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Mipomersen in Familial Hypercholesterolemia: An Update on Health-Related Quality of Life and Patient-Reported Outcomes

*Corresponding author for this work
  • ,
  • Ridge High School
    ,
  • Harvard T.H. Chan School of Public Health
    ,
  • Baylor Scott and White Health Heart Hospital Baylor Plano
Research Output:
Contribution to journal
Article
Peer-review

Open access

Publication Information

Output type

Research Output:
Contribution to journal
Article
Peer-review

Original language

English

Pages from-to (Number of pages)

Pages 73-80 (8 pages)

Journal (Volume, Issue Number)

Vascular Health and Risk Management (Volume 18)

Publication milestones

  • Published - 2022

Publication status

Published - 2022

ISSN

1176-6344

Publication IDs

  • Scopus: 85125136270
  • PubMed: 35221690

Abstract

Familial hypercholesterolemia (FH) is an autosomal dominant condition that leads to significantly elevated low-density lipoprotein cholesterol (LDL-C) levels and an elevated risk for cardiovascular disease. Mipomersen is an antisense oligonucleotide inhibitor targeted to apolipoprotein B-100 (apoB-100) mRNA that is administered via subcutaneous injection. Once administered, mipomersen causes selective degradation of the apoB-100 mRNA and inhibition of protein translation. This ultimately results in substantial reductions in LDL-C and other lipoprotein levels. Mipomersen is approved for the treatment of homozygous FH. In this review, we discuss its mechanism, current evidence, limitations of use including adverse events, and impact on health-related quality of life.

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Sustainable Development Goals

  • SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well