Transition from Restrictive to Obstructive Lung Function Impairment During Treatment and Follow-Up of Active Tuberculosis
Received 16 December 2019
Accepted for publication 10 March 2020
Published 11 May 2020 Volume 2020:15 Pages 1039—1047
Checked for plagiarism Yes
Review by Single anonymous peer review
Peer reviewer comments 2
Editor who approved publication: Dr Richard Russell
Brian W Allwood,1,2 Elizna Maasdorp,3 Grace J Kim,4,5 Christopher B Cooper,6 Jonathan Goldin,4 Richard N van Zyl-Smit,2 Eric D Bateman,2 Rodney Dawson2
1Division of Pulmonology, Department of Medicine, Stellenbosch University, Cape Town, South Africa; 2University of Cape Town Lung Institute, and Division of Pulmonology, Department of Medicine, University of Cape Town, Cape Town, South Africa; 3DST/NRF Centre of Excellence for Biomedical Tuberculosis Research; South African Medical Research Council Centre for Tuberculosis Research; Division of Molecular Biology and Human Genetics, Faculty of Medicine and Health Sciences, Stellenbosch University, Cape Town, South Africa; 4Center for Computer Visions and Imaging Biomarkers, Department of Radiology, David Geffen School of Medicine, University of California, Los Angeles, CA, USA; 5Department of Biostatistics, Fielding School of Public Health, University of California, Los Angeles, CA, USA; 6Departments of Medicine and Physiology, David Geffen School of Medicine, University of California, Los Angeles, CA, USA
Correspondence: Brian W Allwood
Division of Pulmonology, Department of Medicine, Stellenbosch University, Rm 3013 3rd Floor; Clinical Building; Francie Van Zijl Drive; Medical School, Tygerberg 7505, South Africa
Email [email protected]
Background: Pulmonary tuberculosis (PTB) is associated with many forms of chronic lung disease including the development of chronic airflow obstruction (AFO). However, the nature, evolution and mechanisms responsible for the AFO after PTB are poorly understood. The aim of this study was to examine the progression of changes in lung physiology in patients treated for PTB.
Methods: Immunocompetent, previously healthy, adult patients receiving ambulatory treatment for a first episode of tuberculosis were prospectively followed up with serial lung physiology and quantitative computed tomography (CT) lung scans performed at diagnosis of tuberculosis, 2, 6, 12 and 18 months during and after the completion of treatment.
Results: Forty-nine patients (median age 26 years; 37.2% males) were included, and 43 were studied. During treatment, lung volumes improved and CT fibrosis scores decreased, but features of AFO and gas trapping emerged, while reduced diffusing capacity (DLco) seen in a majority of patients persisted. Significant increases in total lung capacity (TLC) by plethysmography were seen in the year following treatment completion (median change 5.9% pred., P< 0.01) and were driven by large increases in residual volume (RV) (median change +19%pred., P< 0.01) but not inspiratory capacity (IC; P=0.41). The change in RV/TLC correlated with significant progression of radiological gas trapping after treatment (P=0.04) but not with emphysema scores. One year after completing treatment, 18.6% of patients had residual restriction (total lung capacity, TLC < 80%pred), 16.3% had AFO, 32.6% had gas trapping (RV/TLC> 45%), and 78.6% had reduced DLco.
Conclusion: Simple spirometry alone does not fully reveal the residual respiratory impairments resulting after a first episode of PTB. Changes in physiology evolve after treatment completion, and these findings when taken together, suggest emergence of gas trapping after treatment likely caused by progression of small airway pathology during the healing process.
Keywords: tuberculosis, post-tuberculosis, chronic obstructive pulmonary disease, lung function, computed tomography, airflow obstruction
Plain Language Summary
Pulmonary tuberculosis is known to cause permanent damage to the lungs in some individuals. This study shows that in previously healthy, young (median age of 26 years), immunocompetent adults, routine spirometry underestimates the amount of residual damage after a first episode of tuberculosis, when more specialized physiology tests are also used to assess patients. More importantly, it shows that changes to the lung occur even after treatment completion. In the year after finishing treatment, there were significant increases in lung volumes, and these increases were largely due to increases in residual volume (the volume remaining in the lung after full expiration). This physiological change implies that after treatment completion gas trapping may emerge. This was confirmed on CT scanning of the lung in a subset of patients where physiological changes correlated significantly with imaging changes of gas trapping. When taken together, this physiological-radiological comparison suggests that after tuberculosis, changes may occur to the small airways, likely narrowing, resulting in the development of gas trapping and airflow obstruction.
