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Selenoprotein P in Patients on Home Parenteral Nutrition

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Background: The purpose of this study was to evaluate the use of selenoprotein P as an indicator of selenium status in patients receiving home parenteral nutrition. Methods: Adult patients (n = 38) who had been on parenteral nutrition with no addition of selenium for 3 to 216 months were included in the study. Plasma samples were analyzed for selenium, selenoprotein P, and extracellular glutathione peroxidase (eGSHPx) using fluorimetry and newly developed radioimmunoassays. Results: The mean plasma (± SD) eGSHPx and selenoprotein P in the patients were 1.9 ± 1.2 mg/L and 0.7 ± 0.4 arbitrary units, respectively, which corresponds to about 50% of the concentration measured in the plasma of the reference subjects (4.0 ± 1.0 mg/L and 1.50 ± 0.17 arbitrary units). The mean plasma selenium concentration was 0.5 ± 0.4 μmol/L, which was approximately half of the concentration measured in the healthy subjects (1.1 ± 0.2 μmol/ L). Thirty‐four (89%) and 20 (53%) patients, respectively, had selenoprotein P and eGSHPx values lower than mean ‐ 2 SD of the reference material. The lowest values observed for selenoprotein P and eGSHPx were 3% and 2% of the reference mean. Selenoprotein P levels correlated significantly to eGSHPx (p = 0.88, p <.0001) and plasma selenium (p = 0.91, p <.0001). Conclusions: The positive correlations between selenoprotein P and eGSHPX and plasma selenium indicates that selenoprotein P may be used as a marker of selenium status in selenium‐depleted patients. (Journal of Parenteral and Enteral Nutrition 20:287–291, 1996)
Title: Selenoprotein P in Patients on Home Parenteral Nutrition
Description:
Background: The purpose of this study was to evaluate the use of selenoprotein P as an indicator of selenium status in patients receiving home parenteral nutrition.
Methods: Adult patients (n = 38) who had been on parenteral nutrition with no addition of selenium for 3 to 216 months were included in the study.
Plasma samples were analyzed for selenium, selenoprotein P, and extracellular glutathione peroxidase (eGSHPx) using fluorimetry and newly developed radioimmunoassays.
Results: The mean plasma (± SD) eGSHPx and selenoprotein P in the patients were 1.
9 ± 1.
2 mg/L and 0.
7 ± 0.
4 arbitrary units, respectively, which corresponds to about 50% of the concentration measured in the plasma of the reference subjects (4.
0 ± 1.
0 mg/L and 1.
50 ± 0.
17 arbitrary units).
The mean plasma selenium concentration was 0.
5 ± 0.
4 μmol/L, which was approximately half of the concentration measured in the healthy subjects (1.
1 ± 0.
2 μmol/ L).
Thirty‐four (89%) and 20 (53%) patients, respectively, had selenoprotein P and eGSHPx values lower than mean ‐ 2 SD of the reference material.
The lowest values observed for selenoprotein P and eGSHPx were 3% and 2% of the reference mean.
Selenoprotein P levels correlated significantly to eGSHPx (p = 0.
88, p <.
0001) and plasma selenium (p = 0.
91, p <.
0001).
Conclusions: The positive correlations between selenoprotein P and eGSHPX and plasma selenium indicates that selenoprotein P may be used as a marker of selenium status in selenium‐depleted patients.
(Journal of Parenteral and Enteral Nutrition 20:287–291, 1996).

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