Blue Cross of Idaho Logo

Express Sign-on

Thank you for registering with Blue Cross of Idaho

If you are an Individual or Family Member under age 65, please register here.

If you are an Medicare or Medicare Supplement member, please register here.

New Options for Affordable Health Insurance

 

MP 2.04.70 Genetic Testing for Lipoprotein(a) Variant(s) as a Decision Aid for Aspirin Treatment

 

Medical Policy    
Section
Medicine
 
Original Policy Date
05/2011
Last Review Status/Date
Created with literature search/5:2013
Issue
5:2013
  Return to Medical Policy Index

Disclaimer

Our medical policies are designed for informational purposes only and are not an authorization, or an explanation of benefits, or a contract. Receipt of benefits is subject to satisfaction of all terms and conditions of the coverage. Medical technology is constantly changing, and we reserve the right to review and update our policies periodically.

 


Description

Lipoprotein(a) (LPA) is a lipid-rich particle similar to low-density lipoprotein (LDL) and has been determined to be an independent risk factor for coronary artery disease (CAD). Patients with a positive test for the LPA genetic variant rs3798220 have a higher risk for thrombosis and therefore may derive more benefit from the anti-thrombotic properties of aspirin. As a result, testing for the rs3798220 variant has been proposed as a method of stratifying benefit from aspirin treatment.

Background

A large amount of epidemiologic evidence has determined that LPA blood level is an independent risk factor for cardiovascular disease. The overall degree of risk associated with LPA levels appears to be modest, and the degree of risk may be mediated by other factors such as LDL levels and/or hormonal status.

Levels of LPA are relatively stable in individuals over time but vary up to 1,000-fold between individuals, presumably on a genetic basis. A single nucleotide polymorphism (LPA rs3798220) has been identified in the LPA gene that has been associated with both elevated levels of lipoprotein(a) and an increased risk of cardiovascular disease. Mendelian randomization studies have supported the hypothesis that these genetic variants, and the subsequent increase in LPA levels, are causative of cardiovascular disease.

Aspirin is a well-established treatment for patients with known coronary artery disease (CAD). It is also prescribed as primary prevention for some patients who are at increased risk of CAD. Current recommendations for primary prevention consider the future risk of cardiovascular events weighed against the bleeding risk of aspirin. U.S. Preventive Services Task Force (USPSTF) guidelines from 2009 recommend aspirin for men between the ages of 45-79 years when the benefit in reducing myocardial infarction (MI) exceeds the risk of bleeding, particularly gastrointestinal hemorrhage; and for women between the ages of 55-79 years when the benefit in reducing stroke exceeds the risk of gastrointestinal bleeding. Given guidelines such as these that recommend individualizing the risk/benefit ratio of aspirin therapy, additional tools that would aid in better defining the benefits of aspirin, and/or the risk of bleeding, have potential utility for clinicians who are making decisions on aspirin therapy.

LPA-Aspirin Check® is a commercially available genetic test (Berkeley HeartLab) that detects the presence of the rs3798220 allele. Patients with a positive test for rs3798220 have a higher risk for thrombosis and therefore may derive more benefit from the anti-thrombotic properties of aspirin. It has been proposed that the additional information obtained from the LPA-Aspirin Check test may aid physicians in better estimating the benefit/risk of aspirin therapy and therefore may aid in deciding whether to prescribe aspirin for individual patients.


Policy

The use of genetic testing for the rs3798220 allele (LPA-Aspirin Check®) is considered investigational in patients who are being considered for treatment with aspirin to reduce risk of cardiovascular events.


Policy Guidelines

There is no specific CPT code for this test. A series of molecular diagnostic codes (83890-83912) or an unlisted code such as 84999 (unlisted chemistry procedure) would likely be used.

An example of a possible series of CPT codes for this test would be:

83891

83892 x 2

83896 x 2

83898

83903

83912

 


Benefit Application

BlueCard/National Account Issues

None identified.


Rationale

This policy was created in May 2011 and updated periodically with literature review. The most recent update covers the period from March 2012 through March 2013.

Genetic testing for the LPA rs3798220 can be evaluated in a similar framework as other novel cardiac risk factors. There are several conditions that must be met in order for a cardiovascular risk factor to demonstrate clinical utility. A 2002 TEC Assessment (1) summarized three steps necessary for clinical utility:

  • Standardization of measurement of the risk factor.
  • Determination of its contribution to risk assessment. As a risk factor, it is important to determine whether the novel risk factor contributes independently to risk assessment compared to established risk factors.
  • Determination of how the novel risk factor will be used in the management of the patient, compared to standard methods of assessing risk, and whether any subsequent changes in patient management result in an improvement in patient outcomes.

Literature review

1) Is the measurement of the LPA rs3798220 allele standardized?

