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    "textoCompleto" => "<span class="elsevierStyleSections"><p id="par0005" class="elsevierStylePara elsevierViewall">We read with interest the paper by Brand&#227;o et al&#46; entitled <span class="elsevierStyleItalic">&#8220;</span>Lipoprotein&#40;a&#41; as a key target in combined therapeutic approaches for cardiovascular disease<span class="elsevierStyleItalic">&#8221;</span><a class="elsevierStyleCrossRef" href="#bib0060"><span class="elsevierStyleSup">1</span></a> highlighting&#44; in the era of new lipid-lowering drugs&#44;<a class="elsevierStyleCrossRefs" href="#bib0065"><span class="elsevierStyleSup">2&#44;3</span></a> the value of Lipoprotein&#40;a&#41; &#91;Lp&#40;a&#41;&#93; as a risk factor for atherosclerotic cardiovascular disease<a class="elsevierStyleCrossRef" href="#bib0075"><span class="elsevierStyleSup">4</span></a> and the importance of its measurement in the cascade screening of familial hypercholesterolemia &#40;FH&#41;&#46;<a class="elsevierStyleCrossRefs" href="#bib0080"><span class="elsevierStyleSup">5&#44;6</span></a> We were comforted by these results because we have been dosing Lp&#40;a&#41; at our Institute for this specific purpose for many years now&#46; Indeed&#44; already in the 1980s&#44; the central role of Lp&#40;a&#41; in cardiovascular disease was demonstrated by various lines of research &#8211; epidemiology&#44; biochemistry&#44; pathophysiology<a class="elsevierStyleCrossRef" href="#bib0090"><span class="elsevierStyleSup">7</span></a> and&#44; unsurprisingly&#44; measurement of Lp&#40;a&#41; has been strongly advocated in FH&#44; as well as in other more frequent forms of dyslipidemia&#46;<a class="elsevierStyleCrossRef" href="#bib0095"><span class="elsevierStyleSup">8</span></a></p><p id="par0010" class="elsevierStylePara elsevierViewall">Subsequent studies reinforced the importance of Lp&#40;a&#41;&#44; which should be assessed in all patients with premature coronary artery disease &#40;CAD&#41; in the absence of major coronary risk factors&#46; Moreover&#44; Lp&#40;a&#41; levels have been found to have a causal role in CAD and the relationship is so strong that&#44; in some countries &#40;such as Germany&#41;&#44; Lp&#40;a&#41;-lowering therapy &#40;i&#46;e&#46; lipoprotein apheresis&#41; is reimbursed by the public health system&#46;<a class="elsevierStyleCrossRef" href="#bib0100"><span class="elsevierStyleSup">9</span></a></p><p id="par0015" class="elsevierStylePara elsevierViewall">The paper by Ellis et al&#46; has the merits of unifying the vision of Lp&#40;a&#41; across the Atlantic and draws attention to an argument which&#44; still today&#44; represents a missed opportunity in cardiovascular medicine&#44; especially considering that we finally have the therapeutic means to intervene in patients with elevated Lp&#40;a&#41;&#46; In addition&#44; the study provides the impetus to associate cascade screening with personalized therapy&#44; as exemplified by the case of a family cared for at our Institute &#40;<a class="elsevierStyleCrossRef" href="#fig0005">Figure 1</a>&#41;&#46; In these cases&#44; we were able to obtain an optimal balance between maximally tolerated lipid-lowering therapy&#44; proprotein convertase subtilisin kexin type 9 inhibitors &#40;PCSK9i&#41; and lipoprotein apheresis&#46; It should be borne in mind that PCSK9i therapy can be titrated to maintain adequate LDL-C levels while increasing the administration interval&#44;<a class="elsevierStyleCrossRef" href="#bib0105"><span class="elsevierStyleSup">10</span></a> although the effect on Lp&#40;a&#41; levels may be unpredictable&#46;<a class="elsevierStyleCrossRef" href="#bib0110"><span class="elsevierStyleSup">11</span></a></p><elsevierMultimedia ident="fig0005"></elsevierMultimedia><span id="sec0005" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0005">Funding sources</span><p id="par0020" class="elsevierStylePara elsevierViewall">No financial support was received&#46;</p></span><span id="sec0010" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0010">Conflicts of interest</span><p id="par0025" class="elsevierStylePara elsevierViewall">The authors have no conflicts of interest to declare&#46;</p></span></span>"