Pulmonary tuberculosis (PTB) may cause permanent impairment of lung function and is associated with several forms of chronic lung disease.1–8 An association between past PTB and chronic airflow obstruction (AFO) has been reported in large population-based epidemiological studies3–6 and contributes to the heavy burden of chronic airways disease seen in high PTB prevalence communities. A causal relationship is suggested by studies examining changes in lung function in patients completing PTB.7,9–13 There is, however, little published evidence for the mechanisms responsible for the impairment of lung function and its clinical course. A common assumption is that the more striking and characteristic sequelae of PTB, namely bronchiectasis, fibrosis, and bronchial stenosis are the major mechanisms responsible for AFO,2,3,14 but few studies have attempted a more thorough assessment of regional structure–function relationships within affected lungs. Nor has it been established whether lung function impairment progresses after the active TB infection has been successfully treated. In a previous observational study of patients with a past history of PTB and spirometric evidence of AFO, we have confirmed that static gas trapping and reduced diffusing capacity (DLco) are common findings, and we have hypothesized that this is best explained by widespread cicatricial changes in or surrounding bronchovascular bundles containing small airways.15 Further, this process may progress over time and contribute to chronic airflow obstruction seen later after treatment has been completed. This observation raises the possibility of considering interventions that might limit these late effects of PTB.
We report here the results of a prospective study of the serial changes in lung function and quantitative CT findings in a cohort of patients with active PTB treated for six months and followed for one year after completion of treatment for PTB, and describe the nature and course of the pulmonary sequelae of PTB during and after completion of treatment.
Materials and Methods
Patients with newly diagnosed drug-sensitive pulmonary TB were recruited from two local ambulatory TB clinics. Eligible patients gave written consent, were 18 years or older with active PTB diagnosed on sputum nucleic acid-amplification testing, confirmed by microscopy and culture. Patients were required to be HIV negative or HIV positive with a CD4 count of over 250 cell/μL. Exclusion criteria were a history of previous PTB, known chronic lung disease or malignancy; a history of illicit drug use; pregnant at the time of diagnosis; or a diagnosis of drug-resistant tuberculosis. Consecutive patients meeting enrollment criteria on recruitment days were invited to participate, with a maximum of three patients recruited per day. For inclusion in the analysis, patients were required to complete an outpatient course of standard anti-tuberculosis therapy (6 months).
Enrolled patients attended for five study visits: On the day of PTB diagnosis (Visit 1), and at 2, 6, 12 and 18 months thereafter (Visits 2 to 5, respectively). At each visit, subjects performed a six-minute walk test, and spirometry before and after administration of an inhaled bronchodilator salbutamol 200ug from a pressurized metered-dose inhaler (pMDI), according to ATS/ERS standards, and16 Global Lung Initiative (GLI) reference equations were used. Body plethysmography and diffusing capacity for carbon monoxide (DLco) corrected for hemoglobin, were performed at 2, 6 and 18 months, and the St. George’s Respiratory Questionnaire (SGRQ) at 6 and 18 months. Plethysmography and DLco were not performed prior to 2 months to reduce the risk of infection to staff.
Chronic obstructive pulmonary disease is currently defined by the presence of airflow obstruction identified by having FEV1/FVC <0.70,17 however, this may underestimate disease in younger persons. Airflow obstruction was defined as a post-bronchodilator ratio of forced expiratory volume in 1 sec (FEV1) to forced vital capacity (FVC) (ie, FEV1/FVC) of less than the predicted lower limit of normal (LLN). Restriction was defined as total lung capacity (TLC) less than 80% predicted, and gas trapping on plethysmography was defined as a residual volume (RV) to TLC ratio (RV/TLC) of greater than 45%. A low DLco (corrected for hemoglobin) and DLco with alveolar volume (VA) correction (ie, DLco/VA) were defined as values of less than 80% predicted.
All patients underwent three high-resolution computed tomography (HRCT) scans of the chest, using a low-dose, non-contrasted protocol that included both inspiratory and expiratory scans. Patients were randomized (1:1:2) into three groups. Group 1 had HRCT scans at Visit 1 (baseline) and after 2 weeks and one month of treatment, Group 2 had scans at baseline, 1 and 2 months, and Group 3 had scans at 2 (Visit 2), 6 (Visit 3) and 18 months (Visit 5).
CT scan images were analyzed quantitatively using in-house software (Los Angeles, USA).18 Using inspiratory scans (ie, TLC scans), percentages of low-attenuation areas (LAAs) <–950 HU were used to define emphysema, and fibrosis was measured as the quantity of lung fibrosis (QLF) of high-attenuation areas (HAAs) >200 HU, either as a percentage (QLF (%)) or millilitre volume (QLF (mL)). On the expiratory scans (ie, RV scans), the percentage of LAAs <–856 HU on expiratory (RV) scans was used to calculate the gas-trapping score (GTS).
