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Inverse relationship between high-density lipoprotein cholesterol raising and high-sensitivity C-reactive protein
W Virgil Brown1, JoAnne M Foody2, Franklin J Zieve3
1Emory University School of Medicine, Atlanta, GA, USA.
Insights
Inflammation marker high-sensitivity C-reactive protein (hsCRP) showed weak baseline links with lipids in older adults. After statin therapy, correlations strengthened, particularly with high-density lipoprotein cholesterol (HDL-C).
Area of Science:
- Cardiology
- Clinical Lipidology
- Inflammation Biomarkers
Background:
- Limited understanding of high-sensitivity C-reactive protein (hsCRP) associations with lipoproteins beyond LDL-C.
- High-density lipoprotein (HDL) is of interest due to its anti-inflammatory and cholesterol-mediating roles.
- Exploratory analysis in older adults at cardiovascular risk.
Purpose of the Study:
- Assess relationships between hsCRP and various lipids.
- Evaluate these associations before and after lipid-lowering therapy.
- Focus on patients aged over 65 with moderate to high cardiovascular disease risk.
Main Methods:
- Analysis of a 12-week, multicenter, randomized, double-blind study.
- Correlations assessed in 1054 patients with baseline and 12-week hsCRP ≤ 10 mg/L.
- Pooled data from ezetimibe/simvastatin (E/S) and atorvastatin (ATV) treatment groups, with significance set at P < .01.
Main Results:
- Weak, nonsignificant baseline correlations between hsCRP and LDL-C, non-HDL-C, or apolipoprotein B.
- Significantly stronger correlations after 12 weeks of treatment for most lipid parameters.
- Inverse correlation between HDL-C and hsCRP observed at baseline and post-treatment across groups.
Conclusions:
- Lipid factor associations with hsCRP were weak initially but strengthened post-treatment in older patients.
- High-density lipoprotein cholesterol (HDL-C) showed consistent inverse correlation with hsCRP.
- Changes in HDL-C and hsCRP were correlated, particularly in E/S and combined treatment groups.
Background:
Little is known regarding relationships between high-sensitivity C-reactive protein (hsCRP) and lipoproteins other than low-density lipoprotein cholesterol (LDL-C). High-density lipoprotein (HDL), with both anti-inflammatory and cholesterol-mediating effects, is of particular interest. This exploratory analysis assessed associations between hsCRP and lipids in older (>65 years) patients with moderate and/or high cardiovascular disease risk, before and after treatment with ezetimibe/simvastatin (E/S) or atorvastatin (ATV).
Methods:
An analysis of a multicenter, randomized, double-blind, 12-week study. Correlations were assessed in 1054 patients with both baseline and 12-week hsCRP ≤ 10 mg/L, pooled across doses of E/S (10/20 and 10/40 mg) and ATV (10, 20, and 40 mg), and combined E/S + ATV treatments. Because of multiple comparisons, observed relationships were considered significant only if P values were < .01.
Results:
Correlations between baseline levels of hsCRP and either LDL-C, non-HDL-C, or apolipoprotein B were weak and nonsignificant in the E/S, ATV, and E/S + ATV groups. After 12 weeks of treatment, these correlations increased slightly and significantly in all groups, except for LDL-C in the ATV group. HDL-C was significantly but inversely correlated with hsCRP in the ATV and E/S + ATV groups at baseline, and in all groups at 12 weeks. Only with HDL-C did change correlate with change in hsCRP in both the E/S and combined groups.
Conclusions:
Relationships between hsCRP and lipid factors in older patients were weak at baseline and somewhat stronger after treatment. HDL-C was inversely and consistently correlated with baseline and 12-week on-treatment hsCRP and with therapy-induced changes in HDL-C and hsCRP.
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