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Utility and prognostic value of diagnosing MAFLD in patients undergoing liver transplantation for alcohol-related liver disease
被引:4
|作者:
Vanlerberghe, Benedict T. K.
[1
,2
,3
,4
,7
]
van Malenstein, Hannah
[1
,2
]
Sainz-Bariga, Mauricio
[5
,6
]
Jochmans, Ina
[5
,6
]
Cassiman, David
[1
,2
]
Monbaliu, Diethard
[5
,6
]
van der Merwe, Schalk
[1
,2
]
Pirenne, Jacques
[5
,6
]
Nevens, Frederik
[1
,2
]
Verbeek, Jef
[1
,2
]
机构:
[1] Univ Hosp Leuven, Dept Gastroenterol & Hepatol, Leuven, Belgium
[2] Katholieke Univ Leuven, Dept Chron Dis & Metab CHROMETA, Lab Hepatol, Leuven, Belgium
[3] Maastricht Univ, Med Ctr, Dept Internal Med, Div Gastroenterol & Hepatol, Maastricht, Netherlands
[4] Univ Maastricht, Sch Nutr & Translat Res Metab NUTRIM, Maastricht, Netherlands
[5] Univ Leuven, KU Leuven, Lab Abdominal Transplantat, Transplantat Res Grp,Dept Microbiol & Transplantat, Leuven, Belgium
[6] Univ Hosp Leuven, Dept Abdominal Transplant Surg, Leuven, Belgium
[7] Univ Hosp Leuven, Dept Gastroenterol & Hepatol, Herestr 49, B-3000 Leuven, Belgium
关键词:
alcohol-related liver disease;
liver transplantation;
metabolic-dysfunction related liver disease;
METABOLIC SYNDROME;
NONALCOHOLIC STEATOHEPATITIS;
CONSUMPTION;
D O I:
10.1111/ctr.14965
中图分类号:
R61 [外科手术学];
学科分类号:
摘要:
BackgroundRecently, the term metabolic dysfunction-associated fatty liver disease (MAFLD) was proposed to replace non-alcoholic fatty liver disease (NAFLD). This concept enables diagnosing liver disease associated with metabolic dysfunction in patients with alcohol-related liver disease (ALD), a main indication for liver transplantation (LTx). We assessed MAFLD prevalence in ALD patients undergoing LTx and its prognostic value on post-LTx outcomes. MethodsWe retrospectively analyzed all ALD patients transplanted at our center between 1990 and August 2020. MAFLD was diagnosed based on the presence or history of hepatic steatosis and a BMI > 25 or type II diabetes or >= 2 metabolic risk abnormalities at LTx. Overall survival and risk factors for recurrent liver and cardiovascular events were analyzed by Cox regression. ResultsOf the 371 included patients transplanted for ALD, 255 (68.7%) had concomitant MAFLD at LTx. Median follow-up post-LTx was 72 months (IQR: 34.50-122). Patients with ALD-MAFLD were older at LTx (p = .001), more often male (p < .001) and more frequently had hepatocellular carcinoma (p < .001). No differences in perioperative mortality and overall survival were found. ALD-MAFLD patients had an increased risk of recurrent hepatic steatosis, irrespective of alcohol relapse, but no superimposed risk of cardiovascular events. ConclusionsThe co-presence of MAFLD at LTx for ALD is associated with a distinct patient profile and is an independent risk factor for recurrent hepatic steatosis. The use of MAFLD criteria in ALD patients might increase awareness and treatment of specific hepatic and systemic metabolic abnormalities before and after LTx.
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