Testing for the LPA rs3798220 allele is commercially available through Berkeley HeartLab® under the name LPA-Aspirin Check®. DNA is extracted from a buccal swab sample taken from the inner cheek. Genetic testing is performed by real-time polymerase chain reaction (PCR) in conjunction with several control samples. (2) Real-time PCR is expected to be more accurate than traditional PCR, since it preserves the exquisite sensitivity of PCR, while reducing the probability of cross-contamination that can result in false-positive results. (3) According to these authors the main limitations to real-time PCR accuracy are human factors such as improper assay development, incorrect data analysis, or unwarranted interpretation.

There were no published studies identified that evaluated the accuracy of real-time PCR testing for the specific rs3798220 allele. According to the manufacturer’s website, (2) “The Real-Time PCR assay is extremely reproducible and has been validated for LPA genotyping by testing over 1,000 specimens from patients whose LPA status was already known. The test accuracy was 100% in validation studies.”

Conclusions. This limited information is sufficient to conclude that real-time PCR is an accurate method for identifying genetic polymorphisms such as the rs3798220 allele but is not sufficient to conclude that the measurement of LPA rs3798220 is standardized.

2) Is LPA rs3798220 an independent risk factor for coronary artery disease?

Several observational studies have evaluated whether LPA rs3798220 is an independent risk factor for coronary artery disease (CAD). Shiffman et al. (4) used data from the Cardiovascular Health Study, a prospective cohort study of risk factors for myocardial infarction (MI) in 4,522 individuals who were 65 years or older, to examine the association of rs3798220 with MI. These authors tested 74 single nucleotide polymorphisms (SNPs) that had been genotyped as part of the Cardiovascular Health Study. After 13 years of follow-up, 539 patients (12%) had developed MI. There were 8 SNPs that were independent predictors of MI, with hazard ratios (HRs) varying from 1.13-1.62. The rs3798220 variant was one of the independent predictors and had the highest HR (1.62 95% confidence interval [CI]: 1.09-2.42). The authors also calculated the false-positive reporting rate for each SNP and estimated this to be 1% for rs3798220.

Clarke et al. (5) used a case-control design to examine the association of rs3798220 with CAD in 3,145 case patients and 3,352 control subjects from 4 European countries. They initially examined 48,742 SNPs in 2,100 genes that had some association with heart disease, including 40 SNPs from the lipoprotein(a) (LPA) gene. The rs3798220 SNP was found in 2% of patients and had the strongest association with CAD, with a HR of 1.92 (95% CI: 1.48-2.49). This association was then replicated in 3 independent populations from cohort studies, with a total of 4,846 case patients and 4,594 controls. In these populations, the rs3798220 variant remained an independent risk factor for CAD, with an odds ratio (OR) that was somewhat lower than in the derivation population (OR: 1.68 95% CI: 1.43-1.98).

Luke et al. (6) examined the association of SNPs with severe CAD as determined by coronary angiography. These authors used populations from 3 case control studies in sequence to determine the SNPs that were most strongly associated with severe CAD. Starting with over 12,000 SNPs, the authors identified 302 SNPs associated with severe disease; following verification in the second study, there were 5 SNPs that remained independent predictors; and after verification in the third study, only rs3798220 remained as the SNP most strongly associated with severe CAD. The adjusted OR for rs3798220 was 3.14 (95% CI: 1.51-6.56).

In a similar case-control design, Shiffman et al. (7) examined the association between the rs3798220 allele and MI in 3 case-control studies totaling 762 cases and 857 controls. Starting from a total of 1,949 SNPs associated with MI, the authors identified 5 SNPs that were mostly strongly associated with MI. One of these was rs3798220, which had ORs in the 3 separate study populations of 1.59 (95% CI: 1.03-2.48), 1.72 (95% CI: 1.19-2.49), and 3.52 (95% CI: 1.85-6.69).

The risk associated with genetic variants of LPA in diabetic patients may be different from that in the general population. A large prospective study performed in 2011 evaluated 2,308 patients with diabetes for LPA variants. (8) There was no significant association between genetic variants and cardiovascular risk or mortality. Odds ratios for coronary heart disease, cardiovascular disease, and cardiovascular death were 0.94 (95% CI: 0.69-1.28), 0.97 (95% CI: 0.72-1.29), and 1.23 (95% CI: 0.79-1.92), respectively. The authors also examined the degree of variability in risk between the diabetic and nondiabetic populations and reported that there was significant heterogeneity between the 2 groups (p=0.006).

