Literature DB >> 33541866

Caucasian lean subjects with non-alcoholic fatty liver disease share long-term prognosis of non-lean: time for reappraisal of BMI-driven approach?

Ramy Younes1,2,3, Olivier Govaere1, Salvatore Petta4, Luca Miele5,6, Dina Tiniakos1,7, Alastair Burt1, Ezio David3, Fabio Maria Vecchio5,8, Marco Maggioni9, Daniela Cabibi10, Duncan McLeod11, Maria Jesus Pareja12, Anna Ludovica Fracanzani13, Rocio Aller14, Chiara Rosso3, Javier Ampuero15, Rocío Gallego-Durán15, Angelo Armandi3, Gian Paolo Caviglia3, Marco Y W Zaki1,16, Antonio Liguori5, Paolo Francione13, Grazia Pennisi4, Antonio Grieco5,6, Giovanni Birolo3, Piero Fariselli3, Mohammed Eslam17, Luca Valenti18, Jacob George17, Manuel Romero-Gómez15, Quentin Mark Anstee19,20, Elisabetta Bugianesi21.   

Abstract

OBJECTIVE: The full phenotypic expression of non-alcoholic fatty liver disease (NAFLD) in lean subjects is incompletely characterised. We aimed to investigate prevalence, characteristics and long-term prognosis of Caucasian lean subjects with NAFLD.
DESIGN: The study cohort comprises 1339 biopsy-proven NAFLD subjects from four countries (Italy, UK, Spain and Australia), stratified into lean and non-lean (body mass index (BMI) </≥25 kg/m2). Liver/non-liver-related events and survival free of transplantation were recorded during the follow-up, compared by log-rank testing and reported by adjusted HR.
RESULTS: Lean patients represented 14.4% of the cohort and were predominantly of Italian origin (89%). They had less severe histological disease (lean vs non-lean: non-alcoholic steatohepatitis 54.1% vs 71.2% p<0.001; advanced fibrosis 10.1% vs 25.2% p<0.001), lower prevalence of diabetes (9.2% vs 31.4%, p<0.001), but no significant differences in the prevalence of the PNPLA3 I148M variant (p=0.57). During a median follow-up of 94 months (>10 483 person-years), 4.7% of lean vs 7.7% of non-lean patients reported liver-related events (p=0.37). No difference in survival was observed compared with non-lean NAFLD (p=0.069).
CONCLUSIONS: Caucasian lean subjects with NAFLD may progress to advanced liver disease, develop metabolic comorbidities and experience cardiovascular disease (CVD) as well as liver-related mortality, independent of longitudinal progression to obesity and PNPLA3 genotype. These patients represent one end of a wide spectrum of phenotypic expression of NAFLD where the disease manifests at lower overall BMI thresholds. LAY
SUMMARY: NAFLD may affect and progress in both obese and lean individuals. Lean subjects are predominantly males, have a younger age at diagnosis and are more prevalent in some geographic areas. During the follow-up, lean subjects can develop hepatic and extrahepatic disease, including metabolic comorbidities, in the absence of weight gain. These patients represent one end of a wide spectrum of phenotypic expression of NAFLD. © Author(s) (or their employer(s)) 2022. No commercial re-use. See rights and permissions. Published by BMJ.

Entities:  

Keywords:  fatty liver; nonalcoholic steatohepatitis

Mesh:

Year:  2021        PMID: 33541866     DOI: 10.1136/gutjnl-2020-322564

Source DB:  PubMed          Journal:  Gut        ISSN: 0017-5749            Impact factor:   23.059


  19 in total

1.  Metabolic dysfunction-associated fatty liver disease (MAFLD) and non-alcoholic fatty liver disease (NAFLD): distinct fatty liver entities with different clinical outcomes?

Authors:  Eda Kaya; Aleko Zedginidze; Lars Bechmann; Ali Canbay
Journal:  Hepatobiliary Surg Nutr       Date:  2022-04       Impact factor: 7.293

2.  AGA Clinical Practice Update: Diagnosis and Management of Nonalcoholic Fatty Liver Disease in Lean Individuals: Expert Review.

Authors:  Michelle T Long; Mazen Noureddin; Joseph K Lim
Journal:  Gastroenterology       Date:  2022-07-14       Impact factor: 33.883

Review 3.  Metabolic (dysfunction)-associated fatty liver disease in individuals of normal weight.

Authors:  Mohammed Eslam; Hashem B El-Serag; Sven Francque; Shiv K Sarin; Lai Wei; Elisabetta Bugianesi; Jacob George
Journal:  Nat Rev Gastroenterol Hepatol       Date:  2022-06-16       Impact factor: 73.082

4.  What are the clinical settings and outcomes of lean NAFLD?

Authors:  Tian-Yi Ren; Jian-Gao Fan
Journal:  Nat Rev Gastroenterol Hepatol       Date:  2021-05       Impact factor: 46.802

5.  Ammonia Scavenger Restores Liver and Muscle Injury in a Mouse Model of Non-alcoholic Steatohepatitis With Sarcopenic Obesity.

Authors:  Zi-Xuan Wang; Meng-Yu Wang; Rui-Xu Yang; Ze-Hua Zhao; Feng-Zhi Xin; Yu Li; Tian-Yi Ren; Jian-Gao Fan
Journal:  Front Nutr       Date:  2022-03-17

6.  Non-invasive tests for liver fibrosis assessment in patients with chronic liver diseases: a prospective study.

Authors:  Kessarin Thanapirom; Sirinporn Suksawatamnuay; Natthaporn Tanpowpong; Bundit Chaopathomkul; Supachaya Sriphoosanaphan; Panarat Thaimai; Nunthiya Srisoonthorn; Sombat Treeprasertsuk; Piyawat Komolmit
Journal:  Sci Rep       Date:  2022-03-22       Impact factor: 4.379

Review 7.  Beyond the Paradigm of Weight Loss in Non-Alcoholic Fatty Liver Disease: From Pathophysiology to Novel Dietary Approaches.

Authors:  Angelo Armandi; Jörn M Schattenberg
Journal:  Nutrients       Date:  2021-06-08       Impact factor: 5.717

Review 8.  The Potential Role of Cellular Senescence in Non-Alcoholic Fatty Liver Disease.

Authors:  Cornelius Engelmann; Frank Tacke
Journal:  Int J Mol Sci       Date:  2022-01-07       Impact factor: 5.923

Review 9.  NAFLD in normal weight individuals.

Authors:  Johanna K DiStefano; Glenn S Gerhard
Journal:  Diabetol Metab Syndr       Date:  2022-03-24       Impact factor: 5.395

Review 10.  From NAFLD to MAFLD: Aligning Translational In Vitro Research to Clinical Insights.

Authors:  Alexandra Gatzios; Matthias Rombaut; Karolien Buyl; Joery De Kock; Robim M Rodrigues; Vera Rogiers; Tamara Vanhaecke; Joost Boeckmans
Journal:  Biomedicines       Date:  2022-01-12
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