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<article article-type="abstract" dtd-version="1.0" xml:lang="en" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:mml="http://www.w3.org/1998/Math/MathML">
<front>
<journal-meta>
<journal-id journal-id-type="publisher-id">CC</journal-id>
<journal-id journal-id-type="nlm-ta">Cardiol Croat</journal-id>
<journal-title-group>
<journal-title>Cardiologia Croatica</journal-title>
<abbrev-journal-title abbrev-type="pubmed">Cardiol. Croat.</abbrev-journal-title>
</journal-title-group>
<issn pub-type="ppub">1848-543X</issn>
<issn pub-type="epub">1848-5448</issn>
<publisher><publisher-name>Croatian Cardiac Society</publisher-name></publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="publisher-id">CC 2022 17_9-10_279</article-id>
<article-id pub-id-type="doi">10.15836/ccar2022.279</article-id>
<article-categories><subj-group subj-group-type="heading"><subject>Extended Abstract</subject></subj-group>
<subj-group subj-group-type="subheading"><subject>Novelties in cardiovascular pharmacotherapy</subject></subj-group>
</article-categories>
<title-group>
<article-title>New prospects in treatment of dyslipidaemia &#x2013; putting patient compliance first</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-3977-9712</contrib-id><name><surname>Striki&#x0107;</surname><given-names>Dominik</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref><xref ref-type="corresp" rid="cor1">*</xref></contrib>
<contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-6622-7572</contrib-id><name><surname>Sli&#x0161;kovi&#x0107;</surname><given-names>Ana Marija</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib>
<contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-2123-5979</contrib-id><name><surname>Vujevi&#x0107;</surname><given-names>Andro</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib>
<contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-0888-5005</contrib-id><name><surname>Sopek-Merka&#x0161;</surname><given-names>Ivana</given-names></name><xref ref-type="aff" rid="aff2"><sup>2</sup></xref></contrib>
<contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-2824-9222</contrib-id><name><surname>Mer&#x0107;ep</surname><given-names>Iveta</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref><xref ref-type="aff" rid="aff3"><sup>3</sup></xref></contrib>
<aff id="aff1"><label>1</label><institution>University Hospital Centre Zagreb</institution>, <addr-line>Zagreb</addr-line>, <country country="hr">Croatia</country></aff>
<aff id="aff2"><label>2</label><institution>Special Hospital for Medical Rehabilitation Krapinske Toplice, Krapinske Toplice</institution>, <country country="hr">Croatia</country>,</aff>
<aff id="aff3"><label>3</label><institution>University of Zagreb</institution>, <institution content-type="dept">School of Medicine</institution>, <addr-line>Zagreb</addr-line>, <country country="hr">Croatia</country></aff>
</contrib-group>
<author-notes>
<corresp id="cor1"><label>*</label>ADDRESS FOR CORRESPONDENCE: Dominik Striki&#x0107;, Klini&#x010D;ki bolni&#x010D;ki centar Zagreb, Ki&#x0161;pati&#x0107;eva 12, HR-10000 Zagreb, Croatia. / Phone: +385-98-9906-200 / E-mail: <email xlink:href="strikic.dominik@gmail.com">strikic.dominik@gmail.com</email></corresp></author-notes>
<pub-date pub-type="epub-ppub"><month>11</month><year>2022</year></pub-date>
<volume>17</volume>
<issue>9-10</issue>
<fpage>279</fpage>
<lpage>279</lpage>
<history>
<date date-type="received"><day>25</day><month>10</month><year>2022</year></date>
<date date-type="accepted"><day>10</day><month>11</month><year>2022</year></date>
</history>
<permissions>
<copyright-year>2022</copyright-year>
<copyright-holder>Croatian Cardiac Society</copyright-holder>
</permissions>
<kwd-group kwd-group-type="author"><title>KEYWORDS: </title><kwd>dyslipidaemia</kwd><kwd>statins</kwd><kwd>inclisiran</kwd><kwd>PCSK9 inhibitors</kwd><kwd>patient compliance</kwd></kwd-group>
</article-meta>
</front>
<body>
<p><bold>Introduction</bold>: Dyslipidaemia is one of the leading cardiovascular risk factors. For a long time, successful treatment options were used, with statin therapy being the cornerstone. Nowadays, more and more new agents are being discovered and approved for the treatment of dyslipidaemia. This summary provides a brief overview of newly approved drugs and those still in development. Methods: For this review, online databases were searched using the keywords &#x201C;dyslipidaemia&#x201D;, &#x201C;statins&#x201D;, &#x201C;PCSK9 inhibitors&#x201D;, &#x201C;inclisiran&#x201D; and &#x201C;new agents&#x201D;.</p>
<p><bold>Discussion</bold>: Statins have been used to treat dyslipidaemia for over 30 years. Studies have shown excellent results in lowering LDL cholesterol levels and reducing cardiovascular risk (<xref ref-type="bibr" rid="r1"><italic>1</italic></xref>). Therefore, statins have become the most important preventive therapeutics for high-risk patients. However, changes in people&#x2019;s lifestyles and the fast pace of life have presented us with new challenges and shown us that statins are not enough in some cases. The first monoclonal antibodies approved for the treatment of dyslipidaemia were the PCSK9 inhibitors evolocumab and alirocumab (<xref ref-type="bibr" rid="r1"><italic>1</italic></xref>, <xref ref-type="bibr" rid="r2"><italic>2</italic></xref>). Studies have shown very good results in lowering blood LDL cholesterol levels, so PCSK9 inhibitors, given once weekly, have gradually become a second-line treatment option (<xref ref-type="bibr" rid="r2"><italic>2</italic></xref>). Recently, the EMA approved a new siRNA molecule called inclisiran that interferes with PCSK9 mRNA translation, thereby lowering LDL cholesterol levels. The main advantage of inclisiran is its dosing scheme of once every three months<bold><sup>3</sup></bold>. Volanesorsen is the first drug to target chylomicrons and lower triglyceride levels. The latest agent in the pipeline is evinacumab, an ANGPLT-3 inhibitor that has shown excellent potential in clinical trials (<xref ref-type="bibr" rid="r3"><italic>3</italic></xref>).</p>
<p><bold>Conclusion</bold>: The reduction in cardiovascular risk with PCSK9 inhibition and inclisiran therapy is not yet known, but its effect on lowering LDL cholesterol is evident. Conventional statin treatment requires everyday oral administration and highly motivated patients, whereas novel agents administered weekly or even monthly are putting patient compliance first.</p>
</body>
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<ref-list>
<title>LITERATURE</title>
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