The Role of Nutrition as a Determinant of Immune Function and Pharmacological Outcome Amongst HIV Infected Malnourished Children in Uganda
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Child Nutrition Disorders
- Sponsor
- Infectious Diseases Institute
- Enrollment
- 150
- Locations
- 2
- Primary Endpoint
- Changes in numbers of circulating immune cell population and their capacity to release cytokines
- Last Updated
- 11 years ago
Overview
Brief Summary
This will be cohort study design with both qualitative and quantitative methods of data collection. The investigators are aiming to study 64 HIV positive children as healthy controls either initiating ART or already on ART and 86 malnourished HIV infected children on ART or naïve initiating ART and RUTF aged between 6 months to 12 years. Primary carers will be asked to provide informed consent whereby the children and primary carers will be enrolled into the study and followed up for 12 weeks.
Detailed Description
BACKGROUND: Malnutrition and Human Immunodeficiency Virus (HIV) infection are intimately linked and present a serious health challenge in Africa. Approximately 30-50% of children in Uganda with severe acute malnutrition (SAM) are HIV infected. Studies on nutrition as a determinant of immune response and drug metabolism in malnourished children are unknown. GAP: Clinicians have noted that certain patients deteriorate after starting ART and nutritional supplementation despite viralogical suppression and immunological improvement with a paradoxical emergence of certain opportunistic infections, electrolyte derangement and malnutrition hence IRIS or re-feeding syndrome (RF). There is paucity of data on nutrition as a determinant of immune and pharmacological response amongst HIV infected malnourished children despite malnutrition being common. HYPOTHESIS: Well-nourished HIV infected children ART naïve or experienced will have a better nutritional, clinical, immunological and pharmacological outcome than malnourished children ART naïve or experienced. METHODS: A cohort design studying 75 malnourished HIV infected children on ART and RUTF comparing them to 75 well-nourished children ART naive or experienced aged between 6 months to 12 years after primary carers have provided informed consent will be enrolled into the study and followed up for 12 weeks. IMPACT: This study will endeavor to provide appropriate information that will enhance the management of malnourished HIV infected children in the context of both ART and RUTF and their impact on immune response and drug metabolism. The study will also generate other research questions that need to be addressed in order to optimize HIV services amongst malnourished children.
Investigators
Infectious Diseases Institute
PhD Candidate
Makerere University
Eligibility Criteria
Inclusion Criteria
- •HIV-infected children aged 6 months to 12 years, including Well Nourished (WN), Moderately Acute Malnutrition (MAM) and Severe Acute Malnutrition (SAM) patients initiating on ART within 2 weeks, whose carer is aged ≥18 years and has provided informed consent.
- •Malnourished HIV-infected children aged 6 months to 12 years stabilized on ART for at least 6 months and initiating on RUTF, whose carer is aged ≥18 years and has provided informed consent.
Exclusion Criteria
- •Previous enrollment in a nutritional therapeutic program in the last 3 months
- •Children involved in an on-going nutrition study
- •Children who have previously received the tuberculin skin test (TST) or mantoux or purified protein derivative (PPD) in the last 3 months.
- •Children with clinically suspected or confirmed malignancy
- •Children exhibiting any specific food intolerance
- •Children who are vomiting profusely (over 3 times daily)
- •Children living outside 50 km radius from Infectious Diseases Institute at Mulago, Kampala
- •Children whose carers do not want to disclose their home address.
- •Children whose cause of malnutrition is compounded by congenital malformations, chromosomal disorders, metabolic disorders, congenital immune disorders, cerebral palsy
- •Children with a severe disability limiting the possibility of investigations
Outcomes
Primary Outcomes
Changes in numbers of circulating immune cell population and their capacity to release cytokines
Time Frame: 12 weeks
Immune response
Secondary Outcomes
- Occurrence of Immune reconstitution inflammatory syndrome (IRIS)(12 weeks)
- Pharmacological: Cmax(12 weeks)
- Number of participants with adverse events(12 weeks)
- Occurrence of re-feeding syndrome(12 weeks)
- Pharmacological: AUC(12 weeks)