This study was conducted in accordance with the Declaration of Helsinki, patient consent was written informed consent and ethical approval for the study was obtained from the University of Cape Town Human Ethics Committee (REF: 248/2013).
Statistical analysis was performed in the statistical programming language R version 3.4.1 (www.r-project.org/) and STATA version 12 (StataCorp, Texas, USA). Descriptive statistics are reported as means and standard deviations when variables are approximately normally distributed and as medians and interquartile ranges when not. Testing for significant differences was done using the Wilcoxon Signed-Rank test for paired data that was not normally distributed. For the difference testing, no correction for multiplicity was applied (38 comparisons were made). Simple linear regression was used for correlations between lung function and radiological variables. Sensitivity analysis for the influence of outliers on the regression was performed, and alpha for all tests was set at 0.05.
A total of 49 patients were recruited. Six patients were excluded from the long-term outcome analysis (see Figure 1). For the remaining 43 subjects, 16 (37.2%) were male, median age of 26 years and 31 (72.1%) were aged 40 years or less. Baseline characteristics and smoking status are reported in Table 1. The mean time to Visits 2, 3 and Visit 5 were 8.1 weeks, 26.3 weeks and 81.1 weeks, respectively. Four subjects delayed Visit 5 due to pregnancy (all conceived after treatment completion).
Table 1 Baseline Demographic and Spirometric Characteristics
Figure 1 Recruitment and exclusion of subjects.
Physiological Changes Over Time (Table 2)
Between baseline and 6 months values for FEV1, FVC but not for FEV1/FVC increased. The majority of the improvements occurred in the first two months of treatment for both FEV1 (median change = 4.6% pred., P<0.01) and FVC (median change = 4.5% pred., P<0.01). Smaller, but statistically significant changes were also observed between 2 and 6 months for FEV1 (median change = 2.9%pred., P<0.01) and FVC (median change = 4.9%pred., P<0.01), but not for FEV1/FVC (P=0.39). Between 6 months and 18months (Visit 5), there were additional significant increases in FEV1 (median change = 3.5%pred., P<0.01), FVC (median change = 3.5%pred., P=0.07) and a non-significant increase in FEV1/FVC (P=0.25).
Table 2 Lung Physiology Data at 2, 6 (Treatment Completion) and 18 Months (One Year After Treatment Completion)
On plethysmography (Figure 2), there was a small but significant increase in TLC and FRC between 2 months and 6 months (median change 3.5% of pred. (P=0.02); and median change 2.3% of pred. (P=0.05), respectively), but non-significant increases in RV (P=0.35). Between 6 and 18 months (ie, after treatment completion), a statistically significant increase in TLC (median change 5.9% pred., P<0.01), RV (median change 19.4% of pred., P<0.01) and FRC (median change 9.3% pred. P<0.01) was observed. There was no significant change in IC between 2 and 6 months, or between 6 and 18 months (P=0.55 and P=0.41, respectively) (see Table 2).
The DLco (%pred.) did not change significantly between 2 and 6months (P=0.18), or between 6 and 18 months (P=0.07).
The six-minute walk distance did not improve significantly at two months (median change 15 m, P=0.06), or thereafter. A statistically significant but not clinically important decrease (improvement) in SGRQ total score was observed between 6 and 18 months (−1.0 units, P<0.01).
One year after completion of treatment (ie, Visit 5), seven patients (16.3%) had AFO, and in six (14.0%) FEV1/FVC was <0.70. Gas trapping was found in 14 (32.6%), and restriction in eight (18.6%) patients. DLco was reduced in 33 of 42 patients (78.6%), and DLco/VA was reduced in 14 of 42 patients (33.3%). The combinations of AFO, restriction, gas trapping and reduced DLco are shown in Figure 3.
Changes in Quantitative Imaging Over Time (Table 3)
On CT imaging the TLC increased significantly between 2 and 6 months (median change 0.22L, P=0.01), but not between 6 and 18 months (P=0.99).
Table 3 Quantitative Computed Tomography Values for Subjects with Scans Performed at 2, 6 (Treatment Completion) and 18 Months (One Year After Treatment Completion)
The median gas-trapping scores (ie, <-856HU on RV scan) measured at 2 and 6 months were not significantly different (P=0.19), but showed small but significant increases between 6 and 18 months (P=0.04). The median difference in emphysema score (ie, LAA<-950HU) between 2 and 6 months and between 6 and 18 months were non-significant (0.92%, P=0.20 and 0.90%, P=0.11, respectively). The median fibrosis score decreased significantly between 2 and 6 months (P<0.01), but changes between 6 and 18 months were non-significant (P=0.07).
