Utility of Hematological Indices in Predicting the Sputum Conversion at the End of the Intensive Phase of Treatment for Patients With Pulmonary TB
DOI:
https://doi.org/10.21276/apalm.3789Keywords:
sputum Conversion, predictor, Hematological, Pulmonary TBAbstract
Background: Early sputum conversion is a crucial marker of treatment response and infectivity reduction in pulmonary tuberculosis (TB). However, conventional microbiological monitoring methods such as culture are time-consuming and resource-intensive. Hematological indices derived from routine complete blood counts are simple, inexpensive markers of systemic inflammation and immune response and may provide additional prognostic information during treatment.Aim: To evaluate the predictive value of baseline hematological indices and their dynamic changes in identifying sputum conversion at the end of the intensive phase of anti-tubercular therapy (ATT) in patients with pulmonary TB.
Methods: This observational longitudinal study included 56 treatment-naïve, CBNAAT-positive pulmonary TB patients. Neutrophil-to-lymphocyte ratio (NLR), monocyte-to-lymphocyte ratio (MLR), platelet-to-lymphocyte ratio (PLR), neutrophil-monocyte-to-lymphocyte ratio (NMLR), and systemic immune-inflammation index (SII) were assessed at baseline and after two months of ATT. Sputum conversion was determined using smear microscopy and culture. Predictive performance was evaluated using receiver operating characteristic (ROC) curve analysis and logistic regression.
Results: Sputum conversion was achieved in 47 (83.9%) patients. Baseline values of all hematological indices were significantly higher in non-converters (p < 0.001) and declined significantly among converters following treatment. NMLR demonstrated the strongest predictive performance (AUC 0.922; OR 180), followed by MLR and NLR.
Conclusion: Hematological indices, particularly NMLR, MLR, and NLR, are effective, low-cost predictors of early microbiological response in pulmonary TB and may serve as useful adjuncts to routine treatment monitoring, especially in resource-limited settings.
References
1. Berida T, Lindsley CW. Move over COVID, tuberculosis is once again the leading cause of death from a single infectious disease. J Med Chem. 2024;67(24):21633–21640. doi:10.1021/acs.jmedchem.4c02876
2. World Health Organization. Global tuberculosis report 2023 [Internet]. Geneva: World Health Organization; 2023 [cited 2026 Jan 30]. Available from: https://www.who.int/teams/global-programme-on-tuberculosis-and-lung-health/tb-reports/global-tuberculosis-report-2023
3. Centers for Disease Control and Prevention (CDC). 2021 state and city TB report: sputum culture conversion [Internet]. Atlanta (GA): CDC; 2024 [cited 2026 Jan 30]. Available from: https://www.cdc.gov/tb-data/2021-state-city-report/sputum-culture-conversion.html
4. Shibabaw A, Gelaw B, Wang SH, et al. Time to sputum smear and culture conversions in multidrug resistant tuberculosis at University of Gondar Hospital, Northwest Ethiopia. PLoS One. 2018;13(6):e0198080. doi:10.1371/journal.pone.0198080
5. Bhatti Z, Khan AH, Sulaiman SAS, et al. Determining the risk factors associated with delayed sputum conversion at the end of the intensive phase among tuberculosis patients. East Mediterr Health J. 2021;27(8):755–763. doi:10.26719/2021.27.8.755
6. Nahid P, Dorman SE, Alipanah N, et al. Official American Thoracic Society/Centers for Disease Control and Prevention/Infectious Diseases Society of America clinical practice guidelines: treatment of drug-susceptible tuberculosis. Clin Infect Dis. 2016;63(7):e147–e195. doi:10.1093/cid/ciw376
