Residual Cardiovascular Risk at Low LDL: Remnants, Lipoprotein(a), and Inflammation

Abstract

Background

Current guidelines target low-density lipoprotein cholesterol (LDL-C) concentrations to reduce atherosclerotic cardiovascular disease (ASCVD) risk, and yet clinical trials demonstrate persistent residual ASCVD risk despite aggressive LDL-C lowering.

Content

Non–LDL-C lipid parameters, most notably triglycerides, triglyceride-rich lipoproteins (TGRLs), and lipoprotein(a), and C-reactive protein as a measure of inflammation are increasingly recognized as associated with residual risk after LDL-C lowering. Eicosapentaenoic acid in statin-treated patients with high triglycerides reduced both triglycerides and ASCVD events. Reducing TGRLs is believed to have beneficial effects on inflammation and atherosclerosis. High lipoprotein(a) concentrations increase ASCVD risk even in individuals with LDL-C < 70 mg/dL. Although statins do not generally lower lipoprotein(a), proprotein convertase subtilisin/kexin type 9 inhibitors reduce lipoprotein(a) and cardiovascular outcomes, and newer approaches are in development. Persistent increases in C-reactive protein after intensive lipid therapy have been consistently associated with increased risk for ASCVD events.

Summary

We review the evidence that biochemical assays to measure TGRLs, lipoprotein(a), and C-reactive protein are associated with residual risk in patients treated to low concentrations of LDL-C. Growing evidence supports a causal role for TGRLs, lipoprotein(a), and inflammation in ASCVD; novel therapies that target TGRLs, lipoprotein(a), and inflammation are in development to reduce residual ASCVD risk.

Introduction

Based on the well-established relation between increased blood cholesterol, particularly cholesterol in low-density lipoproteins (LDL-C), and atherosclerotic cardiovascular disease (ASCVD) morbidity and mortality, current treatment guidelines focus on reducing LDL-C concentration to reduce ASCVD risk (1, 2). However, numerous clinical trials of statin, nonstatin, and combination therapy have shown persistent residual ASCVD risk despite aggressive LDL-C lowering (3–5), leading to efforts to identify determinants of residual ASCVD risk, including those that can be measured by clinical chemistry methods. Recently, the multidisciplinary consensus panel of the European Atherosclerosis Society and the European Federation of Clinical Chemistry and Laboratory Medicine published their recommendations on the quantification of atherogenic lipoproteins beyond LDL-C for lipid-lowering strategies (6).

We will review the evidence for triglycerides (TGs) and triglyceride-rich lipoproteins (TGRLs), lipoprotein(a) [Lp(a)], and inflammation as residual risk factors. In particular, we discuss the association of measurements obtained by available biochemical assays for these factors (Table 1) with ASCVD risk in statin-treated patients, the increasing data supporting a causal role for these factors in ASCVD, and novel therapies in development that target these factors to reduce residual ASCVD risk.

Role of Triglycerides and Remnant Lipoproteins in Atherosclerotic Cardiovascular Disease

In recent years, growing evidence suggests that TGs and TGRLs may contribute to residual ASCVD risk. TGRLs are a heterogeneous population of lipoprotein particles that consist of remnant lipoproteins derived from either chylomicrons synthesized in the intestine or very-low-density lipoproteins (VLDL) synthesized in the liver (Fig. 1). Increased production and delayed catabolism of TGRLs lead to increased TG-enriched remnant lipoproteins, with increased concentrations of remnant-like particle cholesterol (RLP-C). In hypertriglyceridemia, cholesteryl ester transfer protein–mediated transfer of TGs from chylomicrons and VLDL to LDL and high-density lipoprotein (HDL) in exchange for cholesteryl esters from LDL and HDL leads to TG-enriched VLDL remnants, intermediate-density lipoprotein (IDL), LDL, and small dense LDL. Although all remnant particles have a relatively high TG content, it is not fully understood to what extent the TGs and cholesterol of remnant lipoproteins each contribute to ASCVD risk. The cholesterol content of remnant lipoproteins, broadly defined as remnant cholesterol (RC) and sometimes described as RLP-C, is highly atherogenic. Numerous studies have focused on the atherogenic potential of remnant lipoproteins and RLP-C (8, 9). However, few data describe the association between TGs in LDL (LDL-TG) and future ASCVD risk.