At 18 months, 14 of 19 (73.7%) patients had >5% GTS on expiratory CT scan, seven of whom (36.8%) had a GTS value >10%, and two (10.5%) GTS>20%. Fibrosis scores, and radiological volumes are reported in Table 3.
Correlation Between Physiologic and Radiologic Measures Over Time
The overall change in RV/TLC (measured by plethysmography) between 2 and 18 months correlated with changes in radiological GTS (R2= 0.23, P=0.04). This correlation was observed only after 6 months (R2=0.36, P=0.01), and not at earlier time points (P=0.90). By contrast, the correlation between change in RV/TLC (plethysmography) and change in LAA between 2 and 18 months was not significant (R2=0.19, P=0.052). The change in FEV1/FVC between 2 and 18 months correlated poorly with change in radiological GTS (R2= 0.10, P=0.18), and with change in LAA (emphysema score; P=0.11).
As for RV/TLC, change in RV measured by plethysmography correlated significantly with changes in radiological GTS (R2=0.31, P=0.01), and this was similarly attributable to changes occurring after 6 months (R2=0.43, P<0.01), and not before (P=0.99)
There was no correlation between the change in QLF (mL) from 2 to 18 months, and any of the following plethysmography measures: change in TLC %pred. (P=0.91), change in RV/TLC ratio (P=0.17) or change in IC/TLC (P= 0.24).
Correlation of Physiology and Radiological Measures at 18 Months
At 18 months, the FEV1/FVC correlated with radiological GTS (R2 = 0.37, P=0.01) but not with LAA (emphysema score: R2 = 0.17, P=0.07). There was also a correlation between RV/TLC measured by plethysmography and GTS on CT scan (R2 = 0.28, P=0.02), but not LAA (R2 = 0.001, P= 0.89).
The TLC values obtained by plethysmography and CT scan correlated well (R2 = 0.55, P < 0.01) at 18 months. However, the correlation between RV/TLC measured by plethysmography and by CT scan did not correlate significantly (P=0.12). This was primarily due to the poorer correlation between the measurement of RV with the two techniques (R2=0.22, P=0.04), and is likely explained by the difference in body position between plethysmography and CT scans (ie, erect vs supine).
There was no correlation between fibrosis scores (QLF (mL)) and either the TLC or the IC/TLC (P=0.12 and P= 0.93, respectively).
The results of this 18-month prospective study of young, immune-competent patients experiencing their first episode of pulmonary tuberculosis provides several insights into the pathogenesis of lung function impairment and the development of chronic lung disease during and following treatment. Firstly, at one year after completing tuberculosis treatment three quarters of patients had at least one type of lung abnormality as defined in this study. The most common abnormality at 18 months (in 33 of 42 patients; 78.6% of the cohort) was reduced diffusing capacity for carbon monoxide. This was most commonly associated with evidence of gas trapping (in 14 of 33 patients), confirmed on quantitative CT. Seven patients (16.3%) also had evidence of chronic airflow obstruction (FEV1/FVC below the LLN). Restriction was detected in 8 subjects with reduced DLco, most of whom had no evidence of gas trapping or airflow obstruction.
Secondly, the changes in lung volumes progressed in the year after completion of anti-tuberculous treatment, presumably as a consequence of gas trapping rather than emphysema. The increase in TLC one year after treatment completion was largely due to a large increase in RV that was not associated with an increase in IC. The CT imaging confirmed that this increase in RV/TLC ratio correlated more closely with radiological gas-trapping scores, than with either emphysema or fibrosis scores. No correlation was found between the fibrosis scores and any physiological parameter, including TLC and IC/TLC. Together, these findings suggest that the physiological gas trapping is independent of emphysema, and may point to developing airflow limitation at the level of small airways. This hypothesis is supported by lung images in individual patients showing gas trapping on expiratory lung scans one year after treatment, in spite of good resolution of tuberculous pulmonary infiltrates (Figure 4). This explanation is plausible given the extensive bronchiolar involvement seen in more than 90% of patients with active tuberculosis disease.11 The mechanisms responsible for the consistently observed finding of reduced DLCO is less clear, but potential involvement of vasculature within the bronchovascular bundle in and around small airways is one potential mechanism.15
Several large multi-centre studies and systematic reviews have demonstrated the association of previous tuberculosis and spirometric abnormalities.3–6,13,14,19,20 However, these and several smaller studies have been performed without the use of plethysmography or quantitative imaging. In this present study, we found spirometry to be relatively insensitive in identifying post-tuberculosis physiological abnormalities; almost twice as many patients had plethysmographic evidence of gas trapping as compared with spirometry, and almost 80% had a reduction in diffusing capacity.
