Your browser doesn't support javascript.
loading
Significant fibrosis predicts new-onset diabetes mellitus and arterial hypertension in patients with NASH.
Ampuero, Javier; Aller, Rocío; Gallego-Durán, Rocío; Crespo, Javier; Calleja, José Luis; García-Monzón, Carmelo; Gómez-Camarero, Judith; Caballería, Joan; Lo Iacono, Oreste; Ibañez, Luis; García-Samaniego, Javier; Albillos, Agustín; Francés, Rubén; Fernández-Rodríguez, Conrado; Diago, Moisés; Soriano, Germán; Andrade, Raúl J; Latorre, Raquel; Jorquera, Francisco; Morillas, Rosa María; Escudero, Desamparados; Estévez, Pamela; Guerra, Manuel Hernández; Augustín, Salvador; Banales, Jesús M; Aspichueta, Patricia; Benlloch, Salvador; Rosales, José Miguel; Salmerón, Javier; Turnes, Juan; Romero Gómez, Manuel.
Afiliação
  • Ampuero J; Hospital Universitario Virgen del Rocío, Universidad de Sevilla, Sevilla, Spain; SeLiver group, Instituto de Biomedicina de Sevilla, Spain; CIBERehd, Spain. Electronic address: jampuero-ibis@us.es.
  • Aller R; Hospital Clínico Universitario de Valladolid, Centro de Investigación de Endocrinología y Nutrición, Universidad de Valladolid, Spain.
  • Gallego-Durán R; SeLiver group, Instituto de Biomedicina de Sevilla, Spain; CIBERehd, Spain.
  • Crespo J; Hospital Universitario Marqués de Valdecilla, Santander, Spain.
  • Calleja JL; Hospital Universitario Puerta de Hierro, Madrid, Spain.
  • García-Monzón C; Liver Research Unit, Hospital Universitario Santa Cristina Instituto de Investigación Sanitaria Princesa Madrid, Spain.
  • Gómez-Camarero J; Hospital Universitario de Burgos, Spain.
  • Caballería J; CIBERehd, Spain; Liver Unit. Hospital Clínic, Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBPAS), Barcelona, Spain.
  • Lo Iacono O; Hospital Universitario Tajo, Aranjuez, Spain.
  • Ibañez L; CIBERehd, Spain; Hospital Gregorio Marañón, Madrid, Spain.
  • García-Samaniego J; CIBERehd, Spain; Hospital Universitario La Paz, IdiPAZ, Madrid, Spain.
  • Albillos A; CIBERehd, Spain; Hospital Universitario Ramón y Cajal, Madrid, Spain.
  • Francés R; CIBERehd, Spain; Hospital General Universitario de Alicante, Universidad Miguel Hernández, Spain.
  • Fernández-Rodríguez C; Hospital Universitario Fundación de Alcorcón, Universidad Rey Juan Carlos, Spain.
  • Diago M; Hospital General Universitario de Valencia, Spain.
  • Soriano G; Hospital de la Santa Creu i San Pau, Barcelona, Spain.
  • Andrade RJ; CIBERehd, Spain; Unidad de Gestión Clínica de Enfermedades Digestivas, Instituto de Investigación Biomédica de Málaga-IBIMA, Hospital Universitario Virgen de la Victoria, Universidad de Málaga, Málaga, Spain.
  • Latorre R; Hospital Universitari Son Llátzer, Mallorca, Spain.
  • Jorquera F; Servicio de Aparato Digestivo, Complejo Asistencial Universitario de León, IBIOMED y CIBERehd, León, España.
  • Morillas RM; Hospital Germans Trias i Pujol, Badalona, Spain.
  • Escudero D; Hospital Clínico de Valencia, Spain.
  • Estévez P; Complejo Hospitalario Universitario de Vigo, Spain.
  • Guerra MH; Hospital Universitario de Canarias, Santa Cruz de Tenerife, Spain.
  • Augustín S; Hospital Vall d'Hebrón, Barcelona, Spain.
  • Banales JM; CIBERehd, Spain; Department of Liver and Gastrointestinal Diseases, Biodonostia Research Institute - Donostia University Hospital, University of the Basque Country (UPV/EHU), Ikerbasque, San Sebastian, Spain.
  • Aspichueta P; Biocruces Research Institute, Barakaldo, Department of Physiology, Faculty of Medicine and Nursing, University of Basque Country UPV/EHU, Leioa, Spain.
  • Benlloch S; Hospital Universitari i Politecnic La Fe, Valencia, Spain.
  • Rosales JM; Agencia Sanitaria Costa del Sol, Marbella, Spain.
  • Salmerón J; Hospital Universitario San Cecilio, Granada, Spain.
  • Turnes J; Complejo Hospitalario de Pontevedra, Spain.
  • Romero Gómez M; Hospital Universitario Virgen del Rocío, Universidad de Sevilla, Sevilla, Spain; SeLiver group, Instituto de Biomedicina de Sevilla, Spain; CIBERehd, Spain. Electronic address: mromerogomez@us.es.
J Hepatol ; 73(1): 17-25, 2020 07.
Article em En | MEDLINE | ID: mdl-32147361
ABSTRACT
BACKGROUND &

