Glutathione, glutathione peroxidase, and selenium status in HIV-positive and HIV-negative adolescents and young adults

Charles B. Stephensen, Grace S. Marquis, Steven D. Douglas, Laurie A. Kruzich, Craig M. Wilson

Research output: Contribution to journalArticle

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Abstract

Background: Antioxidant nutrient deficiencies may hasten the progression of HIV disease by impairing antioxidant defenses. Objective: The objective of the study was to determine whether HIV infection is associated with poor selenium status and low antioxidant protection by glutathione and glutathione peroxidase (GPX). Design: In a cross-sectional study of 365 HIV-positive and HIV-negative adolescents and young adults, we examined the relation of plasma selenium, whole-blood glutathione, and whole-blood GPX to HIV status, disease severity, immune activation, and oxidative damage. Results: Selenium deficiency (plasma selenium <0.070 μg/mL) was not seen in any subjects, and plasma selenium in 244 HIV-positive subjects (0.120 ± 0.0013 μg/mL) did not differ significantly (P = 0.071) from that in 121 HIV-negative subjects (0.125 ± 0.0020 μg/mL) . However, multiple regression analysis after adjustment for covariates showed a significant (P = 0.002) negative association between HIV-associated immune activation (plasma neopterin) and plasma selenium concentrations. GPX activity was highest in HIV-positive subjects taking antiretroviral therapy (median: 14.2; 25th, 75th percentiles: 11.1, 18.7 U/mL; n = 130), intermediate in HIV-positive subjects not taking antiretroviral therapy (11.8; 9.4, 15.1 U/mL; n = 114), and lowest in HIV-negative subjects (10.6; 8.6, 12.7 U/mL; n = 121; P < 0.05 for all comparisons). GPX was also positively associated with malondialdehyde, a marker of oxidative damage. Conclusions: Subjects had adequate selenium status, although HIV-related immune activation was associated with lower plasma selenium concentrations. GPX activity appears to have been induced by the oxidative stress associated with HIV infection and use of antiretroviral therapy. Thus, young, well-nourished subjects can mount a compensatory antioxidant response to HIV infection.

Original languageEnglish (US)
Pages (from-to)173-181
Number of pages9
JournalAmerican Journal of Clinical Nutrition
Volume85
Issue number1
StatePublished - Jan 1 2007

Fingerprint

Selenium
Glutathione Peroxidase
young adults
glutathione peroxidase
selenium
Glutathione
glutathione
Young Adult
HIV
HIV infections
Antioxidants
HIV Infections
antioxidants
therapeutics
neopterin
blood
nutrient deficiencies
Neopterin
cross-sectional studies
disease severity

Keywords

  • Glutathione
  • Glutathione peroxidase
  • HIV
  • Oxidative stress
  • Selenium

ASJC Scopus subject areas

  • Medicine (miscellaneous)
  • Food Science

Cite this

Stephensen, C. B., Marquis, G. S., Douglas, S. D., Kruzich, L. A., & Wilson, C. M. (2007). Glutathione, glutathione peroxidase, and selenium status in HIV-positive and HIV-negative adolescents and young adults. American Journal of Clinical Nutrition, 85(1), 173-181.

Glutathione, glutathione peroxidase, and selenium status in HIV-positive and HIV-negative adolescents and young adults. / Stephensen, Charles B.; Marquis, Grace S.; Douglas, Steven D.; Kruzich, Laurie A.; Wilson, Craig M.

In: American Journal of Clinical Nutrition, Vol. 85, No. 1, 01.01.2007, p. 173-181.

Research output: Contribution to journalArticle

Stephensen, CB, Marquis, GS, Douglas, SD, Kruzich, LA & Wilson, CM 2007, 'Glutathione, glutathione peroxidase, and selenium status in HIV-positive and HIV-negative adolescents and young adults', American Journal of Clinical Nutrition, vol. 85, no. 1, pp. 173-181.
Stephensen, Charles B. ; Marquis, Grace S. ; Douglas, Steven D. ; Kruzich, Laurie A. ; Wilson, Craig M. / Glutathione, glutathione peroxidase, and selenium status in HIV-positive and HIV-negative adolescents and young adults. In: American Journal of Clinical Nutrition. 2007 ; Vol. 85, No. 1. pp. 173-181.
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