Impact of Pulmonary Tuberculosis Activity on Exhaled Breath Markers Levels in the Egyptian Population

Introduction: Tuberculosis still characterizes till now a major respiratory insult with concurrent pulmonary manifestations and later disability. Aim of Work: To evaluate the level of exhaled fraction of nitric oxide (FENO) and fraction of exhaled carbon monoxide (FECO) as markers of pulmonary tuberculosis TB activity in patients under chemotherapy in comparison to healthy negative patients and latent TB patients. Patients and Methods: This cross-sectional study was conducted on 130 patients recruited from the outpatient clinic of Mansoura Chest hospital during the period from May 2019 to December 2019. They were categorized into the three groups: 1) Pulmonary tuberculous patients PTB (group1) which included 48 cases with positive sputum for TB bacilli in the initiation phase after 1 month of starting anti-tuberculous chemotherapy; 2) Latent patients (group 2): included 40 patients with positive tuberculin skin test (Mantoux test) > 10 mm. 3) Control patients (group 3) which included 42 healthy volunteers with negative sputum for TB bacilli. They were subjected to portable spirogram as well as exhaled fractional NO and CO measurement. Results: FECO and FENO levels prevailed in pulmonary TB patients followed by


Introduction
Eminent diagnosis of pulmonary TB, primarily at the critical care level, counted on obtaining an adequate sample of the bronchial airway as enough expectorated sputum. The basic typical tool for diagnosis of active pulmonary TB relied on the bacteriological culture, alongside with nucleic acid amplification test (NAAT) plus microscopic examination of obtained smear however in one-third of TB patients no adequate biological sputum sample could be acquired [1].
This dictated more different sampling methodologies for fear of failure of diagnosis altogether that was recognized in many low resource communities. Thus, alternate non-invasive techniques, such as blood, urine samples [2] and exhaled breath condensate [3] supported aides in TB diagnosis.
Numerous research teams had utilized gas chromatography (GC) interrelated to mass spectrometry (MS), for inspecting the volatile molecules detected in breath in cases with active pulmonary TB, and detected diverse forms of marker compounds [4] [5] [6] owing to different sampling methods and analytical approaches along with patient population heterogeneity and patient comorbidities [7].
Overall, breath chemical composition could be affected by varied respiratory infections, food, drug medications, and smoking habits in addition to age and gender [8], but less prominent as smoking behaviors do [9]. Also, the profile of compounds possibly created during MTB infection may be altered by the host at different phases of infection and could be variable during the progression/regression of TB disease [5].
Currently, most researchers had focused on exhaled nitric oxide (NO), although recently quite a lot of other volatile gases (carbon monoxide, pentane, ethane) had also been investigated. Moreover, multiple endogenous substances (inflammatory mediators, cytokines, oxidants) were identified in expired breath condensates. In patients with active tuberculosis elevated exhaled NO and NOS2 presentation in alveolar macrophages was established and seemed to vanish with antituberculosis therapy [10].
On the other hand, elevated exhaled CO levels offered an initial warning indicator for an acute pulmonary infection, which was associated with exacerbation of an existing respiratory disease, moreover lower respiratory tract infections other than pulmonary TB [11], thus our study aimed to evaluate the level of exhaled fraction of nitric oxide (NO) and carbon monoxide CO as markers of pulmonary

Patients and Methods
This an observational cross-sectional concurrent parallel study.

Patients:
This study was conducted on 130 patients who were recruited from the Outpatient Clinic of Mansoura Chest Hospital. The practical part of this study was carried out from May 2019 to August 2019 while the theoretical and statistical part was conducted during the period from August 2019 to December 2019. The selected patients were at age (13 -55 years) who were referred for medical advice for TB treatment at Mansoura Chest Hospital Outpatient Clinic, National TB program. Control patients were selected from patients' relatives with a negative history of pulmonary diseases and a negative (tuberculine Monteux test and sputum smear) and nonsmokers with the same age group.
They were categorized into three groups:    To ensure a breath sample was right at the correct flow rate, the monitor was held upright all the time during the test. Repeated measurements were done after 10 minutes until two acceptable comparable values (±2.5 part per billion (ppb) for measurements <35 ppb and ±5% for measurements ≥ 35 ppb) were performed (maximum 3 attempts) [11].

