https://orcid.org/0000-0002-3202-6307
Figures
Abstract
Background
The validity of cardiovascular disease (CVD) risk calculators in decision for statin therapy has not been fully evaluated at a population level. This study aimed to examine the net benefits of statins according to predicted CVD risk.
Methods and findings
A cohort of 40 to 79-year-old Korean adults without CVD was generated from the National Health Information Database 2006–2017. Major CVD event rates and all-cause mortality in 58,265 users who initiated statins during 2007–2010 were compared with those in 58,265 nonusers matched on propensity scores, from January 1, 2012 through December 31, 2017. Additionally, simulation was performed for the population-based cohort of 659,759 adults. CVD risk was predicted using the 2018 revised Pooled Cohort Equations. In propensity score-matched cohort, the CVD hazard ratios (95% CIs) in occasional, intermittent, and regular statin users were 1.06 (0.93–1.20), 0.82 (0.70–0.97), and 0.57 (0.50–0.64), respectively. The corresponding mortality hazard ratios were 1.01 (0.92–1.10), 0.87 (0.78–0.98), and 0.71 (0.66–0.77), respectively. In stratified analyses, the relative risk reductions were similar, irrespective of age, sex, or predicted CVD risk. Accordingly, absolute risk reductions were greater in higher risk categories. In 6-year follow-up simulation cohorts, regular statin use could reduce 17 CVDs and 28 deaths in 1000 adults with a 10-year risk of ≥10.0% vs 10 CVDs and 14 deaths in 1000 with ≥2 major risk factors. However, in actual adults with a risk of ≥10%, statin use was insufficient and estimated to reduce 3 CVDs and 4 deaths in 1000. Limitations of this study include assessment of medication use based on the prescription data, lack of information on the intensity of statins, and limited generalizability to individuals with very old age or other ethnicity.
Citation: Jung HH (2021) Statin use and outcome risks according to predicted CVD risk in Korea: A retrospective cohort study. PLoS ONE 16(1): e0245609. https://doi.org/10.1371/journal.pone.0245609
Editor: Katriina Aalto-Setala, University of Tampere, FINLAND
Received: November 10, 2020; Accepted: January 4, 2021; Published: January 15, 2021
Copyright: © 2021 Hae Hyuk Jung. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Data Availability: The author cannot legally distribute the data. The data contain potentially identifying or sensitive patient information. The National Health Information Database can be requested from the National Health Insurance Sharing Service (http://nhiss.nhis.or.kr) and are provided in a “Data analysis room” located within the National Health Insurance Service (https://nhiss.nhis.or.kr/bd/ab/bdaba032eng.do).
Funding: The author received no specific funding for this work.
Competing interests: The author has declared that no competing interests exist.
Introduction
Statins are widely used to prevent cardiovascular disease (CVD) events: many studies have shown that statins reduce CVD-related morbidity and mortality in patients with or without prior CVD [1–3]. However, the questions about their harmful effects and beneficiaries have remained unresolved.
In terms of decision-making for statin therapy, it would be important to know whether an absolute risk reduction is worth the potential harms or inconvenience of daily statin use. The relative risk reductions for CVD events in statin vs placebo groups were similar across the majority of primary prevention trials [3–8]. Furthermore, a recent review of statin trials reported that the relative risk reductions were similar across age-, sex-, and other risk-based categories [2]. Given similar relative risk reductions, the absolute benefits of statins will be greater among patients at higher risk. Thus, current guidelines recommend predicting CVD risk with a risk calculator and initiating primary prevention statin therapy in individuals at higher predicted risk [9–11]. However, there remain debates about the risk of statin-related adverse events [12–14], and the validity of CVD risk calculators in decision for statin therapy has not been fully evaluated at a population level.
To assess the net benefit of primary prevention statin therapy according to the predicted risk for CVD, this study examined the associations between statin use status and outcome risks across the predicted risk categories, in a retrospective cohort of Korean adults with no prior CVD.
Methods
Participants
This study was conducted from June 2018 to December 2019 using the National Health Information Database (NHID), which is a database for the entire population of Korea managed by the National Health Insurance Service (NHIS) [15]. After the preliminary analysis, the final analysis was performed from February 2019. The Institutional Review Board of Kangwon National University Hospital (IRB File No: KNUH-2018-06-013-001, KNUH-2019-02-001) approved this study and waived the need for informed consent as the data were de-identified prior to analysis. This study is reported as per the Strengthening the Reporting of Observational Studies in Epidemiology (STROBE) for cohort study (S1 Checklist).
