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Effects of Camellia tea and herbal tea on cardiometabolic risk in patients with type 2 diabetes mellitus: A systematic review and meta-analysis of randomized controlled trials. | LitMetric

AI Article Synopsis

  • Research on the anti-diabetic effects of camellia and herbal tea in diabetic patients has been reviewed, focusing on randomized trials that assess their impact on various health factors.
  • Sixteen studies involving 832 participants were analyzed, measuring results like body weight, blood glucose levels, and blood pressure, but no significant effects were found on total cholesterol or waist size.
  • While camellia and herbal teas showed moderate benefits for metabolic regulation, further high-quality studies are required to strengthen these findings and inform clinical practice.

Article Abstract

Evidence for the anti-diabetic actions of camellia and herbal tea in diabetic patients has not been summarized. Several data sources were searched for randomized trials assessing the effect of different teas on cardiometabolic risk factors in T2D subjects. Two independent reviewers extracted relevant data and assessed the risk of bias. Results were summarized using mean differences (MDs) based on a random model. Sixteen studies (19 trials, N = 832) fulfilled the eligibility criteria. Mean differences were measured for body weight, body mass index, fasting blood glucose, glycosylated hemoglobin, a homeostatic model for insulin resistance, high and low-density lipoproteins, triglycerides, and systolic and diastolic blood pressure. No effects on total cholesterol and waist circumference were observed when either camellia or herbal tea was consumed. Tea produced moderate regulatory effects on adipose, glycemic control, lipid profiles, and blood pressure. In terms of efficacy, camellia and herbal teas yield different benefits in regulating metabolism. This discovery has some implications for clinical research and drug development. However, more high-quality trials are needed to improve the certainty of our estimates.

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Source
http://dx.doi.org/10.1002/ptr.7572DOI Listing

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