Lung function and CT lung densitometry in 37- to 39-year-old individuals with alpha-1-antitrypsin deficiency

Behrouz Mostafavi,1 Sandra Diaz,2 Eeva Piitulainen,1 Berend C Stoel,3 Per Wollmer,4 Hanan A Tanash1 1Department of Respiratory Medicine and Allergology Malmö, Skåne University Hospital, Lund University, Malmö, Sweden; 2Department of Clinical Physiology Malmö, Sk...

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Main Authors: Mostafavi B, Diaz S, Piitulainen E, Stoel BC, Wollmer P, Tanash HA
Format: Article
Language:English
Published: Dove Medical Press 2018-11-01
Series:International Journal of COPD
Subjects:
Online Access:https://www.dovepress.com/lung-function-and-ct-lung-densitometry-in-37--to-39-year-old-individua-peer-reviewed-article-COPD
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spelling doaj-ca528738a5cf4599b47dca02b393281d2020-11-25T02:17:26ZengDove Medical PressInternational Journal of COPD1178-20052018-11-01Volume 133689369842112Lung function and CT lung densitometry in 37- to 39-year-old individuals with alpha-1-antitrypsin deficiencyMostafavi BDiaz SPiitulainen EStoel BCWollmer PTanash HABehrouz Mostafavi,1 Sandra Diaz,2 Eeva Piitulainen,1 Berend C Stoel,3 Per Wollmer,4 Hanan A Tanash1 1Department of Respiratory Medicine and Allergology Malmö, Skåne University Hospital, Lund University, Malmö, Sweden; 2Department of Clinical Physiology Malmö, Skåne University Hospital, Lund University, Malmö, Sweden; 3Division of Image Processing, Department of Radiology, Leiden University Medical, Leiden, the Netherlands; 4Department of Translational Medicine, Lund University, Malmö, Sweden Background: Alpha-1-antitrypsin (AAT) deficiency is a hereditary disorder that predisposes to emphysema. A cohort of severe (PiZZ) and moderate (PiSZ) AAT-deficient newborn infants was identified by the Swedish national neonatal AAT screening program in 1972–1974 and has been followed-up since birth. Our aim was to study whether the cohort has signs of emphysema in pulmonary function tests (PFTs) and computed tomography (CT) densitometry at 38 years of age in comparison with an age-matched control group, randomly selected from the population registry. Methods: Forty-one PiZZ, 18 PiSZ, and 61 control subjects (PiMM) underwent complete PFTs, measurement of resistance and reactance in the respiratory system by impulse oscillometry (IOS)/forced oscillation technique (FOT), and CT densitometry. The results were related to self-reported smoking habits. Results: The total lung capacity (TLC) % of the predicted value was significantly higher in the PiZZ ever-smokers than in the PiZZ never-smokers (P<0.05), PiSZ never-smokers (P=0.01) and the PiMM never-smokers (P=0.01). The residual volume (RV) % of the predicted value was significantly higher in the PiZZ ever-smokers compared to the PiMM never-smokers (P<0.01). The PiZZ ever-smokers had a significantly lower carbon monoxide transfer coefficient (Kco) than the PiSZ never-smokers (P<0.01) and PiMM never-smokers (P<0.01). Respiratory system resistance at 5 Hz (P<0.01), at 20 Hz (P<0.01), and the area of low reactance (Alx; P<0.05) were significantly lower and respiratory system reactance at 5 Hz (P<0.05) was significantly higher in PiZZ subjects compared to the PiMM subjects. No statistically significant differences in the CT densitometry parameters were found between the Pi subgroups. Conclusion: The physiological parameters in the PiZZ ever-smokers showed evidence of hyperinflation and emphysema before the age of 40 years. Keywords: alpha-1-antitrypsin deficiency, lung function, lung disease, screening, impulse oscillometryhttps://www.dovepress.com/lung-function-and-ct-lung-densitometry-in-37--to-39-year-old-individua-peer-reviewed-article-COPDAlpha-1-antitrypsin deficiencylung functionlung diseasescreeningImpulse Oscillometry (IOS).
