Long-Term Benefit and Withdrawal Effect of Statins After Percutaneous Coronary Intervention: A Nationwide Population-Based Cohort Study

Abstract

Purpose

Despite indubitable evidence for the cardiovascular benefits of statins, there have been concerns that statin discontinuation may cause negative effects known as “statin withdrawal syndrome.” This study aimed to assess the benefit and the withdrawal effect of statins after percutaneous coronary intervention (PCI).

Patients and Methods

We conducted a retrospective cohort study on 5218 patients who underwent PCI between 2002 and 2013 using the nationwide health insurance claim data in Korea. Based on the prescription data, the use of statins during follow-up was classified into three risk periods: “statin period” (period with statin cover), “statin withdrawal period” (withdrawal of statin within 30 days), and “no statin period” (no exposure to statin for longer than 30 days). The primary outcome was the composite outcome of myocardial infarction, coronary revascularization, stroke, and all-cause death. We performed multivariate Cox proportional regression analyses which treated the use of statins as a time-dependent variable.

Results

During the follow-up period of 3.54 ± 2.91 years (mean ± standard deviation), 1515 (29.0%) patients sustained a primary outcome. Compared with the “no statin period,” the “statin period” was associated with lower risk of the primary outcome (adjusted hazard ratio [HR] 0.72, 95% confidence interval [CI, 0.63–0.81]). While the “statin withdrawal period” posed a significantly increased risk (adjusted HR 1.87, 95% CI [1.52–2.29]). With respect to the intensity of statins associated with withdrawal, dose-dependent increased risk was observed for withdrawal of low-, moderate-, and high-intensity statins; adjusted HR [95% CI] were 1.45 [0.74–2.86], 1.86 [1.49–2.32], and 2.61 [1.41–4.81], respectively.

Conclusion

After PCI, there was an increased cardiovascular risk during the statin withdrawal period, especially with the use of high-intensity statins. To maximize the beneficial effect and to avoid the withdrawal effect of statins, high-risk patients need to adhere to taking statins without discontinuation.

Introduction

Coronary artery disease (CAD) is the leading cause of morbidity and mortality worldwide. Statins (3-hydroxy-3-methylglutaryl-CoA reductase inhibitor) are a class of lipid-lowering agents, which have been established to be effective in reducing cardiovascular risk.^1–3 Current guidelines strongly recommend lifelong statin therapy for high-risk patients with established CAD.^4,5 Despite the established cardiovascular benefits, statin use is dynamic or intermittent in clinical practice, and suboptimal statin use is frequent.^6–8 There is cumulative evidence that discontinuation and non-adherence to the use of statins are strongly associated with poor cardiovascular prognosis.^9–11 However, knowledge of statin use is still limited throughout the long-term follow-up period in patients with CAD. Furthermore, sudden discontinuation of statins may cause additional adverse effects (statin rebound or withdrawal syndrome).^12–14 To evaluate the benefit and the withdrawal effect of statins in a long-term follow-up period, we conducted a retrospective cohort study on patients who underwent percutaneous coronary intervention (PCI) using the nationwide health insurance claim data.

Materials and Methods

Data Source

In this study, we used the data from the National Health Insurance Service‑National Sample Cohort (NHIS‑NSC) in Korea.¹⁵ South Korea has universal health insurance coverage by the NHIS under their national plans. The NHIS-NSC included 1,025,340 individuals selected in 2002 (2.2% of the total eligible Korean population) by stratified random sampling according to sex, age, and household income. The NHIS-NSC contains information on all health claim data between 2002 and 2013 including hospital visits, medical procedures, drug prescriptions, diagnoses, and mortality (cause and date of death). The diagnosis at each hospital visit was recorded according to the International Classification of Diseases, 10th revision (ICD-10).

