Hepatocellular carcinoma in patients with metabolic dysfunctionassociated fatty liver disease: Can we stratify at-risk populations?
- Autores
- Fassio, Eduardo; Barreyro, Fernando Javier; Pérez, Mariana Soledad; Dávila, Diana; Landeira, Graciela; Gualano, Gisela; Ruffillo, Gabriela
- Año de publicación
- 2022
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- Metabolic dysfunction-associated fatty liver disease (MAFLD) is a new nomenclature recently proposed by a panel of international experts so that the entity is defined based on positive criteria and linked to pathogenesis, replacing the traditional non-alcoholic fatty liver disease (NAFLD), a definition based on exclusion criteria. NAFLD/MAFLD is currently the most common form of chronic liver disease worldwide and is a growing risk factor for development of hepatocellular carcinoma (HCC). It is estimated than 25% of the global population have NAFLD and is projected to increase in the next years. Major Scientific Societies agree that surveillance for HCC should be indicated in patients with NAFLD/ MAFLD and cirrhosis but differ in non-cirrhotic patients (including those with advanced fibrosis). Several studies have shown that the annual incidence rate of HCC in NAFLD-cirrhosis is greater than 1%, thus surveillance for HCC is cost-effective. Risk factors that increase HCC incidence in these patients are male gender, older age, presence of diabetes and any degree of alcohol consumption. In non-cirrhotic patients, the incidence of HCC is much lower and variable, being a great challenge to stratify the risk of HCC in this group. Furthermore, large epidemiological studies based on the general population have shown that diabetes and obesity significantly increase risk of HCC. Some genetic variants may also play a role modifying the HCC occurrence among patients with NAFLD. The purpose of this review is to discuss the epidemiology, clinical and genetic risk factors that may influence the risk of HCC in NAFLD/MAFLD patients and propose screening strategy to translate into better patient care.
Fil: Fassio, Eduardo. Hospital Nacional Profesor Alejandro Posadas; Argentina
Fil: Barreyro, Fernando Javier. Universidad Nacional de Misiones; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Nordeste; Argentina
Fil: Pérez, Mariana Soledad. Hospital Nacional Profesor Alejandro Posadas; Argentina
Fil: Dávila, Diana. Hospital Nacional Profesor Alejandro Posadas; Argentina
Fil: Landeira, Graciela. Hospital Nacional Profesor Alejandro Posadas; Argentina
Fil: Gualano, Gisela. Hospital Nacional Profesor Alejandro Posadas; Argentina
Fil: Ruffillo, Gabriela. Hospital Nacional Profesor Alejandro Posadas; Argentina - Materia
-
HEPATOCELLULAR CARCINOMA
INCIDENCE OF HEPATOCELLULAR CARCINOMA
METABOLIC DYSFUNCTION-ASSOCIATED FATTY LIVER DISEASE
NONALCOHOLIC STEATOHEPATITIS
SURVEILLANCE FOR HEPATOCELLULAR CARCINOMA - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- https://creativecommons.org/licenses/by-nc/2.5/ar/
- Repositorio
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/215929
Ver los metadatos del registro completo
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CONICET Digital (CONICET) |
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Hepatocellular carcinoma in patients with metabolic dysfunctionassociated fatty liver disease: Can we stratify at-risk populations?Fassio, EduardoBarreyro, Fernando JavierPérez, Mariana SoledadDávila, DianaLandeira, GracielaGualano, GiselaRuffillo, GabrielaHEPATOCELLULAR CARCINOMAINCIDENCE OF HEPATOCELLULAR CARCINOMAMETABOLIC DYSFUNCTION-ASSOCIATED FATTY LIVER DISEASENONALCOHOLIC STEATOHEPATITISSURVEILLANCE FOR HEPATOCELLULAR CARCINOMAhttps://purl.org/becyt/ford/3.2https://purl.org/becyt/ford/3Metabolic dysfunction-associated fatty liver disease (MAFLD) is a new nomenclature recently proposed by a panel of international experts so that the entity is defined based on positive criteria and linked to pathogenesis, replacing the traditional