7. Mitchison DA. Role of individual drugs in the chemotherapy of tuberculosis. Int J Tuberc Lung Dis. 2000;4(9):796–806.
8. World Health Organization. Treatment of tuberculosis: guidelines. 4th ed. Geneva: World Health Organization; 2010 [Internet]. [cited 2026 Jan 30]. Available from: https://www.ncbi.nlm.nih.gov/books/NBK138748/
9. Alene KA, Viney K, Yi H, et al. Comparison of the validity of smear and culture conversion as a prognostic marker of treatment outcome in patients with multidrug-resistant tuberculosis. PLoS One. 2018;13(5):e0197880. doi:10.1371/journal.pone.0197880
10. Parmar MM, Sachdeva KS, Dewan PK, et al. Unacceptable treatment outcomes and associated factors among India’s initial cohorts of multidrug-resistant tuberculosis (MDR-TB) patients under the revised national TB control programme (2007–2011): evidence leading to policy enhancement. PLoS One. 2018;13(4):e0193903. doi:10.1371/journal.pone.0193903
11. Sekaggya-Wiltshire C, von Braun A, Lamorde M, et al. Delayed sputum culture conversion in tuberculosis–human immunodeficiency virus–coinfected patients with low isoniazid and rifampicin concentrations. Clin Infect Dis. 2018;67(5):708–716. doi:10.1093/cid/ciy179
12. Lawn SD, Zumla AI. Tuberculosis. Lancet. 2011;378(9785):57–72. doi:10.1016/S0140-6736(10)62173-3
13. Parsons LM, Somoskövi A, Gutierrez C, et al. Laboratory diagnosis of tuberculosis in resource-poor countries: challenges and opportunities. Clin Microbiol Rev. 2011;24(2):314–350. doi:10.1128/CMR.00059-10
14. Weyer K, Mirzayev F, Migliori GB, et al. Rapid molecular TB diagnosis: evidence, policy making and global implementation of Xpert MTB/RIF. Eur Respir J. 2013;42(1):252–271. doi:10.1183/09031936.00157212
15. Das P, Horton R. Tuberculosis—getting to zero. Lancet. 2015;386(10010):2231–2232. doi:10.1016/S0140-6736(15)00401-8
16. Alpua M, Say B, Yardimci I, et al. Response to letter to the editor: “First admission neutrophil-lymphocyte ratio may indicate acute prognosis of ischemic stroke.” Rambam Maimonides Med J. 2021;12(4):e0036. doi:10.5041/RMMJ.10457
17. Hu B, Yang XR, Xu Y, et al. Systemic immune-inflammation index predicts prognosis of patients after curative resection for hepatocellular carcinoma. Clin Cancer Res. 2014;20(23):6212–6222. doi:10.1158/1078-0432.CCR-14-0442
18. Fois AG, Paliogiannis P, Scano V, et al. The systemic inflammation index on admission predicts in-hospital mortality in COVID-19 patients. Molecules. 2020;25(23):5725. doi:10.3390/molecules25235725
19. Yoon NB, Son C, Um SJ. Role of the neutrophil-lymphocyte count ratio in the differential diagnosis between pulmonary tuberculosis and bacterial community-acquired pneumonia. Ann Lab Med. 2013;33(2):105–110. doi:10.3343/alm.2013.33.2.105
20. Abakay O, Abakay A, Sen HS, et al. The relationship between inflammatory marker levels and pulmonary tuberculosis severity. Inflammation. 2015;38(2):691–696. doi:10.1007/s10753-014-9978-y
21. Elmas Bozdemir Ş, Aslaner H. Can neutrophil to lymphocyte ratio and monocyte to lymphocyte ratio be used in the diagnosis of childhood tuberculosis? Online Turk Saglik Bilim Derg. 2021;6(4):521–527. doi:10.26453/otjhs.903130
22. Omair M, Baig MS, Farooqui WA, et al. Relationship of neutrophil lymphocyte ratio, monocyte lymphocyte ratio and neutrophil monocyte ratio with treatment response in pulmonary tuberculosis patients during intensive phase treatment. BMC Infect Dis. 2024;24(1):615. doi:10.1186/s12879-024-09454-2
23. Suryana K, Dharmesti NWW, Rai IN. High pretreatment level of neutrophil to lymphocyte ratio, monocyte to lymphocyte ratio and other factors associated with delayed sputum conversion in patients with pulmonary tuberculosis. Infect Drug Resist. 2022;15:5455–5462. doi:10.2147/IDR.S380166
24. Wang W, Wang LF, Liu YY, et al. Value of the ratio of monocytes to lymphocytes for monitoring tuberculosis therapy. Can J Infect Dis Med Microbiol. 2019;2019:3270393. doi:10.1155/2019/3270393
25. Iqbal S, Ahmed U, Khan MA. Haematological parameters altered in tuberculosis. Pak J Physiol. 2015;11(1):13–16. doi:10.69656/pjp.v11i1.375
26. Putri WR, Hernaningsih Y, et al. Neutrophil to lymphocyte ratio and immature granulocyte: assessing for promising parameters to monitor tuberculosis-diabetes mellitus patients. Romanian J Infect Dis. 2023;26(2):68–72. doi:10.37897/RJID.2023.2.6
27. Kobayashi N, Tanaka K, Muraoka S, et al. Influence of age, IGRA results, and inflammatory markers on mortality in hospitalized tuberculosis patients. J Infect Chemother. 2024;30(1):48–52. doi:10.1016/j.jiac.2023.09.011
28. Okeke CO, Amilo GI, Ifeanyichukwu MO, Obi EO. Longitudinal assessment of the impact of tuberculosis infection and treatment on monocyte–lymphocyte ratio, neutrophil–lymphocyte ratio, and other white blood cell parameters. Egypt J Haematol. 2020;45(2):97–102. doi:10.4103/ejh.ejh_62_19.