A case-control study of 2,136 cases and 1,211 controls evaluated if SNPs rs3798220 and rs10455872 were associated with an increased risk of coronary disease. (9) Genotyping of these SNPs rs3798220 and rs10455872 and 7 other LPA variants believed to be associated with coronary disease was done by Taqman assay. After adjusting for conventional risk factors, the authors found an increased odds of MI of 2.14 (95% CI: 1.37-3.33, p=0.00080) and 1.45 (95% CI: 1.36-2.24, p <0.00001) for rs3798220 and rs10455872 respectively. Two additional SNPs, rs3127599 and rs9346818, were also found to be associated with risk of MI, with odds ratios of 1.18 (95% CI: 1.06-1.32) and 0.88 (95% CI: 0.79-0.97), respectively.

A Danish cohort study of 8,720 participants was followed for 10 years to determine if LPA variants or lipoprotein(a) levels increased the risk of a first-time MI or CHD event. (10) Genotyping of rs3798220, rs10455872 and LPA-KIV-2 repeat genotype was performed by PCR. The authors found that 21% of the total variation in lipoprotein(a) levels was explained by the LPA-KIV-2, that 5% of the variation was explained by rs3798220 genotype, and that 27% of the variation was explained by rs10455872 genotype. The hazard ratio for carriers of rs3798220 was 1.3 (95% CI: 0.8-2.1) for MI and 1.4 (95% CI: 1.1-1.9) for CHD compared to noncarriers. LPA rs10455872 carriers had hazard ratios of 1.3 (95% CI: 1.1-1.6) for MI and 1.1 (95% CI: 0.9-1.3) for CHD compared to noncarriers, whereas homozygous rs10455872 patients had hazard ratios of 1.2 (95% CI: 0.5-3.3) for MI and 1.1 (95% CI: 0.5-2.1) for CHD compared to noncarriers.

Conclusions. This information is sufficient to conclude that the genetic variant rs3798220 is an independent risk factor for cardiovascular disease. It has not been determined whether measurement of the genetic variant is superior to measurement of LPA levels as an independent risk factor for cardiovascular disease.

3) Will identification of the rs3798220 variant lead to changes in management, and will these changes in management lead to improved patient outcomes?

The Women’s Health Study (WHS) examined the efficacy of aspirin treatment versus placebo for primary prevention of cardiovascular events in healthy women. Chasman et al. (11) published a post hoc analysis of 28,345 participants in the WHS who were genotyped for the presence of the LPA rs3798220 minor allele. The allele was present in 3.7% of the population, 3.6% who were heterozygotes and 0.06% who were homozygotes. As expected, LPA levels in carriers of the allele were markedly elevated compared to noncarriers, and carriers had a 2-fold increased risk for subsequent cardiovascular events compared to noncarriers.

The authors reported an interaction between the presence of the LPA rs378220 allele and response to aspirin therapy. In carriers there was a significant risk reduction associated with aspirin (ASA) treatment, with cardiovascular events occurring in 4.8% of patients in the placebo group compared to 2.1% in the aspirin group (HR: 0.44, 95% CI: 0.20-0.94, p=0.03). For noncarriers of the allele, there was no significant reduction in cardiovascular events associated with aspirin treatment, with cardiovascular events occurring in 2.3% of the placebo group compared to 2.1% of the aspirin group (HR: 0.91, 95% CI: 0.77-1.08, p=0.30).

Shiffman et al. (12) reported data on the interaction of the LPA rs3798220 variant and aspirin use from the Atherosclerosis Risk in Communities (ARIC) study. The ARIC study was a prospective cohort study of risk factors for CAD in 15,792 individuals. The LPA genetic substudy of ARIC included 6,752 individuals with data available for LPA genotype and ASA use, including 221 individuals with the LPA rs3798220 genotype. Among carriers of rs3798220, the risk of cardiovascular events was compared in aspirin users and non-users. The hazard ratio for non-aspirin users (n=168) was elevated at 1.57 but did not reach statistical significance (95% CI: 0.92-2.69), while the HR for users of aspirin was not elevated at 0.86 (95% CI: 0.38-1.95).

Conclusions. These data are supportive, but not conclusive, of the hypothesis that carriers of the rs3798220 allele may derive greater benefit from aspirin therapy compared to noncarriers. It is not clear how this information would be used in clinical care. For patients who are currently recommended to receive aspirin, a negative genetic test is probably not sufficient to warrant withholding aspirin. Similarly, for patients who are not currently recommended to receive aspirin, a positive genetic test is probably not sufficient to warrant starting aspirin. Therefore, it remains to be determined whether results of rs3798220 testing leads to changes in management and whether these changes in management improve outcomes.

Practice Guidelines and Position Statements

Guidelines exist that contain recommendations for testing of lipoprotein(a) (LPA) serum levels, but no guidelines were identified with recommendations for genetic testing. (13, 14)

Summary

The LPA minor allele rs3798220 is associated with higher levels of LPA and a higher risk for cardiovascular events. This allele is infrequent in the population and is associated with a modest increase in cardiovascular risk in the general population. Testing for this allele is commercially available, but the performance characteristics are uncertain and standardization of testing has not been demonstrated. Several observational studies have established that this genetic variant is an independent risk factor for cardiovascular disease.

