|Year : 2017 | Volume
| Issue : 3 | Page : 260-267
Bedside inflammatory mediators in pulmonary tuberculosis
Samiaa H Sadek1, Shereen Farghaly MD 1, Madleen A.A. Abdou2, Mona H.M. Abdel-Rahim3
1 Department of Chest, Faculty of Medicine, Assiut University, Assiut, Egypt
2 Department of Clinical Pathology, Faculty of Medicine, Assiut University, Assiut, Egypt
3 Department of Medical Microbiology and Immunology, Faculty of Medicine, Assiut University, Assiut, Egypt
|Date of Submission||23-Nov-2016|
|Date of Acceptance||13-Jan-2017|
|Date of Web Publication||24-Jul-2017|
Chest Department, Faculty of Medicine, Assiut University Hospital, Assiut - 71111
Source of Support: None, Conflict of Interest: None
Background Monitoring of pulmonary tuberculosis (PTB) especially in poor countries is a major challenge aiming to find cheap valuable indices.
Objective The objective of this study was to evaluate the use of simple laboratory parameters as complete blood count (CBC), especially platelet (PLT) indices, for assessment and monitoring of PTB activity.
Patients and methods Totally, 140 PTB patients in addition to 30 healthy individuals as a control group were included in this case–control study. Patients were divided into three groups: 66 newly diagnosed active patients (group I), 39 patients after sputum and culture conversion (group II), and 35 patients defined as cured cases (group III). On the basis of chest radiography, only active PTB patients were classified into minimal, moderate, and far advanced cases. Laboratory parameters including CBC with PLT indices, erythrocyte sedimentation rate, and C-reactive protein (CRP) were performed for all enrolled participants.
Results Compared with the control group, hemoglobin, mean PLT volume, and platelet distribution width (PDW) were significantly lower in group I and increased after treatment in groups II and III. On the other hand, PLT count, platelet crit %, CRP, and erythrocyte sedimentation rate were significantly higher in group I compared with the control group and decreased after treatment. In addition, there were significant correlations between CRP and all PLT indices. Regarding radiological extension, hemoglobin and mean PLT volume were significantly lower in far advanced PTB compared with both moderate and mild PTB, whereas PLT crit was significantly higher in moderate PTB compared with minimal PTB.
Conclusion CBC, especially PLT indices, could be considered valuable cheap markers in assessment and monitoring of PTB activity.
Keywords: C-reactive protein, platelet indices, pulmonary tuberculosis
|How to cite this article:|
Sadek SH, Farghaly S, Abdou MA, Abdel-Rahim MH. Bedside inflammatory mediators in pulmonary tuberculosis. Egypt J Bronchol 2017;11:260-7
| Introduction|| |
Tuberculosis (TB) is a common infectious disease caused by Mycobacterium tuberculosis, and despite developments in its diagnosis and treatment it remains an important public health problem. The presence of 9.6 million new TB cases has been reported in 2014 and 1.5 million TB deaths (1.1 million among HIV-negative people and 0.4 million among HIV-positive people). To control TB efficiently, proper identification and cure of infectious pulmonary tuberculosis (PTB) patients should be done . In addition, monitoring TB patients during treatment is important to establish patients’ treatment outcomes .
Because of activation of the immune system in TB patients, excessive cytokines such as interleukin (IL)-1, IL-2, interferon-γ, and tumor necrosis factor-α (TNF-α) are produced. These cytokines enhance hepatic synthesis of acute-phase proteins, such as C-reactive protein (CRP), as well as in the erythrocyte sedimentation rate (ESR). CRP and ESR have been used in the diagnosis and follow-up of patients with TB beside the routinely done sputum for acid-fast bacilli (AFB) and sputum culture . These cytokines also have a role in maturation of thrombopoietic cells and secretion of platelets (PLTs) into the circulation . In recent years, it has been shown that PLTs can act as inflammatory cells releasing various chemokines and cytokines. Changes in PLT counts may be associated with the severity of TB infection and mortality. A change in PLT size has been shown to be associated with numerous inflammatory diseases including TB ,,,,. To the best of our knowledge, these changes in PLTs were not studied as inflammatory markers on monitoring patients on anti-TB treatment.
