2021
DOI: 10.4254/wjh.v13.i12.1991
|View full text |Cite
|
Sign up to set email alerts
|

De novo and recurrence of metabolic dysfunction-associated fatty liver disease after liver transplantation

Abstract: Metabolic dysfunction-associated fatty liver disease (MAFLD) is a new acronym adopted from the consensus of international experts. Given the increasing prevalence of MAFLD in pre-transplant settings, de novo and recurrent graft steatosis/MAFLD are common in post-transplant settings. The impact of graft steatosis on long-term outcomes is unclear. The current knowledge of incidence rate, risk factors, diagnosis, long-term outcomes, and management of graft steatosis (both de nov… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
3
1
1

Citation Types

0
5
0

Year Published

2023
2023
2025
2025

Publication Types

Select...
4

Relationship

0
4

Authors

Journals

citations
Cited by 4 publications
(5 citation statements)
references
References 80 publications
(124 reference statements)
0
5
0
Order By: Relevance
“…Amongst patients who receive a liver transplant for HCC, MAFLD is an increasingly common cause of underlying liver disease, increasing from 1.3% in 2002–2004 to 8.3% from 2014–2016 in a European registry study [ 146 ]. There were no significant differences in post liver transplant survival outcomes or graft survival outcomes between MAFLD and non-MAFLD recipients reported, either for recipients with or without HCC [ 146 ] although recurrence of MAFLD is known to be common post-transplant [ 147 ]. A United Network for Organ Sharing (UNOS) database did report superior overall survival in patients transplanted for MAFLD, however, in the sub-population who received transplant for HCC, there was no difference in overall survival by liver disease aetiology [ 148 ].…”
Section: Discussionmentioning
confidence: 99%
“…Amongst patients who receive a liver transplant for HCC, MAFLD is an increasingly common cause of underlying liver disease, increasing from 1.3% in 2002–2004 to 8.3% from 2014–2016 in a European registry study [ 146 ]. There were no significant differences in post liver transplant survival outcomes or graft survival outcomes between MAFLD and non-MAFLD recipients reported, either for recipients with or without HCC [ 146 ] although recurrence of MAFLD is known to be common post-transplant [ 147 ]. A United Network for Organ Sharing (UNOS) database did report superior overall survival in patients transplanted for MAFLD, however, in the sub-population who received transplant for HCC, there was no difference in overall survival by liver disease aetiology [ 148 ].…”
Section: Discussionmentioning
confidence: 99%
“…The condition affects approximately 25% of the general population [87], and as mentioned earlier, cirrhosis related to it is becoming the leading cause of liver transplantation [8]. The development of de novo MASL or recurrent graft steatosis is relatively common in LT recipients [88]. In detail, after 5 years from LT, recurrent graft steatosis and NASH may be present in approximately 80% and 60% of patients transplanted for NASH cirrhosis, respectively.…”
Section: De Novo and Recurrent Maslmentioning
confidence: 99%
“…Weight loss drugs are commonly used in overweight or obese patients with NAFLD. Other than orlistat, no other oral weight loss agents have been studied in LT recipients [18]. Newer medications, like glucagon-like peptide 1 (GLP-1) agonists, have shown promising results and have led to significant weight loss, improvement in liver transaminases, and steatosis stage when studied in non-transplant patients with NAFLD but are not yet approved [19].…”
Section: Mitigating the Riskmentioning
confidence: 99%
“…Currently, data on the utility of GLP-1 agonists in patients with post-LT steatosis are lacking, but this is subject to change as these medications undergo more widespread use. Surgical or endoscopic bariatric interventions can also be considered in carefully selected LT patients [18]. Finally, close follow-up with initiation or maintenance of guideline-based drugs for management of type 2 diabetes, hypertension, and dyslipidemia is essential.…”
Section: Mitigating the Riskmentioning
confidence: 99%
See 1 more Smart Citation