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. 2010 Nov 2;6:997–1005. doi: 10.2147/VHRM.S7802

Pitavastatin approved for treatment of primary hypercholesterolemia and combined dyslipidemia

Jun Sasaki 1,✉
PMCID: PMC2988623  PMID: 21127702

Abstract

Pitavastatin was first developed in Japan and is expanding the regions in which it is clinically available. A considerable number of clinical studies have been conducted and published to date on the usefulness of pitavastatin for patients with primary hypercholesterolemia or combined dyslipidemia. Pitavastatin demonstrates potent low-density lipoprotein cholesterol reduction at low doses of 1–4 mg/day. It also affects the regression of coronary plaques, as observed in intravascular ultrasound-guided percutaneous coronary intervention studies. Moreover, the persistent, long-term high-density lipoprotein cholesterol elevation observed in the populations treated with pitavastatin is worthy of further attention. The reported improvements in lipid profiles are consistent among the studies conducted in Japan, Korea, Thailand, and Europe. In light of accumulating clinical experience worldwide, pitavastatin is now expected to establish its position for preventing and treating cardiovascular disease.

Keywords: randomized clinical trial, Japan, Korea, Thailand, Europe

Introduction

Statins have contributed greatly to medical care since the late twentieth century through their role in the primary and secondary prevention of cardiovascular disease and reduction in total mortality. Compactin, the first statin, was discovered in the mid-1970s by Akira Endo, who had been exploring a substance from fungi that inhibited 3-hydroxy-3-methylglutaryl-coenzyme A (HMG-CoA) reductase, a rate-determining enzyme in the cholesterol synthesis pathway.1 Thereafter, lovastatin, pravastatin, and simvastatin became clinically available in 1987, 1989, and 1992, respectively. Moreover, large-scale clinical studies, including the West of Scotland Coronary Prevention Study,2 the Air Force/Texas Coronary Atherosclerosis Prevention Study,3 Cholesterol and Recurrent Events,4 and Scandinavian Simvastatin Survival Study5 were successfully conducted, leading to the era of statin therapy. Thereafter, fluvastatin, cerivastatin (withdrawn from the worldwide market in 2001), atorvastatin, pitavastatin, and rosuvastatin were developed.

Aggressive lowering of low-density lipoprotein cholesterol (LDL-C) levels is thought to be associated with a greater risk reduction for cardiovascular disease. Hence, aggressive lowering of LDL-C levels may benefit patients believed to be at risk for cardiovascular disease, even if their LDL-C levels are within the normal range for the general population, as well as patients with high LDL-C levels.6 Statins developed more recently exert more potent LDL-C reduction, allowing for more aggressive LDL-C-lowering therapy.

The withdrawal of cerivastatin was due to reports that the risk for fatal rhabdomyolysis might be increased when it was used concomitantly with gemfibrozil.7 Since this incident, drug–drug interactions have attracted attention. Pitavastatin is the only statin (including its lactone form) that is scarcely metabolized by cytochrome P450 (CYP), a drug-metabolizing enzyme in the liver.8 Hence, pitavastatin is thought to be minimally involved in drug–drug interactions mediated by CYP. This is an important property of pitavastatin because a lot of drug–drug interactions are recognized as a result of interferences in the metabolic pathway, the majority of which involve CYP isoenzymes. In fact, physicians should always take potential drug interactions into account with any drug to be administered, because multiple medications are often needed for patients with elevated cholesterol. As with other statins, other major causes of drug–drug interactions, ie, drug transporters, such as organic anion transporting polypeptide, also need to be carefully considered for pitavastatin.9

Pitavastatin was first developed and launched in Japan in 2003. Its safety and efficacy in Japan was established by the large-scale, prospective, post-marketing LIVES (LIValo Effectiveness and Safety) study, conducted in 20,000 patients with a two-year follow-up for each patient over six years since 2003.10 Pitavastatin’s usefulness has been reported in the results of many other clinical studies. To date, the findings indicate that pitavastatin has not only a potent LDL-C-lowering effect but also a long-term high-density lipoprotein cholesterol (HDL-C)-elevating effect.11 Pitavastatin became available in Korea in 2005, followed by approval in Thailand and China. It was recently approved by the Food and Drug Administration (FDA) in the US in August 2009. Pitavastatin is also being reviewed in Europe, and is expected to be approved there in 2010. Therefore, pitavastatin’s usefulness is expected to be confirmed worldwide in the future. This paper reviews the clinical studies conducted and published to date on the usefulness of pitavastatin for patients with primary hypercholesterolemia and those with combined dyslipidemia, for which pitavastatin is indicated.

