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assay is increasingly used as a marker for cardiac risk assessment and as a prognostic tool in heart disease&#46;<a class="elsevierStyleCrossRefs" href="#bib0030"><span class="elsevierStyleSup">6&#8211;8</span></a> The aim of this study was to analyze the prognostic value of hsCRP values to predict follow-up outcomes in ACS patients regardless of the GRACE &#40;Global Registry of Acute Coronary Events&#41; risk score&#46;<a class="elsevierStyleCrossRef" href="#bib0030"><span class="elsevierStyleSup">6</span></a></p></span><span id="sec0010" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Methods</span><span id="sec0015" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Study population</span><p id="par0045" class="elsevierStylePara elsevierViewall">We included 151 consecutive patients admitted to the coronary care unit with a diagnosis of ACS&#46; Patients with previous ACS&#44; peripheral arterial disease and impaired renal function &#40;estimated glomerular filtration rate by the MDRD-4 equation &#60;60<span class="elsevierStyleHsp" style=""></span>ml&#47;min&#47;1&#46;73<span class="elsevierStyleHsp" style=""></span>m<span class="elsevierStyleSup">2</span>&#41; 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HbA1c of &#8805;6&#46;5&#37;&#44; or treatment with insulin or hypoglycemic agents&#46; Hypertension was defined as systolic&#47;diastolic blood pressure<span class="elsevierStyleHsp" style=""></span>&#62;<span class="elsevierStyleHsp" style=""></span>140&#47;90<span class="elsevierStyleHsp" style=""></span>mmHg or current use of any antihypertensive medication&#46; LVEF<span class="elsevierStyleHsp" style=""></span>&#60;45&#37; was considered to be depressed&#46;</p><p id="par0060" class="elsevierStylePara elsevierViewall">The primary endpoint was the combination of cardiac death and myocardial reinfarction during the follow-up period &#40;median 19&#46;8 months&#44; interquartile range 16&#46;3&#8211;23&#46;7 months&#41;&#46; Reinfarction was defined as the appearance of new symptoms of myocardial ischemia or electrocardiographic ischemic changes accompanied by re-elevation of cardiac biomarkers &#40;high-sensitivity troponin I&#41;&#46;</p></span><span id="sec0030" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Determination of CRP</span><p id="par0065" class="elsevierStylePara elsevierViewall">Blood samples were stored in evacuated tubes at &#8722;20<span class="elsevierStyleHsp" style=""></span>&#176;C and were processed within 24<span class="elsevierStyleHsp" style=""></span>hours by automated microparticle immunoassay &#40;ELISA&#41;&#46; The CRP detection range corresponds to values of 0&#46;1&#8211;12&#46;0<span class="elsevierStyleHsp" style=""></span>mg&#47;dl&#44; with an interassay variation coefficient of &#60;5&#37; &#40;normal values<span class="elsevierStyleHsp" style=""></span>&#60;0&#46;3<span class="elsevierStyleHsp" style=""></span>mg&#47;dl&#41;&#46;</p></span><span id="sec0035" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Statistical analysis</span><p id="par0070" class="elsevierStylePara elsevierViewall">All information was prospectively recorded in a database created with Microsoft Office Access 2007&#46; The statistical analyses were performed with SPSS &#40;Statistical Package for the Social Sciences&#41; version 17&#46;0&#46; Categorical or dichotomous variables are expressed as absolute values and percentages&#44; and were compared with Pearson&#39;s chi-square test&#46; Continuous variables with a normal distribution are expressed as mean<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>standard deviation&#44; and the Student&#39;s <span class="elsevierStyleItalic">t</span> test was used for comparisons between groups&#46; Continuous variables without normal distribution are expressed as median and interquartile range&#46; Pearson&#39;s test was used to study the correlation between quantitative variables&#46; A multivariate logistic regression model was used to evaluate the independent contribution of hsCRP levels to the risk of new events during follow-up&#46; Univariate predictors of potential significance and hsCRP values were included in multivariate analysis &#40;backward