Triglyceride-Rich Lipoproteins and Inflammation

Both LDL-TG (10) and RLP-C, but not cholesterol in LDL (LDL-C) (11), are related to systemic low-grade inflammation and vascular damage, and it has been proposed that the TG content of LDL may be a marker for delayed remnant particle catabolism (10). Consistent with these observations (7), individuals with increased LDL-TG and RLP-C concentrations also had increased concentrations of inflammatory markers high-sensitivity C-reactive protein (hs-CRP) and white blood cell count (7), which may reflect an adverse impact on inflammation.

Laboratory Tests for Triglyceride-Rich Lipoprotein Measurements

It is generally believed that the circulating concentration of TGs serves as a surrogate measure for TGRLs. Plasma TG concentration predominantly reflects the TG content of hepatic-derived VLDL remnants (i.e., VLDL-TG, IDL-TG, and LDL-TG) in the fasting state but also includes the TG content of intestinal-derived chylomicron remnants in the nonfasting state or in the altered fasting state in hypertriglyceridemic individuals. Plasma TGs are most commonly measured using automated chemistry methods and involve the quantification of glycerol upon lipolytic conversion of TGs (12). Methods for the measurement of plasma TG concentrations are standardized through the distribution of commercially available standardized reference materials and are governed by clinical laboratory accreditation and certification agencies. A variety of methods have been used to measure the TG content of specific lipoprotein fractions, particularly LDL-TG content, to investigate the efficacy of these TGRL measures for ASCVD risk prediction. These methodologies generally use some form of conventional equilibrium density-gradient ultracentrifugation to isolate the lipoprotein fraction of interest (e.g., LDL), combined with an enzymatic method for TG quantification (10). More recently, an automated detergent-based homogeneous assay for LDL-TG was developed, which was validated against the standard sequential density ultracentrifugation method (13).

To determine the cholesterol content of TGRLs, a number of different methods have been described. The simplest method, which has been most commonly used, involves a formula for calculating RC by simply subtracting LDL-C and HDL-C from total cholesterol. Calculated RC is a more accurate estimate if directly measured LDL-C is used instead of LDL-C calculated based upon the Friedewald equation, as the Friedewald equation becomes unreliable when TG concentrations are 400 mg/dL or higher (14). It is important to note that calculated RC simply equals TG/5 (i.e., a fixed factor for the TG-to-VLDL-C ratio in mg/dL) when Friedewald-estimated LDL-C is used, and in this case it does not add clinical information beyond TG concentration (15). A newer method for estimating LDL-C using an adjustable factor for the TG-to-VLDL-C ratio based on TG and non–high-density lipoprotein cholesterol (non-HDL-C) concentrations (16) may more accurately estimate calculated RC, particularly in hypertriglyceridemic individuals. Laboratory methods for direct measurement of RC typically involve separation of remnant lipoprotein fractions based on density-gradient ultracentrifugation followed by measurement of their cholesterol content. Several studies, including the VLDL-3 Study, Jackson Heart Study, and Framingham Offspring Cohort Study, have used this method, in which RC was determined by the sum of cholesterol in the densest VLDL subfraction (VLDL₃‐C) and IDL (9, 17). Other laboratory methods for direct measurement of RC are based on immunoseparation of apolipoprotein (apo) E–enriched remnant particles by removing lipoproteins containing apo A-I and some apo B-100–containing lipoproteins and subsequent determination of their cholesterol content (18). More recently, a fully automated homogeneous assay was developed for the direct measurement of RLP-C (19). Although the lack of standardization of methods for the measurements of TGRLs hampers their use in ASCVD risk assesment, the recent availability of validated fully automated procedures for measuring LDL-TG and RLP-C should facilitate widespread use in routine clinical chemistry laboratories and may aid in evaluating the use of TGRLs in ASCVD risk assesment.

Nuclear magnetic resonance (NMR) spectroscopy has been used since the early 1990s to obtain quantitative lipoprotein measurements. Although several research teams have applied NMR spectroscopy for lipoprotein quantification, mostly on smaller numbers of study subjects, the development of commercial NMR-based lipoprotein quantification methods pioneered by Otvos and colleagues at LipoScience (now LabCorp, Raleigh, NC) allowed for a broader application of this method in large population-based studies and clinical trials. Studies using NMR-derived lipoprotein quantification focus on characterization of both particle size and concentration rather than lipoprotein lipid composition. The concentration of each lipoprotein particle subfraction is calculated and particles are classified based on size as VLDL (VLDL-P, including 5 subclasses), LDL (LDL-P, including 3 subclasses), and HDL (HDL-P, including 3 subclasses). Several studies have shown that NMR-derived lipoprotein measures are associated with future ASCVD events (20, 21) and diabetes (22).

