Many different inflammatory cells and mediators play role in pathogenesis of COPD [12]. Recent studies revealed that markers of systemic inflammation such as CRP, fibrinogen and leukocyte count seem as helpful tools in indentifying COPD patients with poor prognosis in terms of comorbidities, frequent exacerbations and overall mortality [13].

Preliminary evidence has suggested that leukocyte subtypes can be used as a measure of systemic inflammation in some chronic diseases. Neutrophil to lymphocyte ratio and platalet to lymphocyteratio have gained significant attention as readily available, cheap and easy to calculate markers.

Various inflammatory events lead to a physiological increase in circulating leukocytes and platelets and a decline in the release of lymphocytes into the circulation [14]. Inflammatory cytokines such as TNF-α and IL6, which also implicated in the patogenesis of COPD, affect the maturation and secretion of platelets [15]. Margination, redistribution and accelerated apoptosis cause lymphocytopenia, whereas demargination, delayed apoptosis and stimulation of stem cells by growth factors lead to neutrophilia [14].

In 1995, first Goodman et al. [16] described NLR as a potential marker in diagnosis of appendicitis. Subsequent studies proved its prognostic value in cardiovascular diseases and its capacity in predicting cardiovascular comorbidities [4,9,17,18]. Its use as a marker of systemic inflammation was further explored by a study of Zahorec et al. [19]. Another study indicated a significant correlation between the criteria of metabolic syndrome and inflammation on the basis of NLR [2]. In a study of Imtiaz et al. [20], an obvious association between NLR and likelihood of having hypertension and diabetes mellitus was shown. De Jager et al. [14] showed that in patients with community acquired pneumonia, increased NLR was correlated with poor clinical outcome. NLR was also shown as a predictor of survival and response to treatment in many cancers such as non-small cell lung cancer, colorectal carcinoma, hodgkin lymphoma and cervical carcinoma [3,5,8,10,21]. The results of a recent study indicated NLR as a predictor of 30-day mortality in acute pulmonary embolism [22].

Likewise, PLR has emerged as a prognostic marker in cadiovascular disease and some cancers. PLR proved to be a marker of long-term mortality in patients presented with non-ST segment elevation myocardial infarction and in-hospital mortality in acute coronary syndrome [1,23]. Higher levels of PLR was associated with poor prognosis in various cancers such as colorectal carcinoma, pancreatic ductal adenocarcinoma, gastric carcinoma, hepatoceluler carcinoma, ovarian cancer and non-small cell lung cancer [7,24-26].

Increased platelet activation in patients with stable stage and acute exacerbation of COPD was shown in a study by Maclay et al. [27]. However, the place of these new inflammatory markers in diagnosis and follow-up of the patients with COPD has not been investigated so far. To our knowledge there is only one study which showed a significant increase in NLR in COPD patients compared to healthy controls. This study also showed that there was a further increase in NLR during acute exacerbation [28]. In this study, we investigated the relationship between clinical characteristics and the level of these markers. PLR, was elevated in male patients with severe airway limitation (FEV1 < 50%) and in GOLD stage C and D. Thus, in stable stage, PLR can be a candidate for defining COPD patients with high risk. To our knowledge, this is the first study showing the possible clinical value of PLR in stable COPD.


Limitations of the Study

The number of study subjects was lower than we expected due to missing data. The study group included only male patients. The study design is retrospective and thus causative inferences cannot be made based on our results. Despite these limitations the results are promising but must be further investigated in a prospective study.


References
  1. Azab B, Shah N, Akerman M, McGinn JT Jr (2012) Value of platelet/lymphocyte ratio as a predictor of all-cause mortality after non-ST-elevation myocardial infarction. J Thromb Thrombolysis 34: 326-334.

  2. Buyukkaya E, Karakas MF, Karakas E, Akçay AB, Tanboga IH, et al. (2014) Correlation of neutrophil to lymphocyte ratio with the presence and severity of metabolic syndrome. ClinApplThrombHemost 20: 159-163.

  3. Cedrés S, Torrejon D, Martínez A, Martinez P, Navarro A, et al. (2012) Neutrophil to lymphocyte ratio (NLR) as an indicator of poor prognosis in stage IV non-small cell lung cancer. ClinTranslOncol 14: 864-869.

