Safety and efficacy of long-term combination therapy with bezafibrate and ezetimibe in patients with dyslipidemia in the prospective, observational J-COMPATIBLE study

Low-density lipoprotein-cholesterol (LDL-C) is one of the most important factors for evaluating the risk associated with cardiovascular disorders. Statins are the most commonly used drug for treating elevated LDL-C, and reduce the risk of cardiovascular events, as demonstrated in large-scale clinical trials [1].

Although statin therapy reduces the risk of cardiovascular events by approximately 30%, the residual risk of cardiovascular events is approximately 70% [2]. Therefore, it is necessary to consider additional interventions to reduce the residual risk. In addition to LDL-C, low levels of high-density lipoprotein-cholesterol (HDL-C) and high triglyceride (TG) concentrations are considered to be risk factors for coronary artery disease [3‐5]. For this reason, it is increasingly being acknowledged that integrated management of dyslipidemia targeting LDL-C as well as HDL-C and TG is necessary [6, 7]. In particular, the European Society of Cardiology/the European Atherosclerosis Society [8] and the Japan Atherosclerosis Society [9] recommend fibrates as the Class I pharmaceutical therapy for treating hypertriglyceridemia.

Fibrates activate peroxisome proliferator-activated receptor (PPAR) alpha, a nuclear receptor that affects the transcriptional regulation of many genes governing lipoprotein metabolism, thereby decreasing TG levels while increasing HDL-C levels [10]. One of these drugs, bezafibrate, is a ligand for three PPAR subtypes (alpha, gamma, and delta) and exerts unique actions that differ from those of other fibrates [10, 11]. In contrast, ezetimibe is an inhibitor of Niemann-pick C1 like 1 protein (NPC1L1), an intestinal cholesterol transporter that is localized to the small intestinal mucosa. By inhibiting NPC1LI, ezetimibe reduces lipid uptake from the intestine, and thereby reduces hepatic cholesterol content and circulating LDL-C levels [12].

Because of these independent mechanisms of action, a combination of bezafibrate and ezetimibe is expected to provide a comprehensive treatment option for dyslipidemia by decreasing LDL-C, increasing HDL-C, and markedly decreasing TG levels. In fact, several studies have already documented the efficacy of fenofibrate in combination with ezetimibe [13‐15]. In contrast, a study combining bezafibrate and ezetimibe has not yet been conducted. For this reason, we conducted a 12-month prospective observational study (J-COMPATIBLE study; Japanese safety and efficacy of long-term COMbination theraPy with bazafibrAte and ezeTImiBe in patients with dysLipidEmia study) the safety and efficacy of bezafibrate in combination with ezetimibe for the treatment of dyslipidemia.

Fibrates are thought to be the most effective drugs for treating low HDL-C and high TG levels [18, 19]. Bezafibrate (400 mg/day) was reported to decrease TG levels by 45.4% and increase HDL-C levels by 14.0% in the J-BENEFIT study [20]. Concurrent administration of a fibrate and a statin might be a feasible treatment option for patients with mixed dyslipidemia who also have relatively high LDL-C levels. However, some caution is necessary because a high risk of rhabdomyolysis was reported during concurrent use of these drugs, especially in patients with renal dysfunction complications [21].

Ezetimibe acts by inhibiting the enterohepatic recirculation of lipids. In post-kidney transplantation patients, ezetimibe was found to stabilize creatinine clearance and also to suppress further decreases in renal function [22]. It differs from fibrates, which pass through the kidneys and are excreted in urine. A meta-analysis revealed that 10 mg/day ezetimibe as monotherapy decreased LDL-C by 18.58%, increased HDL-C by 3.00%, and decreased TG by 8.06% [23]. Therefore, bezafibrate in combination with ezetimibe is thought to be a feasible approach to reducing residual cardiovascular risk because this combination is expected to improve low HDL-C and high TG levels and to decrease LDL-C levels, while providing a good safety profile.

Fibrates reportedly increase the excretion of cholesterol into bile and may promote gallstone formation [24]. Ezetimibe does not promote cholelithiasis, according to one study [25]. To date, however, the risk of gallstones with bezafibrate in combination with ezetimibe has not been adequately evaluated. Therefore, in this study, we performed ultrasonography at baseline and at the end of the observation period to detect gallstones which had developed during combination therapy. We also evaluated the efficacy of this combination therapy in terms of improvements in lipid levels.

ADRs occurred in 6.4% of patients, which was similar to the value of 5.1% reported in our previous study (J-BENEFIT) in which bezafibrate was administered alone [20], and to the rate of 7.0% in patients treated with fenofibrate in combination with ezetimibe [13]. Severe ADRs occurred in three patients and the administration of these drugs was terminated in all three. None of the patients in this study experienced rhabdomyolysis.

All four patients with gallstones (0.6%) had diabetes in addition to dyslipidemia and were > 50 years old. Three of these patients were obese with BMIs of 28.6, 29.6, and 30.1 kg/m². Because dyslipidemia, diabetes, advanced age, and obesity are known risk factors for gallstones [26], it seems likely that these subjects had physiological features that predisposed them to gallstone formation. The gallstone incidence based on the study duration was 1.1 per 100 person-years. The incidence of gallstones in the general population was reported to be 1.4 per 100 person-years [27] or 3.56%/year in an epidemiological study conducted in Taiwan that examined diabetic patients without gallstones [28]. Thus, the gallstone incidence in this study did not differ from that in the general population.

