Effect of Zinc and Selenium Supplementation on HIV+ Individuals on Antiretroviral Treatment.
- Conditions
- Metabolic ComplicationInflammationHIVZinc DeficiencyARTSelenium Deficiency
- Registration Number
- NCT03421314
- Lead Sponsor
- Instituto Nacional de Enfermedades Respiratorias
- Brief Summary
The aim of this study is to evaluate the effect of zinc gluconate and/or selenium yeast supplementation during six months on clinical (glucose, cholesterol, triglycerides, bone mineral density and body composition) and immunological (oxidative stress, CD4+ count and pro-inflammatory cytokines) parameters in a population with HIV diagnosis on antiretroviral treatment.
- Detailed Description
HIV-infected individuals on antiretroviral treatment have lowest risk of AIDS events and more life expectancy. However, antiretroviral treatment does not fully restore the immune system in all individuals due to persistent immune activation and inflammation, increasing the risk of non-AIDS complications, such as insulin resistance, diabetes, hypertension, dyslipidemia, obesity, low bone mass density, oxidative stress and micronutrient deficiencies. Several studies showed that HIV+ patients present zinc and selenium deficiency. Those micronutrients are involved in the pathogenesis of metabolic complications and have a major role in maintaining immune system function. It remains unknown the effect of zinc and selenium supplementation on metabolic and immunological parameters associated to non-AIDS complications.
Recruitment & Eligibility
- Status
- UNKNOWN
- Sex
- Male
- Target Recruitment
- 37
- HIV infected
- >200 CD4+ cells/mL
- >2 years under antiretroviral treatment
- >2 years under virology control (HIV RNA <40 copies/mL)
- Patients with opportunistic infection
- Patients taking vitamin-mineral supplements
- Patients with moderate or high cardiovascular risk (Framingham score higher than 10%) and cholesterol LDL >190 mg/dL or triglycerides >500 mg/dL.
- Patients with diabetes or hypertension diagnosis.
- Patients taking drugs for diabetes, hypertension, dyslipidemia or low bone mass density.
- Low adherence to supplementation.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Primary Outcome Measures
Name Time Method Changes from baseline in zinc and selenium plasmatic levels Baseline and 24 weeks We evaluated the effects of zinc (30mg/d) and selenium (200μg/d) supplementation on plasma zinc and selenium levels.
- Secondary Outcome Measures
Name Time Method Counts of CD4+ T cells Baseline,12 and 24 weeks Changes in LDL cholesterol Baseline,12 and 24 weeks in mg/dL
Changes in triglycerides Baseline,12 and 24 weeks in mg/dL
Frequency of CD4+ T cells Baseline,12 and 24 weeks Measure by flow cytometry
Changes in HDL cholesterol Baseline,12 and 24 weeks in mg/dL
Changes in fat mass Baseline,12 and 24 weeks in Kg
Changes in fasting serum glucose Baseline,12 and 24 weeks Changes in and bone mineral density Baseline,12 and 24 weeks g/cm3
Changes in lipid peroxidation Baseline and 24 weeks Measure by TBARS
Changes in proinflammatory cytokine profile Baseline and 24 weeks Measure by LUMINEX
Changes in total cholesterol Baseline,12 and 24 weeks in mg/dL
Changes in blood pressure Baseline,12 and 24 weeks Changes in bone metabolism biomarkers Baseline and 24 weeks Changes in osteoprotegerin and RANKL levels
Changes in lean soft tissue Baseline,12 and 24 weeks in Kg
Changes in body weight Baseline,12 and 24 weeks in Kg
Related Research Topics
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Trial Locations
- Locations (1)
Centro de Investigaciones en Enfermedades Infecciosas
🇲🇽Mexico city, DF, Mexico
Centro de Investigaciones en Enfermedades Infecciosas🇲🇽Mexico city, DF, MexicoIvan Osuna Padilla, MDSub InvestigatorGustavo Reyes-Terán, MDPrincipal InvestigatorOlivia Briceño Cárdenas, PhDSub InvestigatorNadia Rodriguez Moguel, MDSub InvestigatorAdriana Aguilar Vargas, MDSub Investigator