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Impact of PNPLA3 (rs738409-G) polymorphism on post-transplant outcomes after liver transplantation for alcohol-related liver disease
被引:0
作者:
Yoo, Tae
[1
,2
]
Lee, Kwang-Woong
[1
]
Yi, Nam-Joon
[1
]
Hong, Suk Kyun
[1
]
Lee, Jeong-Moo
[1
]
Kim, Hyeyoung
[3
]
Lim, Jieun
[1
]
Seo, Sooin
[1
]
Suh, Kyung-Suk
[1
]
机构:
[1] Seoul Natl Univ, Coll Med, Dept Surg, 101 Daehak No, Seoul 110744, South Korea
[2] Hallym Univ, Coll Med, Dept Surg, Gyeonggi Do, South Korea
[3] Eulji Univ, Coll Med, Dept Surg, Daejeon, South Korea
关键词:
alcohol recidivism;
alcoholic liver disease;
liver transplantation;
RELAPSE;
RISK;
ASSOCIATION;
BIOMARKERS;
CIRRHOSIS;
VARIANT;
GRAFT;
D O I:
10.1111/ctr.14011
中图分类号:
R61 [外科手术学];
学科分类号:
摘要:
Introduction We aimed to evaluate the association between PNPLA3 polymorphism and post-liver transplantation (LT) outcomes related to alcohol relapse (AR). Method We retrospectively analyzed data from patients receiving LT for alcoholic liver disease (ALD) from 04/2014 to 12/2017. Liver-related clinical outcomes were assessed by the gamma-glutamyltransferase (GGT) level and alcohol-related liver failure (ARLF). Genotyping was performed using prospectively collected DNA samples in both donors and recipients. Results A total of 83 recipients were enrolled. Post-LT AR occurred in 31 patients (37.3%). Thirty-one patients (14 AR, 9 abstainers) showed elevated GGT levels, and 3 AR patients experienced ARLF. In the multivariate analysis, rs738409 G allele carrier and heavy drinking (HRAR score >= 4) were independent risk factors for elevated GGT levels (odds ratio [OR] = 8.69,P < .01; OR = 13.07,P = .01) and ARLF (OR = 4.52,P = .04; OR = 19.62,P = .03). Among 15 heavy AR patients, being an rs738409 G allele carrier was related to GGT elevation (P = .03) and ARLF (P = .04), but it was not related to GGT elevation in mild drinkers (n = 16) or abstainers (n = 52). Conclusion PNPLA3 polymorphism of the recipient genotype can independently affect the post-LT prognosis of LT patients for ALD, especially in heavy AR patients. Therefore, strong abstinence education is recommended in patients with this single nucleotide polymorphism.
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