A propensity score-matched cohort was generated from the NHID, to compare the outcomes in statin users with those in nonusers. First, one million adults were randomly selected from 7.13 million citizens aged 40–79 years who underwent nationwide health screening in 2009, since when high-density lipoprotein (HDL) cholesterol and creatinine levels have been measured (Fig 1). The health screening and NHIS reimbursement records were collected from 2006 to 2017. I excluded the following cases from these one million adults: 57,201 with missing or outlier data; 150,072 with a medical history of heart disease, stroke, or cancer or with an estimated glomerular filtration rate (eGFR) of <30 ml/min/1.73 m2; and 83,877 who died or developed CVD, major cancers, or end-stage kidney disease (ESKD) before the baseline (i.e., January 1, 2012). From the remaining 708,850 adults, 61,665 users who had initiated statins during the 2007–2010 period and 601,494 nonusers who had never or rarely used statins before the baseline were identified. As past statin users might be more likely to have unmeasured health problems, the users who received statins in the year of cohort entry were excluded to minimize residual confounding. The analysis also excluded the users who initiated statins in the last year before baseline, since their statin use status could not reliably be assessed at the baseline. The propensity score (i.e., the predicted probability that a person would be a statin user) among 663,159 adults was calculated using a logistic regression with measured baseline covariates (i.e., age, sex, family history of CVD, income, physical exercise, alcohol consumption, smoking, body mass index, systolic blood pressure, fasting blood glucose, untreated total cholesterol, HDL cholesterol, proteinuria, and eGFR). Then, the pairs of statin users and nonusers were created requesting exact matches for the CVD risk categories and employing a greedy, nearest-neighbor matching algorithm with a caliper width of 0.2.
Exposures and covariates
In each year of follow-up, statin use status (regular, intermittent, occasional, or nonuse; S1 Table in S1 File) was determined as the primary exposure of interest, using information on the prescription of drugs (S2 Table in S1 File). Regular use was determined if statins were used for >2/3 of each period of statin therapy (from the initiation of medication to each year of follow-up), intermittent use if the drugs were used for 1/3–2/3 of each period, occasional use if the drugs were used for <1/3 of each period, and nonuse if the drugs were not used for ≥90 days per year. In each year, antihypertensive and antidiabetic use statuses (regular, irregular, or non-use) were also determined: regular or irregular use was determined if a case received these drugs for >1/2 or ≤1/2 of each period of medication, correspondingly. Meanwhile, non-use was determined if a case did not receive these drugs for ≥90 days per year.
Using the baseline data, I categorized age (40–44, 45–49, 50–54, 55–59, 60–64, 65–69, 70–74, or 75–79 years), sex (men or women), family history of CVD (yes or no), income (high, middle, or low), physical exercise (<1, 1–2, 3–4, or ≥5 days/week), alcohol consumption (0, 0.1–0.4, 0.5–1.4, 1.5–2.9, or ≥3.0 drinks/day), smoking (never, former, or current smoker), body mass index (10.0–18.4, 18.5–22.9, 23.0–24.9, 25.0–29.9, or 30.0–50 kg/m2), systolic blood pressure (90–109, 110–119, 120–129, 130–139, 140–149, 150–159, or 160–200 mm Hg), fasting blood glucose (1.7–4.3, 4.4–5.5, 5.6–6.9, 7.0–7.7, 7.8–8.8, 8.9–9.9, 10.0–50.0 mmol/l), untreated total cholesterol (3.37–4.13, 4.14–5.17, 5.18–6.21, 6.22–7.24, or 7.25–8.29 mmol/l; for a missing value, I imputed the product of treated total cholesterol and 1.10 which was the mean ratio of untreated to treated levels in participants in whom both levels were available), HDL cholesterol (0.52–1.03, 1.04–1.54, or 1.55–2.59 mmol/l), proteinuria (yes or no), and eGFR (30–44, 45–59, 60–89, or ≥90 ml/min/1.73 m2). Details on baseline covariates are provided in S1 Text and S3 Table in S1 File.