Our study has a number of strengths, these include its prospective nature and the enrollment of a young population without previous episodes of PTB, and without known chronic respiratory or cardiac diseases, or recognized impaired immune-incompetency. All PTB infections were drug-sensitive and only those who completed treatment and follow-up were included in analysis. Smoking although not an exclusion criterion, was light (median 3.0 pack-years in those who smoked). It is thus reasonable to assume, that despite the small sample size, the majority of findings are likely primarily attributable to the chronic consequence of tuberculosis.
However, there are also a number of weaknesses, which include its small size with the potential for selection bias, loss of six patients in follow-up, and significant but small correlations. The size of the study may have been underpowered to assess smaller effect of potential co-factors (eg, smoking). Further, in order to limit radiation exposures, timepoints for CT imaging were varied to capture different stages of treatment and follow-up. Finally, owing to potential infection risk, diffusing capacity and body plethysmography were not performed at the baseline visit. However, in spite of these limitations, statistically significant trends were observed.
This young, previously healthy, adult population, demonstrated a significant burden of airflow obstruction (one in six) and residual chronic changes one year after the first episode of treated tuberculosis. The residual disease burden was underestimated by spirometry. Gas trapping (in one third) and reduced DLco (in three quarters) were more common than restriction (one in five). The RV and RV/TLC continued to increase in the year after treatment completion and correlated best with radiological gas trapping. This is consistent with the hypothesis of residual and evolving obstructive changes in the small airways after tuberculosis.
AFO, airflow obstruction; CT, computed tomography; DLco, diffusing capacity for carbon monoxide; FEV1, forced expiratory volume in 1 sec; FVC, forced vital capacity; GLI, Global Lung Initiative; GTS, gas-trapping score; HAA, high-attenuation areas; HRCT, high-resolution computed tomography; IC, inspiratory capacity; L, liters; LAA, low-attenuation areas; LLN, limit of normal; PTB, pulmonary tuberculosis; pMDI, pressurized metered dose inhaler; QLF, quantity of lung fibrosis; QLF (%), quantity of lung fibrosis (percentage); QLF (mL), quantity of lung fibrosis (millilitre volume); RV, residual volume; SGRQ, St. George’s Respiratory Questionnaire; TLC, total lung capacity; VA, alveolar volume.
Notification of Prior Abstract Publication/Presentation
This data has not been published elsewhere but was presented as abstract for the European Respiratory Society Meeting, September 2019.
Role of sponsors:
Funders did not have any role in the study design, data collection, data analysis, manuscript preparation or decision to publish.
We would like to acknowledge the technical assistance of Bronwyn Hendricks, Helena Olckers, Nolubabalu Bam and La-Donna Kappa, at the University of Cape Town Lung Institute.
Protocol design: BA, CC, JG, RvZS, EB, RD; Data Collection: BA, RvZS, RD; Analysis: BA, EM, GK, JG, CC, EB; Manuscript Preparation: BA, EM, GK, CC, JG, RvZS, EB, RD. All authors contributed to data analysis, drafting or revising the article, gave final approval of the version to be published, and agree to be accountable for all aspects of the work.
Funding received from the University of Cape Town Lung Institute for funding the radiology component and Global Alliance for TB Drug Development for access to their bio-storage cohort. E.M. is funded by a Strategic Health Innovation Partnership (SHIP) grant from the South African (SA) Department of Science and Technology (DST) and SA Medical Research Council (SAMRC) to the South African Tuberculosis Bioinformatics Initiative (SATBBI), and E.B. received funding from the National Research Foundation (NRF).
Dr Brian Allwood reports speaker honoraria from Novartis, outside the submitted work. Professor Kim reports personal fee from MedQIA outside the submitted work.
Professor Richard van Zyl-Smit reports personal fees from AstraZeneca CIPLA, Roche, Novartis, Pfizer, ASPEN/GSK and MSD outside the submitted work.
Dr. Cooper reports grants from NIH/NHLBI, Foundation NIH and COPD Foundation, during the conduct of the study; personal fees from PulmonX, GlaxoSmithKline, NUVAIRA and MGC Diagnostics, outside the submitted work.
Professor Eric Bateman reports personal fees from ALK, AstraZeneca, Boehringer Ingelheim, Menarini, Novartis, Orion, Regeneron and Sanofi outside the submitted work.
The authors report no other conflicts of interset in this work.
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