Exploring the Effects of Short-Term Daily Intake of Nitraria retusa Tea on Lipid Profile: A Pre-Post, Uncontrolled Pilot Study in Both Healthy and Overweight/Obese Adults

In the present study, we aimed to explore the feasibility, compliance, and potential benefits of Nitraria retusa extract (NRE) intervention in both healthy (BMI = 24.9 Kg/m(2)) and overweight/obese adults (BMI > 25 Kg/m(2)). A total of 98 participants, including 37 healthy individuals and 61 overweight/obese adults, were randomly assigned to either a low-dose (500 mg/day) or a high-dose (2000 mg/day) NRE intervention group. Plasma lipid biomarkers, liver and kidney functions, general hematology, and blood glucose levels were measured at the baseline and 10 days after intervention. While the lipid profile of the healthy participants did not show any statistically significant changes, the obese participants in the high-dose group experienced a significant decrease in triglyceride levels (within-group difference p value = 0.004) and an increase in HDL levels (within-group p value < 0.001). No significant differences were observed in other parameters, indicating that NRE at the given doses was safe. Furthermore, the study had impressive compliance and acceptability, with over 90% of participants completing the intervention and diligently following the study protocol. This pilot study represents the first investigation into the feasibility, acceptability, and potential benefits of NRE intervention on lipid profiles in human volunteers.

Automated summary

In this study, the feasibility, compliance, and potential benefits of Nitraria retusa extract (NRE) intervention were explored in both healthy and overweight/obese adults. Participants were randomly assigned to either a low-dose or a high-dose NRE intervention group. Results showed that the high-dose group of overweight/obese participants experienced a significant decrease in triglyceride levels and an increase in HDL levels. The study demonstrated good compliance and acceptability, with over 90% of participants completing the intervention.