Study Design

This was a retrospective cohort study based on the NHIS-NSC. We included subjects who were aged ≥20 years and who underwent PCI (angioplasty with or without stent; they had health claim codes of “M6561”, “M6562”, “M6563”, “M6564”, “M6551”, and “M6552”) in 2002–2013. To minimize confounding bias by cancer, we excluded patients who had a diagnosis code of malignant neoplasms (C00–C97) during the study period. Index date for each patient was defined as the admission date for PCI. The primary outcome was a composite of myocardial infarction (MI), coronary revascularization, stroke (ischemic and hemorrhagic), and all-cause mortality, whichever occurred first after the index date. MI was defined as hospitalization (admission or emergency department visit) with a primary diagnosis of I21. Coronary revascularization was determined by health claim codes of PCI (“M6561,” “M6562,” “M6563,” “M6564,” “M6551,” “M6552”) and coronary artery bypass graft (“OA631*–OA639*”, “OB631*–OB639*”, “OA641*”, “OA642*”, “OA647*”, “O0161*–O0171*”, “O1641*–O1647*”.¹⁶ If a patient admitted with MI and received coronary revascularization during the hospitalization period, the case was classified as MI. Stroke was diagnosed in patients hospitalized with a primary diagnosis of I60–63 (ischemic stroke, I63; hemorrhagic stroke, I60–62) and who underwent brain CT or MRI during the hospital visit. In previous validation studies with the NHIS, the diagnostic accuracy of I21 for MI was reported as 73–93%, and I60–I63 for stroke as over 80%.^17–20 Several research articles have been published based on the NHIS health claim data on MI and stroke.^21–23 Unless the patient was disqualified from the NHIS because of death or emigration, all included patients were followed until December 2013 or the date of the primary outcome. As a very short period of follow-up was inadequate to evaluate long-term prognosis following the use and the withdrawal of statins, those followed up for ≤30 days were excluded. All data in the NHIS-NSC were fully anonymized. Therefore, this study was approved, and informed consent was waived, by the Institutional Review Board of Bundang CHA Medical Center (CHAMC 2017-03-021).

Prescription Data Including Statin

All prescription data of included patients are available in the NHIS-NSC. According to the prescription data of statins, statin treatment during follow-up was classified into three risk periods: “statin period” (days covered by statins), “statin withdrawal period” (within 30 days from the end of the most recent statin exposure), and “no statin period” (no statin exposure for more than 30 days). Figure 1 illustrates examples of the risk periods according to the respective statin treatment regimes. In the “statin withdrawal period,” the intensity of the last used statins (low, intermediate, or high) was determined by the daily dose and type (atorvastatin, fluvastatin, rosuvastatin, pitavastatin, pravastatin, simvastatin, and lovastatin) according to the classification in the 2013 American Heart Association guideline on the treatment of high blood cholesterol.⁴ As a covariate, we also collected data on the use of aspirin and adenosine diphosphate (ADP) receptor antagonist (clopidogrel, ticlopidine, ticagrelor and prasugrel). The use of statins and antiplatelets during follow-up was treated as a time-dependent variable for analyses.

Figure 1.

Examples of the definition of risk periods according to statin treatment.

Abbreviation: PCI, percutaneous coronary intervention.

Other Covariates

We identified the data on sex, age (classified into five-year groups in the NHIS-NSC), and household income as a marker of socioeconomic status in the year in which PCI was undertaken. Household income obtained from the NHIS-NSC was subdivided into tertile groups (low, middle, and high) for analytical convenience. Hypertension (I10–15), diabetes mellitus (E08–11, E13–14), and atrial fibrillation (I48) were defined based on the presence of the diagnostic codes (ICD-10) in the NHIS-NSC before or at the time of discharge after PCI. Hypertension and diabetes mellitus were recognized as relevant only if the subjects received antihypertensive (calcium-channel blockers, angiotensin-converting enzyme inhibitors, angiotensin-receptor blockers, diuretics, beta-blockers, alpha-blockers, or vasodilators) or antidiabetic (sulfonylureas, biguanides, alpha-glucosidase inhibitors, thiazolidinediones, meglitinides, glucagon-like peptide-1 receptor agonists, dipeptidyl peptidase-4 inhibitors, or insulin) agents in combination with the respective diagnostic codes.²⁴ A history of MI was determined when a patient was admitted with a diagnosis of “I21” before or upon the decision to perform PCI.

