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The Use of Risk-Enhancing Factors to Personalize ASCVD Risk Assessment: Evidence and Recommendations from the 2018 AHA/ACC Multi-Society Cholesterol Guidelines

  • Anandita Agarwala
  • Jing Liu
  • Christie M. Ballantyne
  • Salim S. ViraniEmail author
Lipids (E Michos, Section Editor)
Part of the following topical collections:
  1. Topical Collection on Lipids

Abstract

Purpose of Review

In 2018, the AHA/ACC Multi-Society Cholesterol Guidelines introduced the novel concept of risk-enhancing factors to be used as a supplement to the pooled cohort risk equations to personalize atherosclerotic cardiovascular disease risk assessment in primary prevention. In this review, we discuss the rationale and evidence behind each of the risk-enhancing factors to help clinicians perform a more personalized cardiovascular risk assessment.

Recent Findings

The risk-enhancing factors are high-risk features that may guide the use of lipid-lowering therapy particularly in intermediate and select borderline-risk patients. For the purpose of this review, these factors are divided into five categories: (i) race and genetics, (ii) conditions specific to women, (iii) lipid-related risk, (iv) concurrent high-risk medical conditions, and (v) biomarkers.

Summary

The addition of the risk-enhancing factors to the pooled cohort equations provides a more individualized and comprehensive approach to cardiovascular disease risk assessment.

Keywords

Risk-enhancing factors Atherosclerotic cardiovascular disease Risk assessment Race and genetics Biomarkers Lipid 

Notes

Funding

This study was supported by Abbott Diagnostic, Akcea, Amgen, Esperion, Novartis, Regeneron, Roche Diagnostic, Sanofi-Synthelabo, NIH, AHA, and ADA. All were paid to institution, not individual.

The following acted as consultants: Abbott Diagnostics, Akcea, Amarin, Amgen, Astra Zeneca*, Boehringer Ingelheim, Denka Seiken, Esperion, Intercept, Janssen, Matinas BioPharma Inc., Merck*, Novartis, Novo Nordisk, Regeneron, Roche Diagnostic, and Sanofi-Synthelabo* (*significant where noted (> $10,000); remainder modest (< $10,000)).

Compliance with Ethical Standards

Conflict of Interest

Anandita Agarwala MD, Jing Liu MD, and Salim S. Virani MD declare that they have no conflict of interest. Dr. Virani was supported by research funding from the Department of Veterans Affairs Health Services Research & Development Service Investigator Initiated Grant, World Heart Federation, and the Jooma and Tahir Family. Dr. Ballantyne was supported by R01-HL134320.

Human and Animal Rights and Informed Consent

This article does not contain any studies with human or animal subjects performed by any of the authors.

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Copyright information

© This is a U.S. Government work and not under copyright protection in the US; foreign copyright protection may apply 2019

Authors and Affiliations

  • Anandita Agarwala
    • 1
  • Jing Liu
    • 2
  • Christie M. Ballantyne
    • 2
    • 3
  • Salim S. Virani
    • 2
    • 3
    • 4
    Email author
  1. 1.Division of CardiologyWashington University School of MedicineSt. LouisUSA
  2. 2.Section of Cardiology, Department of MedicineBaylor College of MedicineHoustonUSA
  3. 3.Section of Cardiovascular Research, Department of MedicineBaylor College of MedicineHoustonUSA
  4. 4.Section of Cardiology, Health Services Research and DevelopmentMichael E. DeBakey Veterans Affairs Medical CenterHoustonUSA

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