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The ULFI study is in agree with the SANTORINI study<a class="elsevierStyleCrossRef" href="#bib0055"><span class="elsevierStyleSup">2</span></a> who reported that a considerable proportion of subjects at high and very high cardiovascular risk fail to reach the LDL-cholesterol goals established by the guidelines (<70 and <55<span class="elsevierStyleHsp" style=""></span>mg/dL, respectively) although prescribing attitudes changed over time, with a rising, trend toward more aggressive LLT interventions. Recently, ESC indications<a class="elsevierStyleCrossRef" href="#bib0060"><span class="elsevierStyleSup">3</span></a> highlighting the importance of periodic reassessment of chronic cardiovascular therapy especially after a lengthy period of treatment. However, between the several discussed cardiovascular medications, some further considerations need to be made regarding the LLT:<ul class="elsevierStyleList" id="lis0005"><li class="elsevierStyleListItem" id="lsti0005"><span class="elsevierStyleLabel">i)</span><p id="par0010" class="elsevierStylePara elsevierViewall"><span class="elsevierStyleBold">Niacin</span> treatment, although able to increase HDL cholesterol levels especially in familial hypoalphalipoproteinemia, increase the frequency of serious adverse events with an unfavorable risk/benefit ration and the <span class="elsevierStyleBold">fish oil supplementation</span> (<1<span class="elsevierStyleHsp" style=""></span>g/day) has an irrelevant therapeutic effect although a very high daily dose is not recommended, especially in patients with heart disease, due to the risk of atrial fibrillation.<a class="elsevierStyleCrossRef" href="#bib0065"><span class="elsevierStyleSup">4</span></a></p></li><li class="elsevierStyleListItem" id="lsti0010"><span class="elsevierStyleLabel">ii)</span><p id="par0015" class="elsevierStylePara elsevierViewall">Statin-associated muscle symptoms (SAMS) are a major determinant of poor treatment adherence and/or statin discontinuation but this condition can benefit from <span class="elsevierStyleBold">coenzyme Q10 supplementation</span> especially when CPK values are high before start statin therapy.<a class="elsevierStyleCrossRef" href="#bib0070"><span class="elsevierStyleSup">5</span></a> Moreover, SAMS could be the opportunity to identify, through <span class="elsevierStyleBold">vitamin D</span> dosage, states of vitamin deficiency in order to start specific therapy.</p></li><li class="elsevierStyleListItem" id="lsti0015"><span class="elsevierStyleLabel">iii)</span><p id="par0020" class="elsevierStylePara elsevierViewall">Among patients with atherosclerotic cardiovascular disease (ASCVD), hypertriglyceridemia is common, and is associated with higher ASCVD risk across a range of TG.<a class="elsevierStyleCrossRef" href="#bib0075"><span class="elsevierStyleSup">6</span></a> Lowering triglycerides with <span class="elsevierStyleBold">fibrates</span> reduces the risk of cardiovascular events by the same amount as LDL-C-lowering therapies when measured per unit change of non-HDL-C. Combinations of statins with gemfibrozil may enhance the risk for myopathy but this risk seems to be small using fenofibrate and routinary monitoring CPK.<a class="elsevierStyleCrossRef" href="#bib0080"><span class="elsevierStyleSup">7</span></a></p></li><li class="elsevierStyleListItem" id="lsti0020"><span class="elsevierStyleLabel">iv)</span><p id="par0025" class="elsevierStylePara elsevierViewall"><span class="elsevierStyleBold">Simvastatin</span> has a good safety profile, especially in chronic kidney disease,<a class="elsevierStyleCrossRef" href="#bib0085"><span class="elsevierStyleSup">8</span></a> and adding ezetimibe allowed an LDL-cholesterol reduction great then 50% in a large number of high cardiovascular risk subjects.</p></li></ul></p><p id="par0030" class="elsevierStylePara elsevierViewall">All strategies, according to the operative international lipid expert panel indication and with protocol to valorized the therapeutic adherence,<a class="elsevierStyleCrossRefs" href="#bib0050"><span class="elsevierStyleSup">1,9</span></a> have a role to improve the LLT effectiveness don’t forget, in the era of “new” lipid-lowering drugs, cornerstone data regarding “old” LLT.</p><span id="sec0005" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0005">Funding sources</span><p id="par0035" class="elsevierStylePara elsevierViewall">No financial support was received.</p></span><span id="sec0010" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0010">Author approval</span><p id="par0040" class="elsevierStylePara elsevierViewall">All authors have seen and approved the study submitted.</p><p id="par0045" class="elsevierStylePara elsevierViewall">No part of the submitted work has been published or is under consideration for publication elsewhere.</p></span><span id="sec0015" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0015">Authors’ contribution</span><p id="par0050" class="elsevierStylePara elsevierViewall">FS and BDP: contributed to conception or design, drafted and critically revised the manuscript. All authors read and approved the final version of the manuscript.</p></span><span id="sec0020" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0020">Notes</span><p id="par0055" class="elsevierStylePara elsevierViewall">Data have not been presented at any congress.</p></span><span id="sec0025" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0025">Consent for publication</span><p id="par0060" class="elsevierStylePara elsevierViewall">The patient signed the informed consent from form for anonymous medical data usage in our paper.</p></span><span id="sec0030" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0030">Conflict of interest</span><p id="par0065" class="elsevierStylePara elsevierViewall">No conflict of interest for each author.</p></span></span>" "textoCompletoSecciones" => array:1 [ "secciones" => array:8 [ 0 => array:2 [ "identificador" => "sec0005" "titulo" => "Funding sources" ] 1 => array:2 [ "identificador" => "sec0010" "titulo" => "Author approval" ] 2 => array:2 [ "identificador" => "sec0015" "titulo" => "Authors’ contribution" ] 3 => array:2 [ "identificador" => "sec0020" "titulo" => "Notes" ] 4 => array:2 [ "identificador" => "sec0025" "titulo" => "Consent for publication" ] 5 => array:2 [ "identificador" => "sec0030" "titulo" => "Conflict of interest" ] 6 => array:2 [ "identificador" => "xack771916" "titulo" => "Acknowledgements" ] 7 => array:1 [ "titulo" => "References" ] ] ] "pdfFichero" => "main.pdf" "tienePdf" => true "bibliografia" => array:2 [ "titulo" => "References" "seccion" => array:1 [ 0 => array:2 [ "identificador" => "bibs0015" "bibliografiaReferencia" => array:9 [ 0 => array:3 [ "identificador" => "bib0050" "etiqueta" => "1" "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:2 [ "titulo" => "Observational study of patients from a Lipid Unit on lipid-modifying therapy for primary and secondary prevention: ULFI study" "autores" => array:1 [ 0 => array:2 [ "etal" => false "autores" => array:6 [ 0 => "À. 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Letter to the Editor
Disponible online el 10 de septiembre de 2024
When “old” lipid lowering therapies not should be discontinued
Cuándo no se deben suspender las terapias hipolipemiantes «antiguas»
Francesco Sbrana
, Beatrice Dal Pino
Autor para correspondencia
Lipoapheresis Unit and Reference Center for Inherited Dyslipidemias, Fondazione Toscana Gabriele Monasterio, Pisa, Italy