stepwise Cox proportional hazard analysis&#41;&#46; Adjusted hazard ratios and 95&#37; confidence intervals &#40;CI&#41; are presented&#46; Kaplan&#8211;Meier curves were constructed to evaluate the prognostic value of hsCRP during follow-up&#46; A p value<span class="elsevierStyleHsp" style=""></span>&#60;0&#46;05 was considered statistically significant&#46;</p></span></span><span id="sec0040" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Results</span><span id="sec0045" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Baseline characteristics</span><p id="par0075" class="elsevierStylePara elsevierViewall"><a class="elsevierStyleCrossRef" href="#tbl0005">Table 1</a> describes the baseline characteristics of the population&#46; CRP values &#40;median and 25&#8211;75&#37; interquartile range&#41; on admission were 0&#46;9 &#40;0&#46;3&#8211;1&#46;9&#41;<span class="elsevierStyleHsp" style=""></span>mg&#47;dl&#46; Of the patients recruited&#44; 80 had STEMI&#46; Although hsCRP values were higher in patients with STEMI &#40;2&#46;6<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>4&#46;2<span class="elsevierStyleHsp" style=""></span>mg&#47;dl&#41;&#44; there was no statistically significant difference compared with NSTE-ACS patients &#40;1&#46;8<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>2&#46;9<span class="elsevierStyleHsp" style=""></span>mg&#47;dl&#44; p&#61;0&#46;161&#41;&#46;</p><elsevierMultimedia ident="tbl0005"></elsevierMultimedia></span><span id="sec0050" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Correlation with in-hospital events</span><p id="par0080" class="elsevierStylePara elsevierViewall">During the follow-up period&#44; 18 &#40;11&#46;9&#37;&#41; patients presented cardiac events &#40;six cardiac deaths&#44; 11 re-infarctions&#41;&#46; These patients had a higher percentage of diabetes&#44; higher Killip functional class&#44; greater proportion of depressed LVEF and higher GRACE risk score&#46; The occurrence of follow-up events was significantly related to admission hsCRP level&#44; which was an excellent predictor of cardiac death and re-infarction during follow-up &#40;HR 1&#46;091&#44; 95&#37; CI 1&#46;014&#8211;1&#46;174&#59; p&#61;0&#46;019&#41;&#46; Stratifying the population based on type of ACS&#44; we found that hsCRP predicted outcome only in the NSTE-ACS group &#40;HR 1&#46;174&#44; 95&#37; CI 1&#46;076&#8211;1&#46;280&#59; p&#61;0&#46;004&#41;&#44; not in patients with STEMI &#40;HR 0&#46;999&#44; 95&#37; CI 0&#46;859&#8211;1&#46;163&#59; p&#61;0&#46;990&#41;&#46; Likewise hsCRP and GRACE risk score at discharge showed a significant positive correlation &#40;r&#61;0&#46;226&#44; p&#61;0&#46;005&#41; &#40;<a class="elsevierStyleCrossRef" href="#fig0005">Figure 1</a>&#41;&#46;</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia><p id="par0085" class="elsevierStylePara elsevierViewall">In ROC analysis&#44; the area under the curve for hsCRP in predicting follow-up outcomes was 0&#46;75<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>0&#46;05&#46; The best cutoff level of hsCRP was 1&#46;1<span class="elsevierStyleHsp" style=""></span>mg&#47;dl&#44; with sensitivity of 77&#46;8&#37; and specificity of 63&#46;2&#37; &#40;<a class="elsevierStyleCrossRef" href="#fig0010">Figure 2</a>&#41;&#46; <a class="elsevierStyleCrossRef" href="#fig0015">Figure 3</a> shows the Kaplan&#8211;Meier survival curves according to hsCRP levels above and below this cutoff &#40;1&#46;1<span class="elsevierStyleHsp" style=""></span>mg&#47;dl&#41;&#46;</p><elsevierMultimedia ident="fig0010"></elsevierMultimedia><elsevierMultimedia ident="fig0015"></elsevierMultimedia></span><span id="sec0055" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Multivariate analysis</span><p id="par0090" class="elsevierStylePara elsevierViewall">In our model &#40;<a class="elsevierStyleCrossRef" href="#tbl0010">Table 2</a>&#41;&#44; adjusted by variables associated with cardiac events &#40;hsCRP&#44; diabetes&#44; depressed LVEF and GRACE risk score&#41;&#44; hsCRP &#40;as a continuous variable&#41; was an independent predictor of follow-up outcomes only in NSTE-ACS patients &#40;HR 1&#46;217&#44; 95&#37; CI&#58; 1&#46;093&#8211;1&#46;356&#44; p&#60;0&#46;001&#41;&#46;</p><elsevierMultimedia