The objectives of this study were to evaluate the use of simple laboratory parameters such as complete blood count (CBC), especially PLT indices, as markers for assessment and monitoring of PTB activity.
| Patients and methods|| |
This case–control study was carried out on 140 PTB patients who were selected from chest outpatient clinic in a tertiary hospital. The study included patients with PTB with positive sputum smear for AFB and positive culture . PTB patients included 66 patients who were newly diagnosed (active TB − in which a biological specimen obtained from the patient is positive by smear microscopy or culture)  and about to begin treatment (group I), 39 patients after sputum and culture conversion (the point at which samples taken from a patient infected with TB can no longer produce TB cell cultures)  (group II), and 35 patients defined as cured cases (a PTB patient with bacteriologically confirmed TB at the beginning of treatment who was smear-negative or culture-negative in the last month of treatment and on at least one previous occasion) (group III). In addition, 30 apparently healthy, age-matched and sex-matched individuals were included in this study as a control group. Informed written consent was obtained from each participants, and the study was approved by the Faculty of Medicine Ethics Committee. Patients who had other respiratory diseases, thromboembolic disorders, valvular or ischemic heart disease, associated hepatic or renal diseases, acute inflammatory disease, immunological disease, recent surgery and malignancy, receiving anticoagulant, anti-PLT, nonsteroidal anti-inflammatory, or antidepressant medications were excluded from the study.
Sputum collection, sputum analysis, and culture
Morning sputum specimens submitted to the laboratory were processed for AFB microscopy and mycobacterial culture. Direct smears were stained by Ziehl–Neelsen technique. A smear was declared to be positive if at least 1–9 AFB in 100 fields were found on microscopy ,.
For sputum culture, specimens were treated with 2% N-acetyl-l-cysteine–sodium hydroxide, followed by centrifugation . The sediment was inoculated on Lowenstein–Jensen medium and incubated at 37°C for a maximum of 8 weeks. Cultures were read weekly for 2 months. Buffy, granular colonies appearing after 3–7 weeks were confirmed for their acid fastness. Culture was declared to be positive if colonies appear on AFB-positive smears. Liquefied or discolored Lowenstein–Jensen medium indicated contamination. Cultures that showed no growth after 8 weeks of incubation were reported as negative .
Clinical and radiological assessment
All the enrolled participants had their medical history taken and underwent physical examination. Chest radiography was performed for the PTB patients to assess severity of radiological involvement. On the basis of chest radiography, PTB patients were classified into minimal (radiography lesion of slight to moderate density, no cavitation, lesions in one or both lungs, and extent of the lesion less than the part above the second chondrosternal junction of lung on one side), moderate (lesions were in one or both lungs, lesions of slight to moderate density involved total volume of one lung or equivalent in both lung cavities, whereas dense lesions were limited to one-third of one lung cavity; when it was present its diameter was less than 4 cm), and far advanced PTB, which included lesions more extensive than moderate .
On the day of testing, patients were resting, fasting, and were refrained from smoking and any caffeine ingestion where a 7 ml sample of venous blood was collected from both patients and control groups by venipuncture of the anticubital fossa under complete antiseptic protocol with minimum tourniquet pressure using 19–21 G syringes. After discarding specimens containing any evidence of clotting, other specimens were maintained at room temperature (20–25°C), not placed on ice, refrigerator, or water bath. Tubes were kept capped upright at room temperature not exposed to vibration, excessive mixing, or agitation . The samples were divided into three parts for analysis of CBC and biochemical analysis of CRP and ESR.
For estimation of CBC, 2 ml of venous blood was placed in standard tubes containing K3 EDTA anticoagulant. Samples were processed within 1 h to avoid bias due to excessive PLT swelling and to minimize variation due to sample aging ,. CBC for patients and control was done by ABX Pentra XL80 (HORIBA group, Montpellier, France). To obtain serum for CRP, 3 ml of venous blood was placed in plain tubes and left to clot at room temperature for at least 30 min, and then centrifuged at 1500 rpm for 15 min. It was determined by using AVITEX CRP Ref OD037/OD023/OD023/E (Omega Diagnostics, UK) according to the methods described by the manufacturer (in-vitro diagnostic reagent for the quantitative determination of CRP). The last 2 ml of venous blood was directly collected in 0.5 ml of 3.8% trisodium citrate for estimation of ESR. Samples were processed within 6 h of collection, and blood was collected to the mark in the tube, as specified by the manufacturer.
