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Clinical Relevance of Liver Involvement in the Clinical Course of Systemic Sclerosis
Liver involvement in systemic sclerosis (SSc) is rare. We evaluated the prevalence of liver fibrosis and hepatic autoimmunity in SSc patients in a retrospective observational cohort (97 SSc or mixed connective tissue disease with sclerodermic manifestations patients undergoing transient elastography...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8879679/ https://www.ncbi.nlm.nih.gov/pubmed/35207242 http://dx.doi.org/10.3390/jcm11040966 |
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author | Lorena, Maria Bellan, Mattia Lepore, Maia Sola, Daniele Pedrazzoli, Roberta Rigamonti, Cristina De Benedittis, Carla Manfredi, Giulia Francesca Acquaviva, Antonio Tonello, Stelvio Rizzi, Manuela Minisini, Rosalba Pirisi, Mario Sainaghi, Pier Paolo |
author_facet | Lorena, Maria Bellan, Mattia Lepore, Maia Sola, Daniele Pedrazzoli, Roberta Rigamonti, Cristina De Benedittis, Carla Manfredi, Giulia Francesca Acquaviva, Antonio Tonello, Stelvio Rizzi, Manuela Minisini, Rosalba Pirisi, Mario Sainaghi, Pier Paolo |
author_sort | Lorena, Maria |
collection | PubMed |
description | Liver involvement in systemic sclerosis (SSc) is rare. We evaluated the prevalence of liver fibrosis and hepatic autoimmunity in SSc patients in a retrospective observational cohort (97 SSc or mixed connective tissue disease with sclerodermic manifestations patients undergoing transient elastography, evaluating liver stiffness (LS) and controlled attenuation parameter (CAP), due to clinical indications along with biochemistry assessments and major antibodies associated to liver autoimmunity). Among them, 11 had LS ≥ 7.5 kPa and 5 showed an LS compatible with cirrhosis (LS ≥ 12.5 kPa). Predictors of LS ≥ 7.5 fibrosis were alcohol consumption (>14 or >7 alcoholic units/week for men and women, respectively), waist circumference (>102 or >88 cm for men and women, respectively), elevated alkaline phosphatase, and anti-La and anti-mitochondrial antibody (AMA) positivity. Six patients had CAP values compatible with severe steatosis (≥280 dB/m). Waist circumference, body mass index and diabetes mellitus were significant predictors of steatosis. Out of 97 patients, 19 were positive for AMA, 4 for anti-Sp100, 1 for anti-Gp210 and 7 were diagnosed with primary biliary cholangitis. Among SSc patients, hepatic fibrosis biomarkers and AMA prevalence are relatively high, suggesting the opportunity of performing a transient elastography and a screening for hepatic autoimmunity at diagnosis and/or during disease progression. |
format | Online Article Text |
id | pubmed-8879679 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-88796792022-02-26 Clinical Relevance of Liver Involvement in the Clinical Course of Systemic Sclerosis Lorena, Maria Bellan, Mattia Lepore, Maia Sola, Daniele Pedrazzoli, Roberta Rigamonti, Cristina De Benedittis, Carla Manfredi, Giulia Francesca Acquaviva, Antonio Tonello, Stelvio Rizzi, Manuela Minisini, Rosalba Pirisi, Mario Sainaghi, Pier Paolo J Clin Med Article Liver involvement in systemic sclerosis (SSc) is rare. We evaluated the prevalence of liver fibrosis and hepatic autoimmunity in SSc patients in a retrospective observational cohort (97 SSc or mixed connective tissue disease with sclerodermic manifestations patients undergoing transient elastography, evaluating liver stiffness (LS) and controlled attenuation parameter (CAP), due to clinical indications along with biochemistry assessments and major antibodies associated to liver autoimmunity). Among them, 11 had LS ≥ 7.5 kPa and 5 showed an LS compatible with cirrhosis (LS ≥ 12.5 kPa). Predictors of LS ≥ 7.5 fibrosis were alcohol consumption (>14 or >7 alcoholic units/week for men and women, respectively), waist circumference (>102 or >88 cm for men and women, respectively), elevated alkaline phosphatase, and anti-La and anti-mitochondrial antibody (AMA) positivity. Six patients had CAP values compatible with severe steatosis (≥280 dB/m). Waist circumference, body mass index and diabetes mellitus were significant predictors of steatosis. Out of 97 patients, 19 were positive for AMA, 4 for anti-Sp100, 1 for anti-Gp210 and 7 were diagnosed with primary biliary cholangitis. Among SSc patients, hepatic fibrosis biomarkers and AMA prevalence are relatively high, suggesting the opportunity of performing a transient elastography and a screening for hepatic autoimmunity at diagnosis and/or during disease progression. MDPI 2022-02-12 /pmc/articles/PMC8879679/ /pubmed/35207242 http://dx.doi.org/10.3390/jcm11040966 Text en © 2022 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 Lorena, Maria Bellan, Mattia Lepore, Maia Sola, Daniele Pedrazzoli, Roberta Rigamonti, Cristina De Benedittis, Carla Manfredi, Giulia Francesca Acquaviva, Antonio Tonello, Stelvio Rizzi, Manuela Minisini, Rosalba Pirisi, Mario Sainaghi, Pier Paolo Clinical Relevance of Liver Involvement in the Clinical Course of Systemic Sclerosis |
title | Clinical Relevance of Liver Involvement in the Clinical Course of Systemic Sclerosis |
title_full | Clinical Relevance of Liver Involvement in the Clinical Course of Systemic Sclerosis |
title_fullStr | Clinical Relevance of Liver Involvement in the Clinical Course of Systemic Sclerosis |
title_full_unstemmed | Clinical Relevance of Liver Involvement in the Clinical Course of Systemic Sclerosis |
title_short | Clinical Relevance of Liver Involvement in the Clinical Course of Systemic Sclerosis |
title_sort | clinical relevance of liver involvement in the clinical course of systemic sclerosis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8879679/ https://www.ncbi.nlm.nih.gov/pubmed/35207242 http://dx.doi.org/10.3390/jcm11040966 |
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