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Effects of Royal Jelly Supplementation in Chronic Kidney Disease

Not Applicable
Recruiting
Conditions
Hemodialysis
Oxidative Stress
Kidney Failure, Chronic
Interventions
Dietary Supplement: Placebo
Dietary Supplement: Real Jelly
Registration Number
NCT06438445
Lead Sponsor
Universidade Federal Fluminense
Brief Summary

The objective of this study is to evaluate the effects of royal jelly on inflammation and cellular senescence in patients with chronic kidney disease (CKD) on hemodialysis (HD).

Detailed Description

Royal jelly is a substance produced in the hypopharyngeal glands of bees that operate young, and rich in bioactive compounds such as polyphenols, free fatty acids and exclusive peptides capable of mitigating inflammation and premature aging (genomic instability, mitochondrial dysfunction, shortening of telomeres) existing in patients with chronic kidney disease (CKD) on hemodialysis. However, to date there are no studies evaluating the effects of royal jelly on such complications in patients with RDC. Objectives: To evaluate the effects of royal jelly on inflammation and cellular senescence in patients with CKD. Methods: Clinical, longitudinal, randomized study, with washout and crossover period. Patients with CKD on HD received 140 mL bottles containing propolis and turmeric, and were instructed to take 10 mL/day (dosing cup), containing a dose equivalent to 110 mg/day of standardized green propolis extract (EPP-AF) plus 130 mg of curcuminoids/day or placebo for 8 weeks. After this supplementation, patients will enter the washout period (8 weeks) and after this period, the intervention group will receive placebo and vice versa. The collection of biological material (blood and feces) will be done before and after each study period. The mRNA expression of the transcription factors Nrf2 and NF-κB, as well as their target genes, antioxidant enzymes, inflammatory cytokines and the expression of genes and proteins that modulate the protein will be evaluated using rtPCR, western blotting and assay methods. multiplex. Uremic toxins from the intestinal microbiota such as indoxyl sulfate (IS), p-cresyl sulfate (p-CS) and Indole-3-acetic acid (IAA) will be confirmed by HPLC and plasma lipopolysaccharide (LPS) levels will be analyzed by ELISA. The determination of antioxidant capacity will be determined by the FRAP, ORAC AND DPPH methods. The analysis of the composition of the intestinal microbiota will be evaluated by high-throughput sequencing of the V4-V5 region of the 16S ribosomal RNA gene. Nutritional status and dietary intake will also be assessed.

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
30
Inclusion Criteria
  • patients with CKD undergoing hemodialysis for more than 6 months
  • patients with arteriovenous fistula (AVF) as vascular access.
Exclusion Criteria
  • pregnant,
  • lactating,
  • smoker
  • patients using antibiotics and antioxidant supplements in the last three months
  • patients with autoimmune and infectious diseases,
  • patients with cancer, liver disease, and AIDS

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Placebo groupPlaceboPatients with chronic kidney disease on hemodialysis will receive capsules containing 500mg of placebo/ day for two months.
Real Jelly GroupReal JellyPatients with chronic kidney disease on hemodialysis will receive capsules containing 500mg of royal jelly/day for two months.
Primary Outcome Measures
NameTimeMethod
Change in inflammatory biomarkers6 weeks

Changes in the mRNA levels of Nrf2, Keap1, Bach1, NLPR3, NF-kB, HO-1, NQO1, p14, p16, p21 and p53 as well as VCAM, ICAM and E-selectin and TLR-4, TNFR and AhR receptors, which will be evaluated from peripheral blood mononuclear cells.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Denise Mafra

🇧🇷

Rio de Janeiro, RJ, Brazil

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