PAGE 3
HIV NUTRITION UPDATE
VOLUME 7, ISSUE 5
 Selenium And HIV Disease
(Continued from page 2)
 

Low levels of selenium are associated with numerous detrimental conditions (Table 2). (2, 4, 5) Research in Miami led to the belief that low levels of selenium might influence HIV disease progression. (9, 10) HIV, as well as other viruses, might reduce the ability to mount an effective immune response by depleting the host's selenium supply. (5) Low selenium is 15 times more significant than low CD4 count as a risk factor for mortality. (10) Baum and colleagues continue to investigate the role of selenium in HIV disease. (12) 
 

SELENIUM DEFICIENCY

Results from numerous cross-sectional studies reported that AIDS patients exhibit clinical selenium deficiency (defined as < 85 micrograms (µg) Se/L) or plasma selenium concentrations lower than non-infected controls. Selenium deficiency reported in HIV-infected patients in both early and end-stage disease (6, 13-17) may be due to reduced intake and absorption and increased use and loss of nutrients. (5) 

In HIV infection, decreased serum or erythrocyte selenium levels have been associated with (1) increased progression to AIDS, (2) greater incidence of OI and (3) decreased survival. Selenium deficiency appears to be related to poor prognosis and to specific clinical characteristics of HIV disease. (9, 18-22) Additionally, it has been demonstrated that selenium deficiency, independent of CD4+ T-cell counts and antiretroviral treatment, is a significant predictor of HIV-related mortality. (9) Of interest to those with HIV and Hepatitis C co-infection, a study by Look and colleagues showed that the decline in selenium levels was greater than that of individuals without Hepatitis C. (21) In pediatric HIV-infection, a low plasma level of selenium is an independent predictor of mortality and appears to be associated with faster disease progression. (23-25) In a three-year, observational study on the effects of highly active antiretroviral therapy (HAART) on micronutrient profiles, the authors concluded that (1) selenium and zinc deficiencies are dependent on immune status and sex and (2) HAART reduced selenium and zinc deficiencies are independent of CD4+ T-cell counts. (26)
 
 

 


 
 
(Continued on page 4)
Results from numerous cross-sectional studies reported that AIDS patients exhibit clinical selenium deficiency (defined as < 85 micrograms (µg) Se/L) or plasma selenium concentrations lower than non-infected controls. 

 
 
 
TABLE 2. CONDITIONS ASSOCIATED WITH SELENIUM DEFICIENCY
Cardiomyopathy
Congestive Heart Failure
Hypothyroid syndrome
Immune dysfunction
Increased risk of thrombosis 
Mycobacterial disease 
Myopathy
Psoriasis


 
 
 

 
 
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3/30/2003