  4. Kaya MG, Akpek M, Lam YY, Yarlioglues M, Celik T, et al. (2013) Prognostic value of neutrophil/lymphocyte ratio in patients with ST-elevated myocardial infarction undergoing primary coronary intervention: a prospective, multicenter study. Int J Cardiol 168:1154-1159.

  5. Koh YW, Kang HJ, Park C, Yoon DH, Kim S, et al. (2012) Prognostic significance of the ratio of absolute neutrophil count to absolute lymphocyte count in classic Hodgkin lymphoma. Am J Clin Pathol 138: 846-854.

  6. Kuyumcu ME, Yesil Y, Ozturk ZA, Kizilarslanoqlu C, EtgulS, et al. (2012) The evaluation of neutrophil-lymphocyte ratio in Alzheimer's disease. Dement GeriatrCognDisord 34: 69-74.

  7. Kwon H-C, Kim SH, Oh SY, Lee S, Lee JH, et al. (2012) Clinical significance of preoperative neutrophil-lymphocyte versus platelet-lymphocyte ratio in patients with operable colorectal cancer. Biomarkers 17:216-222.

  8. Lee YY, Choi CH, Kim HJ, Kim TJ, Lee JW, et al. (2012) Pretreatment neutrophil:lymphocyte ratio as a prognostic factor in cervical carcinoma. Anticancer Res 32: 1555-1561.

  9. Solak Y, Yilmaz M, Sonmez A, Saglam M, Cakir E, et al. (2013) Neutrophil to lymphocyte ratio independently predicts cardiovascular events in patients with chronic kidney disease. ClinExpNephrol 17:532-540.

  10. Yao Y, Yuan D, Liu H, Gu X, Song Y (2013) Pretreatment neutrophil to lymphocyte ratio is associated with response to therapy and prognosis of advanced non-small cell lung cancer patients treated with first-line platinum-based chemotherapy. Cancer Immunol Immunother 62: 471-479.

  11. The global initiative for chronic obstructive lung disease (GOLD).Global strategy for diagnosis, management and prevention of chronic obstructive pulmonary disease.

  12. Zhang Y, Bunjhoo H, Xiong W, Xu Y, Yang D (2012) Association between C-reactive protein concentration and chronic obstructive pulmonary disease: a systematic review and meta-analysis. J Int Med Res 40:1629-1635.

  13. Thomsen M, Ingebrigtsen TS, Marott JL, Dahl M, Lange P, et al. (2013) Inflammatory biomarkers and exacerbations in chronic obstructive pulmonary disease. JAMA 309: 2353-2361.

  14. de Jager CP, Wever PC, Gemen EF, Kusters R, van Gageldonk-Lafeber AB, et al. (2012) The neutrophil-lymphocyte count ratio in patients with community-acquired pneumonia. PLoS One 7: e46561.

  15. Kaushansky K (2005) The molecular mechanisms that control thrombopoiesis. J Clin Invest 115: 3339-3347.

  16. Goodman DA, Goodman CB, Monk JS (1995) Use of the neutrophil:lymphocyte ratio in the diagnosis of appendicitis. Am Surg 61: 257-259.

  17. Acanfora D, Gheorghiade M, Trojano L, Furgi G, Pasini E, et al. (2001) Relative lymphocyte count: a prognostic indicator of mortality in elderly patients with congestive heart failure. Am Heart J 142: 167-173.

  18. Tamhane UU, Aneja S, Montgomery D, Rogers EK, Eagle KA, et al. (2008) Association between admission neutrophil to lymphocyte ratio and outcomes in patients with acute coronary syndrome. Am J Cardiol 102: 653-657.

  19. Zahorec R (2001) Ratio of neutrophil to lymphocyte counts--rapid and simple parameter of systemic inflammation and stress in critically ill. BratislLekListy 102: 5-14.

  20. Imtiaz F, Shafique K, Mirza SS, Ayoob Z, Vart P, et al. (2012) Neutrophil lymphocyte ratio as a measure of systemic inflammation in prevalent chronic diseases in Asian population. Int Arch Med 5: 2.

  21. Walsh SR, Cook EJ, Goulder F, Justin TA, Keeling NJ (2005) Neutrophil-lymphocyte ratio as a prognostic factor in colorectal cancer. J SurgOncol 91: 181-184.