Methods

Articles for this review were selected to examine LDL-C reduction by dose, safety, and the long-term HDL-C-elevating effect of pitavastatin in patients with primary hypercholesterolemia or combined dyslipidemia.

To examine LDL-C reduction and safety of pitavastatin at different doses, a systematic review was conducted on randomized active-controlled studies that compared the effects of pitavastatin with those of other statins in patients with primary hypercholesterolemia or combined dyslipidemia. Relevant articles were searched for in PubMed on 26 April 2010, using the search term “pitavastatin” and “randomized”. Thirty-seven papers11–47 were found. Four of these papers were reviews,11–14 two were articles on rationale and design of clinical studies,15,16 two were nonclinical studies,17,18 and five were pharmacokinetic studies,19–23 so were excluded. One interventional study of an unspecified statin,24 two clinical studies using unspecified doses of pitavastatin,25,26 and three studies that did not report percent change in LDL-C with different doses of pivastatin27–29 were also excluded. In addition, one nonrandomized comparative study and seven studies that compared pitavastatin treatment with nonstatin treatment, lifestyle modification, or combined treatment with pitavastatin and other agents were further excluded,30–36 as were two studies conducted in patients with familial hypercholesterolemia. 37,38 However, one study conducted in patients who had glucose intolerance and baseline lipid levels similar to those in the other included articles39 and another two studies conducted in patients with acute coronary syndrome (ACS)40,41 were included. Moreover, two Phase III studies reported in Europe that were not found from the search results (one found in a review article and the other reported in a congress meeting were included).48,49 Thus, a total of 11 articles39–47 were reviewed.

Five studies of the long-term treatment with pitavastatin39,48– 53 were reviewed. These papers were selected in a similar way to the abovementioned clinical studies, and all had study durations of more than 52 weeks or 12 months. Of those identified in PubMed using the keyword “pitavastatin”, review articles, commentaries, nonclinical and pharmacokinetic studies, and those focusing on rationale and/or study were excluded. Articles on HDL-C were also excluded if patients were treated with unspecified statins, data for HDL-C levels were not available for more than three visits, or the paper was a case report for one or two patients. A further study not identified on PubMed, but in which one of the authors of the present review participated, was included.50

LDL-C reduction and safety of pitavastatin

Randomized controlled studies that compared the effects of pitavastatin with those of other statins in patients with primary hypercholesterolemia or combined dyslipidemia, including some patients with glucose intolerance or ACS, were reviewed (Table 1). Relatively high percent reductions in LDL-C were reported, including 37.4% using 1 mg/day pitavastatin in Thailand,42 42.6% using 2 mg/day pitavastatin in CHIBA (Collaborative Study on Hypercholesterolemia Drug Intervention and their Benefits for Atherosclerosis Prevention)43 conducted in Japan, and 44.4% using 2 mg/day pitavastatin in a Korean study that used atorvastatin as a control,44 respectively. The LDL-C-lowering effects of 2 mg/day pitavastatin in other studies conducted in Japan, Korea, and Europe39,43–49 ranged from 36.8% to 39%. The LDL-C-lowering effects of 4 mg/day pitavastatin ranged from 44.0% to 44.6% in the Phase III studies conducted in Europe.47–49 The LDL-C-lowering effects of 1 mg/day pitavastatin was 31.4% in a Phase III study conducted in Europe.49 Randomized controlled studies that compared the LDL-C-lowering effect of 4 mg/day pitavastatin with that of other statins in patients with primary hypercholesterolemia or combined dyslipidemia have not been reported in Japan, Korea, or Thailand. However, two studies conducted in patients with ACS in Japan showed that LDL-C levels were reduced by 36% from 131 mg/dL at baseline and by 31% from 115 mg/dL at baseline.40,41

Table 1.

