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Randomized Controlled Trial
. 2011 Aug 13:12:192.
doi: 10.1186/1745-6215-12-192.

Effect of selenium supplementation on CD4 T-cell recovery, viral suppression, morbidity and quality of life of HIV-infected patients in Rwanda: study protocol for a randomized controlled trial

Affiliations
Randomized Controlled Trial

Effect of selenium supplementation on CD4 T-cell recovery, viral suppression, morbidity and quality of life of HIV-infected patients in Rwanda: study protocol for a randomized controlled trial

Julius Kamwesiga et al. Trials. .

Abstract

Background: Low levels of serum selenium are associated with increased risk of mortality among HIV+ patients in East Africa. We aim to assess the effect of selenium supplementation on CD4 cell count, HIV viral load, opportunistic infections, and quality of life in HIV-infected patients in Rwanda.

Methods and design: A 24-month, multi-centre, patient and provider-blinded, randomized, placebo-controlled clinical trial involving 300 pre-antiretroviral therapy (ART) HIV-infected patients will be carried out at two sites in Rwanda. Patients ≥ 21 years of age with documented HIV infection, CD4 cell count of 400-650 cells/mm3, and not yet on ART will be recruited. Patients will be randomized at each study site using a randomized block design to receive either the selenium micronutrient supplement or an identically appearing placebo taken once daily. The primary outcome is a composite of time from baseline to reduction of CD4 T lymphocyte count below 350 cells/mm3 (confirmed by two measures at least one week apart), or start of ART, or the emergence of a documented CDC-defined AIDS-defining illness. An intention-to-treat analysis will be conducted using stepwise regression and structural equation modeling.

Discussion: Micronutrient interventions that aim to improve CD4 cell count, decrease opportunistic infections, decrease HIV viral load, and ultimately delay initiation of more costly ART may be beneficial, particularly in resource-constrained settings, such as sub-Saharan Africa. Additional trials are needed to determine if micro-supplementation can delay the need for more costly ART among HIV-infected patients. If shown to be effective, selenium supplementation may be of public health importance to HIV-infected populations, particularly in sub-Saharan Africa and other resource-constrained settings.

Trial registration: ClinicalTrials.gov NCT01327755.

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Figures

Figure 1
Figure 1
Study flow diagram. This figure displays the intended recruitment and measurement points in this trial.

References

    1. Piwoz EG, Preble EA. A review of the literature and recommendations for nutritional care and support in sub-Saharan Africa. Support for Analysis and Research in Africa, SARA/USAID. 2000.
    1. Semba RD, Tang AM. Micronutrients and the pathogenesis of human immunodeficiency virus infection. Br J Nutr. 1999;81:181–189. doi: 10.1017/S0007114599000379. - DOI - PubMed
    1. Gross RL, Newberne PM. Role of nutrition in immunologic function. Physiol Rev. 1980;60:188–302. - PubMed
    1. Bendich A. Micronutrients and immune responses. Ann N Y Acad Sci. 1990;587:168–180. - PubMed
    1. Beisel WR. Single nutrients and immunity. Am J Clin Nutr. 1982;35(suppl):417–468. - PubMed

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