More recently, the Nightingale Health Company has developed a NMR spectroscopy method to measure >200 metabolic plasma biomarkers, including lipoprotein particle size and 14 lipoprotein subclasses. In addition, for each lipoprotein subclass, total, free, and esterified cholesterol, triglycerides, phospholipids, fatty acids, apolipoproteins, and particle concentration are measured (23). The Nightingale Health NMR methodology has been used to measure directly the contribution of cholesterol content in remnant lipoproteins to plasma total cholesterol concentrations in the general population (24). Lipoprotein particle concentrations in clinical laboratories are also measured using electrospray differential mobility analysis, also known as ion mobility, which can be used for the direct quantification of lipoprotein particles in the range of 17.2–540.0 Å, spanning from small, dense HDL to large buoyant VLDL and providing information on both particle size and concentration (25). The method is based on the principle that particles of a given size and uniform charge behave in a predictable manner when carried in a laminar air flow and subjected to an electrical field. The use of ion mobility for quantification of lipoprotein particle subfractions has been validated against other methods such as NMR and gradient density (vertical auto profile) ultracentrifugation; small dense LDL particles were consistently associated with greater coronary atherosclerosis progression independent of standard lipid measurements (26).

Although commercially available high-throughput NMR spectroscopy and ion mobility are promising methods for quantifying lipoprotein subclasses, including remnant lipoproteins, several obstacles prevent their broad application in routine clinical chemistry laboratories, including lack of standardization for lipoprotein subclasses, proprietary software, issues related to sensitivity (variability in 600- to 800-MHz NMR instruments used), high costs for instruments, and complexity of the methods.

Epidemiologic Studies of Triglycerides and Triglyceride-Rich Lipoproteins and Atherosclerotic Cardiovascular Disease Risk

Large epidemiologic studies provide accumulating evidence for the role of TG in ASCVD risk (27). Few data are available on clinical utility of LDL-TG concentrations in ASCVD risk prediction, possibly because of the complexity of measuring LDL-TG (28). In a cross-sectional study of cases with stable coronary heart disease (CHD), in which LDL-TG was measured after fractionation of LDL by equilibrium density-gradient centrifugation, altered LDL metabolism characterized by high LDL-TG was correlated with prevalent CHD and systemic low-grade inflammation independent of LDL-C (10). The Atherosclerosis Risk in Communities (ARIC) study, was the first to demonstrate a significant association of LDL-TG concentrations with incident CHD and stroke in middle-aged adults (mean age 63 years) followed up to 16 years (7). Similarly, the Ludwigshafen Risk and Cardiovascular Health (LURIC) study in 3316 subjects (mean age 63 years) also showed that high concentrations of LDL-TG were associated with increased risk for cardiovascular mortality, independent of LDL-C, during approximately 10-year follow-up (29). In a study of older ARIC participants (mean age 76 years, half of whom were taking statin therapy, LDL-TG and RLP-C, markers of TGRL, were associated with TG, and higher LDL-TG concentration was associated with higher risk for CHD and ASCVD independent of traditional risk factors, indicating a role of LDL-TG in residual ASCVD risk in individuals on lipid-lowering therapy and suggesting additional targets for ASCVD risk reduction. In a biracial cohort from the Jackson Heart Study and Framingham Offspring Cohort Study, RLP-C was positively associated with incident CHD in unadjusted models (9). The ARIC study showed that high concentrations of small dense LDL-C, but not large buoyant LDL-C, were associated with increased risk of ASCVD even in individuals considered to be at low cardiovascular risk based on their LDL-C concentrations (30). The Copenhagen General Population Study recently showed that individuals with high concentrations of small dense LDL-C had higher risks for myocardial infarction (MI) and ASCVD (31). The Women’s Health Study recently found that TGRL-C was strongly associated with future MI and peripheral artery disease events, whereas small dense LDL-C was associated with MI alone (32). The authors suggested that the cholesterol content of TGRLs and small dense LDL might therefore influence atherogenesis with potentially different potency across vascular beds.