ident="tbl0010"></elsevierMultimedia></span></span><span id="sec0060" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Discussion</span><p id="par0095" class="elsevierStylePara elsevierViewall">In this single-center study we showed that hsCRP was significantly associated with adverse follow-up outcomes in patients with NSTE-ACS&#44; independently of GRACE risk score&#44; but not in patients with STEMI&#46;</p><p id="par0100" class="elsevierStylePara elsevierViewall">Many studies have assessed the prognostic value of CRP in the hospital phase of ACS&#46;<a class="elsevierStyleCrossRefs" href="#bib0045"><span class="elsevierStyleSup">9&#8211;12</span></a> However&#44; fewer studies have examined its prognostic value in follow-up&#44; and very few have investigated its prognostic role over the entire spectrum of ACS patients&#44; classified as NSTE-ACS or non-STEMI&#46;</p><p id="par0105" class="elsevierStylePara elsevierViewall">The hypothesis that inflammatory reactions promote plaque fissuring&#44; erosion&#44; ulceration&#44; and rupture of the plaque surface should in most cases be applicable to both settings of ACS&#46;<a class="elsevierStyleCrossRefs" href="#bib0105"><span class="elsevierStyleSup">13&#44;14</span></a> They may share the same underlying pathophysiologic processes&#44; with coronary plaque disruption and consequent platelet aggregation and thrombosis&#46; However&#44; the differences found in our study between the two types of ACS were in agreement with previous studies in which hsCRP was a predictor of negative outcome&#44; especially in patients with unstable angina and non-STEMI&#46; Kuch et al&#46;<a class="elsevierStyleCrossRef" href="#bib0065"><span class="elsevierStyleSup">15</span></a> reported data on an unselected sample of patients with myocardial infarction admitted to a community hospital&#44; showing that CRP was significantly associated with adverse short-term outcome&#46; Their multivariate analysis showed that both troponin positivity and CRP positivity were associated with a 2-fold increased risk of dying within 28 days after the acute event for all patients with myocardial infarction&#46; Stratifying by myocardial infarction type showed that in patients with STEMI&#44; troponin positivity&#44; but not CRP positivity&#44; independently predicted 28-day case fatality&#44; while in patients with non-STEMI&#44; CRP positivity&#44; but not troponin positivity&#44; predicted outcome&#46; They concluded that admission CRP is a powerful parameter for risk stratification of patients with myocardial infraction&#44; with better stratification in patients with non-STEMI&#46;</p><p id="par0110" class="elsevierStylePara elsevierViewall">Morrow et al&#46;&#44; using a cutoff of 1&#46;5<span class="elsevierStyleHsp" style=""></span>mg&#47;dl &#40;similar to ours&#41;&#44; observed that elevated CRP at admission was associated with higher mortality at 14 days&#46; Schoos et al&#46;<a class="elsevierStyleCrossRef" href="#bib0080"><span class="elsevierStyleSup">16</span></a> demonstrated that preprocedure hsCRP is an independent and strong predictor of a composite endpoint of death&#44; nonfatal recurrent myocardial infarction&#44; and stent thrombosis after percutaneous intervention with coronary stent implantation&#46; Abbate et al&#46; confirmed the prognostic value of CRP in predicting short- and long-term outcomes after ACS&#46; Our group has shown that hsCRP was a predictor of adverse outcomes in the in-hospital phase of ACS independently of GRACE risk score&#46; However&#44; to date&#44; no studies have analyzed the follow-up prognostic value of hsCRP regardless of GRACE risk score at discharge&#46;</p><p id="par0115" class="elsevierStylePara elsevierViewall">There is an intracardiac inflammatory response in ACS that appears to be the result of the evolution of myocardial necrosis&#44; as shown by higher CRP&#44; TNF&#945; and IL-6 levels in patients with major adverse cardiac events&#46; Patients with ACS and higher CRP may represent a group with hyperresponsiveness of the inflammatory system&#44; which might exaggerate the acute-phase reaction and increase immune system activation&#44; which may in turn mediate myocardial damage