Statistical analysis was performed using the statistical package for the social sciences, version 20, software (SPSS; SPSS Inc., Chicago, Illinois, USA). The results were expressed as mean±SD or frequencies. Kruskal–Wallis one-way analysis of variance was used for comparison of continuous variables among the study groups. Spearman’s correlation analysis was used to evaluate the correlations between both CRP and ESR and CBC parameters; P-values less than 0.05 were considered significant.
| Results|| |
This study included 66 newly diagnosed active TB patients (group I), 39 patients after sputum and culture conversion (group II), and 35 cured patients after completion of anti-TB treatment (group III). These three groups are matched as regards age, sex, smoking habit, and BMI (P>0.05). Demographic data are shown in [Table 1].
[Table 2] demonstrated the laboratory parameters among the study groups. Hemoglobin (HB) was significantly lower in group I than in the control group (11.57±2.25 vs. 13.39±1.58 gm/dl, P=0.001) but relatively higher in other groups after treatment. Total leukocytic count was also significantly lower in group I than in the control group (5.39±1.23 vs. 7.00±1.76×109/l, P=0.038) and significantly increased with treatment. Among PLT indices, total PLT count and platelet crit (PCT) % were significantly higher in group I compared with the control group (365.2±184.2 vs. 235.17±60.98, P=0.001; 0.299±0.098 vs. 0.21±0.07, P=0.008, respectively) but showed a relative decrease in group II (365.2±184.2 vs. 295.9±106.57, P=0.212; 0.27±0.12 vs 0.299±0.098, P=0.545, respectively) and group III (365.2±184.2 vs. 341.71±147.07, P=0.755; 0.299±0.098 vs. 0.27±0.12, P=0626, respectively). On the other hand, mean platelet volume (MPV) was significantly lower in group I than in the control group (7.5±1.198 vs. 8.597±1.199, P=0.001) but significantly increased after completion of anti-TB treatment in group III compared with group I (8.43±0.68 vs. 7.5±1.198, P=0.021). In addition, PDW % was significantly lower in group I compared with the control group (14.73±2.54 vs. 16.42±1.97, P=0.005). As expected, CRP and ESR first and second were significantly higher in group I compared with the control group (16.56±14.79 vs. 3.77±1.22, P=0.004; 58.65±27.88 vs. 10.53±5.44, P<0.001; 90.53±29.90 vs. 22.20±11.36, P<0.001, respectively) and lower in both group II (16.56±14.79 vs. 9.22±8.42, P=0.168; 58.65±27.88 vs. 34.27±19.96, P=0.010; 90.53±29.90 vs. 57.0±20.16, P=0.01, respectively) and group III (16.56±14.79 vs. 2.29±0.76, P=0.002; 58.65±27.88 vs. 17.0±9.73, P<0.001; 90.53±29.90 vs. 22.20±11.36, P<0.001, respectively) compared with group I (i.e. significantly decreased with treatment).
According to radiological extension in group I, we observed that HB was significantly lower in far advanced PTB compared with minimal and moderate PTB (9.95±1.37 vs. 12.8±2.46 gm/dl, P=0.003; 9.95±1.37 vs. 12.06±1.9, P=0.005, respectively). No significant differences were detected between radiological groups regarding total leukocytic count (P>0.05). Among PLT indices, MPV was significantly lower in far advanced and moderate PTB compared with minimal PTB (6.7±1.84 vs. 8.18±0.79 fl, P=0.019; 7.4±0.95 vs. 8.18±0.79, P=0.045, respectively), whereas PCT% was significantly higher in moderate PTB compared with minimal PTB (0.29±0.12 vs. 0.22±0.072, P=0.24). Although it was not significant, PLT count increased and PDW% decreased with increased radiological extension ([Table 3]).
