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Low Serum Levels of Alpha(1) Anti-trypsin (α(1)-AT) and Risk of Airflow Obstruction in Non-Primary α(1)-AT-Deficient Patients with Compensated Chronic Liver Disease
BACKGROUND: Alpha(1) anti-trypsin (α(1)-AT), a serine protease inhibitor synthesized in the liver, is a major circulating antiprotease that provides defense against proteolytic damage in several tissues. Its deficiency is associated with airflow obstruction. The present study aimed to explore the ro...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Scientific Literature, Inc.
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4424928/ https://www.ncbi.nlm.nih.gov/pubmed/25913248 http://dx.doi.org/10.12659/MSM.893350 |
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author | Rodríguez-Romero, Elizabeth Suárez-Cuenca, Juan Antonio Elizalde-Barrera, César Iván Mondragón-Terán, Paul Martínez-Hernández, José Enrique Gómez-Cortés, Eduardo de Vaca, Rebeca Pérez-Cabeza Hernández-Muñoz, Rolando E. Melchor-López, Alberto Jiménez-Saab, Nayeli Gabriela |
author_facet | Rodríguez-Romero, Elizabeth Suárez-Cuenca, Juan Antonio Elizalde-Barrera, César Iván Mondragón-Terán, Paul Martínez-Hernández, José Enrique Gómez-Cortés, Eduardo de Vaca, Rebeca Pérez-Cabeza Hernández-Muñoz, Rolando E. Melchor-López, Alberto Jiménez-Saab, Nayeli Gabriela |
author_sort | Rodríguez-Romero, Elizabeth |
collection | PubMed |
description | BACKGROUND: Alpha(1) anti-trypsin (α(1)-AT), a serine protease inhibitor synthesized in the liver, is a major circulating antiprotease that provides defense against proteolytic damage in several tissues. Its deficiency is associated with airflow obstruction. The present study aimed to explore the role of α(1)-AT as a biomarker of airflow performance in chronic liver disease (CLD). MATERIAL/METHODS: Serum α(1)-AT levels and lung function (spirometry) were evaluated in non-primary α(1)-AT-deficient, alcoholic CLD patients without evident respiratory limitations. RESULTS: Thirty-four patients with airflow obstruction (n=11), airflow restriction (n=12), and normal airflow (n=11, age-matched controls) were eligible. α1-AT was decreased in the airflow obstruction group. ROC-cutoff α(1)-AT=24 mg/dL effectively discriminated airflow obstruction (AUC=0.687) and was associated with a 10-fold higher risk (p=0.0007). CONCLUSIONS: Lower α(1)-AT increased the risk of airflow obstruction in CLD patients without primary α(1)-AT deficiency. |
format | Online Article Text |
id | pubmed-4424928 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | International Scientific Literature, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-44249282015-05-11 Low Serum Levels of Alpha(1) Anti-trypsin (α(1)-AT) and Risk of Airflow Obstruction in Non-Primary α(1)-AT-Deficient Patients with Compensated Chronic Liver Disease Rodríguez-Romero, Elizabeth Suárez-Cuenca, Juan Antonio Elizalde-Barrera, César Iván Mondragón-Terán, Paul Martínez-Hernández, José Enrique Gómez-Cortés, Eduardo de Vaca, Rebeca Pérez-Cabeza Hernández-Muñoz, Rolando E. Melchor-López, Alberto Jiménez-Saab, Nayeli Gabriela Med Sci Monit Clinical Research BACKGROUND: Alpha(1) anti-trypsin (α(1)-AT), a serine protease inhibitor synthesized in the liver, is a major circulating antiprotease that provides defense against proteolytic damage in several tissues. Its deficiency is associated with airflow obstruction. The present study aimed to explore the role of α(1)-AT as a biomarker of airflow performance in chronic liver disease (CLD). MATERIAL/METHODS: Serum α(1)-AT levels and lung function (spirometry) were evaluated in non-primary α(1)-AT-deficient, alcoholic CLD patients without evident respiratory limitations. RESULTS: Thirty-four patients with airflow obstruction (n=11), airflow restriction (n=12), and normal airflow (n=11, age-matched controls) were eligible. α1-AT was decreased in the airflow obstruction group. ROC-cutoff α(1)-AT=24 mg/dL effectively discriminated airflow obstruction (AUC=0.687) and was associated with a 10-fold higher risk (p=0.0007). CONCLUSIONS: Lower α(1)-AT increased the risk of airflow obstruction in CLD patients without primary α(1)-AT deficiency. International Scientific Literature, Inc. 2015-04-27 /pmc/articles/PMC4424928/ /pubmed/25913248 http://dx.doi.org/10.12659/MSM.893350 Text en © Med Sci Monit, 2015 This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported License |
spellingShingle | Clinical Research Rodríguez-Romero, Elizabeth Suárez-Cuenca, Juan Antonio Elizalde-Barrera, César Iván Mondragón-Terán, Paul Martínez-Hernández, José Enrique Gómez-Cortés, Eduardo de Vaca, Rebeca Pérez-Cabeza Hernández-Muñoz, Rolando E. Melchor-López, Alberto Jiménez-Saab, Nayeli Gabriela Low Serum Levels of Alpha(1) Anti-trypsin (α(1)-AT) and Risk of Airflow Obstruction in Non-Primary α(1)-AT-Deficient Patients with Compensated Chronic Liver Disease |
title | Low Serum Levels of Alpha(1) Anti-trypsin (α(1)-AT) and Risk of Airflow Obstruction in Non-Primary α(1)-AT-Deficient Patients with Compensated Chronic Liver Disease |
title_full | Low Serum Levels of Alpha(1) Anti-trypsin (α(1)-AT) and Risk of Airflow Obstruction in Non-Primary α(1)-AT-Deficient Patients with Compensated Chronic Liver Disease |
title_fullStr | Low Serum Levels of Alpha(1) Anti-trypsin (α(1)-AT) and Risk of Airflow Obstruction in Non-Primary α(1)-AT-Deficient Patients with Compensated Chronic Liver Disease |
title_full_unstemmed | Low Serum Levels of Alpha(1) Anti-trypsin (α(1)-AT) and Risk of Airflow Obstruction in Non-Primary α(1)-AT-Deficient Patients with Compensated Chronic Liver Disease |
title_short | Low Serum Levels of Alpha(1) Anti-trypsin (α(1)-AT) and Risk of Airflow Obstruction in Non-Primary α(1)-AT-Deficient Patients with Compensated Chronic Liver Disease |
title_sort | low serum levels of alpha(1) anti-trypsin (α(1)-at) and risk of airflow obstruction in non-primary α(1)-at-deficient patients with compensated chronic liver disease |
topic | Clinical Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4424928/ https://www.ncbi.nlm.nih.gov/pubmed/25913248 http://dx.doi.org/10.12659/MSM.893350 |
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