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Effects of simvastatin on pro-inflammatory cytokines in patients with hypercholesterolemia
Barbara Zubelewicz-Szkodzińska1, Janusz Szkodziński, Aleksander Danikiewicz
1Department of Internal Diseases, Silesian Medical Academy, Bytom, Poland.
Insights
Simvastatin significantly reduced interleukin-2 (IL-2) levels in hypercholesterolemia patients, while diet alone decreased tumor necrosis factor-alpha (TNFalpha). Simvastatin further reduced IL-2 but not TNFalpha post-diet.
Area of Science:
- Cardiology
- Immunology
- Pharmacology
Background:
- Inflammation plays a key role in atherosclerosis development.
- Pro-inflammatory cytokines are implicated in cardiovascular disease.
- Cytokine imbalance may contribute to myocardial ischemia.
Purpose of the Study:
- To evaluate the impact of simvastatin on interleukin-2 (IL-2) and tumor necrosis factor-alpha (TNFalpha) levels.
- To assess the effects of simvastatin in patients with hypercholesterolemia.
Main Methods:
- A study involving 64 males with hypercholesterolemia and 10 healthy controls.
- Measurements of lipids, IL-2, and TNFalpha at baseline, after diet, and after simvastatin therapy.
- Comparison of cytokine levels between hypercholesterolemic patients and healthy individuals.
Main Results:
- Simvastatin significantly reduced total and LDL-cholesterol.
- Simvastatin therapy led to a significant decrease in IL-2 plasma concentration.
- Diet significantly decreased TNFalpha serum concentration, with a non-significant further reduction by simvastatin.
Conclusions:
- A hypolipemic diet effectively lowers TNFalpha but does not impact IL-2 levels.
- Simvastatin therapy significantly reduces IL-2 levels compared to post-diet values.
- Simvastatin did not significantly alter TNFalpha levels beyond the effects of diet.
Background:
The role of inflammation in the development of atherosclerosis and its complications has been recently documented. Pro-inflammatory cytokines are among many postulated factors. It is possible that the imbalance between protective cytokines and cytokines affecting endothelial function is one of the underlying mechanisms of myocardial ischaemia.
Aim:
To examine the effects of simvastatin on IL-2 and TNFalpha levels in patients with hypercholesterolemia.
Methods:
The study group consisted of 64 males (age 20-65 years) with hypercholesterolemia. The control group was composed of 10 healthy male volunteers (age 25-40 years) with normal lipid profile. Total cholesterol, LDL-cholesterol, IL-2 and TNFalpha were measured in both groups at baseline, after three months of dietary treatment, and after a further three months of simvastatin therapy.
Results:
Simvastatin caused a significant decrease in the total and LDL-cholesterol levels compared both with baseline measurements (p=0.0001) and after dietary treatment (p=0.0001). Moreover, simvastatin significantly reduced the IL-2 plasma concentration (p=0.0003). There were no significant differences between IL-2 levels before and following dietary treatment. The TNFalpha serum concentration significantly decreased following the implementation of diet (p=0.0001). Subsequent simvastatin therapy caused further decrease in the TNFalpha serum concentration but this difference did not achieve statistical significance.
Conclusions:
A hypolipemic diet significantly decreases TNFalpha serum concentration without affecting the IL-2 level. The subsequent simvastatin therapy significantly reduces IL-2 but not TNFalpha when compared with the post-diet values.
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