|Table 3 Comparison of laboratory data among different groups of radiological extension|
Click here to view
Moreover, significant positive correlations were observed between CRP and each of total PLT count (r=0.512, P=0.009) ([Figure 1]a) and PCT% (r=0.444, P=0.001) ([Figure 1]b). However, CRP was negatively correlated with each of MPV (although not significant) (r=−0.260, P=0.060) ([Figure 1]c) and PDW% (r=−0.362, P=0.008) ([Figure 1]d). ESR second showed only a significant positive correlation with total PLT count (r=0.269, P=0.019) ([Figure 2]a) and negative correlation with MPV (r=−0.369, P=0.001) ([Figure 2]c), with no significant correlation with other PLT indices ([Figure 2]b and [Figure 2]d).
|Figure 1 Correlations between C-reactive protein (mg/l) and each of (a) platelet count (×109/l), (b) platelet crit percentage, (c) mean platelet volume (fl), and (d) platelet distribution width percentage. CRP, C-reactive protein; PCT, platelet crit; PDW, platelet distribution width; PLT, platelet|
Click here to view
|Figure 2 Correlations between erythrocyte sedimentation rate second and each of (a) platelet count (×109/l), (b) platelet crit percentage, (c) mean platelet volume (fl), and (d) platelet distribution width percentage. CRP, C-reactive protein; ESR, erythrocyte sedimentation rate; PCT, platelet crit; PDW, platelet distribution width; PLT, platelet|
Click here to view
| Discussion|| |
TB is an infectious common disease affecting as many as one-third of the world population, with population growth number of new cases continuing to increase . Proper identification and monitoring of TB patients during treatment are important to establish patients’ treatment outcomes .
Many markers of acute inflammation are available to assess activity and monitoring of PTB, but specific markers are expensive  and cannot be done routinely. Hematological changes have been documented in PTB infection . In recent years, PLTs are considered inflammatory cells releasing chemokines and cytokines ,,,,. CBC is a simple laboratory test and PLT indices (MPV, PCT%, PDW) are readily measured by clinical hematology analyzers and are indicators of PLT activation. Thus, this study was designed to investigate the simple CBC parameters, especially PLT indices, in assessment of activity and in follow-up of PTB patients.
Out of the hematological abnormalities, HB was significantly lower in group I (active PTB) than in the control group and relatively increased in other groups after anti-TB therapy. The prevalence of anemia was observed in previous studies ,,, and it was thought to be due to a blunted response of bone marrow to anemia or suppression of erythropoietin production by TNF-α and other cytokines released by activated monocytes . Total leukocytic count was also significantly lower in group I than in the control group (5.39±1.23 vs. 7.00±1.76, P=0.038) and significantly increased with treatment. Mild leukocytosis was documented in 8–40%  and leukopenia in 1–4% of patients with PTB. Leukopenia in active PTB was thought to be a consequence of marrow granulopoietic failure or associated malnutrition. Nevertheless, the role of cytokine including TNF in the pathogenesis of lymphocytopenia has been suggested .
Among PLT indices, total PLT count was significantly higher in group I compared with the control group (365.2±184.2 vs. 235.17±60.98, P=0.001), but it showed a relative decrease with treatment. Thrombocytosis was commonly reported in active PTB patients ,,. Increased PLT count before treatment would usually return to normal after anti-TB therapy ,. Inflammatory cytokines, especially IL-6 (one of the inflammatory markers involved in TB granuloma formation), have been known to stimulate PLT production .
On the other hand, the present study revealed significantly lower MPV in group I compared with the control group (7.5±1.198 vs. 8.597±1.199, P=0.001), which relatively increased with treatment in group III compared with group I (8.43±0.68 vs. 7.5±1.198, P=0.021). Gunluoglu et al.  agree with our results; they observed that MPV significantly reduced in PTB patients compared with healthy controls. Similarly, Baynes et al.  found the MPV to be low in patients with active PTB and suggested that although thrombopoiesis increased in patients with TB the PLTs’ lifetime may have been shortened and that this may simply reflect the thrombocytosis, as there is normally an inverse correlation between the number and volume of PLTs. As they suppress other blood elements, excessive production of cytokines and acute-phase reactants affect megakaryopoiesis and decrease PLT size released from bone marrow . Contrary to our study, Tozkoparan et al.  found that the MPV was significantly higher in patients with active PTB than in control patients and decreased with anti-TB treatment. However, Sahin et al.  observed no significant difference between healthy control and active PTB. Variability of these results may be attributed to the difference in patient characteristics − e.g. BMI or comorbidities − which could affect the results of PLT indices.