Statistical Analysis

We computed the hazard ratio (HR) and 95% confidence interval (CI) for the primary outcome using time-dependent Cox proportional hazard regression analyses. The assumption of proportional hazards in the Cox models was tested by evaluating scaled Schoenfeld residuals, which were found to be satisfactory. Adjustments were performed for sex; age (as continuous variables); level of household income; presence of hypertension, diabetes mellitus, atrial fibrillation, and MI (as time-independent variables); and use of antiplatelets, and statins during follow-up (as time-dependent variables). As secondary outcome analysis, we constructed individual Cox regression models for each clinical outcome (MI, coronary revascularization, stroke, and all-cause mortality). The data manipulation and statistical analyses were performed with PostgreSQL version 10.1 (The PostgreSQL Global Development Group; https://www.postgresql.org/) and R software version 3.4.1 (The R Foundation for Statistical Computing, Vienna, Austria; http://www.R-project.org/). A two-sided P-value of <0.05 was considered statistically significant.

Data Availability

Requests for access to the NHIS data can be made through the homepage of National Health Insurance Sharing Service [http://nhiss.nhis.or.kr/bd/ab/bdaba021eng.do]. To gain access to the data, a completed application form, a research proposal, and the applicant’s approval document from the institutional review board should be submitted to and reviewed by the inquiry committee of research support in the NHIS. The NHIS-NSC data were fully anonymized and did not contain any information that allowed patient identification.

Results

In the NHIS-NSC, there were 7682 adult patients (age ≥20 years) who underwent PCI between 2002 and 2013. After excluding 2464 patients who were followed up for ≤30 days or who had diagnosis of malignant neoplasms, we finally included 5218 patients. Among the 5218 included patients, 65.2% were male, and the median age was 60–64 years (Table 1). The total study follow-up period of study patients was 18,049 person-years. Of them, the proportion of days-covered by any statins were 71.3% (12,866 person-years). In terms of the percentage of individual statins used, atorvastatin was the highest (44.9%), and rosuvastatin (23.0%) and simvastatin (16.1%) were second and third. During the follow–up period of 3.54 ± 2.91 years (mean ± standard deviation), there were 1515 patients (29.0%) who suffered primary outcome events (358 with MI, 670 with coronary revascularization, 181 with stroke, and 303 with all-cause mortality; considering only the earliest outcome for each patient).

Table 1.

Clinical Characteristics of Patients Who Received Percutaneous Coronary Intervention

Variable	[All] N = 5218
Sex, male	3402 (65.2)
Age	60–64 [50–54; 70–74]
Hypertension	4511 (86.5)
Diabetes mellitus	1742 (33.4)
Atrial fibrillation	436 (8.4)
Myocardial infarction	2380 (45.6)
Household Income
Low	1535 (29.4)
Middle	1908 (36.6)
High	1775 (34.0)
Year of Admission
2002–2005	1059 (20.3)
2006–2009	1805 (34.6)
2010–2013	2354 (45.1)

Note: Data are number (%) or median [interquartile range].

In a time-dependent Cox regression analysis (Table 2), the “statin period” was significantly associated with lower risk of the primary outcome after PCI compared with the “no statin period” (adjusted HR [95% CI], 0.72 [0.63–0.81], p < 0.001). While the “statin withdrawal period” resulted in a significantly increased risk of the primary outcome (adjusted HR [95% CI], 1.87 [1.50–2.29], p < 0.001). Further analysis with respect to the intensity of the statin used just before withdrawal revealed an inverse dose–response relationship between risk of the primary outcome and the intensity of statin. Adjusted HR [95% CI] for withdrawal of “low-,” “moderate-,” and “high-intensity” statin compared to that in the “no statin period” were 1.45 [0.74–2.86], 1.86 [1.49–2.32], and 2.61 [1.41–4.81], respectively (Figure 2). This finding suggested a greater rebound phenomenon with discontinuation of a high-intensity statin compared to the rebound observed with discontinuation of a low-intensity statin. In the secondary outcome analysis for individual outcomes, statin withdrawal was significantly associated with increased risk for MI, coronary revascularization, and all-cause death (Table 3).

Table 2.