Risk categories
Participants were assigned to one of three categories according to the 10-year risk for CVD (high,10.0–90.0%; moderate, 5.0–9.9%; or low, 0.1–4.9%) predicted using the 2018 revised Pooled Cohort Equations (S2 Text in S1 File) [16]. Participants were also categorized by the number of risk factors present at the baseline (≥3, 2, or ≤1 of the 5 risk factors―hypertension, diabetes, dyslipidemia, proteinuria, and active smoking; S1 Table in S1 File).
Outcomes
The study outcomes were identified using NHIS reimbursement record-retrieved information on in-hospital procedures, surgeries, and medications (S2 Table in S1 File), along with the diagnosis codes in the NHID (S4 Table in S1 File). The primary outcomes were major CVD events and all-cause deaths by December 31, 2017. Major CVD event was identified as a composite of acute myocardial infarction, acute ischemic stroke, and cardiovascular death: i.e., revascularization or critical care unit admission for myocardial infarction, revascularization or critical care unit admission for ischemic stroke, and death from CVD. Vital status was confirmed using death certificates from Statistics Korea.
The secondary outcomes comprised five non-CVD events. Diabetes mellitus was identified as a fasting glucose of ≥7.0 mmol/l during biennial health screenings or a prescription of antidiabetics for ≥90 days per year. Dementia cases were defined as those that received cholinesterase inhibitors or memantine for dementia: in Korea, the medications could be reimbursed in the cases with mini mental state exam ≤26, clinical dementia rating ≤3, or global deterioration scale ≤7. Severe cataract cases were defined as those that underwent first surgery for cataract: it comprised cataract surgery, primary intraocular lens implantation, or lens-phacoemulsification. ESKD was defined as dialysis for ≥90 days per year or kidney transplantation and identified using information about hemodialysis, prescribed peritoneal dialysates, and kidney transplantation. Major cancers comprised the seven most common causes of cancer death in Korea: i.e., lung cancer, hepatoma, colon cancer, stomach cancer, pancreatic cancer, gallbladder and bile duct cancer, and breast cancer.
Statistical analysis
The primary analyses compared the outcome risks in users who had recently initiated statins with those in nonusers who had never or rarely received statins at the baseline. To avoid selection bias due to loss of follow-up, baseline nonusers, including those who received statins thereafter, were used as references throughout the study period. In propensity score-matched 58,265 pairs, the hazard ratios were estimated using Cox regression with time-varying covariates to incorporate changes in medication use over time. The yearly updated statin, antihypertensive, and antidiabetic use status were entered as time-lagged covariates for subsequent years (S5 Table in S1 File) [17]. The categorized baseline covariates were entered as fixed covariates to address potential imbalance resulting from further classification of statin users according to statin use status [18]. The analyses were conducted for all participants combined and for subgroups stratified by age (≥65 or <65 years), sex (men or women), or predicted CVD risk.
Secondary analyses were conducted to explore residual confounding related to statin indication. The hazard ratios of regular use were estimated in comparison with occasional rather than nonuse in a 61,665 users having initiated statins in the 2007–2010 period. The Cox models included the yearly medication use status as time-varying covariates and the baseline status along with the year of statin initiation as fixed covariates. To explore the robustness of the results, the hazard ratios were reanalyzed in a NHIS-generated sample cohort (S3 Text in S1 File). Further, to explore the validity of the revised Pooled Cohort Equations, the hazard ratios for major CVD events were estimated with the predicted 10-year risk for CVD using restricted cubic spline functions, in response to peer reviewer comments.
To estimate the absolute benefits of statins in the Korean population, simulation analyses were conducted combining the 601,494 baseline nonusers of the full cohort and the 58,265 pairs of the propensity score-matched cohort: the 58,265 nonusers of the matched cohort were double counted as simulated nonusers to replace 58,265 statin users. Statistical analyses were performed using SAS (version 9.4; SAS Institute, Cary, NC, USA) and SPSS (version 25.0; SPSS Inc, Chicago, IL, USA). Data are presented as numbers and percentages, means and SDs, or hazard ratios and 95% CIs.
Results
Baseline characteristics
The propensity score-matched cohort included 58,265 pairs of statin users and nonusers. They had baseline characteristics with standardized differences of mostly less than 0.10 (Table 1) [19]. Among statin users, the occasional, intermittent, and regular user groups had comparable demographic characteristics. The regular statin user group had higher proportions of regular antihypertensive and antidiabetic users than the other two groups.