  22. Kayrak M, Erdogan HI, Solak Y, Akilli H, Gul EE, et al. (2014) Prognostic value of neutrophil to lymphocyte ratio in patients with acute pulmonary embolism: a restrospective study. Heart Lung Circ 23: 56-62.

  23. Oylumlu M, Yildiz A, Oylumlu M, Yuksel M, Polat N, et al. (2015) Platelet-to-lymphocyte ratio is a predictor of in-hospital mortality patients with acute coronary syndrome. Anatol J Cardiol 15: 277-283.

  24. Raungkaewmanee S, Tangjitgamo S, Manusirivithaya S, Srijaipracharoen S, Thavaramara T (2012) Platelet to lymphocyte ratio as a prognostic factor for epithelial ovarian cancer. J GynecolOncol 23: 265-273.

  25. Smith RA, Bosonnet L, Raraty M, Sutton R, Neoptolemos JP, et al. (2009) Preoperative platelet-lymphocyte ratio is an independent significant prognostic marker in resected pancreatic ductal adenocarcinoma. Am J Surg 197:466-472.

  26. Zhou X, Du Y, Huang Z, Xu J, Qiu T, et al. (2014) Prognostic value of PLR in various cancers: a meta-analysis. PLoS One 9: e101119.

  27. Maclay JD, McAllister DA, Johnston S, Raftis J, McGuinnes C, et al. (2011) Increased platelet activation in patients with stable and acute exacerbation of COPD. Thorax 66: 769-774.

  28. Gunay E, SarincUlasli S, Akar O, Ahsen A, Gunay S, et al. (2014) Neutrophil-to-lymphocyte ratio in chronic obstructive pulmonary disease: a retrospective study. Inflammation 37: 374-380.

International Journal of Anesthetics and Anesthesiology (ISSN: 2377-4630)
International Journal of Blood Research and Disorders   (ISSN: 2469-5696)
International Journal of Brain Disorders and Treatment (ISSN: 2469-5866)
International Journal of Cancer and Clinical Research (ISSN: 2378-3419)
International Journal of Clinical Cardiology (ISSN: 2469-5696)
Journal of Clinical Gastroenterology and Treatment (ISSN: 2469-584X)
Clinical Medical Reviews and Case Reports (ISSN: 2378-3656)
Journal of Dermatology Research and Therapy (ISSN: 2469-5750)
International Journal of Diabetes and Clinical Research (ISSN: 2377-3634)
Journal of Family Medicine and Disease Prevention (ISSN: 2469-5793)
Journal of Genetics and Genome Research (ISSN: 2378-3648)
Journal of Geriatric Medicine and Gerontology (ISSN: 2469-5858)
International Journal of Immunology and Immunotherapy (ISSN: 2378-3672)
International Journal of Medical Nano Research (ISSN: 2378-3664)
International Journal of Neurology and Neurotherapy (ISSN: 2378-3001)
International Archives of Nursing and Health Care (ISSN: 2469-5823)
International Journal of Ophthalmology and Clinical Research (ISSN: 2378-346X)
International Journal of Oral and Dental Health (ISSN: 2469-5734)
International Journal of Pathology and Clinical Research (ISSN: 2469-5807)
International Journal of Pediatric Research (ISSN: 2469-5769)
International Journal of Respiratory and Pulmonary Medicine (ISSN: 2378-3516)
Journal of Rheumatic Diseases and Treatment (ISSN: 2469-5726)
International Journal of Sports and Exercise Medicine (ISSN: 2469-5718)
International Journal of Stem Cell Research & Therapy (ISSN: 2469-570X)
International Journal of Surgery Research and Practice (ISSN: 2378-3397)
Trauma Cases and Reviews (ISSN: 2469-5777)
International Archives of Urology and Complications (ISSN: 2469-5742)
International Journal of Virology and AIDS (ISSN: 2469-567X)
More Journals

Contact Us

ClinMed International Library | Science Resource Online LLC
3511 Silverside Road, Suite 105, Wilmington, DE 19810, USA
Email: contact@clinmedlib.org
 

Feedback

Get Email alerts
 
Creative Commons License
Open Access
by ClinMed International Library is licensed under a Creative Commons Attribution 4.0 International License based on a work at https://clinmedjournals.org/.
Copyright © 2017 ClinMed International Library. All Rights Reserved.