Lipid baselines, percent changes, and safety results of randomized clinical studies of pitavastatin compared with the other statin

Subject Study Lipid criteria (mg/dL) Study drug Duration n Percent change from baseline Baseline level (mg/dL) Safety
LDL-C TG HDL-C TC LDL-C TG HDL-C TC
Japan Saito et al45 TC ≥ 220, TG < 400 PTV 2 mg 12 wks 120 −37.6 8.9 −28.0 194.2 158.0 56.8 279.7 Both treatments well tolerated
PRV 10 mg 105 −18.4 9.8 −13.8 195.3 166.8 52.9 278.8
CHIBA43 TC ≥ 220, TG < 400 PTV 2 mg 12 wks 93 −42.6 −17.3 3.2 −29.7 177.1 155.2 58.5 262.8 AST, ALT, γ-GTP elevated in ATV
ATV 10 mg 98 −44.1 −10.7 1.7 −31.1 178.3 138.9 60.2 265.8
PIAT39* LDL-C ≥ 140, HDL-C < 80, TG < 500 PTV 2 mg 8 wks 88 −36.8 8.2 163.7 155.1 51.9 246.9 No significant differences
ATV 10 mg 85 −37.9 3.4 161.9 171.9 51.6 246.7
Korea Park et al46 LDL-C > 130, TG < 600 PTV 2 mg 8 wks 49 −38.2 8.3 −26.9 170.0 168.1 51.0 246.8 More incidence of ADRs in SMV
SMV 20 mg 46 −39.4 3.6 −28.5 165.7 153.6 52.1 240.0
Lee et al44 LDL-C > 130, TG < 400 PTV 2 mg 4 wks 110 −44.4 −13.4 4.6 −30.1 159 142 52 239 No significant differences
ATV 10 mg 112 −43.2 −13.3 5.7 −29.3 160 136 52 239
Thailand Sansanayudh et al42 Indicated for statin therapy by NCEP-ATP III PTV 1 mg 8 wks 50 −37.4 −10.4 2.8 −27.6 176.0 145.2 53.4 258.4 Both treatments well tolerated
ATV 10 mg 50 −45.8 −7.1 −0.4 −32.3 172.9 141.9 53.9 255.2
Europe Budinski et al48 160 ≤ LDL-C ≤ 220, TG ≤ 400 PTV 2 mg 12 wks 315 −37.9 −14.1 4 −27.7 183.6 157.8 48.5 263.6 All treatments well tolerated
ATV 10 mg 102 −37.8 −17.7 3 −28.1 179.8 156.8 50.2 261.3
PTV 4 mg 298 −44.6 −19 5 −32.4 182 156.8 49.9 263.3
ATV 20 mg 102 −43.5 −22.3 2.5 −32.7 181.9 161.9 48.4 262.7
Ose et al47 160 ≤ LDL-C ≤ 220, TG ≤ 400 PTV 2 mg 12 wks 307 −39.0 −15.9 6.0 −27.9 183.6 163.8 51.3 267.6 All treatments well tolerated
SMV 20 mg 107 −35.0 −15.6 5.5 −25.4 184.1 166.7 51.0 268.4
PTV 4 mg 319 −44.0 −16.8 6.2 −31.5 184.1 155.4 52.8 268.0
SMV 40 mg 110 −42.8 −16.1 6.8 −30.5 184.0 153.9 52.3 267.0
Hounslow49 130 ≤ LDL-C ≤ 220 PTV 1 mg 12 wks −31.4 All treatments well tolerated
PRV 10 mg −22.4
PTV 2 mg −39.0 162.8–
PRV 20 mg −28.8 166.6
PTV 4 mg −44.3
PRV 40 mg −34.0
Japan JAPAN-ACS16,40 TC ≥ 180, LDL-C ≥ 100 PTV 4 mg 8–12 mos 125 −36.2 16.2 9.9 −21.6 130.9 119.2 45.0 196.5 No significant differences
ATV 20 mg 127 −35.8 21.2 8.0 −21.9 133.8 116.7 43.9 197.9
Toi et al41 Unspecified PTV 2 mg 2–3 wks 80 −31.0 −8.0 −2.6 −22.5 114.7 86.2 45.5 178.0 NA
ATV 10 mg 80 −27.9 0.8 −5.1 −22.0 122.0 120.3 45.5 191.1
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*

Note: Patients with impaired glucose tolerance or Type 2 diabetes mellitus.