and promote cardiac complications&#46;<a class="elsevierStyleCrossRefs" href="#bib0085"><span class="elsevierStyleSup">17&#8211;20</span></a> This may be more pronounced in patients with NSTE-ACS than in those with STEMI&#44; due to a higher atherosclerotic burden&#46;</p><p id="par0120" class="elsevierStylePara elsevierViewall">hsCRP measurement&#44; as a marker of inflammatory activity&#44; has several advantages&#46; Firstly&#44; it is a stable compound and secondly&#44; it can be measured at any time of day without regard for the biological clock&#44; since unlike measurements of cytokines such as IL-6&#44; no circadian variation appears to exist for hsCRP&#46;</p></span><span id="sec0065" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Conclusions</span><p id="par0125" class="elsevierStylePara elsevierViewall">Although the GRACE risk score is routinely used for stratification of patients with acute coronary syndrome&#44; assessment of hsCRP may provide additional prognostic value&#46; High hsCRP values were an independent and strong predictor of a composite endpoint of death and nonfatal recurrent myocardial infarction&#46; These findings highlight the importance of determining levels of this biomarker for risk stratification of these patients during follow-up&#46;</p></span><span id="sec0070" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Ethical disclosures</span><span id="sec0075" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Protection of human and animal subjects</span><p id="par0130" class="elsevierStylePara elsevierViewall">The authors declare that no experiments were performed on humans or animals for this study&#46;</p></span><span id="sec0080" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Confidentiality of data</span><p id="par0135" class="elsevierStylePara elsevierViewall">The authors declare that no patient data appear in this article&#46;</p></span><span id="sec0085" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Right to privacy and informed consent</span><p id="par0140" class="elsevierStylePara elsevierViewall">The authors declare that no patient data appear in this article&#46;</p></span></span><span id="sec0090" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Conflict of interest</span><p id="par0145" class="elsevierStylePara elsevierViewall">The authors have no conflicts of interest to declare&#46;</p></span></span>"
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            0 => "Elevada sensibilidade de prote&#237;na C-reativa"
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        "titulo" => "Abstract"
        "resumen" => "<span class="elsevierStyleSectionTitle">Introduction</span><p id="spar0005" class="elsevierStyleSimplePara elsevierViewall">Atherosclerosis is an active process and the inflammatory component appears to be particularly correlated with the development of acute coronary syndromes &#40;ACS&#41;&#46; C-reactive protein &#40;CRP&#41; is an acute phase protein that appears in the circulation in response to inflammatory cytokines&#46; The present study investigated the association between high-sensitivity C-reactive protein &#40;hsCRP&#41; on admission and follow-up prognosis after an ACS&#46;</p> <span class="elsevierStyleSectionTitle">Methods</span><p id="spar0010" class="elsevierStyleSimplePara elsevierViewall">We included 151 consecutive patients admitted to the coronary care unit with a diagnosis of ACS &#40;47&#37; ST-segment elevation myocardial infarction &#91;STEMI&#93;&#41;&#46; The primary endpoint was the combination of cardiac death and myocardial reinfarction during the follow-up period &#40;median 19&#46;8 months&#44; interquartile range 16&#46;3&#8211;23&#46;7 months&#41;&#46;</p> <span class="elsevierStyleSectionTitle">Results</span><p id="spar0015" class="elsevierStyleSimplePara elsevierViewall">The occurrence of follow-up events was significantly related to admission hsCRP level&#44; which was an excellent predictor of cardiac death and reinfarction during follow-up &#40;HR 1&#46;091&#44; 95&#37; CI 1&#46;014&#8211;1&#46;174&#59; p&#61;0&#46;019&#41;&#46; Stratifying the population based on type of ACS&#44; adjusted by variables associated with cardiac events in univariate analysis &#40;hsCRP&#44; diabetes&#44; depressed ejection fraction and GRACE risk score&#41;&#44; hsCRP proved to be an independent predictor of follow-up outcomes only in non-STEMI patients &#40;HR 1&#46;217&#44; 95&#37; CI&#58; 1&#46;093&#8211;1&#46;356&#44; p&#60;0&#46;001&#41;&#44; not in STEMI patients&#46; The best cutoff level of hsCRP to predict follow-up outcomes was 1&#46;1<span class="elsevierStyleHsp" style=""></span>mg&#47;dl&#44; with sensitivity of 77&#46;8&#37; and specificity of 63&#46;2&#37;&#46;</p> <span class="elsevierStyleSectionTitle">Conclusion</span><p id="spar0020" class="elsevierStyleSimplePara elsevierViewall">Although the GRACE risk score is routinely used for stratification of patients with ACS&#44; assessment of hsCRP may provide additional prognostic value in the follow-up of non-STEMI patients&#46;</p>"
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        "resumen" => "<span class="elsevierStyleSectionTitle">Introdu&#231;&#227;o</span><p id="spar0025" class="elsevierStyleSimplePara elsevierViewall">A aterosclerose &#233; um processo ativo e a sua componente inflamat&#243;ria parece estar particularmente relacionada com o desenvolvimento de s&#237;ndromes coron&#225;rias agudas &#40;SCA&#41;&#46; A prote&#237;na C-reativa &#40;PCR&#41; &#233; uma prote&#237;na que aparece na circula&#231;&#227;o&#44; na fase aguda do processo inflamat&#243;rio&#46; O presente estudo teve como objetivo analisar a associa&#231;&#227;o entre o valor do teste de alta sensibilidade da prote&#237;na C-reativa &#40;PCR-as&#41; na admiss&#227;o&#44; com o progn&#243;stico no seguimento&#44; em doentes p&#243;s-SCA&#46;</p> <span class="elsevierStyleSectionTitle">M&#233;todos</span><p id="spar0035" class="elsevierStyleSimplePara elsevierViewall">Foram inclu&#237;dos 151 doentes consecutivos&#44; internados na unidade de cuidados coron&#225;rios&#44; com diagn&#243;stico de SCA &#40;47&#37; com enfarte agudo do mioc&#225;rdio com eleva&#231;&#227;o do segmento ST &#8211; STEMI&#41;&#46; O <span class="elsevierStyleItalic">end-point</span> estudado foi a vari&#225;vel composta pela morte associada a patologia card&#237;aca e re-enfarte mioc&#225;rdio durante o per&#237;odo de seguimento &#40;mediana de 19&#44;8 meses&#44; intervalo interquartil 16&#44;3-23&#44;7 meses&#41;&#46;</p> <span class="elsevierStyleSectionTitle">Resultados</span><p id="spar0040" class="elsevierStyleSimplePara elsevierViewall">A ocorr&#234;ncia de eventos apresentou uma forte rela&#231;&#227;o com o valor de CPR-as registado na admiss&#227;o&#44; sendo por isso considerado como um bom preditor para a ocorr&#234;ncia de morte associada a patologia card&#237;aca e a re-enfarte no per&#237;odo de seguimento de doentes p&#243;s-SCA &#40;HR 1&#44;091&#44; CI 95&#37; 1&#44;014-1&#44;174&#59; p<span class="elsevierStyleHsp" style=""></span>&#61;<span class="elsevierStyleHsp" style=""></span>0&#44;019&#41;&#46; Ap&#243;s estratifica&#231;&#227;o da popula&#231;&#227;o pelo tipo de SCA e ajustando as vari&#225;veis associadas &#224; ocorr&#234;ncia de eventos card&#237;acos &#40;an&#225;lise univariada das vari&#225;veis valor de PCR-as&#44; diabetes <span class="elsevierStyleItalic">mellitus</span>&#44; fra&#231;&#227;o de eje&#231;&#227;o deprimida e <span class="elsevierStyleItalic">score</span> de risco GRACE&#41;&#44; o valor de PCR-as destacou-se como preditor independente no seguimento dos doentes com EAM sem eleva&#231;&#227;o ST &#40;HR 1&#44;217&#44; IC 95&#37;&#58; 1&#44;093-1&#44;356&#44; p<span class="elsevierStyleHsp" style=""></span>&#60;<span class="elsevierStyleHsp" style=""></span>0&#44;001&#41;&#46; O valor de <span class="elsevierStyleItalic">cut-off</span> para o n&#237;vel de PCR-as preditor foi de 1&#44;1<span class="elsevierStyleHsp" style=""></span>mg&#47;dl&#44; com uma sensibilidade de 77&#44;8&#37; e uma especificidade de 63&#44;2&#37;&#46;</p> <span class="elsevierStyleSectionTitle">Conclus&#227;o</span><p id="spar0055" class="elsevierStyleSimplePara elsevierViewall">Apesar de o <span class="elsevierStyleItalic">score</span> de risco GRACE ser utilizado&#44; por rotina&#44; para estratificar os doentes com SCA&#44; a medi&#231;&#227;o do valor de PCR-as pode acrescentar valor progn&#243;stico no seguimento de doentes com EAM sem eleva&#231;&#227;o e ST&#46;</p>"