Result of Cox Regression Analyses for Primary Outcome After Percutaneous Coronary Intervention

Variable	Univariate		Multivariate
	Unadjusted HR [95% CI]	p-value	Adjusted HR [95% CI]	p-value
Time-fixed variables
Sex, male	0.98 [0.88–1.08]	0.646	1.06 [0.95–1.19]	0.292
Age, per 5 years	1.07 [1.05–1.10]	< 0.001	1.07 [1.04–1.10]	< 0.001
Hypertension	1.09 [0.93–1.27]	0.302	1.02 [0.87–1.20]	0.082
Diabetes mellitus	1.34 [1.20–1.48]	< 0.001	1.33 [1.19–1.47]	< 0.001
Atrial fibrillation	1.27 [1.08–1.50]	< 0.001	1.16 [0.98–1.37]	0.090
Myocardial infarction	1.42 [1.28–1.57]	< 0.001	1.42 [1.29–1.58]	< 0.001
Household Income
Low	1 (Ref)	–	1 (Ref)	–
Middle	0.99 [0.87–1.12]	0.863	1.03 [0.91–1.17]	0.637
High	1.05 [0.92–1.19]	0.456	1.08 [0.95–1.23]	0.243
Time-dependent Variables
Antiplatelets
No aspirin, no ADPRB	1 (Ref)	–	1 (Ref)	–
Aspirin only	0.49 [0.42–0.57]	< 0.001	0.71 [0.59–0.85]	< 0.001
ADPRB only	0.58 [0.46–0.72]	< 0.001	0.82 [0.64–1.05]	0.120
Aspirin plus ADPRB	0.69 [0.60–0.80]	< 0.001	1.03 [0.86–1.23]	0.730
Statins
No statin	1 (Ref)	–	1 (Ref)	–
Statin use	0.69 [0.62–0.78]	< 0.001	0.72 [0.63–0.81]	< 0.001
Withdrawal	1.90 [1.56–2.32]	< 0.001	1.87 [1.52–2.29]	< 0.001

Note: Data are derived from multivariate time-dependent Cox proportional hazard regression model.

Abbreviations: ADPRB, adenosine diphosphate receptor blocker (clopidogrel, prasugrel, ticlopidine, ticagrelor); CI, confidence interval; HR, hazard ratio.

Figure 2.

Risk for primary outcome according to statin treatment. (A) Adjusted HR for “statin use period” and “withdrawal period” compared to the “no statin period” (Ref). (B) Adjusted HR for statin withdrawal for “low-intensity”, “moderate-intensity”, and “high-intensity” statins compared to the “no statin period” (Ref). Data are derived from multivariate time-dependent Cox proportional hazard regression analysis adjusted for the variables listed in Table 2

Abbreviations: CI, confidence interval; HR, hazard ratio.

Table 3.

Secondary Outcome Analysis for Individual Outcome

Event of Interest	Myocardial Infarction	Coronary Revascularization	Stroke	All-Cause Death
Risk period
No statin	1 (Ref)	1 (Ref)	1 (Ref)	1 (Ref)
Statin use	0.84 [0.64–1.11]	0.79 [0.66–0.94]	0.73 [0.33–1.61]	0.44 [0.34–0.58]
Withdrawal	2.11 [1.39–3.20]	2.43 [1.81–3.26]	0.78 [0.55–1.12]	1.49 [1.02–2.18]

Notes: Data are adjusted hazard ratio [95% confidence interval] derived from multivariate time-dependent Cox proportional hazard regression models for individual outcomes. Adjustments were performed for same variables listed in Table 2.