Abbreviations: ACS, acute coronary syndrome; n, number of patients; PTV, pitavastatin; PRV, pravastatin; ATV, atorvastatin; SMV, simvastatin; NA, data not available; ADRs, adverse drug reactions; TC, toal cholesterol; TG, triglycerides; LDL-C, low-density lipoprotein cholesterol; HDL-C, high-density lipoprotein cholesterol.

The LDL-C-lowering effects following the administration of 2 mg/day and 4 mg/day pitavastatin are thought to be comparable with those observed following the administration of 10 mg/day and 20 mg/day atorvastatin and 20 mg/day and 40 mg/day simvastatin. The safety and tolerability of pitavastatin were similar to those of controls in the randomized controlled studies. Each study is outlined below.

Phase III Japanese study of pitavastatin versus pravastatin

The effects of 2 mg/day pitavastatin were compared with the effects of a regular dose of 10 mg/day pravastatin, which was the most commonly used statin in Japan at the time of this study.45 In 225 patients with total cholesterol (TC) levels ≥ 220 mg/dL and triglyceride (TG) levels < 400 mg/dL, the LDL-C-lowering effect of pitavastatin after administration for 12 weeks was significantly better than that of pravastatin (37.6%, 95% confidence interval [CI] 35.3–39.9 versus 18.4%, 95% CI 16.1–20.7, respectively; the 95% CI of the difference was 11.8–16.5). In patients with baseline TG levels ≥ 150 mg/dL, the TG-lowering-effect was 23.3% (95% CI 13.7–32.9) and 20.2% (95% CI 12.0–28.4) in the pitavastatin group and the pravastatin group, respectively. HDL-C levels increased by 8.9% (95% CI 6.4–11.4) and 9.8% (95% CI 6.4–11.4), respectively.

CHIBA study

Since pitavastatin was launched in Japan in 2003, several investigator-initiated randomized comparative studies have been conducted, including the Chiba trial.43 In this trial, 251 hypercholesterolemic patients with TC levels ≥ 220 mg/dL and TG levels < 400 mg/dL were randomized to receive 2 mg/day pitavastatin or 10 mg/day atorvastatin. The primary endpoint was the percent change in non-HDL-C levels from baseline after 12 weeks of treatment. Non-HDL-C levels were reduced by 39% (P < 0.001) in the pitavastatin group and by 40.3% (P < 0.001) in the atorvastatin group. The percent reduction in non-HDL-C levels showed a statistically significant positive correlation with waist circumference and body mass index (BMI) only in the atorvastatin group (r = 0.33, P = 0.034 and r = 0.279, P = 0.022, respectively); no significant correlation for these parameters was found in the pitavastatin group. There were no statistically significant between-group differences in the percent changes in LDL-C, TG, HDL-C, and non-HDL-C. HDL-C increased significantly only in the pitavastatin group (3.2%, P = 0.033). The percent changes in LDL-C were 42.6% (P < 0.001) and 44.1% (P < 0.001) in the pitavastatin and atorvastatin groups, respectively. Subgroup analysis was also conducted in patients with metabolic syndrome. In this subanalysis, LDL-C reduction in the pitavastatin group showed a tendency to be significantly superior to that in the atorvastatin group (P = 0.050), and the percent change in TG (−25.2%, P < 0.001) as well as HDL-C (6.7%, P = 0.019) was statistically significant only in the pitavastatin group. Both treatments were well tolerated, but aspartate aminotransferase, alanine aminotransferase, and gamma-glutamyl transpeptidase became elevated in atorvastatin group.