In addition, the current study demonstrated significantly higher PCT % in group I compared with the control group (0. 299±0.098 vs. 0.21±0.07, P=0.008), which relatively decreased with treatment but had significantly lower PDW compared with the control group. PCT is an expression of a percentage that reflects the volume occupied by PLTs in blood  and thus it depends on both size and number of PLTs . PDW refers to the variability or the change in uniformity in the PLT size . It might reflect the active role of PLTs in active PTB. Microthrombi (which denoted activity of PLTs) were observed around the cavity of PTB, which prevented dissemination of the disease, and it was suggested as an immunological defense mechanism ,.
As observed in previous studies ,,,,,,, we showed a significant increase in markers of acute-phase reactants CRP and ESR in group I compared with the healthy control group and a significant decrease with treatment. Th1 immunity, which is activated in PTB, results in systemic release of IL-2, IL-6, IL-12, INF-γ, and TNF-α with subsequent increase in ESR and CRP levels ,. Moreover, there are significant correlations between CRP and all PLT indices in our study. Significant correlation was observed between CRP and total PLT count in previous studies ,. Sahin et al.  also found that CRP and PCT% significantly increased in PTB patients with thrombocytosis compared with those with normal PLT count. Similarly, Unsal et al.  observed an increased level of IL-6 in addition to CRP in tuberculous patients with thrombocytosis.
According to radiological extension, HB was significantly lower in severe PTB compared with minimal and moderate PTB (9.95±1.37 vs. 12.8±2.46, P=0.003; 9.95±1.37 vs. 12.06±1.9, P=0.005, respectively). Among PLT indices, MPV (fl) was significantly lower in far advanced and moderate PTB compared with minimal PTB (6.7±1.84 vs. 8.18±0.79, P=0.019; 7.4±0.95 vs. 8.18±0.79, P=0.045, respectively), whereas PCT% was significantly higher in moderate PTB compared with minimal PTB (0.29±0.12 vs. 0.22±0.072, P=0.24). Although it was not significant, PLT count increased and PDW% decreased with increased radiological extension. In their study, Sahin et al.  confirmed that PLT count, PCT%, ESR, and CRP were higher in advanced TB compared with minimal TB, and HB was lower; also, they documented that thrombocytosis in PTB correlated with the disease severity. MPV was also significantly correlated with radiological extent . PLT activation also evaluated by PLT factor 4 was well correlated with radiological extent . On the other hand, Gunluoglu et al.  showed no correlation between radiological extent and each of MPV and PLT count. However, they use radiological classification involving pleural abnormalities that did not match with our study that assess radiology depending only on lung extension and cavitation.
This study concluded that CBC and PLT indices could be considered as simple valuable nonexpensive markers in assessment of activity, extension, and follow-up of PTB patients.
The strength of the current study is as follows: first, it evaluates PTB at three different stages of treatment; second, it evaluates PTB with different radiological extensions; and third, we included healthy individuals as a control group for comparison.
Limitations of this study are as follows: first, we did not study the modifying role of other comorbidities (e.g. diabetes, renal impairment, hepatic disease, and others) in CBC, ESR, and CRP, and thus further studies concentrated on these points may be useful; second, we did not compare inflammation in PTB with other diseases − e.g. pneumonia, chronic obstructive pulmonary disease, and others. Further studies are recommended to evaluate PLT index parameters in extra-PTB.
Dr Samiaa Hamdy Sadek contributed to concepts, design of the study, definition of intellectual content, clinical studies, and data analysis and manuscript review. Dr Shereen Farghaly contributed to definition of intellectual content, literature search, clinical studies, data analysis, statistical analysis, manuscript preparation, and takes responsibility of the integrity of the work as a whole from inception to published article. Dr Madleen A.A. Abdou contributes to data acquisition and manuscript preparation regarding laboratory methods. Dr Mona H.M. Abdel-Rahim contributes to data acquisition and manuscript preparation regarding microbiology methods.
