Llorenç Caballeria

Dr. Llorenç Caballeria

Institut Català de la Salut
orcid

Research Focus & Metrics

Academic Career Length

37Years (1990-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

View All Publications
1 March 2006 in Gastroenterology
Verified
Journal Article
Closed access
APAlbert Parés
Albert Parés
LCLlorenç Caballeria
Llorenç Caballeria
JRJuan Rodés
Juan Rodés

1 December 2014 in Gastroenterology
Verified
Journal Article
Closed access
PDF file
WLWillem J Lammers
Willem J Lammers
HBHenk R Van Buuren
Henk R Van Buuren
GHGideon M Hirschfield
Gideon M Hirschfield
HJHarry L A Janssen
Harry L A Janssen
PIPietro Invernizzi
Pietro Invernizzi
GGGlobal PBC Study Group
Global PBC Study Group

1 December 2015 in Gastroenterology
Verified
Journal Article
Closed access
PDF file
WLWillem J. Lammers
Willem J. Lammers
GHGideon M. Hirschfield
Gideon M. Hirschfield
CCChristophe Corpechot
Christophe Corpechot
FNFrederik Nevens
Frederik Nevens
KLKeith D. Lindor
Keith D. Lindor
HBHenk R. van Buuren
Henk R. van Buuren

1 June 1999 in Journal of Hepatology
Verified
Journal Article
Closed access
JMJose M Mato
Jose M Mato
JCJavier Cámara
Javier Cámara
JPJavier Fernández de Paz
Javier Fernández de Paz
LCLlorenç Caballeria
Llorenç Caballeria
SCSusana Coll
Susana Coll
JRJoan Rodés
Joan Rodés

1 July 2018 in Clinical Gastroenterology and Hepatology
Verified
Journal Article
Open access
LCLlorenç Caballeria
Llorenç Caballeria
GPGuillem Pera
Guillem Pera
IPIngrid Cecibel Arteaga Pillasagua
Ingrid Cecibel Arteaga Pillasagua
LRLluís Rodríguez
Lluís Rodríguez
AAAlba Alumà
Alba Alumà
PGPere Ginès
Pere Ginès
Liver fibrosis is the main determinant of long-term outcome in chronic liver diseases. Little is known about the prevalence of liver fibrosis in the general population. The aim of the study was to investigate the prevalence of liver fibrosis in the general adult population with unknown liver disease. This was a population-based, cross-sectional study performed in the Barcelona metropolitan area. Subjects aged 18 to 75 years old were identified randomly from citizens included in the primary health care registry. Of 4866 subjects invited, 3076 participated (63.2%). Liver fibrosis was estimated by measuring liver stiffness (LS) with transient elastography (TE). Liver histology was assessed in 92 subjects with increased LS. Prevalence estimates of increased LS (≥6.8, ≥8.0, and ≥9.0 kPa) were 9.0%, 5.8%, and 3.6%, respectively. The etiology of liver disease was mainly nonalcoholic fatty liver disease (NAFLD), followed by alcohol risk consumption (consumption of ≥21 standard drinking units/wk in men and ≥14 standard drinking units/wk in women). Factors independently associated with increased LS were male sex, abdominal obesity, type 2 diabetes, serum glucose, high-density lipoprotein, and triglyceride levels. Subjects without risk factors for NAFLD or without alcohol risk consumption had a very low prevalence of increased LS. The best cut-off value of LS for significant liver fibrosis (F2-F4) was 9.2 kPa, with high sensitivity and specificity. TE was more accurate than alanine aminotransferase, NAFLD fibrosis score, or Fibrosis 4. An algorithm for screening for liver fibrosis using TE in the community setting is proposed. These findings show a high prevalence of silent liver disease with advanced fibrosis mainly related to NAFLD in adult European subjects without known liver disease. An LS value less than 9.2 kPa predicts the absence of significant liver fibrosis with high accuracy and could be used for screening purposes.

1 April 2000 in Journal of Hepatology
Verified
Journal Article
Closed access
APAlbert Parés
Albert Parés
LCLlorenç Caballeria
Llorenç Caballeria
JRJuan Rodés
Juan Rodés
MBMiquel Bruguera
Miquel Bruguera
Luis RodrigoLuis Rodrigo
Luis Rodrigo
RVRosario Velicia
Rosario Velicia