Dyslipidemia as a risk factor for liver fibrosis progression in a multicentric population with non-alcoholic steatohepatitis [version 1; peer review: 2 approved]
Nahum Méndez-Sánchez,
Eira Cerda-Reyes,
Fátima Higuera-de-la-Tijera,
Ana K. Salas-García,
Samantha Cabrera-Palma,
Guillermo Cabrera-Álvarez,
Carlos Cortez-Hernández,
Luis A Pérez-Arredondo,
Emma Purón-González,
Edgar Coronado-Alejandro,
Arturo Panduro,
Heriberto Rodríguez-Hernández,
Vania C. Cruz-Ramón,
Alejandro Valencia-Rodríguez,
Xingshun Qi,
Nashla Hamdan-Pérez,
Nancy E. Aguilar-Olivos,
Beatriz Barranco-Fragoso,
Oscar Ramírez-Pérez,
Alfonso Vera-Barajas
Affiliations
Nahum Méndez-Sánchez
Liver Research Unit, Medica Sur Clinic & Foundation, Mexico City, Mexico, 14050, Mexico
Eira Cerda-Reyes
Department of Gastroenterology, Central Military Hospital, Mexico City, Mexico
Fátima Higuera-de-la-Tijera
Department of Gastroenterology, General Hospital of Mexico "Dr. Eduardo Liceaga", Mexico City, Mexico, Mexico
Ana K. Salas-García
Department of Gastroenterology, General Hospital of Mexico "Dr. Eduardo Liceaga", Mexico City, Mexico, Mexico
Samantha Cabrera-Palma
Liver Clinic, General Regional Hospital IMSS 1, Cuernavaca, Morelos, Mexico
Guillermo Cabrera-Álvarez
Liver Clinic, General Regional Hospital IMSS 1, Cuernavaca, Morelos, Mexico
Carlos Cortez-Hernández
Department of Gastroenterology, University Hospital “Jose Eleuterio González”, Monterrey, Nuevo Leon, Mexico
Luis A Pérez-Arredondo
Department of Gastroenterology, University Hospital “Jose Eleuterio González”, Monterrey, Nuevo Leon, Mexico
Emma Purón-González
Department of Internal Medicine, Christus Muguerza “Super Specialty Hospital”, Monterrey, Nuevo Leon, Mexico
Edgar Coronado-Alejandro
Department of Internal Medicine, Christus Muguerza “Super Specialty Hospital”, Monterrey, Nuevo Leon, Mexico
Arturo Panduro
Department of Molecular Biology in Medicine, Civil Hospital of Guadalajara "Fray Antonio Alcalde”, Guadalajara, Jalisco, Mexico
Heriberto Rodríguez-Hernández
Faculty of Medicine and Nutrition, Juarez University of the State of Durango, Durango, Mexico
Vania C. Cruz-Ramón
Liver Research Unit, Medica Sur Clinic & Foundation, Mexico City, Mexico, 14050, Mexico
Alejandro Valencia-Rodríguez
Liver Research Unit, Medica Sur Clinic & Foundation, Mexico City, Mexico, 14050, Mexico
Xingshun Qi
Department of Gastroenterology, General Hospital of Northern Theater Command, Shenyang, Liaoning, 10016, China
Nashla Hamdan-Pérez
Liver Research Unit, Medica Sur Clinic & Foundation, Mexico City, Mexico, 14050, Mexico
Nancy E. Aguilar-Olivos
Liver Research Unit, Medica Sur Clinic & Foundation, Mexico City, Mexico, 14050, Mexico
Beatriz Barranco-Fragoso
Department of Gastroenterology, National Medical Center "20 Noviembre", Mexico City, Mexico, 03229, Mexico
Oscar Ramírez-Pérez
Liver Research Unit, Medica Sur Clinic & Foundation, Mexico City, Mexico, 14050, Mexico
Alfonso Vera-Barajas
Liver Research Unit, Medica Sur Clinic & Foundation, Mexico City, Mexico, 14050, Mexico
Background: Nonalcoholic fatty liver disease (NAFLD) is a serious worldwide health problem, with an estimated global prevalence of 24%; it has a notable relationship with other metabolic disorders, like obesity and type 2 diabetes mellitus (T2DM). Nonalcoholic steatohepatitis (NASH) is one of the most important clinical entities of NAFLD, which is associated with an increased risk of progression to liver cirrhosis and hepatocellular carcinoma (HCC). Mexico is one of the countries with the highest prevalence of metabolic diseases; therefore, we sought to investigate the impact that these clinical entities have in the progression to advanced fibrosis in Mexican patients with NASH. Methods: We performed a multicenter retrospective cross-sectional study, from January 2012 to December 2017. A total of 215 patients with biopsy-proven NASH and fibrosis were enrolled. NASH was diagnosed according NAS score and liver fibrosis was staged by the Kleiner scoring system. For comparing the risk of liver fibrosis progression, we divided our sample into two groups. Those patients with stage F0-F2 liver fibrosis were included in the group with non-significant liver fibrosis (n=178) and those individuals with F3-F4 fibrosis were included in the significant fibrosis group (n=37). We carried out a multivariate analysis to find risk factors associated with liver fibrosis progression. Results: From the 215 patients included, 37 had significant liver fibrosis (F3-4). After logistic regression analysis T2DM (p=0.044), systemic arterial hypertension (p=0.014), cholesterol (p=0.041) and triglycerides (p=0.015) were the main predictor of advanced liver fibrosis. Conclusions: In a Mexican population, dyslipidemia was the most important risk factor associated with advanced liver fibrosis and cirrhosis.