Statin use and outcome risks
In the propensity score matched cohort of 58,265 pairs of statin users and nonusers, major CVD events occurred in 1105 nonusers and 818 statin users, and all-cause deaths were noted in 2246 nonusers and 1797 users, over 6 years of follow-up. Multivariable-adjusted hazard ratios compared with baseline nonusers were estimated according to statin use status (Fig 2). The hazard ratios (95% CI) for major CVD events were 1.06 (0.93–1.20) in occasional users, 0.82 (0.70–0.97) in intermittent users, and 0.57 (0.50–0.64) in regular users. The corresponding hazard ratios (95% CI) for all-cause mortality were 1.01 (0.92–1.10), 0.87 (0.78–0.98), and 0.71 (0.66–0.77), respectively.
Among 58,265 pairs matched on propensity scores, multivariable-adjusted hazard ratios were estimated using Cox models with a time-varying covariate for statin use status. Baseline nonusers served as the reference. The participants who were diagnosed with cataract (or dementia, or diabetes) before the baseline were excluded from the analysis of cataract (or dementia, or diabetes). CVD, cardiovascular disease; ESKD, end-stage kidney disease.
In the secondary analyses that estimated the hazard ratios in comparison with occasional rather than nonusers, the risk reductions for major CVD events and all-cause mortality in regular statin users were substantial with the hazard ratios similar to those in the primary analyses (Fig 3).
Within 61,665 statin users, multivariable-adjusted hazard ratios were estimated using Cox models with a time-varying covariate for statin use status. Occasional users served as the reference. The participants who were diagnosed with cataract (or dementia, or diabetes) before the baseline were excluded from the analysis of cataract (or dementia, or diabetes). CVD, cardiovascular disease; ESKD, end-stage kidney disease.
For non-CVD events, regular statin use was associated with a risk increase for diabetes (hazard ratio 1.16, 95% CI 1.10–1.21) and a risk reduction for dementia (hazard ratio 0.88, 95% CI 0.79–0.98). The trends of the associations persisted in secondary analyses conducted within statin users and in further analyses conducted using the NHIS-generated sample cohort (S1 Fig in S1 File). However, statin use was not consistently associated with the risk for major cancers, ESKD, or cataract surgery.
In stratified analyses, the hazard ratios for major CVD events and all-cause mortality in statin users were similar, irrespective of age, sex, or predicted CVD risk (Fig 4). When the absolute event rates were estimated in statin users with reference to the rates in nonusers, the absolute risk reductions for major CVD events and all-cause mortality were greater among higher risk categories (S2 Fig in S1 File).
Multivariable-adjusted hazard ratios were estimated using Cox models with a time-varying covariate for statin use status, in subgroups stratified by age, sex, or 10-year CVD risk. CVD, cardiovascular disease.
Simulation analyses
Simulation was performed on the assumption that the relative risk reductions of 43.3% for major CVD events and 28.8% for all-cause mortality were not different between the simulated and propensity score-matched cohorts, nor did they vary among the CVD risk categories. When 659,759 simulated pairs were categorized using the Pooled Cohort Equations, the major CVD events were observed or estimated to occur in 3580 nonusers and 2030 regular users among the 90,750 pairs with a 10-year risk of ≥10.0% (Table 2), over 6 years of follow-up. When categorized by the number of risk factors, major CVD events occurred or would occur in 3640 nonusers and 2064 regular users among the 161,071 pairs with ≥2 risk factors. Thus, over the 6-year follow-up, regular statin use could reduce 1550 CVDs and 2573 deaths in 90,750 adults (17 CVDs and 28 deaths in 1000) with a risk of ≥10.0% (Fig 5). Meanwhile, regular use could reduce 1576 CVDs and 2254 deaths in 161,071 adults (10 CVDs and 14 deaths in 1000) with ≥2 risk factors. However, in the actual cohort of adults with a risk of ≥10%, statins were used in 29,299 adults (including occasional, intermittent, and regular users) and estimated to reduce 232 CVDs and 346 deaths (3 CVDs and 4 deaths in 1000).
