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Highly Effective Reduction of C-Reactive Protein in Patients With Coronary Heart Disease by Extracorporeal Low-Density Lipoprotein Apheresis

Atherosclerosis
2002;162:187-191.

Eberhard Wieland, Volker Schettler, Victor William Armstrong

C-reactive protein (CRP) is a sensitive marker of inflammation also found to be associated with coronary heart disease (CHD). CRP has been found in atherosclerotic lesions, and a causal relationship has been suggested between CRP deposition and the inflammatory reaction in the vessel wall. As a result, reduction of CRP levels, even from normal concentrations, may prove to be therapeutic. The authors hypothesized that treatment with the heparin-induced LDL-apheresis method may result in more significant reductions in CRP levels than those seen with statin use alone. CRP concentrations were determined from the serum of hypercholesterolemic patients with CHD (n=13) both pre- and postapheresis. In addition, the effect of the heparin-induced method on serum CRP concentrations in vitro was also determined.

The heparin-induced method significantly reduced CRP concentrations by an average of 65% (3.09 mg/L [0.22-6.11] – 1.07 [0.10-3.08]; P<0.001). This was comparable with the 64% average reduction in LDL-C in the same samples.
CRP was partly co-precipitated with LDL-C in agreement with previous studies, which show that other plasma proteins are co-precipitated with the heparin-induced method. In vitro precipitation achieved 100% removal of LDL-C, whereas CRP concentrations were lowered by approximately 67%.
Kinetic studies demonstrated that, in contrast to LDL-C, the rate of return of CRP concentrations to preapheresis values showed larger fluctuations. A sustained decrease in CRP levels was observed in four of six patients over the first 4 days following apheresis.
The authors conclude that the heparin-induced method efficiently and effectively lowers CRP concentrations in patients with CHD. This information may help explain the stabilization and reduction in atherosclerotic plaques seen in hypercholesterolemic patients following LDL-apheresis treatment.

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