Genetic Studies of Triglycerides and Triglyceride-Rich Lipoproteins and Atherosclerotic Cardiovascular Disease Risk

Genetic studies, in particular Mendelian randomization studies, have been used to investigate the causal relationship between a biomarker and disease risk because they capture the lifetime effect of an exposure without the possibility of reverse causality. Genetic studies provide additional evidence of the association of TGRL with ASCVD (33). Among genes involved in TG and TGRL metabolism, variants of those encoding lipoprotein lipase (LPL) and hepatic lipase (LIPC) and their inhibitors (apo C-III [APOC3], angiopoietin-like protein 3 [ANGPTL3; ANGPTL3]) have been associated with ASCVD risk.

A gain-of-function variant of LPL (rs328) was strongly associated with lower RLP-C and LDL-TG concentrations in ARIC (7) and has been associated with decreased TG and increased HDL-C concentrations (34) and reduced CHD (35). The LIPC variant rs2070895, in the promoter region of the gene, has been associated with decreased hepatic lipase activity (36) and increased LDL-TG concentrations (7). LIPC variants were associated with increased risk for ischemic heart disease risk in the Copenhagen City Heart Study (37), and complete deficiency of hepatic lipase leads to increases in RLP-C and LDL-TG (36).

The inhibitory effect of apo C-III on lipoprotein lipase leads to delayed clearance of TGRLs (38). APOC3 loss-of function variants are associated with decreased concentrations of TGs and small dense LDL-C, increased HDL-C concentration, and reductions in postprandial lipemia and CHD risk (39). In ARIC, APOC3 loss-of-function variants were associated with decreased RLP-C and LDL-TG concentrations.

ANGPTL3 also inhibits lipoprotein lipase and decreases clearance of VLDL-TG (40). Loss-of-function variants in ANGPTL3 have been associated with decreased TG and LDL-C concentrations and reduced ASCVD risk (41).

Evidence from Clinical Trials of Lowering Triglycerides and Triglyceride-Rich Lipoproteins to Reduce Atherosclerotic Cardiovascular Disease Risk

Eicosapentaenoic acid (EPA) reduces TG and RLP-C concentrations (42). In the Reduction of Cardiovascular Events with Icosapent Ethyl–Intervention Trial (REDUCE-IT) (43), patients with high TGs and either ASCVD or high ASCVD risk who were treated with EPA had significant ASCVD risk reduction compared with placebo. In contrast, Statin Residual Risk Reduction with Epanova in High Cardiovascular Risk Patients with Hypertriglyceridemia (STRENGTH; NCT02104817), in which patients with ASCVD, high TG, and low HDL-C were treated with omega-3 carboxylic acids (Epanova; EPA + docosahexaenoic acid) or placebo, was stopped earlier than planned on the recommendation of an independent data monitoring committee because of low likelihood of benefit; trial results have not yet been published.

Fibrates activate peroxisome proliferator-activated receptor–α to downregulate APOC3 expression and upregulate LPL expression, which leads to reductions in TG and TGRL and improvements in LDL phenotype from small dense to more-buoyant particles (44). The ongoing Pemafibrate to Reduce Cardiovascular Outcomes by Reducing Triglycerides In Patients with Diabetes (PROMINENT; NCT03071692) is examining the clinical efficacy of pemafibrate added to statin therapy for ASCVD risk reduction in high-risk patients with diabetes, high TG concentrations, and low HDL-C concentrations.

Emerging therapies use gene silencing that targets APOC3 and ANGPTL3 as potential new approaches for treating hypertriglyceridemia (45). Antisense oligonucleotides in development inhibit APOC3 (APOCIII-L_Rx) (46) and hepatic ANGPTL3 (ANGPTL3-L_Rx) (47), and targeted delivery of small interfering RNAs against APOC3 (ARO-APOC3) (48) and ANGPTL3 (ARO-ANG3) (49) to hepatocytes provides efficient gene silencing. In early-phase clinical trials, both approaches to both targets demonstrated dramatic and durable TG reductions.

