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Lysosomal Acid Lipase Activity Is Reduced Both in Cryptogenic Cirrhosis and in Cirrhosis of Known Etiology

Lysosomal acid lipase deficiency (LAL-d) is a rare autosomal recessive disease in which LAL activity is almost absent, with consequent massive microvesicular steatosis evolving to cirrhosis and liver failure. We aimed to determine LAL-activity, and to investigate the most common single nucleotide po...

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Autores principales: Vespasiani-Gentilucci, Umberto, Gallo, Paolo, Piemonte, Fiorella, Riva, Elisabetta, Porcari, Aldostefano, Vorini, Ferruccio, Tozzi, Giulia, Piccioni, Livia, Galati, Giovanni, De Vincentis, Antonio, Carotti, Simone, Morini, Sergio, D’Amico, Jessica, Angeletti, Silvia, Pedone, Claudio, Picardi, Antonio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4878774/
https://www.ncbi.nlm.nih.gov/pubmed/27219619
http://dx.doi.org/10.1371/journal.pone.0156113
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author Vespasiani-Gentilucci, Umberto
Gallo, Paolo
Piemonte, Fiorella
Riva, Elisabetta
Porcari, Aldostefano
Vorini, Ferruccio
Tozzi, Giulia
Piccioni, Livia
Galati, Giovanni
De Vincentis, Antonio
Carotti, Simone
Morini, Sergio
D’Amico, Jessica
Angeletti, Silvia
Pedone, Claudio
Picardi, Antonio
author_facet Vespasiani-Gentilucci, Umberto
Gallo, Paolo
Piemonte, Fiorella
Riva, Elisabetta
Porcari, Aldostefano
Vorini, Ferruccio
Tozzi, Giulia
Piccioni, Livia
Galati, Giovanni
De Vincentis, Antonio
Carotti, Simone
Morini, Sergio
D’Amico, Jessica
Angeletti, Silvia
Pedone, Claudio
Picardi, Antonio
author_sort Vespasiani-Gentilucci, Umberto
collection PubMed
description Lysosomal acid lipase deficiency (LAL-d) is a rare autosomal recessive disease in which LAL activity is almost absent, with consequent massive microvesicular steatosis evolving to cirrhosis and liver failure. We aimed to determine LAL-activity, and to investigate the most common single nucleotide polymorphism (SNP) affecting the LIPA gene and responsible for 50–70% of LAL-d cases (rs116928232 c.894G>A), in patients with cryptogenic cirrhosis. Sixty-three patients with cryptogenic cirrhosis, 88 cirrhotics of known etiology, and 97 healthy subjects were enrolled. LAL-activity was determined in dried-blood-spot (DBS). The c.894G>A mutation was analyzed by pyrosequencing method in SNP mode. LAL-activity was severely reduced in patients with cryptogenic cirrhosis with respect to healthy subjects [0.62 (0.44–0.86) Vs 0.96 (0.75–1.25) nmol/spot/h, p<0.001)], but it was also reduced in known-etiology cirrhotics [0.54 (0.42–0.79) nmol/spot/h, p<0.001 Vs healthy subjects; p = 0.5 Vs cryptogenic cirrhotics]. Fourteen percent of cryptogenic cirrhotics and 20% of known-etiology cirrhotics showed a LAL-activity in the range of heterozygous carriers of LIPA gene mutations (0.15–0.40 nmol/spot/h). However, none of the subjects with reduced LAL-activity carried the c.894G>A SNP except for one patient with HCV cirrhosis. By multivariate analysis, LAL-activity was not associated with age, sex, liver enzymes, liver function or lipid parameters, while it was independently associated with white blood cell (β = 0.2; p<0.01) and platelet (β = 0.4; p<0.001) counts and with the condition of cirrhosis (β = -0.2; p = 0.04). CONCLUSION: Liver cirrhosis is characterized by a severe acquired reduction of LAL-activity, the precise causes and consequences of which need to be further addressed. DBS-determined lysosomal enzyme activities seem to be affected by white blood cell and platelet counts, and the specificity of these tests can be reduced when applied to determined populations, such as cirrhotics.
