Evaluation of Alpha-1 antitrypsin level in the serum of children with idiopathic bronchiectasis
Background: Bronchiectasis is a clinical syndrome characterized by chronic cough, sputum production, recurrent respiratory infections, and permanent bronchial dilation. The association between the level of alpha-1 antitrypsin (AAT) and bronchiectasis is controversial. In this study, we aimed to inv...
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Tehran University of Medical Sciences
2021
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oai:doaj.org-article:e64febfcf6b54a14bd303b8af532add32021-11-29T06:16:21ZEvaluation of Alpha-1 antitrypsin level in the serum of children with idiopathic bronchiectasis0044-60251735-969410.18502/acta.v59i11.7775https://doaj.org/article/e64febfcf6b54a14bd303b8af532add32021-11-01T00:00:00Zhttps://acta.tums.ac.ir/index.php/acta/article/view/9233https://doaj.org/toc/0044-6025https://doaj.org/toc/1735-9694Background: Bronchiectasis is a clinical syndrome characterized by chronic cough, sputum production, recurrent respiratory infections, and permanent bronchial dilation. The association between the level of alpha-1 antitrypsin (AAT) and bronchiectasis is controversial. In this study, we aimed to investigate this association in children with idiopathic bronchiectasis. Methods: The study was conducted on 20 patients with idiopathic bronchiectasis as the case group (mean age 15.9±2.1) and 20 healthy individuals as the control group (mean age 14.9±2.6). Serum AAT level was measured using nephelometric analysis (g/L). Other criteria including sex, parent consanguinity, number of hospitalization, age of the first symptom were evaluated in both groups related to AAT level. Results: The mean serum level of AAT in the case and control groups were 1.3±0.29; 1.5 ±0.59, respectively with statistical significance (P=0.001). There was a significant difference between the two groups in the AAT level distribution, according to AAT normal range (p=0.01). The case group had a more positive attitude toward consanguinity than the control group (66.7% versus 33.3%; P<0.001). The results showed that 80% of patients had the first symptom of disease under 1 year of age, 6.6% 1- 5 years, 6.6% 5- 10 years, and 6.6% in more than 10 years old. In the case group, 53.3% had a history of medical hospitalization for one time, 26.7% two times, while 20% of the patients had no medical hospitalization. Conclusion: Decreased AAT serum level and high consanguinity rates may be considered as two risk factors for idiopathic bronchiectasis occurrence in children.Maryam BabaeiZahra KanannejadSoheila AlyasinTehran University of Medical Sciencesarticlealpha-1 antitrypsinidiopathic bronchiectasisnephelometryMedicine (General)R5-920ENActa Medica Iranica, Pp 641-644 (2021) |
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alpha-1 antitrypsin idiopathic bronchiectasis nephelometry Medicine (General) R5-920 |
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alpha-1 antitrypsin idiopathic bronchiectasis nephelometry Medicine (General) R5-920 Maryam Babaei Zahra Kanannejad Soheila Alyasin Evaluation of Alpha-1 antitrypsin level in the serum of children with idiopathic bronchiectasis |
description |
Background: Bronchiectasis is a clinical syndrome characterized by chronic cough, sputum production, recurrent respiratory infections, and permanent bronchial dilation. The association between the level of alpha-1 antitrypsin (AAT) and bronchiectasis is controversial. In this study, we aimed to investigate this association in children with idiopathic bronchiectasis.
Methods: The study was conducted on 20 patients with idiopathic bronchiectasis as the case group (mean age 15.9±2.1) and 20 healthy individuals as the control group (mean age 14.9±2.6). Serum AAT level was measured using nephelometric analysis (g/L). Other criteria including sex, parent consanguinity, number of hospitalization, age of the first symptom were evaluated in both groups related to AAT level.
Results: The mean serum level of AAT in the case and control groups were 1.3±0.29; 1.5 ±0.59, respectively with statistical significance (P=0.001). There was a significant difference between the two groups in the AAT level distribution, according to AAT normal range (p=0.01). The case group had a more positive attitude toward consanguinity than the control group (66.7% versus 33.3%; P<0.001). The results showed that 80% of patients had the first symptom of disease under 1 year of age, 6.6% 1- 5 years, 6.6% 5- 10 years, and 6.6% in more than 10 years old. In the case group, 53.3% had a history of medical hospitalization for one time, 26.7% two times, while 20% of the patients had no medical hospitalization.
Conclusion: Decreased AAT serum level and high consanguinity rates may be considered as two risk factors for idiopathic bronchiectasis occurrence in children. |
format |
article |
author |
Maryam Babaei Zahra Kanannejad Soheila Alyasin |
author_facet |
Maryam Babaei Zahra Kanannejad Soheila Alyasin |
author_sort |
Maryam Babaei |
title |
Evaluation of Alpha-1 antitrypsin level in the serum of children with idiopathic bronchiectasis |
title_short |
Evaluation of Alpha-1 antitrypsin level in the serum of children with idiopathic bronchiectasis |
title_full |
Evaluation of Alpha-1 antitrypsin level in the serum of children with idiopathic bronchiectasis |
title_fullStr |
Evaluation of Alpha-1 antitrypsin level in the serum of children with idiopathic bronchiectasis |
title_full_unstemmed |
Evaluation of Alpha-1 antitrypsin level in the serum of children with idiopathic bronchiectasis |
title_sort |
evaluation of alpha-1 antitrypsin level in the serum of children with idiopathic bronchiectasis |
publisher |
Tehran University of Medical Sciences |
publishDate |
2021 |
url |
https://doaj.org/article/e64febfcf6b54a14bd303b8af532add3 |
work_keys_str_mv |
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