PIAT study

The PIAT study was conducted to examine the effects of pitavastatin and atorvastatin on HDL-C levels in patients with elevated LDL-C and glucose intolerance.39 In this study, the primary endpoint was the percent change in HDL-C levels following treatment with 2 mg/day pitavastatin or 10 mg/day atorvastatin for 52 weeks (described further on in this review with regard to the HDL-C-elevating effect of pitavastatin). The subjects were 173 hypercholesterolemic patients with glucose intolerance or Type 2 diabetes mellitus who had LDL-C levels ≥ 140 mg/dL, HDL-C levels < 80 mg/dL, and TG levels < 500 mg/dL. The LDL-C reductions in the pitavastatin group and atorvastatin group after treatment for eight weeks (a treatment duration similar to that used in other studies) were 36.8% and 37.9%, respectively (P = 0.61), which were reported by Sasaki in the XVI International Symposium on Drugs Affecting Lipid Metabolism in New York, USA in 2007. No significant differences between the two groups were observed with regard to worsening of glucose metabolism or incidence of adverse events.

Comparative study of pitavastatin and simvastatin in Korea

In this study, 103 hypercholesterolemic patients with LDL-C levels ≥ 130 mg/dL and TG levels < 600 mg/dL received 2 mg/day pitavastatin or 20 mg/day simvastatin for eight weeks.46 The LDL-C reduction was 38.2% in the pitavastatin group and 39.4% in the simvastatin group; there was no significant difference between the groups (P = 0.648) for percent changes in TC, TG, and HDL-C, or the proportion of patients attaining the LDL-C treatment goals recommended in the National Cholesterol Education Program (NCEP)-Adult Treatment Panel (ATP) III guidelines. The incidence of adverse events was not significantly different between the groups (25.0% in the pitavastatin group and 37.3% in the simvastatin group, P = 0.179). However, the incidence of adverse events that had an undeniable causal relationship with the study drug was 15.4% in the pitavastatin group and 37.3% in the simvastatin group, indicating a significant difference between the groups (P = 0.015).

Comparative study of pitavastatin and atorvastatin in Korea

In this study, 268 hypercholesterolemic patients with LDL-C levels ≥ 130 mg/dL and TG levels < 400 mg/dL received 2 mg/day pitavastatin or 10 mg/day atorvastatin for four weeks, followed another four-week treatment with uptitration when a patient did not achieve the NCEP-ATP III goal.44 Thus, the study drugs were administered for a total of eight weeks. The LDL-C reduction was 44.4% in the pitavastatin group and 43.2% in the atorvastatin group after four weeks, indicating no significant difference between the groups (P = 0.41). Tolerability was good in both groups. The incidence of adverse events was 19.1% in the pitavastatin group and 25.0% in the atorvastatin group. Increased creatine kinase levels equal to or higher than 10 times the upper limit of the normal range, with muscle symptoms, did not occur.

Comparative study of pitavastatin and atorvastatin in Thailand

A study conducted in Thailand compared the LDL-C reduction using 1 mg/day pitavastatin with that of 10 mg/day atorvastatin.42 In a total of 100 patients with hypercholesterolemia, the LDL-C reduction after treatment (P < 0.001) in 74% and 84% of subjects in the pitavastatin and atorvastatin groups, respectively, achieved the LDL-C goal recommended in the NCEP-ATP III guidelines, with no significant difference between the groups (P = 0.220). Tolerability was good in both groups. Elevation of alanine transaminase levels equal to or higher than three times the upper limit of normal or elevation of creatine kinase levels equal to or higher than 10 times the upper limit of normal did not occur. The monthly cost per percent LDL-C reduction by pitavastatin 1 mg/day was less than that for atorvastatin 10 mg/day in Thailand.

Comparative study of pitavastatin and atorvastatin in Europe

This study was conducted in 821 patients with hypercholesterolemia or combined dyslipidemia whose LDL-C levels were between 160 and 220 mg/dL and whose TG levels were ≤400 mg/dL.48 The study aimed to compare the LDL-C reductions following treatment with pitavastatin for 12 weeks with those after atorvastatin treatment for the same duration (pitavastatin 2 mg/day versus atorvastatin 10 mg/day and pitavastatin 4 mg/day versus atorvastatin 20 mg/day). The LDL-C reductions were 37.9% (pitavastatin 2 mg/day), 37.8% (atorvastatin 10 mg/day), 44.6% (pitavastatin 4 mg/day), and 43.5% (atorvastatin 20 mg/day), indicating no significant differences between the pitavastatin and atorvastatin groups (P = 0.93 between the lower dose groups and 0.57 between the higher dose groups, respectively). There were no significant between-group differences in the percent changes in TC, TG, HDL-C, and non-HDL-C or the rates of achievement of the LDL-C goal. Tolerability was good in both groups. The incidence of adverse events was 19.0% (pitavastatin 2 mg/day), 16.7% (atorvastatin 10 mg/day), 16.7% (pitavastatin 4 mg/day), and 22.3% (atorvastatin 20 mg/day).