The numbers of events in simulated regular statin users were estimated on the assumption that the relative risk reductions of 43.3% for CVD and 28.8% for mortality were not different between the simulated and propensity score-matched cohorts, nor were they different among the CVD risk categories. CVD, cardiovascular disease.
Discussion
In this cohort study of Korean adults with no prior CVD, regular statin use was associated with substantial risk reductions for major CVD events and all-cause mortality. For non-CVD events, the effects of statins were neutral. In stratified analyses, statin use was associated with similar relative risk reductions for major CVD events and all-cause mortality, irrespective of age, sex, or predicted CVD risk. Accordingly, the absolute risk reductions with statins were substantially greater in adults at higher risk predicted using CVD risk calculators. However, in this cohort, statin use was insufficient and estimated to reduce much smaller numbers of events among adults at high predicted risk compared with those in simulation analyses.
In both the primary and secondary analyses, regular statin use was associated with substantial risk reductions of CVD events and all-cause mortality. The 43% risk reduction for major CVD events in regular users vs nonusers was similar to the 44% risk reduction for those in the secondary analysis (i.e., in regular vs occasional users) and comparable to the 24%–44% CVD risk reductions observed in primary prevention statin trials [2–8]. Conversely, regular statin use was associated with a 16% risk increase for incident diabetes in the primary analysis (or with an 8% risk increase in the secondary analysis). In 2010 and 2016 meta-analyses of clinical trials, no or only minimal associations were found between statin use and diabetes risk [2,20]. However, some cohort studies reported that statin use was associated with 50%–100% risk increase for diabetes compared with nonuse [21–24]. Unlike previous cohort studies, the present study generated the propensity score-matched cohort among users having recently initiated statins and a relatively large number of nonusers. Furthermore, the secondary analysis compared regular use with occasional rather than nonuse to assess residual confounding related to statin indication. The excess risk of diabetes observed in previous cohort studies of statin users might be exaggerated due to confounding by indication or reverse causality, i.e. participants with impending diabetes would more likely receive statins. Meanwhile, regular statin use was associated with a risk reduction for dementia in this study. Given substantial CVD and mortality benefits of regular use, statins should not be discontinued due to exaggerated fear of non-CVD side effects [25].
In stratified analyses, regular statin use had an association with similar relative risk reductions for CVD events and all-cause mortality, irrespective of age, sex, or predicted CVD risk. The findings were consistent with those of statin trials indicating similarities among relative risk reductions for CVD events across subgroups stratified by baseline characteristics or predicted CVD risk [7,8,26]. Meanwhile, in the present study, regular statin use was not consistently associated with the risk for major cancers, ESKD, or cataract, to which elderly or high risk individuals might be more vulnerable. The relative risk reductions for CVD events were steady, and the effects on non-CVD events were neutral. Therefore, the absolute net benefits of statins were substantially greater among participants at higher risk predicted using CVD risk calculators that accounted for age, sex, and other risk factors. By comparison, a study for antihypertensive users showed that aggressive lowering of blood pressure was associated with a risk increase for adverse outcomes. It also concluded that the risk calculators failed to discriminate the risk groups according to different risk thresholds of treated blood pressure [27]. The present findings strongly support the validity of CVD risk calculators in determining potential beneficiaries of statin use. However, this study does not ensure the role of risk calculators in determining optimal blood pressure for antihypertensive treatment.
In this study, regular statin use was associated with relative risk reductions for CVD events even among individuals at low predicted risk. However, the small absolute benefits could not support the need of primary prevention statin therapy in low risk individuals (S2 Fig in S1 File). In contrast, statins would certainly be beneficial in individuals at high risk. When simulation was performed for the population-based cohort of Korean adults, the absolute risk reductions with statins in the population with a 10-year risk of ≥10% were similar to those in the population with ≥2 risk factors. The similarity existed although the population size ratio of the former to the latter was approximately 50%. This indicates the 10-year risk predicted using CVD risk calculators is more cost-effective in decision-making for statin therapy than the risk assessment by counting risk factors. However, statin use was insufficient and estimated to reduce much smaller numbers of CVDs and deaths among actual adults with a risk of ≥10%. Calculating 10-year CVD risk and regular statin use in individuals at high predicted risk could be an effective strategy to reduce outcome risks much more than present in Korea.
