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dc.contributor.authorChambergo-Michilot, D.
dc.contributor.authorAlur, A.
dc.contributor.authorKulkarni, S.
dc.contributor.authorAgarwala, A.
dc.date.accessioned2025-10-31T18:47:59Z
dc.date.available2025-10-31T18:47:59Z
dc.date.issued2022
dc.identifier.urihttps://hdl.handle.net/20.500.12805/6354
dc.description.abstractFamilial 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.en_US
dc.formatapplication/pdf
dc.language.isoeng
dc.publisherDove Medical Press
dc.relation.ispartofurn:issn:1176-6344
dc.rightshttps://purl.org/coar/access_right/c_abf2
dc.rights.urihttps://creativecommons.org/licenses/by-nc-sa/4.0/
dc.subjectSDG 3en_US
dc.subjectLipoprotein Dynamics and Cardiovascular Risk Managementen_US
dc.subjectMipomersen's Role in Familial Hypercholesterolemia Treatmenten_US
dc.titleMipomersen in Familial Hypercholesterolemia: An Update on Health-Related Quality of Life and Patient-Reported Outcomesen_US
dc.typehttps://purl.org/coar/resource_type/c_dcae04bc
dc.identifier.doihttps://doi.org/10.2147/VHRM.S191965
dc.subject.ocdehttps://purl.org/pe-repo/ocde/ford#3.02.27
dc.type.otherReview
dc.identifier.journalVascular Health and Risk Management
dc.type.versionhttps://purl.org/coar/version/c_970fb48d4fbd8a85


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