non-alcoholic fatty liver disease (NAFLD), a definition based on exclusion criteria. NAFLD/MAFLD is currently the most common form of chronic liver disease worldwide and is a growing risk factor for development of hepatocellular carcinoma (HCC). It is estimated than 25% of the global population have NAFLD and is projected to increase in the next years. Major Scientific Societies agree that surveillance for HCC should be indicated in patients with NAFLD/ MAFLD and cirrhosis but differ in non-cirrhotic patients (including those with advanced fibrosis). Several studies have shown that the annual incidence rate of HCC in NAFLD-cirrhosis is greater than 1%, thus surveillance for HCC is cost-effective. Risk factors that increase HCC incidence in these patients are male gender, older age, presence of diabetes and any degree of alcohol consumption. In non-cirrhotic patients, the incidence of HCC is much lower and variable, being a great challenge to stratify the risk of HCC in this group. Furthermore, large epidemiological studies based on the general population have shown that diabetes and obesity significantly increase risk of HCC. Some genetic variants may also play a role modifying the HCC occurrence among patients with NAFLD. The purpose of this review is to discuss the epidemiology, clinical and genetic risk factors that may influence the risk of HCC in NAFLD/MAFLD patients and propose screening strategy to translate into better patient care.Fil: Fassio, Eduardo. Hospital Nacional Profesor Alejandro Posadas; ArgentinaFil: Barreyro, Fernando Javier. Universidad Nacional de Misiones; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Nordeste; ArgentinaFil: Pérez, Mariana Soledad. Hospital Nacional Profesor Alejandro Posadas; ArgentinaFil: Dávila, Diana. Hospital Nacional Profesor Alejandro Posadas; ArgentinaFil: Landeira, Graciela. Hospital Nacional Profesor Alejandro Posadas; ArgentinaFil: Gualano, Gisela. Hospital Nacional Profesor Alejandro Posadas; ArgentinaFil: Ruffillo, Gabriela. Hospital Nacional Profesor Alejandro Posadas; ArgentinaBaishideng Publishing Group Inc2022-02info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/215929Fassio, Eduardo; Barreyro, Fernando Javier; Pérez, Mariana Soledad; Dávila, Diana; Landeira, Graciela; et al.; Hepatocellular carcinoma in patients with metabolic dysfunctionassociated fatty liver disease: Can we stratify at-risk populations?; Baishideng Publishing Group Inc; World Journal of Hepatology; 14; 2; 2-2022; 354-3711948-5182CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/doi/10.4254/wjh.v14.i2.354info:eu-repo/semantics/altIdentifier/url/https://www.wjgnet.com/1948-5182/full/v14/i2/354.htminfo:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-03T10:02:07Zoai:ri.conicet.gov.ar:11336/215929instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-09-03 10:02:07.969CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
dc.title.none.fl_str_mv |
Hepatocellular carcinoma in patients with metabolic dysfunctionassociated fatty liver disease: Can we stratify at-risk populations? |
title |
Hepatocellular carcinoma in patients with metabolic dysfunctionassociated fatty liver disease: Can we stratify at-risk populations? |
spellingShingle |
Hepatocellular carcinoma in patients with metabolic dysfunctionassociated fatty liver disease: Can we stratify at-risk populations? Fassio, Eduardo HEPATOCELLULAR CARCINOMA INCIDENCE OF HEPATOCELLULAR CARCINOMA METABOLIC DYSFUNCTION-ASSOCIATED FATTY LIVER DISEASE NONALCOHOLIC STEATOHEPATITIS SURVEILLANCE FOR HEPATOCELLULAR CARCINOMA |
title_short |
Hepatocellular carcinoma in patients with metabolic dysfunctionassociated fatty liver disease: Can we stratify at-risk populations? |
title_full |
Hepatocellular carcinoma in patients with metabolic dysfunctionassociated fatty liver disease: Can we stratify at-risk populations? |
title_fullStr |
Hepatocellular carcinoma in patients with metabolic dysfunctionassociated fatty liver disease: Can we stratify at-risk populations? |