AIMS:

Non-alcoholic fatty liver disease (NAFLD) could play a catalytic role in the development of metabolic comorbidities, although the magnitude of this effect in metabolically healthy patients with NAFLD remains unclear. We assessed the role of biopsy-proven NAFLD on the risk of developing type 2 diabetes mellitus (T2DM) and other metabolic comorbidities (arterial hypertension [AHT], and dyslipidemia) in metabolically healthy patients.

METHODS:

We included 178 metabolically healthy-defined by the absence of baseline T2DM, AHT, dyslipidemia-patients with biopsy-proven NAFLD from the HEPAmet Registry (N = 1,030). Hepamet fibrosis score (HFS), NAFLD fibrosis score, and Fibrosis-4 were calculated. Follow-up was computed from biopsy to the diagnosis of T2DM, AHT, or dyslipidemia.

RESULTS:

During a follow-up of 5.6 ± 4.4 years, T2DM occurred in 9% (16/178), AHT in 8.4% (15/178), low HDL in 9.6% (17/178), and hypertriglyceridemia in 23.6% (42/178) of patients. In multivariate analysis, significant fibrosis predicted T2DM and AHT. Independent variables related to T2DM appearance were significant fibrosis (HR 2.95; 95% CI 1.19-7.31; p = 0.019), glucose levels (p = 0.008), age (p = 0.007) and BMI (p = 0.039). AHT was independently linked to significant fibrosis (HR 2.39; 95% CI 1.14-5.10; p = 0.028), age (p = 0.0001), BMI (p = 0.006), glucose (p = 0.021) and platelets (p = 0.050). The annual incidence rate of T2DM was higher in patients with significant fibrosis (4.4 vs. 1.2 cases per 100 person-years), and increased in the presence of obesity, similar to AHT (4.6 vs. 1.1 cases per 100 person-years). HFS >0.12 predicted the risk of T2DM (25% [4/16] vs. HFS <0.12 4.5% [4/88]; logRank 6.658, p = 0.010).

CONCLUSION:

Metabolically healthy patients with NAFLD-related significant fibrosis were at greater risk of developing T2DM and AHT. HFS >0.12, but not NAFLD fibrosis score or Fibrosis-4, predicted the occurrence of T2DM. LAY

SUMMARY:

Patients with biopsy-proven non-alcoholic fatty liver disease and significant fibrosis were at risk of developing type 2 diabetes mellitus and arterial hypertension. The risk of metabolic outcomes in patients with significant fibrosis was increased in the presence of obesity. In addition to liver biopsy, patients at intermediate-to-high risk of significant fibrosis by Hepamet fibrosis score were at risk of type 2 diabetes mellitus.
Assuntos
Palavras-chave

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Diabetes Mellitus Tipo 2 / Hepatopatia Gordurosa não Alcoólica / Hipertensão / Fígado / Cirrose Hepática Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Diabetes Mellitus Tipo 2 / Hepatopatia Gordurosa não Alcoólica / Hipertensão / Fígado / Cirrose Hepática Idioma: En Ano de publicação: 2020 Tipo de documento: Article