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Switching from statin monotherapy to ezetimibe/simvastatin or rosuvastatin modifies the relationships between apolipoprotein B, LDL cholesterol, and non-HDL cholesterol in patients at high risk of coronary disease. | LitMetric

AI Article Synopsis

  • The study aimed to analyze how apolipoprotein B (Apo B), LDL cholesterol (LDL-C), and non-HDL cholesterol (non-HDL-C) relate in high-risk patients on lipid-lowering therapy.
  • It compared LDL-C and non-HDL-C levels after treatment with either a statin alone or a combination therapy at the end of the study.
  • Findings showed that while treatment improved LDL-C and non-HDL-C levels, only a little over 50% of patients achieving LDL-C or non-HDL-C targets also had an Apo B level under the desired threshold, suggesting Apo B could push for stricter lipid management criteria.

Article Abstract

Objective: To evaluate relationships between apolipoprotein B (Apo B), LDL cholesterol (LDL-C), and non-HDL-C in high-risk patients treated with lipid-lowering therapy.

Design And Methods: This post-hoc analysis calculated LDL-C and non-HDL-C levels corresponding to an Apo B of 0.9 g/L following treatment with 1) statin monotherapy (baseline) and 2) ezetimibe/simvastatin 10/20mg or rosuvastatin 10mg (study end). The percentages of patients reaching LDL-C, non-HDL-C, and Apo B targets were calculated at study end.

Results: After switching to ezetimibe/simvastatin or rosuvastatin, the LDL-C and non-HDL-C corresponding to Apo B=0.9 g/L were closer to the more aggressive LDL-C and non-HDL-C goals (1.81 and 2.59 mmol/L, respectively). Only slightly >50% of the patients who reached minimum recommended LDL-C or non-HDL-C at study end also had an Apo B level <0.9 g/L with both treatments.

Conclusion: The use of Apo B for monitoring the efficacy of lipid-altering therapy would likely lead to more stringent criteria for lipid lowering.

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Source
http://dx.doi.org/10.1016/j.clinbiochem.2011.02.008DOI Listing

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