Effects of Candesartan on Insulin Sensitivity in Non-Diabetic Obese Individuals
Author Information
Author(s): López-Jaramillo Patricio, Pradilla Lina P, Lahera Vicente, Sieger Federico A Silva, Rueda-Clausen Christian F, Márquez Gustavo A
Primary Institution: Fundación Cardiovascular de Colombia
Hypothesis
Candesartan (32 mg/day during 6 months) has a beneficial effect on fasting plasma glucose, proinflammatory, prothrombotic and oxidative stress markers in non diabetic, non hypertense subjects, with dysglycemia and abdominal obesity.
Conclusion
Candesartan treatment may improve insulin sensitivity and related markers in non-diabetic, non-hypertensive individuals with dysglycemia and abdominal obesity.
Supporting Evidence
- The study involved a sample size of 100 subjects to ensure adequate power.
- Participants received educational, nutritional, and exercise support during the trial.
- Results indicated a potential reduction in insulin resistance markers with Candesartan treatment.
Takeaway
This study looks at whether a medicine called Candesartan can help people who are not diabetic but have high blood sugar and belly fat to use insulin better.
Methodology
A randomized, double blind, cross-over, placebo-controlled clinical trial assessing the effects of Candesartan on various health markers over 6 months.
Potential Biases
Potential biases related to participant selection and adherence to treatment protocols.
Limitations
The study may not be generalizable to all populations due to specific inclusion criteria.
Participant Demographics
Non-diabetic, non-hypertensive individuals with abdominal obesity and dysglycemia, aged over 18.
Statistical Information
P-Value
0.09
Confidence Interval
95% IC- 2 to 42%
Statistical Significance
p<0.05
Digital Object Identifier (DOI)
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