Financial support and sponsorship
Conflicts of interest
There are no conflicts of interest.
| References|| |
World Health Organization. Global tuberculosis control: 2015 report. Geneva World Health Organization
Senkoro M, Mfinanga SG, Mørkve O. Smear microscopy and culture conversion rates among smear positive pulmonary tuberculosis patients by HIV status in Dares Salaam, Tanzania. BMC Infect Dis
Ottenhoff TH. New pathways of protective and pathological host defense to mycobacteria. Trends Microbiol
Peresi E, Silva SM, Calvi SA, Marcondes-Machado J. Cytokines and acute phase serum proteins as markers of inflammatory regression during the treatment of pulmonary tuberculosis. J Bras Pneumol
Endler G, Klimesch A, Sunder-Plassmann H, Schillinger M, Exner M, Mannhalter C et al.
Mean platelet volume is an independent risk factor for myocardial infarction but not for coronary artery disease. Br J Haematol
Mimidis K, Papadopoulos V, Kotsianidis J, Filippou D, Spanoudakis E, Bourikas G et al.
Alterations of platelet function, number and indexes during acute pancreatitis. Pancreatology
Kisacik B, Tufan A, Kalyoncu U, Karadag O, Akdogan A, Ozturk MA et al.
Mean platelet volume (MPV) as an inflammatory marker in ankylosing spondylitis and rheumatoid arthritis. Joint Bone Spine
Yuksel O, Helvaci K, Basar O, Köklü S, Caner S, Helvaci N et al.
An overlooked indicator of disease activity in ulcerative colitis: mean platelet volume. Platelets
Tuncel T, Uysal P, Hocaoglu AB, Erge DO, Karaman O, Uzuner N. Change of mean platelet volume values in asthmatic children as an inflammatory marker. Allergol Immunopathol (Madr)
Su WJ, Feng JY, Chiu YC, Huang SF, Lee YC. Role of 2-month sputum smears in predicting culture conversion in pulmonary tuberculosis. Eur Respir J
The American Thoracic Society and the Centers for Disease Control and Prevention. Diagnostic standards and classification of tuberculosis in adults and children. Am J Respir Crit Care Med
Huh HJ, Koh WJ, Song DJ, Ki CS, Lee NY. Evaluation of the Cobas TaqMan MTB test for the detection of Mycobacterium tuberculosis complex according to acid-fast-bacillus smear grades in respiratory specimens. J Clin Microbiol
Boum Y, Orikiriza P, Rojas-Ponce G, Riera-Montes M, Atwine D, Nansumba M et al.
Use of colorimetric culture methods for detection of Mycobacterium tuberculosis complex isolates from sputum samples in resource limited settings. J Clin Microbiol
Seaton A, Seaton D, Leitch AG. Crofton and Douglas’s respiratory diseases
. 4th ed. Oxford, UK: Blackwell; 1989. 409–410.
Harrison P, Mackie I, Mumford A, Briggs C, Liesner R, Winter M et al.
Guidelines for the laboratory investigation of heritable disorders of platelet function. Br J Haematol
Kodiatte TA, Manikyam UK, Rao SB, Jagadish TM, Reddy M, Lingaiah HK et al.
Mean platelet volume in type 2 diabetes mellitus. J Lab Physicians
Dastjerdi MS, Emami T, Najafian A, Amini M. Mean platelet volume measurement, EDTA or citrate?. Hematology
Somoskövi A, Zissel G, Zipfel PF, Ziegenhagen MW, Klaucke J, Haas H et al.
Different cytokine patterns correlate with the extension of disease in pulmonary tuberculosis. Eur Cytokine Netw
Ageep AK. Diagnosis of Tuberculous lymphadenitis in Red Sea State, Sudan. Int J Trop Med
Morris CD, Bird AR, Nell H. The hematological and biochemical changes in severe pulmonary tuberculosis. Q J Med
Singh KJ, Ahulwalia G, Sharma SK, Saxena R, Chaudhary VP, Anant M. Significance of hematological manifestations in patients with tuberculosis, J Assoc Physicians India
Lee SW, Kang YA, Yoon YS, Um SW, Lee SM, Yoo CG et al.
The prevalence and evolution of anemia associate with tuberculosis. J Korean Med Sci
Goldenberg AS. Hematologic abnormalities and mycobacterial infection. In: Williams NR, Stuart GM. editors. Tuberculosis
. Boston, MA: Little − Brown Company; 1996. pp. 645–647.
Sharma SK, Pande JN, Singh YN, Verma K, Kathait SS, Khare SD et al.
