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Utility of Transient Elastography for the Screening of Liver Disease in Patients with Alpha1-Antitrypsin Deficiency
Screening of liver disease in alpha-1 antitrypsin deficiency (AATD) is usually carried out with liver enzymes, with low sensitivity. We conducted a multicenter cross-sectional study aiming to describe the utility of transient elastography for the identification of liver disease in patients with AATD...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8073267/ https://www.ncbi.nlm.nih.gov/pubmed/33923569 http://dx.doi.org/10.3390/jcm10081724 |
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author | Pons, Mònica Núñez, Alexa Esquinas, Cristina Torres-Durán, María Rodríguez-Hermosa, Juan Luis Calle, Myriam Tubio-Pérez, Ramón Belmonte, Irene Rodríguez-Frías, Francisco Rodríguez, Esther Genescà, Joan Miravitlles, Marc Barrecheguren, Miriam |
author_facet | Pons, Mònica Núñez, Alexa Esquinas, Cristina Torres-Durán, María Rodríguez-Hermosa, Juan Luis Calle, Myriam Tubio-Pérez, Ramón Belmonte, Irene Rodríguez-Frías, Francisco Rodríguez, Esther Genescà, Joan Miravitlles, Marc Barrecheguren, Miriam |
author_sort | Pons, Mònica |
collection | PubMed |
description | Screening of liver disease in alpha-1 antitrypsin deficiency (AATD) is usually carried out with liver enzymes, with low sensitivity. We conducted a multicenter cross-sectional study aiming to describe the utility of transient elastography for the identification of liver disease in patients with AATD. A total of 148 AATD patients were included. Among these, 54.7% were Pi*ZZ and 45.3% were heterozygous for the Z allele. Between 4.9% and 16.5% of patients had abnormal liver enzymes, without differences among genotypes. Liver stiffness measurement (LSM) was significantly higher in Pi*ZZ individuals than in heterozygous Z (5.6 vs. 4.6 kPa; p = 0.001). In total, in 8 (5%) individuals LSM was >7.5 kPa, considered significant liver fibrosis, and ≥10 kPa in 3 (1.9%) all being Pi*ZZ. Elevated liver enzymes were more frequently observed in patients with LSM > 7.5 kPa, but in 5 out of 8 of these patients all liver enzymes were within normal range. In patients with AATD, the presence of abnormal liver enzymes is frequent; however, most of these patients do not present significant liver fibrosis. Transient elastography can help to identify patients with liver fibrosis even with normal liver enzymes and should be performed in all Z-allele carriers to screen for liver disease. |
format | Online Article Text |
id | pubmed-8073267 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-80732672021-04-27 Utility of Transient Elastography for the Screening of Liver Disease in Patients with Alpha1-Antitrypsin Deficiency Pons, Mònica Núñez, Alexa Esquinas, Cristina Torres-Durán, María Rodríguez-Hermosa, Juan Luis Calle, Myriam Tubio-Pérez, Ramón Belmonte, Irene Rodríguez-Frías, Francisco Rodríguez, Esther Genescà, Joan Miravitlles, Marc Barrecheguren, Miriam J Clin Med Article Screening of liver disease in alpha-1 antitrypsin deficiency (AATD) is usually carried out with liver enzymes, with low sensitivity. We conducted a multicenter cross-sectional study aiming to describe the utility of transient elastography for the identification of liver disease in patients with AATD. A total of 148 AATD patients were included. Among these, 54.7% were Pi*ZZ and 45.3% were heterozygous for the Z allele. Between 4.9% and 16.5% of patients had abnormal liver enzymes, without differences among genotypes. Liver stiffness measurement (LSM) was significantly higher in Pi*ZZ individuals than in heterozygous Z (5.6 vs. 4.6 kPa; p = 0.001). In total, in 8 (5%) individuals LSM was >7.5 kPa, considered significant liver fibrosis, and ≥10 kPa in 3 (1.9%) all being Pi*ZZ. Elevated liver enzymes were more frequently observed in patients with LSM > 7.5 kPa, but in 5 out of 8 of these patients all liver enzymes were within normal range. In patients with AATD, the presence of abnormal liver enzymes is frequent; however, most of these patients do not present significant liver fibrosis. Transient elastography can help to identify patients with liver fibrosis even with normal liver enzymes and should be performed in all Z-allele carriers to screen for liver disease. MDPI 2021-04-16 /pmc/articles/PMC8073267/ /pubmed/33923569 http://dx.doi.org/10.3390/jcm10081724 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Pons, Mònica Núñez, Alexa Esquinas, Cristina Torres-Durán, María Rodríguez-Hermosa, Juan Luis Calle, Myriam Tubio-Pérez, Ramón Belmonte, Irene Rodríguez-Frías, Francisco Rodríguez, Esther Genescà, Joan Miravitlles, Marc Barrecheguren, Miriam Utility of Transient Elastography for the Screening of Liver Disease in Patients with Alpha1-Antitrypsin Deficiency |
title | Utility of Transient Elastography for the Screening of Liver Disease in Patients with Alpha1-Antitrypsin Deficiency |
title_full | Utility of Transient Elastography for the Screening of Liver Disease in Patients with Alpha1-Antitrypsin Deficiency |
title_fullStr | Utility of Transient Elastography for the Screening of Liver Disease in Patients with Alpha1-Antitrypsin Deficiency |
title_full_unstemmed | Utility of Transient Elastography for the Screening of Liver Disease in Patients with Alpha1-Antitrypsin Deficiency |
title_short | Utility of Transient Elastography for the Screening of Liver Disease in Patients with Alpha1-Antitrypsin Deficiency |
title_sort | utility of transient elastography for the screening of liver disease in patients with alpha1-antitrypsin deficiency |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8073267/ https://www.ncbi.nlm.nih.gov/pubmed/33923569 http://dx.doi.org/10.3390/jcm10081724 |
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