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Assessment of TLL1 variant and risk of hepatocellular carcinoma in Latin Americans and Europeans.
Fu, Siyu; Karim, Dhamina; Prieto, Jhon; Balderramo, Domingo; Ferrer, Javier Diaz; Mattos, Angelo Z; Arrese, Marco; Carrera, Enrique; Oliveira, Jeffrey; Debes, Jose D; Boonstra, Andre.
Afiliación
  • Fu S; Department of Gastroenterology and Hepatology, Erasmus MC University Medical Center, Rotterdam, The Netherlands.
  • Karim D; School of Public Health, University of Minnesota, Minneapolis, MN, USA.
  • Prieto J; Centro de Enfermedades Hepaticas y Digestivas, Bogota, Distrito Capital de Bogota, Colombia.
  • Balderramo D; Hospital Privado Universitario de Córdoba, Instituto Universitario de Ciencias Biomédicas de Córdoba, Cordoba, Argentina.
  • Ferrer JD; Facultad de Medicina, Universidad de San Martin de Porres, Lima, Perú.
  • Mattos AZ; Graduate Program in Medicine: Hepatology, Federal University of Health Sciences of Porto Alegre, Porto Alegre, Brazil.
  • Arrese M; Departamento de Gastroenterología, Facultad de Medicina, Pontificia Universidad Católica de Chile, Santiago, Chile.
  • Carrera E; Hospital Especialidades Eugenio Espejo, Universidad San Francisco de Quito, Quito, Ecuador.
  • Oliveira J; Department of Gastroenterology and Hepatology, Erasmus MC University Medical Center, Rotterdam, The Netherlands.
  • Debes JD; Department of Gastroenterology and Hepatology, Erasmus MC University Medical Center, Rotterdam, The Netherlands; School of Public Health, University of Minnesota, Minneapolis, MN, USA; Department of Medicine, University of Minnesota, Minneapolis, MN, USA.
  • Boonstra A; Department of Gastroenterology and Hepatology, Erasmus MC University Medical Center, Rotterdam, The Netherlands. Electronic address: p.a.boonstra@erasmusmc.nl.
Ann Hepatol ; 29(2): 101181, 2024.
Article en En | MEDLINE | ID: mdl-37981236
ABSTRACT
INTRODUCTION AND

OBJECTIVES:

Tolloid like protein 1 (TLL1) rs17047200 has been reported to be associated with HCC development and liver fibrosis. However, to our knowledge, no studies have been performed on Latin Americans and comparative differences between TLL1 rs17047200 in HCC patients from Latin America and Europe are undefined. MATERIALS AND

METHODS:

Cross-sectional analysis was performed on Latin American and European individuals. We analyzed TLL1 rs17047200 on DNA from 1194 individuals, including 420 patients with HCC (86.0 % cirrhotics) and 774 without HCC (65.9 % cirrhotics).

RESULTS:

TLL1 rs17047200 genotype AT/TT was not associated with HCC development in Latin Americans (OR 0.699, 95 %CI 0.456-1.072, p = 0.101) or Europeans (OR 0.736, 95 %CI 0.447-1.211, p = 0.228). TLL1 AT/TT was not correlated with fibrosis stages among metabolic dysfunction-associated steatotic liver disease (MASLD) patients from Latin America (OR 0.975, 95 %CI 0.496-1.918, p = 0.941). Among Europeans, alcohol-related HCC had lower TLL1 AT/TT frequencies than cirrhosis (18.3 % versus 42.3 %, OR 0.273, 95 %CI 0.096-0.773, p = 0.015).

CONCLUSIONS:

We found no evidence that the TLL1 rs17047200 AT/TT genotype is a risk factor for HCC development in Latin Americans or Europeans. A larger study integrating ethnic and etiology backgrounds is needed to determine the importance of the TLL1 SNP in HCC development.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Carcinoma Hepatocelular / Neoplasias Hepáticas Límite: Humans Idioma: En Revista: Ann Hepatol Asunto de la revista: GASTROENTEROLOGIA Año: 2024 Tipo del documento: Article País de afiliación: Países Bajos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Carcinoma Hepatocelular / Neoplasias Hepáticas Límite: Humans Idioma: En Revista: Ann Hepatol Asunto de la revista: GASTROENTEROLOGIA Año: 2024 Tipo del documento: Article País de afiliación: Países Bajos