Donor PNPLA3 and TM6SF2 Variant Alleles Confer Additive Risks for Graft Steatosis After Liver Transplantation
Jazyk angličtina Země Spojené státy americké Médium print
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
31356578
DOI
10.1097/tp.0000000000002876
PII: 00007890-202003000-00019
Knihovny.cz E-zdroje
- MeSH
- acyltransferasy MeSH
- alely MeSH
- alografty patologie MeSH
- biopsie MeSH
- dárci tkání statistika a číselné údaje MeSH
- dospělí MeSH
- fosfolipasy A2 nezávislé na vápníku MeSH
- genotypizační techniky statistika a číselné údaje MeSH
- játra patologie MeSH
- jednonukleotidový polymorfismus MeSH
- lidé středního věku MeSH
- lidé MeSH
- lipasa genetika MeSH
- membránové proteiny genetika MeSH
- mladý dospělý MeSH
- následné studie MeSH
- nealkoholová steatóza jater diagnóza epidemiologie genetika patologie MeSH
- pooperační komplikace diagnóza epidemiologie genetika patologie MeSH
- prevalence MeSH
- příjemce transplantátu statistika a číselné údaje MeSH
- rizikové faktory MeSH
- stupeň závažnosti nemoci MeSH
- transplantace jater škodlivé účinky MeSH
- Check Tag
- dospělí MeSH
- lidé středního věku MeSH
- lidé MeSH
- mladý dospělý MeSH
- mužské pohlaví MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- acyltransferasy MeSH
- fosfolipasy A2 nezávislé na vápníku MeSH
- lipasa MeSH
- membránové proteiny MeSH
- PNPLA3 protein, human MeSH Prohlížeč
- TM6SF2 protein, human MeSH Prohlížeč
BACKGROUND: The rs58542926 polymorphism in transmembrane 6 superfamily member 2 (TM6SF2) is a genetic factor predisposing to nonalcoholic fatty liver disease. We aimed to explore the effect of recipient and donor TM6SF2 rs58542926 genotypes on liver graft fat content after liver transplantation. METHODS: Steatosis was evaluated in liver biopsies from 268 adult recipients. The influence of recipient and donor TM6SF2 genotypes, patatin-like phospholipase domain-containing 3 (PNPLA3) rs738409 genotypes, and nongenetic factors on the steatosis grade assessed 6-30 months after transplantation was analyzed by ordinal logistic regression. RESULTS: The presence of the TM6SF2 c.499A allele in the donor (P = 0.014), PNPLA3 c.444G allele in the donor (P < 0.001), posttransplant body mass index (P < 0.001), and serum triglycerides (P = 0.047) independently predicted increased liver fat content on multivariable analysis, whereas noncirrhotic liver disease, as an indication for liver transplantation, was associated with lower risk of steatosis (P = 0.003). The effects of the donor TM6SF2 A and PNPLA3 G alleles were additive, with an odds ratio of 4.90 (95% confidence interval, 2.01-13.00; P < 0.001), when both minor alleles were present compared with an odds ratio of 2.22 (95% confidence interval, 1.42-3.61; P = 0.002) when only one of these alleles was present. CONCLUSIONS: The donor TM6SF2 c.499A allele is an independent risk factor of liver graft steatosis after liver transplantation that is additive to the effects of donor PNPLA3 c.444G allele.
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