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Atorvastatin effect on circulating and leukocyte-produced CD40 ligand concentrations in people with normal
Issam Zineh1, Gregory J Welder, Amy E DeBella
1Department of Pharmacy Practice and Center for Pharmacogenomics, College of Pharmacy, University of Florida, Gainesville, Florida 32610, USA. zineh@cop.ufl.edu
Insights
Atorvastatin significantly reduced leukocyte-produced CD40 ligand (CD40L) in normocholesterolemic individuals, independent of cholesterol reduction. These findings suggest a potential benefit of atorvastatin beyond lipid lowering, warranting further investigation in non-dyslipidemic populations.
Area of Science:
- Cardiovascular Pharmacology
- Immunology
- Lipid Metabolism
Background:
- CD40 ligand (CD40L) plays a role in atherothrombosis.
- Statins are primarily used to lower low-density lipoprotein cholesterol (LDL).
- The effect of statins on CD40L in individuals without dyslipidemia is not well understood.
Purpose of the Study:
- To determine if atorvastatin reduces serum and leukocyte-produced CD40L levels.
- To assess if these effects are dependent on LDL cholesterol reduction.
- To investigate atorvastatin's impact in normocholesterolemic individuals.
Main Methods:
- Prospective pilot study involving 25 normocholesterolemic volunteers.
- Atorvastatin 80 mg/day administered orally for 16 weeks.
- Measurement of serum and leukocyte-produced CD40L concentrations and lipid profiles.
Main Results:
- Atorvastatin significantly reduced leukocyte-produced CD40L by 57% (p=0.045).
- Serum CD40L levels showed a non-significant decrease.
- Lipid-lowering effects included a 59% reduction in LDL cholesterol.
- Observed CD40L reduction was independent of LDL cholesterol changes.
Conclusions:
- Atorvastatin effectively reduces leukocyte-derived CD40L production in normocholesterolemic individuals.
- This effect appears independent of LDL cholesterol reduction.
- Further research is warranted to explore the potential cardiovascular benefits of atorvastatin in this population.
Study Objectives:
To investigate whether atorvastatin decreases serum or leukocyte-produced CD40 ligand (CD40L) levels and whether these effects are dependent on reduction in low-density lipoprotein cholesterol (LDL) levels in people without overt dyslipidemia.
Design:
Prospective pilot study.
Setting:
University research center.
Subjects:
Twenty-five normocholesterolemic volunteers (mean age 32 +/- 11 yrs; 15 women, 10 men) without cardiovascular disease.
Intervention:
After a 2-week drug-free run-in period, subjects received atorvastatin 80 mg/day orally for 16 weeks.
Measurements And Main Results:
All lipoprotein level measurements were performed with the subject in the fasting state. The CD40L concentrations were measured by immunofluorescence detection in serum and leukocyte culture supernates after 24-hour incubation, and treatment effect was analyzed. Baseline mean +/- SD total cholesterol, LDL, high-density lipoprotein cholesterol, and triglyceride levels were 179 +/- 33, 97 +/- 29, 62 +/- 20, and 102 +/- 69 mg/dl, respectively. Mean changes in each of these levels, respectively, after 16 weeks of atorvastatin were -34%, -59%, +3%, and -23%. The median serum CD40L level was lower at 16 weeks (2.3 ng/ml, interquartile range [IQR] 1.2-5.0 ng/ml) than at baseline (3.0 ng/ml, IQR 2.1-3.7 ng/ml), but the change was not significant (p=0.24). However, atorvastatin significantly lowered CD40L produced from leukocytes by 57% (21 pg/mg of protein [IQR 10-38 pg/mg] vs 49 pg/mg [IQR 21-149 pg/mg], p=0.045). Effects were independent of reduction in cholesterol levels.
Conclusion:
Although atorvastatin did not significantly lower serum CD40L levels, significant reduction in leukocyte production was seen independent of degree of LDL reduction. These pilot data suggest a potential benefit in normocholesterolemic individuals that should be further investigated, and that leukocyte CD40L concentrations should be considered in the drug response.
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