The Pooled Cohort Equations risk calculator was designed to predict 10-year risk for fatal and non-fatal myocardial infarction and stroke that could be reduced by statin therapy. The calculator was developed and validated in several US cohorts comprising Caucasians and African Americans [16,28]. In this Korean cohort, the predicted risk scores were linearly associated with the hazard ratios for CVD events reflecting consistent discrimination over the risk scores (Fig 6), although the finding did not ensure individual-level accuracy or exclude a need of calibration to predict absolute risk. The use of the risk calculator to determine appropriate candidates for statin therapy, who will have a substantial net benefit with minimal harm or discomfort, requires additional study in both the US and other countries. Of the participants at intermediate risk predicted using the Pooled Cohort Equations, approximately 50% had no coronary artery calcification on computed tomography scanning [29], in an analysis of the Multi-Ethnic Study of Atherosclerosis. Moreover, CVD events were scarcely observed in those with no coronary artery calcification [29]. If statins were allocated to such patients, a large number of patients would be treated for a long time to prevent one CVD event. Accordingly, it would lead to many patients taking medicine daily, visiting medical offices periodically, and being exposed to potential side effects, while the CVD benefit of absolute risk reduction would be very small. Consideration of additional measures like coronary calcification might be needed for patients at intermediate predicted risk.
Among propensity score-matched statin users (A) and nonusers (B), unadjusted hazard ratios (solid line) and 95% CIs (dotted line) were estimated using a restricted cubic spline function with five knots placed at the 5th, 25th, 50th, 75th, and 95th percentile CVD risk scores. CVD, cardiovascular disease.
This study encountered several limitations that need addressing. First, despite the propensity score-matching, there might be residual confounding by unmeasured factors or inadequate matching. Specifically, this analysis did not address performance status or hospital visits that could potentially be related to regular use of statins, although the variables of physical exercise and medications use status were included in the models. Second, it did not evaluate muscle pain or damage, or liver injury, which might have a potential link with statin use. Moreover, the reasons for statin discontinuation (i.e., occasional or intermittent use) were not provided due to lack of the records in the NHID. Third, medication use status was assessed based on prescription data, and the analysis did not examine dose-dependent or drug-specific relationships of statins with outcome risks as doses of different statins varied with different periods of time. Finally, caution is required when generalizing the findings to individuals with very old age or other ethnic groups. The reason was that the study included 40 to 79-year-old adults residing in Korea. Because the accuracy or validity of CVD risk calculators could be different according to race or ethnicity [30–32], the findings should be confirmed in other populations.
Conclusions
The findings highlight the importance of regular statin use and strongly support the validity of CVD risk calculators in determining the potential benefits of statin use in Asian populations. The proper CVD risk assessment and regular statin use in patients at high predicted risk should be emphasized as an effective strategy for public health. Nevertheless, additional deliberation may be needed for patients at intermediate predicted risk, and further research is required to confirm the findings in populations with very old age or other ethnic groups.
Supporting information
References
- 1. Cholesterol Treatment Trialists’ (CTT) Collaboration, Baigent C, Blackwell L, Emberson J, Holland LE, Reith C, et al. Efficacy and safety of more intensive lowering of LDL cholesterol: a meta-analysis of data from 170,000 participants in 26 randomised trials. Lancet. 2010;376: 1670–1681. pmid:21067804