collection DOAJ
language English
format Article
sources DOAJ
author Mostafavi B
Diaz S
Piitulainen E
Stoel BC
Wollmer P
Tanash HA
spellingShingle Mostafavi B
Diaz S
Piitulainen E
Stoel BC
Wollmer P
Tanash HA
Lung function and CT lung densitometry in 37- to 39-year-old individuals with alpha-1-antitrypsin deficiency
International Journal of COPD
Alpha-1-antitrypsin deficiency
lung function
lung disease
screening
Impulse Oscillometry (IOS).
author_facet Mostafavi B
Diaz S
Piitulainen E
Stoel BC
Wollmer P
Tanash HA
author_sort Mostafavi B
title Lung function and CT lung densitometry in 37- to 39-year-old individuals with alpha-1-antitrypsin deficiency
title_short Lung function and CT lung densitometry in 37- to 39-year-old individuals with alpha-1-antitrypsin deficiency
title_full Lung function and CT lung densitometry in 37- to 39-year-old individuals with alpha-1-antitrypsin deficiency
title_fullStr Lung function and CT lung densitometry in 37- to 39-year-old individuals with alpha-1-antitrypsin deficiency
title_full_unstemmed Lung function and CT lung densitometry in 37- to 39-year-old individuals with alpha-1-antitrypsin deficiency
title_sort lung function and ct lung densitometry in 37- to 39-year-old individuals with alpha-1-antitrypsin deficiency
publisher Dove Medical Press
series International Journal of COPD
issn 1178-2005
publishDate 2018-11-01
description Behrouz Mostafavi,1 Sandra Diaz,2 Eeva Piitulainen,1 Berend C Stoel,3 Per Wollmer,4 Hanan A Tanash1 1Department of Respiratory Medicine and Allergology Malmö, Skåne University Hospital, Lund University, Malmö, Sweden; 2Department of Clinical Physiology Malmö, Skåne University Hospital, Lund University, Malmö, Sweden; 3Division of Image Processing, Department of Radiology, Leiden University Medical, Leiden, the Netherlands; 4Department of Translational Medicine, Lund University, Malmö, Sweden Background: Alpha-1-antitrypsin (AAT) deficiency is a hereditary disorder that predisposes to emphysema. A cohort of severe (PiZZ) and moderate (PiSZ) AAT-deficient newborn infants was identified by the Swedish national neonatal AAT screening program in 1972–1974 and has been followed-up since birth. Our aim was to study whether the cohort has signs of emphysema in pulmonary function tests (PFTs) and computed tomography (CT) densitometry at 38 years of age in comparison with an age-matched control group, randomly selected from the population registry. Methods: Forty-one PiZZ, 18 PiSZ, and 61 control subjects (PiMM) underwent complete PFTs, measurement of resistance and reactance in the respiratory system by impulse oscillometry (IOS)/forced oscillation technique (FOT), and CT densitometry. The results were related to self-reported smoking habits. Results: The total lung capacity (TLC) % of the predicted value was significantly higher in the PiZZ ever-smokers than in the PiZZ never-smokers (P<0.05), PiSZ never-smokers (P=0.01) and the PiMM never-smokers (P=0.01). The residual volume (RV) % of the predicted value was significantly higher in the PiZZ ever-smokers compared to the PiMM never-smokers (P<0.01). The PiZZ ever-smokers had a significantly lower carbon monoxide transfer coefficient (Kco) than the PiSZ never-smokers (P<0.01) and PiMM never-smokers (P<0.01). Respiratory system resistance at 5 Hz (P<0.01), at 20 Hz (P<0.01), and the area of low reactance (Alx; P<0.05) were significantly lower and respiratory system reactance at 5 Hz (P<0.05) was significantly higher in PiZZ subjects compared to the PiMM subjects. No statistically significant differences in the CT densitometry parameters were found between the Pi subgroups. Conclusion: The physiological parameters in the PiZZ ever-smokers showed evidence of hyperinflation and emphysema before the age of 40 years. Keywords: alpha-1-antitrypsin deficiency, lung function, lung disease, screening, impulse oscillometry
topic Alpha-1-antitrypsin deficiency
lung function
lung disease
screening
Impulse Oscillometry (IOS).
url https://www.dovepress.com/lung-function-and-ct-lung-densitometry-in-37--to-39-year-old-individua-peer-reviewed-article-COPD
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