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                "termino" => "ACS"
                "descripcion" => "<p id="par0005" class="elsevierStylePara elsevierViewall">acute coronary syndrome</p>"
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              1 => array:2 [
                "termino" => "CRP"
                "descripcion" => "<p id="par0010" class="elsevierStylePara elsevierViewall">C-reactive protein</p>"
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              2 => array:2 [
                "termino" => "hsCRP"
                "descripcion" => "<p id="par0015" class="elsevierStylePara elsevierViewall">high-sensitivity C-reactive protein</p>"
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                "termino" => "LVEF"
                "descripcion" => "<p id="par0020" class="elsevierStylePara elsevierViewall">left ventricular ejection fraction</p>"
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                "termino" => "NSTE-ACS"
                "descripcion" => "<p id="par0025" class="elsevierStylePara elsevierViewall">non-ST-elevation acute coronary syndrome</p>"
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                "termino" => "STEMI"
                "descripcion" => "<p id="par0030" class="elsevierStylePara elsevierViewall">ST-elevation myocardial infarction</p>"
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                  \t\t\t\t">hsCRP&nbsp;\t\t\t\t\t\t\n
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                  \t\t\t\t">0&#46;934 &#40;0&#46;806&#8211;1&#46;083&#41;&nbsp;\t\t\t\t\t\t\n
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                  \t\t\t\t  " align="char" valign="\n
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                  \t\t\t\t">0&#46;166&nbsp;\t\t\t\t\t\t\n
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                    0 => array:2 [
                      "titulo" => "Inflammation and atherosclerosis"
                      "autores" => array:1 [
                        0 => array:2 [
                          "etal" => false
                          "autores" => array:3 [
                            0 => "P&#46; Libby"
                            1 => "P&#46;M&#46; Ridker"
                            2 => "A&#46; Maseri"
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                      "Revista" => array:6 [
                        "tituloSerie" => "Circulation"
                        "fecha" => "2002"
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                        "paginaFinal" => "1143"
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                            "url" => "https://www.ncbi.nlm.nih.gov/pubmed/11877368"
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                      "titulo" => "Markers of inflammation and cardiovascular disease&#58; application to clinical and public health practice"
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                        0 => array:2 [
                          "etal" => true
                          "autores" => array:3 [
                            0 => "T&#46;A&#46; Pearson"
                            1 => "G&#46;A&#46; Mensah"
                            2 => "R&#46;W&#46; Alexander"
                          ]
                        ]
                      ]
                    ]
                  ]
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                    0 => array:1 [
                      "Revista" => array:6 [
                        "tituloSerie" => "Circulation"
                        "fecha" => "2003"
                        "volumen" => "107"
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Original article
High-sensitivity C-reactive protein predicts adverse outcomes after non-ST-segment elevation acute coronary syndrome regardless of GRACE risk score, but not after ST-segment elevation myocardial infarction
O valor do teste de alta sensibilidade da proteína C-reativa como preditor de resultados adversos em doentes com síndrome coronária aguda
Sergio Raposeiras Roubína,
Corresponding author
raposeiras26@hotmail.com

Corresponding author.
