4.7 Article

Serum Selenium Status as a Diagnostic Marker for the Prognosis of Liver Transplantation

Journal

NUTRIENTS
Volume 13, Issue 2, Pages -

Publisher

MDPI
DOI: 10.3390/nu13020619

Keywords

trace element; liver transplantation; selenoprotein P; glutathione peroxidase; hepatitis C virus

Funding

  1. Deutsche Forschungsgemeinschaft (DFG) [FOR-2558, Scho 849/6-2, CRC/TR 296]
  2. Open Access Publication Fund of Charite-Universitatsmedizin Berlin

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The study reveals that liver cancer patients undergoing transplantation have lower selenium and SELENOP levels compared to healthy subjects, particularly those with ethanol toxicity as the etiology. Non-survivors show a decreasing trend in selenium concentrations, indicating a pronounced selenium deficit in severe liver disease necessitating organ replacement. A recovering selenium status post-surgery is associated with positive prognosis, suggesting that selenium supplementation could support recovery.
The trace element selenium (Se) is taken up from the diet and is metabolized mainly by hepatocytes. Selenoprotein P (SELENOP) constitutes the liver-derived Se transporter. Biosynthesis of extracellular glutathione peroxidase (GPx3) in kidney depends on SELENOP-mediated Se supply. We hypothesized that peri-operative Se status may serve as a useful prognostic marker for the outcome in patients undergoing liver transplantation due to hepatocellular carcinoma. Serum samples from liver cancer patients were routinely collected before and after transplantation. Concentrations of serum SELENOP and total Se as well as GPx3 activity were determined by standardized tests and related to survival, etiology of cirrhosis/carcinoma, preoperative neutrophiles, lymphocytes, thyrotropin (TSH) and Child-Pugh and Model for End-Stage Liver Disease (MELD) scores. A total of 221 serum samples from 79 transplanted patients were available for analysis. The Se and SELENOP concentrations were on average below the reference ranges of healthy subjects. Patients with ethanol toxicity-dependent etiology showed particularly low SELENOP and Se concentrations and GPx3 activity. Longitudinal analysis indicated declining Se concentrations in non-survivors. We conclude that severe liver disease necessitating organ replacement is characterized by a pronounced Se deficit before, during and after transplantation. A recovering Se status after surgery is associated with positive prognosis, and an adjuvant Se supplementation may, thus, support convalescence.

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