Statin and Ezetimibe Combination Therapy Decreases Mean Platelet Volume Compared to Statin Monotherapy

Article information

J Stroke. 2017;19(1):109-110
Publication date (electronic) : 2017 January 31
doi :
aDepartment of Neurology, Hong-Ik Hospital, Seoul, Korea
bDepartment of Laboratory Medicine, Hong-Ik Hospital, Seoul, Korea
cDepartment of Neurology, Gangnam Severance Hospital, Yonsei University College of Medicine, Seoul, Korea
Correspondence: Jun-beom Lee  Department of Neurology, Hong-Ik Hospital, 225 Mokdong-ro, Yangchun-gu, Seoul 07937, Korea  Tel: +82-2-2600-0578, Fax: +82-2-2697-4605 E-mail:
Received 2016 May 15; Revised 2016 July 21; Accepted 2016 August 30.

Dear Sir:

When platelets are activated, they increase in size and change from a quiescent disc to a swollen sphere. Large platelets are more reactive and likely aggregate more than small ones [1]. Mean platelet volume (MPV), an indicator of platelet size and activation, has been shown to predict ischemic stroke, myocardial infarction, and overall vascular mortality [2,3]. The IMProved Reduction of Outcomes: Vytorin Efficacy International Trial (IMPROVEIT) study showed that ezetimibe added to statin therapy further decreases low density lipoprotein cholesterol (LDL-C) levels and prevented acute coronary syndromes [4]. In this study, we investigated the lowering effect of LDL-C and MPV changes in patients who are on statin-ezetimibe combination therapy and those who receive statin monotherapy.

Patients with acute ischemic cerebral infarctions (n=120) were divided into those who were on statin therapy (n=60) and those on statin plus ezetimibe (n=60). The statin group received either atorvastatin (20 mg; n=13) or rosuvastatin (10 mg; n=48). The statin plus ezetimibe group received ezetimibe (10 mg) on top of the same dose of statin (atorvastatin plus ezetimibe, n=14; rosuvastatin plus ezetimibe, n=47). Student’s t-tests showed that MPV and serum LDL-C levels were more significantly decreased (MPV: P<0.001; LDL-C: P=0.017) by statin plus ezetimibe combination therapy (MPV: from 7.39±1.04 [5.8–9.2] to 6.04±0.58 [4.9–7.3] fL; LDL-C: from 160.1±21.9 [122-212] to 79.5±22.9 [33-158] mg/dL) than statin monotherapy (MPV: from 7.47±0.74 [5.6–11.6] to 6.56±1.04 [4.9–9.2] fL; LDL-C: from 143.4±29.4 [52–238] to 95.6±21.7 [41–150] mg/dL). Total cholesterol and triglycerides, but not high-density lipoprotein-cholesterol, were more significantly altered with combination therapy than with statin monotherapy (Table 1). A multivariate regression analysis showed that only LDL-C in the lipid profile correlated significantly with the MPV change. A Pearson correlation analysis showed a positive correlation between the post-treatment MPV and post-treatment LDL-C levels (r=0.230, P=0.012).

Comparison of Lipid profile and mean platelet volume between statin and ezetimibe combination and statin monotherapy at baseline and post treatment

Statin has pleiotrophic effects and modulates platelet function by direct interactions with platelet membranes or by influencing signaling pathways, irrespective of the cholesterol-lowering effects. Aydin et al. reported that high doses of statin decrease MPV and LDL-C levels in patients with diabetes, but the changes in LDL-C and MPV did not correlate [5]. Nevertheless, Marek et al. reported that MPV was correlated with small dense LDL-C [6]. The possible mechanisms through which small dense LDL-C increases MPV include easier oxidation and glycation, which enhances the mobilization of arachidonic acid from phospholipids and decreases membrane fluidity. However, small dense-LDL-C measurements are time consuming and expensive in real life. In general, statin and ezetimibe induce reductions in all LDL-C subclasses. Ezetimibe blocks the critical mediator of cholesterol absorption, the Niemann-Pick C1-like 1 (NPC1L1) protein, on gastrointestinal tract epithelial cells as well as in hepatocytes, which causes them to absorb more LDL-C from the circulation and lower the circulating cholesterol level.

The previously proposed mechanisms of hypercholesterolemia in platelet activation are increased thromboxane A2 biosynthesis, inhibition of the platelet Na+/H+ antiport, decreased platelet endogenous nitric oxide production, and diminished endothelial nitric oxide synthase (eNOS) protein expression [7]. In addition, platelet activation by high LDL-C through platelet signaling pathways has been reported [8]. The effects of ezetimibe monotherapy on the LDL subclass profile are controversial. Kasper et al. reported that ezetimibe increases small dense LDL-C in healthy men [9]. In contrast, other studies have reported that ezetimibe decreases all LDL-C subclasses, including small dense LDL-C [10].

Our results showed that MPV and LDL-C levels were more significantly decreased by statin and ezetimibe combination therapy than statin monotherapy and that their levels are closely correlated. Our data suggest that the lowering of LDL-C may causally related with MPV changes and support the “Lower LDL-C, better outcome” findings of the IMPROVE-IT study [4].


The authors have no financial conflicts of interest.


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Table 1.

Comparison of Lipid profile and mean platelet volume between statin and ezetimibe combination and statin monotherapy at baseline and post treatment

Statin plus ezetimibe
Stain only
At baseline At follow up Change (%) At baseline At follow up Change (%)
TC (mg/dL) 234.5±36.8 165.3±19.7 -29.5 231.5±37.4 188.3±20.3 -19.6 0.039
LDL-C (mg/dL) 160.1±21.9 79.5±22.9 -50.4 143.4±29.4 95.6±21.7 -33.4 0.017
TG (mg/dL) 189.1±22.4 152.7±18.2 -19.2 183.5±21.9 163.7±13.6 -10.7 0.042
HDL-C (md/dL) 35.2±3.5 44.7±1.9 21.2 39.4±2.5 47.8±5.8 17.6 0.474
MPV (fL) 7.39±1.04 6.04±0.58 -18.3 7.47±0.74 6.56±1.04 -12.2 < 0.001

TC, Total cholesterol; LDL-C, Low density lipoprotein cholesterol; TG, Triglyceride; HDL-C, High density lipoprotein cholesterol; MPV, Mean platelet volume.