Comparative study of pitavastatin and simvastatin in Europe

This study was conducted in 857 patients with hypercholesterolemia or combined dyslipidemia whose LDL-C levels were between 160 and 220 mg/dL and whose TG levels were ≤400 mg/dL.47 The study compared the LDL-C reductions following treatment with pitavastatin for 12 weeks with those after treatment with simvastatin for the same duration (pitavastatin 2 mg/day versus simvastatin 20 mg/day and pitavastatin 4 mg/day versus simvastatin 40 mg/day). The LDL-C reductions were 39.0% (pitavastatin 2 mg/day), 35.0% (simvastatin 20 mg/day), 44.0% (pitavastatin 4 mg/day), and 42.8% (simvastatin 40 mg/day). The LDL-C reduction following treatment with 2 mg/day pitavastatin was significantly better than that after treatment with 20 mg/day simvastatin (P = 0.014). The percent changes in TC and non-HDL-C levels and the rate of achievement of the LDL-C goal recommended in the European Atherosclerosis Society guidelines in the pitavastatin 2 mg/day group were similarly superior to those in the simvastatin 20 mg/day group (P = 0.041, 0.021, and 0.049, respectively). The percent changes in TG and HDL-C and the rate of achievement of the LDL-C goal recommended in the NCEP-ATP III guidelines did not differ significantly between the treatment groups. Tolerability was good in both groups. The incidence of adverse events was 35.4% (pitavastatin 2 mg/day), 33.6% (simvastatin 20 mg/day), 32.2% (pitavastatin 4 mg/day), and 27.3% (simvastatin 40 mg/day).

Comparative study of pitavastatin and pravastatin in Europe

This study was conducted in elderly patients with hypercholesterolemia or combined dyslipidemia whose LDL-C levels were between 130 and 220 mg/dL and whose TG levels were ≤400 mg/dL. The study compared LDL-C reductions following administration of pitavastatin for 12 weeks with those following administration of pravastatin for the same duration (pitavastatin 1 mg/day versus pravastatin 10 mg/day, pitavastatin 2 mg/day versus pravastatin 20 mg/day, and pitavastatin 4 mg/day versus pravastatin 40 mg/day).49 The LDL-C reductions were 31.4% (pitavastatin 1 mg/day), 22.4% (pravastatin 10 mg/day), 39.0% (pitavastatin 2 mg/day), 28.8% (pravastatin 20 mg/day), 44.3% (pitavastatin 4 mg/day), and 34.0% (pravastatin 40 mg/day). The LDL-C reduction following pitavastatin treatment was significantly superior to that following pravastatin treatment at each dose comparison (P < 0.001). Adverse events were similar for the pitavastatin and pravastatin groups. Tolerability was good in both groups.

JAPAN-ACS study

JAPAN-ACS (Japanese Assessment of Pitavastatin and Atorvastatin in ACS) was conducted in 252 patients with ACS who had successfully undergone intravascular ultrasound-guided percutaneous coronary intervention.40 In this study, the percent change in coronary plaque volume after treatment with 4 mg/day pitavastatin for 8–12 months was compared with that after 20 mg/day atorvastatin for the same duration. This study indicated the regressive effect of aggressive lipid-lowering therapy on coronary plaque volume in patients with ACS who had undergone intravascular ultrasound-guided percutaneous coronary intervention. The plaque regressive effect of pitavastatin was equivalent to that of atorvastatin. The LDL-C reduction was equivalent in the pitavastatin and atorvastatin groups (36.2% and 35.8%, respectively, P = 0.9). The LDL-C reductions were relatively smaller than those seen in the other studies because the LDL-C levels were low at baseline (130.9 mg/dL in the pitavastatin group and 133.8 mg/dL in the atorvastatin group). Unlike in other placebo-controlled studies, the percent change in LDL-C was not correlated with the percent change in plaque volume in the JAPAN-ACS study. No significant differences were found in the incidence rate of cardiovascular or adverse events between the treatment groups.