Evidence from a post-hoc analysis of the Women’s Health Study reported that carriers of the allele may derive greater benefit from aspirin treatment compared to noncarriers. It is unclear whether this information derived from genetic testing leads to changes in management. In particular, it cannot be determined from the available evidence whether deviating from current guidelines on treatment with ASA based on LPA genetic testing improves outcomes. Therefore, measurement of the LPA rs3798220 variant as a decision aid for aspirin treatment is considered investigational.

References:

  1. Blue Cross and Blue Shield Association Technology Evaluation Center (TEC). C-Reactive Protein as a Cardiac Risk Marker (Special Report). TEC Assessments 2002; Volume 17, Tab 23.
  2. Berkeley HeartLab® LPA-AspirinCheck Web site. 2011. Available online at: http://lpa-aspirincheck.com/testprocess/processing/. Last accessed April 2011.
  3. Valasek MA, Repa JJ. The power of real-time PCR. Adv Physiol Educ 2005; 29(3):151-9.
  4. Shiffman D, O'Meara ES, Bare LA et al. Association of gene variants with incident myocardial infarction in the Cardiovascular Health Study. Arterioscler Thromb Vasc Biol 2008; 28(1):173-9.
  5. Clarke R, Peden JF, Hopewell JC et al. Genetic variants associated with Lp(a) lipoprotein level and coronary disease. N Engl J Med 2009; 361(26):2518-28.
  6. Luke MM, Kane JP, Liu DM et al. A polymorphism in the protease-like domain of apolipoprotein(a) is associated with severe coronary artery disease. Arterioscler Thromb Vasc Biol 2007; 27(9):2030-6.
  7. Shiffman D, Kane JP, Louie JZ et al. Analysis of 17,576 potentially functional SNPs in three case-control studies of myocardial infarction. PloS One 2008; 3(8):e2895.
  8. Qi Q, Workalemahu T, Zhang C et al. Genetic variants, plasma lipoprotein(a) levels, and risk of cardiovascular morbidity and mortality among two prospective cohorts of type 2 diabetes. Eur Heart J 2012; 33(3):325-34.
  9. Koch W, Mueller JC, Schrempf M et al. Two rare variants explain association with acute myocardial infarction in an extended genomic region including the apolipoprotein(A) gene. Ann Hum Genet 2013; 77(1):47-55.
  10. Kamstrup PR, Tybjaerg-Hansen A, Nordestgaard BG. Extreme lipoprotein(a) levels and improved cardiovascular risk prediction. J Am Coll Cardiol 2013; 61(11):1146-56.
  11. Chasman DI, Shiffman D, Zee RY et al. Polymorphism in the apolipoprotein(a) gene, plasma lipoprotein(a), cardiovascular disease, and low-dose aspirin therapy. Atherosclerosis 2009; 203(2):371-6.
  12. Shiffman D, Chasman DI, Ballantyne CM et al. Coronary heart disease risk, aspirin use, and apolipoprotein(a) 4399Met allele in the Atherosclerosis Risk in Communities (ARIC) study. Thromb Haemost 2009; 102(1):179-80.
  13. Cardiovascular risk reduction in atherogenic dyslipidemia: beyond LDL-C and statins: recommendations from the European Atherosclerosis Society Consensus. 2012. Available online at: http://www.eas-society.org/consensus_position_paper_initiative.asp. Last accessed March 2012.
  14. Helfand M, Buckley DI, Freeman M et al. Emerging risk factors for coronary heart disease: a summary of systematic reviews conducted for the U.S. Preventive Services Task Force. Ann Intern Med 2009; 151(7):496-507.

 

 

Codes

Number

Description

CPT

 

No specific code (See Policy Guidelines)

ICD-9-CM diagnosis

 

Investigational for all relevant diagnoses

ICD-10-CM (effective 10/1/14)   Investigational for all relevant diagnoses
ICD-10-PCS (effective 10/1/14)   Not applicable. ICD-10-PCS codes are only used for inpatient services. There are no ICD procedure codes for laboratory tests.

 


 

Index

Aspirin, Genetic Testing
Lipoprotein(a), Genetic Testing

 


 

Policy History

Date Action Reason
05/12/11 Add to Medicine section, Pathology/Laboratory subsection New policy. 
5/10/12 Replace policy Policy updated with literature search, references 8, 11, 12 added. No change to policy statement.
05/09/13 Replace policy Policy updated with literature search through March 2013, reference 9 and 10 added. No change to policy statement.