- 2. Chou R, Dana T, Blazina I, Daeges M, Jeanne TL. Statins for Prevention of Cardiovascular Disease in Adults: Evidence Report and Systematic Review for the US Preventive Services Task Force. JAMA. 2016;316: 2008–2024. pmid:27838722
- 3. Yusuf S, Bosch J, Dagenais G, Zhu J, Xavier D, Liu L, et al. Cholesterol Lowering in Intermediate-Risk Persons without Cardiovascular Disease. N Engl J Med. 2016;374: 2021–2031. pmid:27040132
- 4. Shepherd J, Cobbe SM, Ford I, Isles CG, Lorimer AR, MacFarlane PW, et al. Prevention of coronary heart disease with pravastatin in men with hypercholesterolemia. West of Scotland Coronary Prevention Study Group. N Engl J Med. 1995;333: 1301–1307. pmid:7566020
- 5. Sever PS, Dahlöf B, Poulter NR, Wedel H, Beevers G, Caulfield M, et al. Prevention of coronary and stroke events with atorvastatin in hypertensive patients who have average or lower-than-average cholesterol concentrations, in the Anglo-Scandinavian Cardiac Outcomes Trial—Lipid Lowering Arm (ASCOT-LLA): a multicentre randomised controlled trial. Lancet. 2003;361: 1149–1158. pmid:12686036
- 6. Colhoun HM, Betteridge DJ, Durrington PN, Hitman GA, Neil HAW, Livingstone SJ, et al. Primary prevention of cardiovascular disease with atorvastatin in type 2 diabetes in the Collaborative Atorvastatin Diabetes Study (CARDS): multicentre randomised placebo-controlled trial. Lancet Lond Engl. 2004;364: 685–696. pmid:15325833
- 7. Ridker PM, Danielson E, Fonseca FAH, Genest J, Gotto AM Jr, Kastelein JJP, et al. Rosuvastatin to prevent vascular events in men and women with elevated C-reactive protein. N Engl J Med. 2008;359: 2195–2207. pmid:18997196
- 8. Downs JR, Clearfield M, Weis S, Whitney E, Shapiro DR, Beere PA, et al. Primary prevention of acute coronary events with lovastatin in men and women with average cholesterol levels: results of AFCAPS/TexCAPS. Air Force/Texas Coronary Atherosclerosis Prevention Study. JAMA. 1998;279: 1615–1622. pmid:9613910
- 9. US Preventive Services Task Force, Bibbins-Domingo K, Grossman DC, Curry SJ, Davidson KW, Epling JW Jr, et al. Statin Use for the Primary Prevention of Cardiovascular Disease in Adults: US Preventive Services Task Force Recommendation Statement. JAMA. 2016;316: 1997–2007. pmid:27838723
- 10. Grundy SM, Stone NJ, Bailey AL, Beam C, Birtcher KK, Blumenthal RS, et al. 2018 AHA/ACC/AACVPR/AAPA/ABC/ACPM/ADA/AGS/APhA/ASPC/NLA/PCNA Guideline on the Management of Blood Cholesterol: A Report of the American College of Cardiology/American Heart Association Task Force on Clinical Practice Guidelines. J Am Coll Cardiol. 2018. pmid:30423393
- 11. Mach F, Baigent C, Catapano AL, Koskinas KC, Casula M, Badimon L, et al. 2019 ESC/EAS Guidelines for the management of dyslipidaemias: lipid modification to reduce cardiovascular risk. Eur Heart J. 2020;41: 111–188. pmid:31504418
- 12. Mach F, Ray KK, Wiklund O, Corsini A, Catapano AL, Bruckert E, et al. Adverse effects of statin therapy: perception vs. the evidence—focus on glucose homeostasis, cognitive, renal and hepatic function, haemorrhagic stroke and cataract. Eur Heart J. 2018;39: 2526–2539. pmid:29718253
- 13. He Y, Li X, Gasevic D, Brunt E, McLachlan F, Millenson M, et al. Statins and Multiple Noncardiovascular Outcomes: Umbrella Review of Meta-analyses of Observational Studies and Randomized Controlled Trials. Ann Intern Med. 2018;169: 543–553. pmid:30304368
- 14. Gurwitz JH, Go AS, Fortmann SP. Statins for Primary Prevention in Older Adults: Uncertainty and the Need for More Evidence. JAMA. 2016;316: 1971–1972. pmid:27838724
- 15. Cheol Seong S, Kim Y-Y, Khang Y-H, Heon Park J, Kang H-J, Lee H, et al. Data Resource Profile: The National Health Information Database of the National Health Insurance Service in South Korea. Int J Epidemiol. 2017;46: 799–800. pmid:27794523
