Differential Hs-CRP Reduction in Patients with Familial Hypercholesterolemia Treated with Aggressive or Conventional Statin Therapy
Overview
Authors
Affiliations
Background: High sensitivity C-reactive protein (hs-CRP) has emerged as the best studied and most promising marker of inflammation in atherosclerotic vascular disease.
Materials And Methods: The ASAP (effects of Atorvastatin vs. Simvastatin on Atherosclerosis Progression) study was a 2-year randomised, double-blind trial with 325 familial hypercholesterolemia patients, treated with torvastatin 80 mg or imvastatin 40 mg. Intima media thickness (IMT) of carotid artery segments and hs-CRP levels were determined at baseline, 1 and 2 years.
Results: Baseline median hs-CRP values were 2.1 mg/l (interquartile range (IQR) 0.9-5.2) and 2.0 mg/l (IQR 0.8-3.0) and after 2 years these levels decreased to 1.1 mg/l (IQR 0.6-2.4) and 1.5 mg/l (IQR 0.6-3.0) in the atorvastatin 80 mg and simvastatin 40 mg group, respectively. These changes were significant within as well as between the two groups. No correlations were observed between change in hs-CRP after 2 years and change in lipids. A significant correlation was found in univariate analysis between the decrease of hs-CRP and the reduction of IMT.
Conclusions: Our results show that atorvastatin 80 mg reduces hs-CRP levels to a greater extent than simvastatin 40 mg. Furthermore, we show that the extent of hs-CRP reduction is associated with the progression rate of the atherosclerotic process as measured by IMT.
Zhang J, Wang X, Tian W, Wang T, Jia J, Lai R Front Cardiovasc Med. 2022; 9:936817.
PMID: 35966518 PMC: 9363636. DOI: 10.3389/fcvm.2022.936817.
How Can We Identify Very High-Risk Heterozygous Familial Hypercholesterolemia?.
Kataoka Y, Funabashi S, Doi T, Harada-Shiba M J Atheroscler Thromb. 2022; 29(6):795-807.
PMID: 35022364 PMC: 9174089. DOI: 10.5551/jat.RV17063.
Statins and C-reactive protein: in silico evidence on direct interaction.
Shakour N, Ruscica M, Hadizadeh F, Cirtori C, Banach M, Jamialahmadi T Arch Med Sci. 2020; 16(6):1432-1439.
PMID: 33224343 PMC: 7667423. DOI: 10.5114/aoms.2020.100304.
Blinc L, Mlinaric M, Battelino T, Groselj U Molecules. 2020; 25(21).
PMID: 33158028 PMC: 7663751. DOI: 10.3390/molecules25215118.
Al-Hail N, Butler A, Dargham S, Abou Seif A, Atkin S Front Endocrinol (Lausanne). 2019; 10:659.
PMID: 31608014 PMC: 6773810. DOI: 10.3389/fendo.2019.00659.