Intensive lipid lowering may reduce progression of carotid atherosclerosis within 12 months of treatment: the METEOR study
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M L Bots1, M K Palmer, S Dogan
1Julius Center for Health Sciences and Primary Care, University Medical Center Utrecht, The Netherlands. m.l.bots@umcutrecht.nl
Insights
Rosuvastatin significantly slowed atherosclerosis progression, with differences in carotid intima media thickness (CIMT) becoming apparent after 12 months. This suggests one-year trials can evaluate lipid-lowering efficacy on CIMT progression.
Area of Science:
- Cardiovascular Medicine
- Pharmacology
- Medical Imaging
Background:
- Vascular event rates in statin trials often diverge around 1 year.
- The precise timing of statin effects on atherosclerosis progression remains undefined.
- The METEOR trial investigated the earliest detection of statin effects on atherosclerosis.
Purpose of the Study:
- To determine the earliest time point for detecting significant differences in atherosclerosis progression rates after statin initiation.
- To evaluate the effect of rosuvastatin on carotid intima media thickness (CIMT) progression.
Main Methods:
- A double-blind, randomized placebo-controlled trial (METEOR) involving 984 low-risk subjects.
- Rosuvastatin (40 mg) was administered to lower LDL-C.
- Carotid intima media thickness (CIMT) was measured by B-mode ultrasound at baseline and every 6 months for 2 years.
Main Results:
- Rosuvastatin significantly reduced LDL-C (-49%), total cholesterol (-34%), and triglycerides (-16%), while increasing HDL-C (+8.0%).
- No significant difference in CIMT progression was observed at 6 months (P=0.34).
- Statistically significant differences in CIMT progression rates emerged at 12 months (P=0.049) and became more pronounced over 24 months.
Conclusions:
- Aggressive LDL-C lowering with rosuvastatin impacts atherosclerosis progression within the first 12 months.
- The timing of CIMT progression changes aligns with observed reductions in vascular events.
- One-year trials with precise measurements and adequate sample size can effectively evaluate lipid-lowering treatment efficacy on CIMT progression.
Background:
In several statin trials, vascular event rates for treatment groups begin to separate 1 year after commencement of treatment. For atherosclerosis progression, the temporal sequence of the effect has not been defined. We used data from the Measuring Effects on intima media Thickness: an Evaluation Of Rosuvastatin (METEOR) trial to determine the earliest time point at which significant differences in atherosclerosis progression rates could be detected after initiation of statin therapy.
Methods:
The METEOR trial was a double-blind, randomized placebo-controlled trial that studied the effect of LDL-C lowering with 40 mg rosuvastatin on the rate of change of carotid intima media thickness (CIMT) measured by B-mode ultrasound amongst 984 low risk subjects. Ultrasound assessments were made at baseline and every 6 months up to 2 years.
Results:
Rosuvastatin treatment was associated with a 49% reduction in LDL-C-C, a 34% reduction in total cholesterol, an 8.0% increase in HDL-C and a 16% reduction in triglycerides (all P < 0.0001 compared with placebo). The difference in rate of mean maximum CIMT progression between the rosuvastatin and placebo groups (based on near and far wall measurements from both left and right common carotid and internal carotid segments and carotid bifurcation) was not statistically significant after 6 months (0.0023 mm year(-1) and 0.0106 mm year(-1), respectively P = 0.34). After 12 months, CIMT progression rates were significantly different between the groups: 0.0032 mm year(-1) and 0.0133 mm year(-1) in the rosuvastatin-treated and placebo-treated groups, respectively (P = 0.049). This divergence grew with further follow-up: -0.0009 mm year(-1) and 0.0131 mm year(-1) after 18 months (P < 0.001) and -0.0014 mm year(-1) and 0.0131 mm year(-1) after 24 months of treatment (P < 0.001). Results were stronger for the mean common CIMT progression (based on near and far wall measurements from both left and right common carotid segments).
Conclusion:
Aggressive LDL-C lowering seems to exert its beneficial effect on atherosclerosis progression during the first 12 months of treatment. This parallels the timing of event reduction seen in clinical trials and suggests that the efficacy of lipid lowering treatment on CIMT progression can be evaluated in trials with a duration of 1 year, given sufficient sample size, high precision of measurements and a treatment effect comparable to that seen in METEOR.
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