In terms of the impact of combination therapy on renal function, we observed a significant increase in creatinine levels between baseline and LOCF, although the magnitude of the increase was not clinically meaningful. However, because we did not determine the estimated glomerular filtration rate (eGFR), further studies will be necessary to evaluate the effects of this combination on renal function. We also considered the impact of combination therapy on liver functions. Co-administration of fenofibrate and ezetimibe reportedly increases the risk of hepatic dysfunction [13, 15]. In our study, however, AST, ALT, GGT, and ALP decreased significantly from baseline to the LOCF. Bezafibrate accelerates fatty acid beta-oxidation by stimulating PPAR alpha receptors in the liver [29], and was reported to have lower hepatotoxicity than fenofibrate in mitochondrial toxicity studies using rat livers [30].

In the safety evaluation, co-administration of bezafibrate and ezetimibe was shown to not increase the risk of gallstone formation. In addition, liver function test values decreased, and BMI, systolic blood pressure, diastolic blood pressure and glycated hemoglobin levels showed no adverse influences. On the other hand, “increased blood CPK” and “myalgia” were noted as ADRs, and creatinine and blood urea nitrogen levels were significantly increased. As described in the exclusion criteria for this study, bezafibrate should not be administered to patients with a serum creatinine level ≥ 2.0 mg/dL.

In the efficacy analysis, LDL-C, TG, and non-HDL-C levels decreased and HDL-C increased significantly from baseline to the LOCF during combination therapy (all, p < 0.001). In particular, non-HDL-C levels decreased significantly from 183.5 mg/dL at baseline to 143.8 mg/dL at the LOCF (change: –39.6 mg/dL). This change is greater than that in the J-BENEFIT study [17], in which 2818 patients received bezafibrate monotherapy and non-HDL-C levels decreased from 178.3 mg/dL at baseline to 160.2 mg/dL at the LOCF (change: –18.1 mg/dL). These observations suggest that the combination therapy used in this study had beneficial effects on lipid profiles. The non-HDL-C fraction contains the lipoproteins that can cause arteriosclerosis, including remnant lipoproteins, and higher non-HDL-C levels were suggested to be associated with greater risk of coronary artery disease [31]. It was also reported that non-HDL-C is a better marker than LDL-C for estimating the risk of arteriosclerotic disease [32]. In particular, the Japan Atherosclerosis Society recommends that, in patients with TG > 400 mg/dL, non-HDL-C should be used rather than LDL-C as a clinical marker.

In the subgroup analysis, when the lipid parameter changes at the LOCF from the baseline level in each of the three groups (EZE + BEZA, BEZA + EZE and BEZA & EZE groups) were compared, significant improvement was seen in all lipid parameters. In addition, comparisons among the three groups revealed no significant differences in LDL-C or non-HDL-C. These efficacies were similar in the three groups and a complementary effect was seen. On the other hand, even after adjusting for baseline values, the analysis of covariance (ANCOVA) method showed significant differences in HDL-C and TG. These observations might be attributable to HDL-C and TG responding differently to the treatment interventions.

Our study has several important limitations. First, this was conducted as a post-marketing, prospective observational study, and was designed to examine and confirm the safety and efficacy of bezafibrate in combination with ezetimibe in patients with dyslipidemia, without a control group. Because it is impossible to remove all of the potential confounding factors, our results should be interpreted with caution until a randomized controlled study with a large number of patients can be performed. Second, for logistic, economic, and other reasons, laboratory parameters were measured at each of the participating institutions, rather than in a central laboratory. Third, LDL-C levels were estimated using the Friedewald formula. Therefore, cases with TG ≥ 400 mg were not evaluated for LDL-C [17]. Fourth, the usefulness of triple combination therapy with fenofibrate, ezetimibe and a statin has recently been reported [33, 34]. Since this study was conducted for the purpose of clarifying the safety and efficacy of combination therapy with bezafibrate and ezetimibe, investigation of triple combination therapy with the addition of a statin was not part of the study design. Even in the case of combination therapy with bezafibrate and ezetimibe, an insufficient effect was seen in some patients. It is therefore necessary to sufficiently investigate triple combination therapy with the addition of a statin in future studies.

Nevertheless, this was the first study to examine the safety and efficacy of bezafibrate in combination with ezetimibe, and we confirmed that this combination achieved significant improvements in LDL-C, HDL-C, TG, and non-HDL-C levels. From the perspective of coronary artery disease prevention, this combination is useful as part of comprehensive management regimen for dyslipidemia.

From the perspective of coronary artery disease prevention, comprehensive management of dyslipidemia is necessary by treating patients with low HDL-C and/or high TG levels in addition to those with high LDL-C levels. Based on our results, bezafibrate in combination with ezetimibe is a safe and effective treatment option that achieved marked improvements in LDL-C levels together with the expected increase in HDL-C levels and a decrease in TG levels.