title_full_unstemmed |
Hepatocellular carcinoma in patients with metabolic dysfunctionassociated fatty liver disease: Can we stratify at-risk populations? |
title_sort |
Hepatocellular carcinoma in patients with metabolic dysfunctionassociated fatty liver disease: Can we stratify at-risk populations? |
dc.creator.none.fl_str_mv |
Fassio, Eduardo Barreyro, Fernando Javier Pérez, Mariana Soledad Dávila, Diana Landeira, Graciela Gualano, Gisela Ruffillo, Gabriela |
author |
Fassio, Eduardo |
author_facet |
Fassio, Eduardo Barreyro, Fernando Javier Pérez, Mariana Soledad Dávila, Diana Landeira, Graciela Gualano, Gisela Ruffillo, Gabriela |
author_role |
author |
author2 |
Barreyro, Fernando Javier Pérez, Mariana Soledad Dávila, Diana Landeira, Graciela Gualano, Gisela Ruffillo, Gabriela |
author2_role |
author author author author author author |
dc.subject.none.fl_str_mv |
HEPATOCELLULAR CARCINOMA INCIDENCE OF HEPATOCELLULAR CARCINOMA METABOLIC DYSFUNCTION-ASSOCIATED FATTY LIVER DISEASE NONALCOHOLIC STEATOHEPATITIS SURVEILLANCE FOR HEPATOCELLULAR CARCINOMA |
topic |
HEPATOCELLULAR CARCINOMA INCIDENCE OF HEPATOCELLULAR CARCINOMA METABOLIC DYSFUNCTION-ASSOCIATED FATTY LIVER DISEASE NONALCOHOLIC STEATOHEPATITIS SURVEILLANCE FOR HEPATOCELLULAR CARCINOMA |
purl_subject.fl_str_mv |
https://purl.org/becyt/ford/3.2 https://purl.org/becyt/ford/3 |
dc.description.none.fl_txt_mv |
Metabolic dysfunction-associated fatty liver disease (MAFLD) is a new nomenclature recently proposed by a panel of international experts so that the entity is defined based on positive criteria and linked to pathogenesis, replacing the traditional non-alcoholic fatty liver disease (NAFLD), a definition based on exclusion criteria. NAFLD/MAFLD is currently the most common form of chronic liver disease worldwide and is a growing risk factor for development of hepatocellular carcinoma (HCC). It is estimated than 25% of the global population have NAFLD and is projected to increase in the next years. Major Scientific Societies agree that surveillance for HCC should be indicated in patients with NAFLD/ MAFLD and cirrhosis but differ in non-cirrhotic patients (including those with advanced fibrosis). Several studies have shown that the annual incidence rate of HCC in NAFLD-cirrhosis is greater than 1%, thus surveillance for HCC is cost-effective. Risk factors that increase HCC incidence in these patients are male gender, older age, presence of diabetes and any degree of alcohol consumption. In non-cirrhotic patients, the incidence of HCC is much lower and variable, being a great challenge to stratify the risk of HCC in this group. Furthermore, large epidemiological studies based on the general population have shown that diabetes and obesity significantly increase risk of HCC. Some genetic variants may also play a role modifying the HCC occurrence among patients with NAFLD. The purpose of this review is to discuss the epidemiology, clinical and genetic risk factors that may influence the risk of HCC in NAFLD/MAFLD patients and propose screening strategy to translate into better patient care. Fil: Fassio, Eduardo. Hospital Nacional Profesor Alejandro Posadas; Argentina Fil: Barreyro, Fernando Javier. Universidad Nacional de Misiones; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Nordeste; Argentina Fil: Pérez, Mariana Soledad. Hospital Nacional Profesor Alejandro Posadas; Argentina Fil: Dávila, Diana. Hospital Nacional Profesor Alejandro Posadas; Argentina Fil: Landeira, Graciela. Hospital Nacional Profesor Alejandro Posadas; Argentina Fil: Gualano, Gisela. Hospital Nacional Profesor Alejandro Posadas; Argentina Fil: Ruffillo, Gabriela. Hospital Nacional Profesor Alejandro Posadas; Argentina |
description |