Discussion
Pulmonary tuberculosis has been boomed for many years as most ancient disease and inveterate infection of humankind for its mass dramatic impact on body systems not only the lungs. Diagnosis of pulmonary tuberculosis has drawn attention for all specialties to attain the access of early diagnostic modalities in order to guard against debilitating sequels.
Inhaled inflammatory markers estimation shared to a greater extent as being evidence of respiratory disease occurrence and a trace of their prognosis.  Multivariate analysis carried out by Jose W. L Opez et al. [18] stated no significant association between diagnosis of TB and FeNO level after correction for age, gender, BMI, height and HIV status.
In our research mean age was insignificantly higher in the LTB group followed by the PTB group (32 ± 11.23 and 29 ± 9.25 years), unlike the control group that presented 26 ± 8.65 years. Females were insignificantly less affected than males in all studied groups and in total patients apart from the control group that were approximate. Depending on the duration of illness as an indicator for disease severity and in correlation with exhaled marker level could not be applied in this study due to difficulties that were encountered in machine calibration, limited number for the device to perform in addition to patient follow up problems.
In L Opez study, on one hand, the median FeNO levels were 13 ppb in TB participants of and 15 ppb in healthy non-diseased controls, without statistically level between pulmonary TB patients and latent Tb patients could be explained by the pathophysiological inflammatory mechanisms of pulmonary parenchyma owing to increased macrophages activity and lack of balance in iNO synthetase enzyme system. In our study patients with immune disorders or other chronic pulmonary disorders were excluded for fear of false-negative results. Previous human studies on FeNO had shown contradictory results. The largest human experiment to date in Indonesia found lower mean FeNO levels in TB cases with no convincing explanation, although data coincided considerably with those in healthy controls, and similar data were observed in an Ethiopian study which included HIV-positive patient [19] [20]. A study in Taiwan had reported increased FeNO levels in active TB patients, assuming increased lung macrophage activity and up-regulation of iNOS [10]. They found a median FeNO value of 15 ppb in healthy control subjects, parallel to values reported in Vietnamese construction workers (15 ppb) and healthy controls in the Indonesian study (16.6 ppb), but higher than that in controls in the Taiwanese study (6.5 ± 0.9 ppb) and lower than mean values observed in Korean controls (27.06 ± 10.8 ppb) and Yhi study 2016 [21] [22]. The FeNO level unevenness in healthy controls was furthermore demonstrated in the Vietnam study: although FeNO was greater in TB participants compared with a subgroup of healthy hospital workers, they were not significantly different on comparison with healthy construction workers [23].
The fractional concentration of exhaled nitric oxide that had been used as a measure of type 2 airway inflammation showed correlations with a sputum eosinophilia and Th2 cytokines including IL-5 and IL-13 [24] [25]. As a Th1 response predominates in TB, this might clarify why they found no difference in FeNO levels between TB patients and controls [26].
In our work in Mansoura chest hospital sputum eosinophilia was identified in pulmonary TB and latent TB patients that might be related to one variant in this type of infection. ESR and sputum eosinophilia presented higher levels in pulmonary TB patients than the other two groups.
Elevated exhaled NO and NOS2 expression in alveolar macrophages is found in patients with active tuberculosis and is decreased with anti-tuberculous therapy [10]. A longitudinal study in Korean TB participants also demonstrated no significant change following 8 weeks of treatment [21]. Likewise, only a very small variation was observed in mean FeNO levels at treatment completion in the Indonesian study, 10.7 -15.1 ppb, which falls within the precision range for the portable NO analyzer device used (±5 ppb for values < 50 ppb).
Carbon monoxide (CO) was recognized as a gas that may be generated endogenously and was detectable in exhaled air. There were three major sources of CO in exhaled air: exogenous CO, enzymatic degradation of heme, non-heme-related release initiated by (lipid peroxidation, bacteria, hypoxia, tumor necrosis factor, reactive nitrogen and oxygen intermediates [27] [28] and also by MTB infection [29] [30]. CO gas resulted from the degradation of hemoglobin by the enzyme heme oxygenase (HO) that was mostly exhaled, and approximately 15% had ari- sen from the degradation of myoglobin, NO synthases, catalase, guanylyl cyclase and cytochromes [31]. Several bacteria yielded CO, and less than 1% is unbound and dissolved in body fluid [32]. Furthermore, in response to PTB infection, host cells produced a variety of toxic compounds to mediate microbial eradication nitric oxide (NO), and carbon monoxide (CO) are some of them. Formerly, multiple studies [28] [29] found that throughout MTB infection, HO-1 enzyme was induced in macrophages in infection suggesting that increased levels of CO might be observed during MTB infection. In our work exhaled CO was statistically higher in PTB group being more than four folds increase in the measured level than normal healthy volunteers and 50% increase than latent tuberculous patients.
Radiological findings were prominent in PTB group, grade III more than 50% was detected in PTB however grade VI accounted for 25%. Grade II and V were identified in lower percentages.
Radiological presentations were evident in latent TB group as (2.38%) in grade I and II and minimal in healthy group. These findings were related to previous pulmonary infections other than TB. These findings were reasonable with most diseased patients and these imaging tools were held in the study to correlate with clinical progression of the disease and to be supporting aids in the diagnosis. Many limitations had been encountered in our study the first one represented in application of serial monitoring that had been canceled due to apparatus calibration as mentioned earlier, the second was in comparison between pulmonary and extrapulmonary patients was it differ, that needed larger multi-organ studies. The third was in the strong need for recent well-documented sterilization techniques for portable spirometer and gas analyzer to hinder the transmission of infection in subsequent studies to save cost of sensors used in the three groups.

Conclusion
Measurement of exhaled NO and CO level in expired air can entitle a simple non-invasive approach in the pathway of diagnosis of pulmonary tuberculosis in both active and latent phases and differentiate them from healthy non-affected cases.