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          "en" => "<p id="spar0005" class="elsevierStyleSimplePara elsevierViewall">Pedigree of the proband family 1&#46;</p> <p id="spar0010" class="elsevierStyleSimplePara elsevierViewall">The proband &#40;subject III&#46;4&#41; was referred to our Institute after percutaneous coronary intervention and was diagnosed with <span class="elsevierStyleItalic">FH LDL-receptor</span> gene &#40;c&#46;1860G&#62;A&#41; mutation&#46; The other family members were identified by cascade screening and consequently treated&#46; Two cousins with extremely high levels of Lp&#40;a&#41; associated with FH were started on lipoprotein apheresis &#40;subject III&#46;5 had undergone percutaneous coronary intervention&#44; whereas subject III&#46;6 had had a rapid progression of carotid atherosclerosis despite statin therapy&#41;&#46; The proband &#40;subject III&#46;4&#41; was treated temporarily with lipoprotein apheresis&#44; which was subsequently replaced with PCSK9i therapy&#46;</p> <p id="spar0015" class="elsevierStyleSimplePara elsevierViewall"><span class="elsevierStyleItalic">Legend</span>&#58; &#42;&#58; Proband&#59; &#9652;&#58; concomitant spinocerebellar ataxias with hyper-CPK&#59; ATS&#58; peripheral atherosclerosis on carotid vessels&#59; CAD&#58; coronary artery disease&#59; HDL-C&#58; high density lipoprotein cholesterol &#40;mg&#47;dl&#41;&#59; LDL-C&#58; low density lipoprotein cholesterol &#40;mg&#47;dl&#41;&#59; Lp&#40;a&#41;&#58; lipoprotein&#40;a&#41; &#40;mg&#47;dl&#41;&#59; TC&#58; total cholesterol &#40;mg&#47;dl&#41;&#59; TG&#58; triglycerides &#40;mg&#47;dl&#41;&#59; <span class="elsevierStyleItalic">y</span>&#58; years&#46;</p>"
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Letter to the Editor
Lipoprotein(a) in familial hypercholesterolemia: Tips from family history
Lipoproteína (a) na hipercolesterolemia familiar: «truques» de histórias familiares
Beatrice Dal Pinoa, Francesco Sbranaa,
Autor para correspondência
francesco.sbrana@ftgm.it

Corresponding author.
, Michele Coceanib, Federico Bigazzia, Tiziana Sampietroa
a Lipoapheresis Unit and Reference Center for Inherited Dyslipidemias, Fondazione Toscana Gabriele Monasterio, Pisa, Italy
b Invasive Cardiology Unit, Fondazione Toscana Gabriele Monasterio, Pisa, Italy
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          "en" => "<p id="spar0005" class="elsevierStyleSimplePara elsevierViewall">Pedigree of the proband family 1&#46;</p> <p id="spar0010" class="elsevierStyleSimplePara elsevierViewall">The proband &#40;subject III&#46;4&#41; was referred to our Institute after percutaneous coronary intervention and was diagnosed with <span class="elsevierStyleItalic">FH LDL-receptor</span> gene &#40;c&#46;1860G&#62;A&#41; mutation&#46; The other family members were identified by cascade screening and consequently treated&#46; Two cousins with extremely high levels of Lp&#40;a&#41; associated with FH were started on lipoprotein apheresis &#40;subject III&#46;5 had undergone percutaneous coronary intervention&#44; whereas subject III&#46;6 had had a rapid progression of carotid atherosclerosis despite statin therapy&#41;&#46; The proband &#40;subject III&#46;4&#41; was treated temporarily with lipoprotein apheresis&#44; which was subsequently replaced with PCSK9i therapy&#46;</p> <p id="spar0015" class="elsevierStyleSimplePara elsevierViewall"><span class="elsevierStyleItalic">Legend</span>&#58; &#42;&#58; Proband&#59; &#9652;&#58; concomitant spinocerebellar ataxias with hyper-CPK&#59; ATS&#58; peripheral atherosclerosis on carotid vessels&#59; CAD&#58; coronary artery disease&#59; HDL-C&#58; high density lipoprotein cholesterol &#40;mg&#47;dl&#41;&#59; LDL-C&#58; low density lipoprotein cholesterol &#40;mg&#47;dl&#41;&#59; Lp&#40;a&#41;&#58; lipoprotein&#40;a&#41; &#40;mg&#47;dl&#41;&#59; TC&#58; total cholesterol &#40;mg&#47;dl&#41;&#59; TG&#58; triglycerides &#40;mg&#47;dl&#41;&#59; <span class="elsevierStyleItalic">y</span>&#58; years&#46;</p>"
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