Role of Lipoprotein(a) in Atherosclerosis

Genetic, epidemiologic, and clinical studies have established that high concentrations of Lp(a) are associated with increased risk for ASCVD. Lp(a) was first described in 1963 and has an apo B lipoprotein moiety with covalent bonding to apo(a), which has homology to plasminogen (50). Apo(a) contains multiple repeating kringle motifs, and the differing number of kringle IV type 2 repeats in apo(a) leads to Lp(a) isoform size heterogeneity. There is a general inverse correlation between apo(a) isoform size and plasma Lp(a) concentration, which is believed to be largely due to less efficient secretion of the larger apo(a) isoforms from hepatocytes. Lp(a) is thought to have pleiotropic effects on ASCVD: promoting atherosclerosis due to its LDL moiety, promoting thrombosis due to the homology with plasminogen, and promoting vascular inflammation due to the oxidized phospholipids (51) which mediate arterial wall inflammation. Targeting Lp(a) may therefore be of incremental value beyond lowering LDL-C, even in individuals without increased LDL-C (52).

Evidence from Epidemiologic and Genetic Studies for a Causal Role of Liprotein(a) in Atherosclerotic Cardiovascular Disease

Numerous epidemiologic studies have shown a relationship between Lp(a) concentrations and MI, stroke, and aortic stenosis (53), and high Lp(a) concentrations have been shown to improve risk assessment (54). Lp(a) concentrations are primarily determined by genetics, and the ability to combine genomic data with epidemiologic data in Mendelian randomization studies has provided evidence that increased concentrations of Lp(a) are causally related to both ASCVD and aortic stenosis (55, 56). The accumulating evidence that Lp(a) is an independent ASCVD risk factor has led to the recent consensus statement from HEART UK, which provides recommendations for its measurement in clinical practice and reviews therapeutic strategies to reduce ASCVD risk in individuals with high Lp(a) concentrations (57).

Lipoprotein(a) Assay Standardization and Cutoffs for Atherosclerotic Cardiovascular Disease Risk Assessment

Measurement of Lp(a) is typically performed with autoanalyzers that use immunological methods usually based on polyclonal antibodies directed against apo(a). Historically, most labs have reported Lp(a) concentrations in mg/dL with target values of the assay calibrators in terms of total Lp(a) mass, which consists of apo(a), apo B, and lipids. The preferred approach is to report values in nmol/L using calibrators traceable to the World Health Organization/International Federation of Clinical Chemistry and Laboratory reference materials (58). There is no conclusive evidence for specific cutpoints based on age, sex, and race. Risk in primary prevention has been documented to increase at Lp(a) concentrations >30 mg/dL or >75 nmol/L in some studies, but the most recent guidelines in the United States and Europe consider a concentration ≥50 mg/dL or ≥125 nmol/L to be at high risk (2, 59).

Efficacy of Lipid-Lowering Therapies in Patients with High Lipoprotein(a) Concentrations

In the past, niacin was frequently used in patients with high concentrations of Lp(a) because it had been shown to reduce Lp(a) by 20%–25%. However, as recently reviewed, both the AIM-HIGH and HPS2-THRIVE trials failed to show any benefit of adding niacin to statin therapy for reducing ASCVD events but showed increased risk for adverse events such as new-onset diabetes and infections (60). Although statins are highly effective therapies for reducing LDL-C and apo B concentrations and reducing ASCVD events, statins do not lower Lp(a), and high-efficacy statin doses may lead to increases in Lp(a) concentrations. Statin therapy has been shown to reduce ASCVD events in patients with high concentrations of Lp(a) in both primary and secondary prevention studies (52, 61).

The approved proprotein convertase subtilisin/kexin type 9 (PCSK9) inhibitors, evolocumab and alirocumab, reduce Lp(a) concentration by 23%–27% (5, 62). In patients with higher baseline Lp(a), PCSK9 inhibitor provided greater absolute Lp(a) reduction and greater absolute risk reduction for cardiovascular events (63, 64). In a subgroup analysis from Odyssey Outcomes, Lp(a) reduction with alirocumab independently contributed to ASCVD reduction beyond the effects of reductions in LDL-C and non-HDL-C (63).