Pulmonary tuberculosis and immunologic abnormalities in miliary tuberculosis. Am Rev Respir Dis
Yaranal PJ, Umashankar T, Harish SG. Hematological profile in pulmonary tuberculosis. Int J Health Rehabil Sci
Tozkoparan E, Deniz O, Ucar E, Bilgic H, Ekiz K. Changes in platelet count and indices in pulmonary tuberculosis. Clin Chem Lab Med
Rahman SP. Haematological profile in pulmonary tuberculosis [dissertation]
. Bangalore, India: St Johns Medical College; 2010.
Kartaloglu Z, Cerrahoglu K, Okutan O, Ozturk A, Aydilek R. Parameters of blood coagulation in patients with pulmonary tuberculosis. Int J Intern Med
Gunluoglu G, Yazar EE, Veske NS, Seyhan EC, Altin S. Mean platelet volume as an inflammation marker in active pulmonary tuberculosis. Multidiscip Respir Med
Baynes RD, Bothwell TH, Flax H, McDonald TP, Atkinson P, Chetty N et al.
Reactive thrombocytosis in pulmonary tuberculosis. J Clin Pathol
Bath PM, Butterworth RJ. Platelet size: measurement, physiology and vascular disease. Blood Coagul Fibrinolysis
Sahin F, Yazar E, Yıldız P. Prominent features of platelet count, plateletcrit, mean platelet volume and platelet distribution width in pulmonary tuberculosis. Multidiscip Respir Med
Beyan C, Kaptan K, Ifran A. Platelet count, mean platelet volume, platelet distribution width, and plateletcrit do not correlate with optical platelet aggregation responses in healthy volunteers. J Thromb Thrombolysis
Wiwanitkit V. Plateletcrit, mean platelet volume, platelet distribution width: its expected values and correlation with parallel red blood cell parameters. Clin Appl Thromb Hemost
Amin MA, Amin AP, Kulkarnite HR. Platelet distribution width (PDW) is increased in vaso-oclusive crisis in sickle cell disease. Ann Hematol
Kuhn C, Askin FB. Lung and mediastinum, Chapter 22. In: Kissane JM, editor. Anderson’s pathology
. 8th ed. St. Louis: CV Mosby; 1985. pp. 838–854.
Khechinashvili GN, Khvitiia NG, Volobuev VI, Sabanadze SA. Protective platelet features in fibrocavernous tuberculosis. Probl Tuberk Bolezn Legk
Haghighi L, Doust JY. C-reactive protein in pulmonary tuberculosis. Dis Chest
Chakrabarti DA, Dasgupta B, Ganguli D, Ghosal AG. Haematological changes in disseminated tuberculosis. Ind J Tub
Nwankwo EK, Kwaru A, Ofulu A, Babashani M. Haematological changes in tuberculosis in Kano, Nigeria. J Med Lab Sci
Choi CM, Kang CI, Jeung WK, Kim DH, Lee CH, Yim JJ. Role of the C-reactive protein for the diagnosis of TB among military personnel in South Korea. Int J Tuberc Lung Dis
Muhammed KS, Javed AS, Bikha RD, Syed ZAS, Samina S, Imran S. C-reactive protein in patients with pulmonary tuberculosis. World Appl Sci J
Zuñiga J, Torres-García D, Santos-Mendoza T, Rodriguez-Reyna TS, Granados J, Yunis EJ. Cellular and humoral mechanisms involved in the control of tuberculosis. Clin Dev Immunol
Kellar KL, Gehrke J, Weis SE, Mahmutovic-Mayhew A, Davila B, Zajdowicz MJ et al.
Multiple cytokines are released when blood from patients with tuberculosis is stimulated with Mycobacterium tuberculosis antigens. PLoS One
Unsal E, Aksaray S, Köksal D, Sipit T. Potential role of interleukin 6 in reactive thrombocytosis and acute phase response in pulmonary tuberculosis. Postgrad Med J
Büyükaşik Y, Soylu B, Soylu AR, Ozcebe OI, Canbakan S, Haznedaroğlu IC et al.
In vivoplatelet and T-lymphocyte activities during pulmonary tuberculosis. Eur Respir J
[Figure 1], [Figure 2]
[Table 1], [Table 2], [Table 3]