Pitavastatin versus atorvastatin using virtual histology intravascular ultrasound

A study conducted in 160 patients with ACS who underwent percutaneous coronary intervention reported the early effects of 2–3 weeks’ treatment with 2 mg/day pitavastatin and 10 mg/day atorvastatin on the components of coronary plaques.41 After treatment, the plaque volume index and fibrofatty plaque (a component of coronary plaques) volume index decreased significantly in the pitavastatin group (P < 0.05). The mean LDL-C level at baseline was 114.7 mg/dL in the pitavastatin group and 122.0 mg/dL in the atorvastatin group; both levels were lower than those in the JAPAN-ACS study. The LDL-C reduction was 31.0% in the pitavastatin group (P < 0.001) and 27.9% in the atorvastatin group (P < 0.001). The percent change in plaque volume index showed a mild positive correlation with the percent change in LDL-C in the pitavastatin group. In a subgroup of patients in the pitavastatin group with a dense calcium plaque ratio less than 10%, the percent change in fibrofatty volume index and the percent change in LDL-C correlated positively.

HDL-C-elevating effect of pitavastatin

HDL-C elevation following treatment with pitavastatin for 4–12 weeks ranged from 3.2% to 8.9% in a population with baseline HDL-C levels between 48.5 and 58.5 mg/dL in the randomized, active-controlled comparative study (see Table 1). The PIAT study39 compared treatment for 52 weeks with 2 mg/day pitavastatin and 10 mg/day atorvastatin. Because pitavastatin has an LDL-C-lowering effect similar to that of atorvastatin but is expected to have a superior HDL-C- elevating effect, PIAT also assessed the effects of pitavastatin and atorvastatin on the HDL-C levels of patients with elevated LDL-C and glucose intolerance.39 Patients with glucose intolerance or Type 2 diabetes mellitus were chosen because HDL-C levels, in addition to LDL-C levels, play a particularly important role in cardiovascular risk in these patients.

Pitavastatin was significantly superior to atorvastatin with regard to the increase in HDL-C levels after 52 weeks (8.8% versus 3.6%, respectively, P = 0.034). This result was sustained throughout the 52 weeks of treatment. The percent change in the level of Apoprotein A-1, a major protein component of HDL-C, was significantly higher in the pitavastatin group than in the atorvastatin group after 52 weeks (5.2% versus 1.1%, respectively, P = 0.031). Pitavastatin had a persistent HDL-C-elevating effect. Moreover, various nonrandomized studies that examined the effects of long-term administration of pitavastatin reported a sustained increase in HDL-C levels with pitavastatin treatment (see Figure 1).39,50–53 In addition to the potent LDL-C-lowering effect of pitavastatin, its long-term HDL-C-elevating effect is expected to provide some long-term benefits, but further confirmation of these results is warranted.

Figure 1.

Figure 1

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Time course of high-density lipoprotein cholesterol levels in long-term clinical studies of pitavastatin.

Note: Data are expressed as mean ± standard deviation. Reference 52 is subanalysis for patients whose baseline high-density lipoprotein cholesterol was <40 mg/dL.

Conclusion

Pitavastatin has a potent serum LDL-C-lowering effect, even at low doses of 1–4 mg/day. Pitavastatin also affects regression of coronary plaques, as observed in intravascular ultrasound-guided percutaneous coronary intervention studies. Moreover, the persistent long-term HDL-C elevation observed in patients treated with pitavastatin is worthy of further attention. The reported improvements in the lipid profile are consistent between the studies conducted in Japan, Korea, Thailand, and Europe. Pitavastatin has a lower propensity for drug–drug interactions via CYP, can exert a potent LDL-C-lowering effect at relatively low doses, and has a favorable effect on coronary plaques. Therefore, it is expected that, as clinical experience of pitavastatin accumulates worldwide, this statin will establish its position as a useful drug for preventing and treating cardiovascular disease.

Acknowledgment

Kowa Company Ltd provided the information on the randomized active-controlled clinical research of pitavastatin already published but not found in the search result in PubMed.

Footnotes

Disclosure

The author reports no conflict of interest in this work.

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