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spelling pubmed-48787742016-06-09 Lysosomal Acid Lipase Activity Is Reduced Both in Cryptogenic Cirrhosis and in Cirrhosis of Known Etiology Vespasiani-Gentilucci, Umberto Gallo, Paolo Piemonte, Fiorella Riva, Elisabetta Porcari, Aldostefano Vorini, Ferruccio Tozzi, Giulia Piccioni, Livia Galati, Giovanni De Vincentis, Antonio Carotti, Simone Morini, Sergio D’Amico, Jessica Angeletti, Silvia Pedone, Claudio Picardi, Antonio PLoS One Research Article Lysosomal acid lipase deficiency (LAL-d) is a rare autosomal recessive disease in which LAL activity is almost absent, with consequent massive microvesicular steatosis evolving to cirrhosis and liver failure. We aimed to determine LAL-activity, and to investigate the most common single nucleotide polymorphism (SNP) affecting the LIPA gene and responsible for 50–70% of LAL-d cases (rs116928232 c.894G>A), in patients with cryptogenic cirrhosis. Sixty-three patients with cryptogenic cirrhosis, 88 cirrhotics of known etiology, and 97 healthy subjects were enrolled. LAL-activity was determined in dried-blood-spot (DBS). The c.894G>A mutation was analyzed by pyrosequencing method in SNP mode. LAL-activity was severely reduced in patients with cryptogenic cirrhosis with respect to healthy subjects [0.62 (0.44–0.86) Vs 0.96 (0.75–1.25) nmol/spot/h, p<0.001)], but it was also reduced in known-etiology cirrhotics [0.54 (0.42–0.79) nmol/spot/h, p<0.001 Vs healthy subjects; p = 0.5 Vs cryptogenic cirrhotics]. Fourteen percent of cryptogenic cirrhotics and 20% of known-etiology cirrhotics showed a LAL-activity in the range of heterozygous carriers of LIPA gene mutations (0.15–0.40 nmol/spot/h). However, none of the subjects with reduced LAL-activity carried the c.894G>A SNP except for one patient with HCV cirrhosis. By multivariate analysis, LAL-activity was not associated with age, sex, liver enzymes, liver function or lipid parameters, while it was independently associated with white blood cell (β = 0.2; p<0.01) and platelet (β = 0.4; p<0.001) counts and with the condition of cirrhosis (β = -0.2; p = 0.04). CONCLUSION: Liver cirrhosis is characterized by a severe acquired reduction of LAL-activity, the precise causes and consequences of which need to be further addressed. DBS-determined lysosomal enzyme activities seem to be affected by white blood cell and platelet counts, and the specificity of these tests can be reduced when applied to determined populations, such as cirrhotics. Public Library of Science 2016-05-24 /pmc/articles/PMC4878774/ /pubmed/27219619 http://dx.doi.org/10.1371/journal.pone.0156113 Text en © 2016 Vespasiani-Gentilucci et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Vespasiani-Gentilucci, Umberto
Gallo, Paolo
Piemonte, Fiorella
Riva, Elisabetta
Porcari, Aldostefano
Vorini, Ferruccio
Tozzi, Giulia
Piccioni, Livia
Galati, Giovanni
De Vincentis, Antonio
Carotti, Simone
Morini, Sergio
D’Amico, Jessica
Angeletti, Silvia
Pedone, Claudio
Picardi, Antonio
Lysosomal Acid Lipase Activity Is Reduced Both in Cryptogenic Cirrhosis and in Cirrhosis of Known Etiology
title Lysosomal Acid Lipase Activity Is Reduced Both in Cryptogenic Cirrhosis and in Cirrhosis of Known Etiology
title_full Lysosomal Acid Lipase Activity Is Reduced Both in Cryptogenic Cirrhosis and in Cirrhosis of Known Etiology
title_fullStr Lysosomal Acid Lipase Activity Is Reduced Both in Cryptogenic Cirrhosis and in Cirrhosis of Known Etiology
title_full_unstemmed Lysosomal Acid Lipase Activity Is Reduced Both in Cryptogenic Cirrhosis and in Cirrhosis of Known Etiology
title_short Lysosomal Acid Lipase Activity Is Reduced Both in Cryptogenic Cirrhosis and in Cirrhosis of Known Etiology
title_sort lysosomal acid lipase activity is reduced both in cryptogenic cirrhosis and in cirrhosis of known etiology
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4878774/
https://www.ncbi.nlm.nih.gov/pubmed/27219619
http://dx.doi.org/10.1371/journal.pone.0156113
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