Emerging Therapies to Reduce High Lipoprotein(a) Concentrations

Because of the limited efficacy of current therapies to lower Lp(a) concentrations, novel approaches are in development that use newer technologies to lower Lp(a) by inhibiting synthesis of apo(a). APO(a)-L_Rx is a GalNAc-conjugated second-generation antisense oligonucleotide that targets apo(a) by reducing the synthesis of apo(a) in the liver. Dose-dependent and sustained Lp(a) reductions of up to 80% were observed in a phase 2 clinical trial, in which the agent was well tolerated, with the major side effect being increased frequency of injection-site erythema reported in those receiving drug compared with placebo (65). The Assessing the Impact of Lipoprotein (a) Lowering With TQJ230 on Major Cardiovascular Events in Patients With CVD (Lp(a)HORIZON; NCT04023552) is a phase 3 outcomes trial enrolling 7860 high-risk secondary prevention patients with Lp(a) concentrations ≥70 mg/dL.

AMG 890 (formerly ARO-LPA) is a GalNAc-conjugated small interfering RNA designed to inhibit Lp(a) production. A phase 1 single ascending dose clinical trial to evaluate the safety, pharmacokinetics, and pharmacodynamics in patients with high Lp(a) (n = 80) has been completed (NCT03626662), and a phase 2 clinical trial to determine dosing is ongoing in patients with high Lp(a) (n = 240; NCT04270760).

Inflammation and Residual Atherosclerotic Cardiovascular Disease Risk with Low Concentrations of Low-Density Lipoprotein Cholesterol

Although numerous biochemical measures related to inflammation have been shown to be associated with increased risk for ASCVD in both epidemiologic studies and clinical trials, hs-CRP is the most widely studied and has the greatest evidence as a useful marker in patients who have been treated to low concentrations of LDL-C. Although hs-CRP has been a useful marker of increased risk, Mendelian randomization studies investigating the association of genetic variants in the CRP gene with risk for CHD suggest that CRP concentration itself is unlikely to be a causal factor in CHD (66). Other Mendelian randomization studies have demonstrated a causal relationship between genetic variation in cytokine signaling, such as interleukin-6 receptor and the risk for CHD (67).

In a post hoc analysis of 10 major statin trials (68) and a prospective analysis the JUPITER study, the greatest benefit of therapy was observed in those who achieved the lowest concentrations of LDL-C and hs-CRP (69). This has also been observed when nonstatin therapies, such as ezetimibe (70) or PCSK9 inhibitors, were added to statin therapy (71). A recent prespecified post hoc secondary analysis of the Assessment of Clinical Effects of Cholesteryl Ester Transfer Protein Inhibition with Evacetrapib in Patients at a High Risk for Vascular Outcomes (ACCELERATE) trial showed that increased Lp(a) concentrations with high-risk vascular disease are related to cardiovascular death, MI, and stroke when hs-CRP concentrations are ≥2 mg/L but not <2 mg/L, suggesting a potential benefit of lowering Lp(a) in patients with residual systemic inflammation despite optimal medical therapy (72).

Canakinumab is a monoclonal antibody against interleukin-1β. In CANTOS, a phase 3 randomized, placebo-controlled clinical trial in 10 061 participants with a history of MI and hs-CRP concentrations >2.0 mg/L, canakinumab 150 mg resulted in a 15% reduction in the primary composite endpoint of MI, stroke, and cardiovascular death (hazard ratio [HR] 0.85, 95% confidence interval [CI] 0.74–0.98) compared with placebo (73). Key secondary endpoints including MI, unstable angina requiring urgent revascularization, and any coronary revascularizations were also reduced. There was no significant reduction in cardiovascular mortality or stroke. CANTOS was a landmark trial because it was the first to show that a therapy specifically targeting inflammation provided clinical benefit independent of lowering lipoproteins. Although canakinumab therapy was associated with increased risk for fatal infection, it was also associated with reduced risk for death from cancer, with a reduction in lung cancer. Furthermore, participants who achieved hs-CRP concentrations <2 mg/L after a single dose of canakinumab had greater reduction in cardiovascular outcomes (by 25%) and all-cause mortality (by 31%) (74). These findings have important clinical implications, as they may help identify a subset of patients in whom canakinumab or other anti-inflammatory therapy may prove particularly clinically effective.

Beyond residual cholesterol risk, these results support the concept of residual inflammatory risk. Residual inflammatory risk is not uncommon; in both Pravastatin or Atorvastatin Evaluation and Infection Therapy (PROVE IT) (75) and IMPROVE-IT (4), almost one-third of statin-treated patients had hs-CRP >2 mg/L. More than one-third of the patients in the PCSK9 mAb cardiovascular outcomes trials met the eligibility criteria for CANTOS despite achieving very low LDL-C (71).

