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Donor mannose-binding lectin gene polymorphisms influence the outcome of liver transplantation

✍ Scribed by Carlos Cervera; Domingo Balderramo; Belén Suárez; Jhon Prieto; Francisco Fuster; Laura Linares; Josep Fuster; Asunción Moreno; Francisco Lozano; Miquel Navasa


Publisher
John Wiley and Sons
Year
2009
Tongue
English
Weight
121 KB
Volume
15
Category
Article
ISSN
1527-6465

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✦ Synopsis


Mannose-binding lectin (MBL) is a C-type lectin produced mainly by the liver that binds to a wide range of pathogens. Polymorphisms at the promoter and exon 1 of the MBL2 gene are responsible for low serum levels of MBL and have been associated with an increased risk of infections. We prospectively analyzed 95 liver transplant recipients. Well-known functionally relevant polymorphisms of the MBL2 gene of the liver donor were examined by gene sequencing. Infectious events were collected prospectively. No differences in the incidence of infections were found according to the donor MBL2 genotypes. Survival was lower in patients receiving a liver graft from a donor with an exon 1 MBL2 variant genotype, and they had higher infection-related mortality (50% versus 14%, P ϭ 0.040). No differences were found according to other polymorphisms involving the promoter and 5Ј-untranslated region. When we analyzed bacterial infection episodes, we found that patients receiving a liver from a donor with an exon 1 variant genotype had a higher incidence of septic shock (46% versus 11%, P ϭ 0.004). Independent variables associated with graft or patient survival were as follows: receiving a graft from a donor with an exon 1 MBL2 variant genotype [adjusted hazard ratio (aHR), 9.64; 95% confidence interval (CI), 2.59-36.0], the Model for End-Stage Liver Disease score (aHR, 1.14; 95% CI, 1.05-1.23), and bacterial infections (aHR, 11.1; 95% CI, 2.73-44.9). Liver transplantation from a donor with a variant MBL2 exon 1 genotype was associated with a worse prognosis, mainly because of infections of higher severity.


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