- 16. Yadlowsky S, Hayward RA, Sussman JB, McClelland RL, Min Y-I, Basu S. Clinical Implications of Revised Pooled Cohort Equations for Estimating Atherosclerotic Cardiovascular Disease Risk. Ann Intern Med. 2018;169: 20–29. pmid:29868850
- 17. Fisher LD, Lin DY. Time-dependent covariates in the Cox proportional-hazards regression model. Annu Rev Public Health. 1999;20: 145–157. pmid:10352854
- 18. Nguyen T-L, Collins GS, Spence J, Daurès J-P, Devereaux PJ, Landais P, et al. Double-adjustment in propensity score matching analysis: choosing a threshold for considering residual imbalance. BMC Med Res Methodol. 2017;17: 78. pmid:28454568
- 19. Austin PC. Balance diagnostics for comparing the distribution of baseline covariates between treatment groups in propensity-score matched samples. Stat Med. 2009;28: 3083–3107. pmid:19757444
- 20. Sattar N, Preiss D, Murray HM, Welsh P, Buckley BM, de Craen AJM, et al. Statins and risk of incident diabetes: a collaborative meta-analysis of randomised statin trials. Lancet. 2010;375: 735–742. pmid:20167359
- 21. Culver AL, Ockene IS, Balasubramanian R, Olendzki BC, Sepavich DM, Wactawski-Wende J, et al. Statin use and risk of diabetes mellitus in postmenopausal women in the Women’s Health Initiative. Arch Intern Med. 2012;172: 144–152. pmid:22231607
- 22. Cederberg H, Stančáková A, Yaluri N, Modi S, Kuusisto J, Laakso M. Increased risk of diabetes with statin treatment is associated with impaired insulin sensitivity and insulin secretion: a 6 year follow-up study of the METSIM cohort. Diabetologia. 2015;58: 1109–1117. pmid:25754552
- 23. Ko MJ, Jo AJ, Kim YJ, Kang SH, Cho S, Jo S-H, et al. Time- and Dose-Dependent Association of Statin Use With Risk of Clinically Relevant New-Onset Diabetes Mellitus in Primary Prevention: A Nationwide Observational Cohort Study. J Am Heart Assoc. 2019;8: e011320. pmid:30982384
- 24. Lee S-E, Sung JM, Cho I-J, Kim HC, Chang H-J. Risk of new-onset diabetes among patients treated with statins according to hypertension and gender: Results from a nationwide health-screening cohort. PLOS ONE. 2018;13: e0195459. pmid:29630642
- 25. Bradley Corey K., Wang Tracy Y., Li Shuang, Robinson Jennifer G, Roger Veronique L., Goldberg Anne C., et al. Patient‐Reported Reasons for Declining or Discontinuing Statin Therapy: Insights From the PALM Registry. J Am Heart Assoc. 2019;8: e011765. pmid:30913959
- 26. Cholesterol Treatment Trialists’ (CTT) Collaborators, Mihaylova B, Emberson J, Blackwell L, Keech A, Simes J, et al. The effects of lowering LDL cholesterol with statin therapy in people at low risk of vascular disease: meta-analysis of individual data from 27 randomised trials. Lancet. 2012;380: 581–590. pmid:22607822
- 27. Jung HH. Association of Optimal Blood Pressure With Critical Cardiorenal Events and Mortality in High-Risk and Low-Risk Patients Treated With Antihypertension Medications. JAMA Netw Open. 2019;2: e199307–e199307. pmid:31441935
- 28. Muntner P, Colantonio LD, Cushman M, Goff DC, Howard G, Howard VJ, et al. Validation of the atherosclerotic cardiovascular disease Pooled Cohort risk equations. JAMA. 2014;311: 1406–1415. pmid:24682252
- 29. Nasir K, Bittencourt MS, Blaha MJ, Blankstein R, Agatson AS, Rivera JJ, et al. Implications of Coronary Artery Calcium Testing Among Statin Candidates According to American College of Cardiology/American Heart Association Cholesterol Management Guidelines: MESA (Multi-Ethnic Study of Atherosclerosis). J Am Coll Cardiol. 2015;66: 1657–1668. pmid:26449135
- 30. Ridker PM, Cook NR. Statins: new American guidelines for prevention of cardiovascular disease. The Lancet. 2013;382: 1762–1765. pmid:24268611
- 31. Jee SH, Jang Y, Oh DJ, Oh B-H, Lee SH, Park S-W, et al. A coronary heart disease prediction model: the Korean Heart Study. BMJ Open. 2014;4: e005025. pmid:24848088
- 32. Kavousi M, Leening MJG, Nanchen D, Greenland P, Graham IM, Steyerberg EW, et al. Comparison of application of the ACC/AHA guidelines, Adult Treatment Panel III guidelines, and European Society of Cardiology guidelines for cardiovascular disease prevention in a European cohort. JAMA. 2014;311: 1416–1423. pmid:24681960