Summary/Conclusions

Accumulating evidence from epidemiologic and genetic studies, as well as randomized clinical trials, suggest that remnant lipoproteins, Lp(a), and inflammation are causally related to risk of ASCVD in individuals already treated with statin therapy. Novel therapies to reduce circulating concentrations of TGRL, Lp(a), and inflammatory markers in these individuals show promising results, although their efficacy in reducing residual cardiovascular risk is still under investigation with several clinical trials currently ongoing. Issues related to the lack of standardization of various clinical tests to measure TGRLs and Lp(a) remain an obstacle to their widespread adoption in clinical practice.

Author Contributions

All authors confirmed they have contributed to the intellectual content of this paper and have met the following 4 requirements: (a) significant contributions to the conception and design, acquisition of data, or analysis and interpretation of data; (b) drafting or revising the article for intellectual content; (c) final approval of the published article; and (d) agreement to be accountable for all aspects of the article thus ensuring that questions related to the accuracy or integrity of any part of the article are appropriately investigated and resolved.

Authors’ Disclosures or Potential Conflicts of Interest

Upon manuscript submission, all authors completed the author disclosure form. Disclosures and/or potential conflicts of interest:

Employment or Leadership

None declared.

Consultant or Advisory Role

R. C. Hoogeveen, Denka Seiken; C. M. Ballantyne, Abbott Diagnostics, Akcea, Amarin, Amgen, AstraZeneca, Boehringer Ingelheim, Corvidia, Denka Seiken, Esperion, Intercept, Janssen, Matinas BioPharma Inc., Merck, Novartis, Novo Nordisk, Regeneron, Roche Diagnostics, and Sanofi-Synthelabo.

Stock Ownership

None declared.

Honoraria

None declared.

Research Funding

R. C. Hoogeveen has received research grants (to institution) from Denka Seiken; C. M. Ballantyne has received National Institutes of Health grant R01HL134320 and has received grants or research support (to institution) from Abbott Diagnostic, Akcea, Amgen, Esperion, Novartis, Regeneron, and Roche Diagnostics.

Expert Testimony

None declared.

Patents

None declared.

References

Nonstandard Abbreviations:

 
• AIM-HIGH

  Atherothrombosis Intervention in Metabolic Syndrome with Low HDL/High

 
• Triglycerides

  Impact on Global Health Outcomes;

 
• ANGPTL3

  angiopoietin-like protein 3;

 
• apo

  apolipoprotein;

 
• ARIC

  Atherosclerosis Risk in Communities;

 
• ASCVD

  atherosclerotic cardiovascular disease;

 
• CHD

  coronary heart disease;

 
• EPA

  eicosapentaenoic acid;

 
• HDL

  high-density lipoprotein;

 
• HPS2-THRIVE

  Heart Protection Study 2-Treatment of HDL to Reduce the Incidence of Vascular Events;

 
• hs-CRP

  high-sensitivity C-reactive protein;

 
• IDL

  intermediate-density lipoprotein;

 
• LDL-C

  low-density lipoprotein cholesterol;

 
• LDL-TG

  low-density lipoprotein triglycerides;

 
• Lp(a)

  lipoprotein (a);

 
• MI

  myocardial infarction;

 
• NMR

  nuclear magnetic resonance;

 
• non-HDL-C

  non–high-density lipoprotein cholesterol;

 
• PCSK9

  proprotein convertase subtilisin/kexin type 9;

 
• PROMINENT

  Pemafibrate to Reduce Cardiovascular Outcomes by Reducing Triglycerides In Patients with Diabetes;

 
• RC

  remnant cholesterol;

 
• REDUCE-IT

  Reduction of Cardiovascular Events with Icosapent Ethyl–Intervention Trial;

 
• RLP-C

  remnant-like particle cholesterol;

 
• STRENGTH

  Statin Residual Risk Reduction with Epanova in High Cardiovascular Risk Patients with Hypertriglyceridemia;

 
• TG

  triglyceride;

 
• TGRL

  triglyceride-rich lipoprotein;

 
• VLDL

  very-low-density lipoproteins