Metabolic dysfunction-associated fatty liver disease (MAFLD) is a new nomenclature recently proposed by a panel of international experts so that the entity is defined based on positive criteria and linked to pathogenesis, replacing the traditional non-alcoholic fatty liver disease (NAFLD), a definition based on exclusion criteria. NAFLD/MAFLD is currently the most common form of chronic liver disease worldwide and is a growing risk factor for development of hepatocellular carcinoma (HCC). It is estimated than 25% of the global population have NAFLD and is projected to increase in the next years. Major Scientific Societies agree that surveillance for HCC should be indicated in patients with NAFLD/ MAFLD and cirrhosis but differ in non-cirrhotic patients (including those with advanced fibrosis). Several studies have shown that the annual incidence rate of HCC in NAFLD-cirrhosis is greater than 1%, thus surveillance for HCC is cost-effective. Risk factors that increase HCC incidence in these patients are male gender, older age, presence of diabetes and any degree of alcohol consumption. In non-cirrhotic patients, the incidence of HCC is much lower and variable, being a great challenge to stratify the risk of HCC in this group. Furthermore, large epidemiological studies based on the general population have shown that diabetes and obesity significantly increase risk of HCC. Some genetic variants may also play a role modifying the HCC occurrence among patients with NAFLD. The purpose of this review is to discuss the epidemiology, clinical and genetic risk factors that may influence the risk of HCC in NAFLD/MAFLD patients and propose screening strategy to translate into better patient care. |
publishDate |
2022 |
dc.date.none.fl_str_mv |
2022-02 |
dc.type.none.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion http://purl.org/coar/resource_type/c_6501 info:ar-repo/semantics/articulo |
format |
article |
status_str |
publishedVersion |
dc.identifier.none.fl_str_mv |
http://hdl.handle.net/11336/215929 Fassio, Eduardo; Barreyro, Fernando Javier; Pérez, Mariana Soledad; Dávila, Diana; Landeira, Graciela; et al.; Hepatocellular carcinoma in patients with metabolic dysfunctionassociated fatty liver disease: Can we stratify at-risk populations?; Baishideng Publishing Group Inc; World Journal of Hepatology; 14; 2; 2-2022; 354-371 1948-5182 CONICET Digital CONICET |
url |
http://hdl.handle.net/11336/215929 |
identifier_str_mv |
Fassio, Eduardo; Barreyro, Fernando Javier; Pérez, Mariana Soledad; Dávila, Diana; Landeira, Graciela; et al.; Hepatocellular carcinoma in patients with metabolic dysfunctionassociated fatty liver disease: Can we stratify at-risk populations?; Baishideng Publishing Group Inc; World Journal of Hepatology; 14; 2; 2-2022; 354-371 1948-5182 CONICET Digital CONICET |
dc.language.none.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
info:eu-repo/semantics/altIdentifier/doi/10.4254/wjh.v14.i2.354 info:eu-repo/semantics/altIdentifier/url/https://www.wjgnet.com/1948-5182/full/v14/i2/354.htm |
dc.rights.none.fl_str_mv |
info:eu-repo/semantics/openAccess https://creativecommons.org/licenses/by-nc/2.5/ar/ |
eu_rights_str_mv |
openAccess |
rights_invalid_str_mv |
https://creativecommons.org/licenses/by-nc/2.5/ar/ |
dc.format.none.fl_str_mv |
application/pdf application/pdf |
dc.publisher.none.fl_str_mv |
Baishideng Publishing Group Inc |
publisher.none.fl_str_mv |
Baishideng Publishing Group Inc |
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reponame:CONICET Digital (CONICET) instname:Consejo Nacional de Investigaciones Científicas y Técnicas |
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CONICET Digital (CONICET) |
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CONICET Digital (CONICET) |
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Consejo Nacional de Investigaciones Científicas y Técnicas |
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CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas |
repository.mail.fl_str_mv |
dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar |
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1842269738809425920 |
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13.13397 |