Discussion

The current study evaluated the beneficial effect and the withdrawal effect of statins in a long-term period after PCI based on real-world data. The current guidelines strongly recommend that high-intensity statin therapy should be continued before and after PCI to reduce the development of cardiovascular adverse events.^25,26 Statins are generally well tolerated, but as many as 20–30% of patients report adverse events, and discontinuation of statin is very common in the clinical setting.^6,12,27 About half of patients starting statin therapy discontinue the statin within the first year, and adherence to the statin decreases with time.²⁸ Despite the emphasis on high-intensity statin use in the guidelines, adherence to high-intensity statins was relatively lower compared with adherence to low- to moderate-intensity statins, and there were more frequent adverse events.^23,29

Suboptimal use and discontinuation of statins have been important clinical issues.^10,30,31 After myocardial infarction, early discontinuation of statins was a significant risk factor for worse clinical outcomes.^32,33 In patients who had undergone major vascular surgery, statin discontinuation during the postoperative period was associated with a higher incidence of myocardial ischemia, nonfatal myocardial infarction, and cardiovascular death.⁹ Previous studies have focused mainly on the risk of statin discontinuation in the early phase after vascular events. Our longitudinal study evaluated the prognosis according to the use and discontinuation of statin during a long-term period. After PCI, patients who received statin treatment were at a significantly lower risk of the primary outcome, which means that statin therapy should be continued to maintain the protective effects on the cardiovascular system.

In this study, statin withdrawal led to an increased risk in excess of that of no statin use. More interestingly, the degree of withdrawal effect was correlated with the intensity of the statin last taken. These findings suggest the presence of a rebound phenomenon in the early period of statin withdrawal, known as “statin withdrawal syndrome.” To maximize the cardiovascular benefits of statin therapy and to avoid the detrimental effect of statin withdrawal, there is a need to develop more practical interventions combining educational and behavioral components.^28,34,35 The European Atherosclerosis Society Consensus Panel recommends brief discontinuation and re-initiation of statin therapy in patients with statin intolerance such as statin-attributed muscle symptoms.³⁶ Based on the results of the present study, we found that a greater rebound effect occurs in association with withdrawal from high-intensity statins, and this is proportional to the statin intensity. Therefore, when statin intolerance develops (except in patients with serious side effects), it might be reasonable to down-titrate the dose initially rather than to abruptly stop the drugs or change to non-statins, especially in those taking high-intensity statins.

Some mechanisms have been proposed to explain the rebound phenomenon caused by statin withdrawal: 1) Induction of vascular dysfunction: The Rho family of guanosine triphosphates (GTP) is a family of small signaling G proteins which modulate the levels of nitric oxide, production of reactive oxygen species, and levels of angiotensin II-AT1 receptors, endothelin-I, adhesion molecules, and inflammatory cytokines.¹² Statins can block isoprenoid-dependent Rho membrane translocation and GTP-binding activity, which leads to upregulation of endothelial nitric oxide synthase expression and accumulation of nonisoprenylated Rho protein in the endothelial cytosol, inducing a vascular protective effect.³⁷ Withdrawing statins can restore the availability of isoprenoids and result in a rebound activation of Rho and downregulation of endothelial nitric oxide production. Acute statin withdrawal increases angiotensin II receptor type 1 activity in smooth muscle cells and exacerbates vascular dysfunction.³⁸ 2) Rebound of inflammatory response: Statin withdrawal could induce a rebound phenomenon of the inflammatory response by increasing expression of inflammatory markers like C-reactive protein and interleukin-6.³⁹ In an experimental study on human and rat vascular smooth muscle cells, statin withdrawal increased levels of proatherogenic substances, such as free radicals, monocyte chemoattractant protein 1, and tissue factor gene expression.⁴⁰ 3) Decreased angiogenesis: Statin discontinuation was purported to reduce angiogenesis, which could delay myocardial recovery after acute coronary syndrome.⁴¹

We should acknowledge the possible limitations of this study. This study had a retrospective cohort design; therefore, it might have confounding effects. Although there are previous validation studies for the outcome measures that used the NHIS database, non-hospitalized outcomes could not be captured with the limitations of the health claim database. We determined statin treatment by accessing the prescription data on the NHIS database. Actual statin use might have been different from the prescription data. Further large clinical and experimental studies are needed to evaluate the effect of “statin withdrawal” on cardiovascular prognosis and the underlying mechanisms.

Conclusion

After PCI, the use of statins showed a significant beneficial effect in the long-term period. Withdrawal of statins resulted in increased risk of cardiovascular events. Clinicians should take comprehensive measures to ensure that continued use of statins is maintained in all patients after PCI.

Disclosure

The authors report no conflicts of interest in this work.