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Pulmonary Functions and Inflammatory Biomarkers in Post-Pulmonary Tuberculosis Sequelae

BACKGROUND: Post-tuberculosis (TB) sequelae is a commonly encountered clinical entity, especially in high TB burden countries. This may represent chronic anatomic sequelae of previously treated TB, with frequent symptomatic presentation. This pilot study was aimed to investigate the pulmonary functi...

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Autores principales: Shanmugasundaram, Kumar, Talwar, Anjana, Madan, Karan, Bade, Geetanjali
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Academy of Tuberculosis and Respiratory Diseases 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8987661/
https://www.ncbi.nlm.nih.gov/pubmed/35232004
http://dx.doi.org/10.4046/trd.2021.0127
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author Shanmugasundaram, Kumar
Talwar, Anjana
Madan, Karan
Bade, Geetanjali
author_facet Shanmugasundaram, Kumar
Talwar, Anjana
Madan, Karan
Bade, Geetanjali
author_sort Shanmugasundaram, Kumar
collection PubMed
description BACKGROUND: Post-tuberculosis (TB) sequelae is a commonly encountered clinical entity, especially in high TB burden countries. This may represent chronic anatomic sequelae of previously treated TB, with frequent symptomatic presentation. This pilot study was aimed to investigate the pulmonary functions and systemic inflammatory markers in patients with post-TB sequelae (PTBS) and to compare them with post-TB without sequelae (PTBWS) participants and healthy controls. METHODS: A total of 30 participants were enrolled, PTBS (n=10), PTBWS (n=10), and healthy controls (n=10). Pulmonary function tests included spirometry and measurement of airway impedance by impulse oscillometry. Serum levels of matrix metalloproteinase (MMP)-1, transforming growth factor-β, and interferon-γ were estimated. RESULTS: Slow vital capacity (SVC), forced vital capacity (FVC), forced expiratory volume in 1 second (FEV(1)), FEV(1)/FVC, and peak expiratory flow were significantly lower in PTBS as compared to controls. SVC and FEV(1) were significantly less in PTBS as compared to PTBWS. Total airway impedance (Z(5)), total airway resistance (R(5)), central airway resistance (R(20)), area of reactance (Ax), and resonant frequency (Fres) were significantly higher and respiratory reactance at 5 and 20 Hz (X(5), X(20)) were significantly lower in PTBS as compared to PTBWS. Spirometry parameters correlated with impulse oscillometry parameters in PTBS. Serum MMP-1 level was significantly higher in PTBS as compared to other groups. CONCLUSION: Significant pulmonary function impairment was observed in PTBS, and raised serum MMP-1 levels compared with PTBWS and healthy controls. Follow-up pulmonary function testing is recommended after treatment of TB for early diagnosis and treatment of PTBS.
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spelling pubmed-89876612022-04-18 Pulmonary Functions and Inflammatory Biomarkers in Post-Pulmonary Tuberculosis Sequelae Shanmugasundaram, Kumar Talwar, Anjana Madan, Karan Bade, Geetanjali Tuberc Respir Dis (Seoul) Original Article BACKGROUND: Post-tuberculosis (TB) sequelae is a commonly encountered clinical entity, especially in high TB burden countries. This may represent chronic anatomic sequelae of previously treated TB, with frequent symptomatic presentation. This pilot study was aimed to investigate the pulmonary functions and systemic inflammatory markers in patients with post-TB sequelae (PTBS) and to compare them with post-TB without sequelae (PTBWS) participants and healthy controls. METHODS: A total of 30 participants were enrolled, PTBS (n=10), PTBWS (n=10), and healthy controls (n=10). Pulmonary function tests included spirometry and measurement of airway impedance by impulse oscillometry. Serum levels of matrix metalloproteinase (MMP)-1, transforming growth factor-β, and interferon-γ were estimated. RESULTS: Slow vital capacity (SVC), forced vital capacity (FVC), forced expiratory volume in 1 second (FEV(1)), FEV(1)/FVC, and peak expiratory flow were significantly lower in PTBS as compared to controls. SVC and FEV(1) were significantly less in PTBS as compared to PTBWS. Total airway impedance (Z(5)), total airway resistance (R(5)), central airway resistance (R(20)), area of reactance (Ax), and resonant frequency (Fres) were significantly higher and respiratory reactance at 5 and 20 Hz (X(5), X(20)) were significantly lower in PTBS as compared to PTBWS. Spirometry parameters correlated with impulse oscillometry parameters in PTBS. Serum MMP-1 level was significantly higher in PTBS as compared to other groups. CONCLUSION: Significant pulmonary function impairment was observed in PTBS, and raised serum MMP-1 levels compared with PTBWS and healthy controls. Follow-up pulmonary function testing is recommended after treatment of TB for early diagnosis and treatment of PTBS. The Korean Academy of Tuberculosis and Respiratory Diseases 2022-04 2022-03-02 /pmc/articles/PMC8987661/ /pubmed/35232004 http://dx.doi.org/10.4046/trd.2021.0127 Text en Copyright © 2022 The Korean Academy of Tuberculosis and Respiratory Diseases https://creativecommons.org/licenses/by-nc/4.0/It is identical to the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ).
spellingShingle Original Article
Shanmugasundaram, Kumar
Talwar, Anjana
Madan, Karan
Bade, Geetanjali
Pulmonary Functions and Inflammatory Biomarkers in Post-Pulmonary Tuberculosis Sequelae
title Pulmonary Functions and Inflammatory Biomarkers in Post-Pulmonary Tuberculosis Sequelae
title_full Pulmonary Functions and Inflammatory Biomarkers in Post-Pulmonary Tuberculosis Sequelae
title_fullStr Pulmonary Functions and Inflammatory Biomarkers in Post-Pulmonary Tuberculosis Sequelae
title_full_unstemmed Pulmonary Functions and Inflammatory Biomarkers in Post-Pulmonary Tuberculosis Sequelae
title_short Pulmonary Functions and Inflammatory Biomarkers in Post-Pulmonary Tuberculosis Sequelae
title_sort pulmonary functions and inflammatory biomarkers in post-pulmonary tuberculosis sequelae
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8987661/
https://www.ncbi.nlm.nih.gov/pubmed/35232004
http://dx.doi.org/10.4046/trd.2021.0127
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