29. Ştefanescu S, Cocoş R, Turcu-Stiolica A, et al. Evaluation of prognostic significance of hematological profiles after the intensive phase treatment in pulmonary tuberculosis patients from Romania. PLoS One. 2021;16(4):e0249301. doi:10.1371/journal.pone.0249301
30. Choudhary RK, Wall KM, Njuguna I, et al. Monocyte-to-lymphocyte ratio is associated with tuberculosis disease and declines with anti-TB treatment in HIV-infected children. J Acquir Immune Defic Syndr. 2019;80(2):174–181. doi:10.1097/QAI.0000000000001893
31. Putra AAGORK, Suryana IK, Rai IBN, et al. The association of monocyte lymphocyte ratio and IFN-γ/IL-4 ratio on status of sputum conversion in tuberculosis patients with post intensive phase. Medico Leg Update. 2022;22(2):1–11. doi:10.37506/mlu.v22i2.3225
32. Shojaan H, Kalami N, Ghasempour Alamdari M, et al. Diagnostic value of the neutrophil lymphocyte ratio in discrimination between tuberculosis and bacterial community-acquired pneumonia: a meta-analysis. J Clin Tuberc Mycobact Dis. 2023;33:100395. doi:10.1016/j.jctube.2023.100395
33. Kissling M, Fritschi N, Baumann P, et al. Monocyte, lymphocyte and neutrophil ratios—easy-to-use biomarkers for the diagnosis of pediatric tuberculosis. Pediatr Infect Dis J. 2023;42(6):520–527. doi:10.1097/INF.0000000000003901
34. Yin Y, Kuai S, Liu J, et al. Pretreatment neutrophil-to-lymphocyte ratio in peripheral blood was associated with pulmonary tuberculosis retreatment. Arch Med Sci. 2017;2:404–411. doi:10.5114/aoms.2016.60822
35. Neutrophil–lymphocyte ratio and prognosis in miliary tuberculosis. Respirology. 2017;22(Suppl 3):216–216. doi:10.1111/resp.13207_336
36. Adane T, Melku M, Ayalew G, et al. Accuracy of monocyte to lymphocyte ratio for tuberculosis diagnosis and its role in monitoring anti-tuberculosis treatment: systematic review and meta-analysis. Medicine (Baltimore). 2022;101(44):e31539. doi:10.1097/MD.0000000000031539
37. He X, Hou H, Jiang Y, et al. Association between indices of peripheral blood inflammation and cavitary pulmonary tuberculosis. Int J Gen Med. 2024;17:5133–5142. doi:10.2147/IJGM.S483185
38. Chen G, Wu C, Luo Z, et al. Platelet–lymphocyte ratios: a potential marker for pulmonary tuberculosis diagnosis in COPD patients. Int J Chron Obstruct Pulmon Dis. 2016;11:2737–2740. doi:10.2147/COPD.S111254
39. Jeon YL, Lee WI, Kang SY, et al. Neutrophil-to-monocyte-plus-lymphocyte ratio as a potential marker for discriminating pulmonary tuberculosis from nontuberculosis infectious lung diseases. Lab Med. 2019;50(3):286–291. doi:10.1093/labmed/lmy083
40. Yu Z, Shang Z, Huang Q, et al. Integrating systemic immune-inflammation index, fibrinogen, and T-SPOT.TB for precision distinction of active pulmonary tuberculosis. Front Microbiol. 2024;15:1382665. doi:10.3389/fmicb.2024.1382665
41. Dong H, Feng J, Chang X, et al. Predictive value of systemic immune-inflammatory biomarkers for drug-induced liver injury in hepatitis B virus surface antigen positive tuberculosis patients: a retrospective observational study. Medicine (Baltimore). 2024;103(45):e40349. doi:10.1097/MD.0000000000040349
Downloads
Published
Issue
Section
License
Copyright (c) 2026 Hage Yaja, Bineeta Kashyap, Mrinalini Kotru

This work is licensed under a Creative Commons Attribution 4.0 International License.
Authors who publish with this journal agree to the following terms:
- Authors retain copyright and grant the journal right of first publication with the work simultaneously licensed under a Creative Commons Attribution License that allows others to share the work with an acknowledgement of the work's authorship and initial publication in this journal.
- Authors are able to enter into separate, additional contractual arrangements for the non-exclusive distribution of the journal's published version of the work (e.g., post it to an institutional repository or publish it in a book), with an acknowledgement of its initial publication in this journal.
- Authors are permitted and encouraged to post their work online (e.g., in institutional repositories or on their website) prior to and during the submission process, as it can lead to productive exchanges, as well as earlier and greater citation of published work (See The Effect of Open Access at http://opcit.eprints.org/oacitation-biblio.html).