, Cristina Barreiro Pardalb, Filomena Roubín-Camiñac, Raymundo Ocaranza Sancheza, Ezequiel Álvarez Castroa, Beatriz Paradela Dobarroa, Jose María García-Acuñaa, Pablo Aguiar Soutoa, Michel Jacquet Herveta, Maria José Castromána, Isabel Arufea, Belén Outesa, María Victoria Reino-Maceirasa, Emad Abu Assia, José Ramón González-Juanateya
a Department of Cardiology, University Clinical Hospital of Santiago de Compostela, A Coruña, Spain
b Department of Anethesiology, Montecelo Hospital, Pontevedra, Spain
c Laboratory Unit, Meixoeiro Hospital, Vigo, Spain
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    "textoCompleto" => "<span class="elsevierStyleSections"><span id="sec0005" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Introduction</span><p id="par0035" class="elsevierStylePara elsevierViewall">Inflammation plays a pivotal role in the pathogenesis of atherosclerosis and its complications&#46; In particular&#44; atherosclerosis is an active process and the inflammatory component appears to be particularly correlated with the development of acute coronary syndromes &#40;ACS&#41;&#46;<a class="elsevierStyleCrossRefs" href="#bib0005"><span class="elsevierStyleSup">1&#44;2</span></a> C-reactive protein &#40;CRP&#41; is an acute phase protein that appears in the circulation in response to inflammatory cytokines&#44; such as interleukin-6&#44; and serves as a biomarker for systemic inflammation&#46;<a class="elsevierStyleCrossRefs" href="#bib0015"><span class="elsevierStyleSup">3&#44;4</span></a> There are also increased concentrations of acute-phase serum reactants such as CRP in patients with ACS&#46;<a class="elsevierStyleCrossRef" href="#bib0025"><span class="elsevierStyleSup">5</span></a></p><p id="par0040" class="elsevierStylePara elsevierViewall">The high-sensitivity CRP &#40;hsCRP&#41; assay is increasingly used as a marker for cardiac risk assessment and as a prognostic tool in heart disease&#46;<a class="elsevierStyleCrossRefs" href="#bib0030"><span class="elsevierStyleSup">6&#8211;8</span></a> The aim of this study was to analyze the prognostic value of hsCRP values to predict follow-up outcomes in ACS patients regardless of the GRACE &#40;Global Registry of Acute Coronary Events&#41; risk score&#46;<a class="elsevierStyleCrossRef" href="#bib0030"><span class="elsevierStyleSup">6</span></a></p></span><span id="sec0010" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Methods</span><span id="sec0015" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Study population</span><p id="par0045" class="elsevierStylePara elsevierViewall">We included 151 consecutive patients admitted to the coronary care unit with a diagnosis of ACS&#46; Patients with previous ACS&#44; peripheral arterial disease and impaired renal function &#40;estimated glomerular filtration rate by the MDRD-4 equation &#60;60<span class="elsevierStyleHsp" style=""></span>ml&#47;min&#47;1&#46;73<span class="elsevierStyleHsp" style=""></span>m<span class="elsevierStyleSup">2</span>&#41; were excluded&#46; We also excluded patients under treatment with anti-inflammatory drugs and those with concomitant inflammatory diseases&#44; cancer&#44; or other significant heart disease&#46; The study was approved by the ethics committee of the University Clinical Hospital of Santiago de Compostela&#44; and all patients gave their written informed consent to participate&#46;</p></span><span id="sec0020" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Study design</span><p id="par0050" class="elsevierStylePara elsevierViewall">All patients were treated invasively by catheterization&#46; The use of beta-adrenergic blocking agents&#44; angiotensin-converting enzyme inhibitors&#44; antiplatelets&#44; diuretics and inotropic drug support was left to the discretion of the coronary care unit cardiologists according to our clinical protocols based on international guidelines&#46; For each patient we estimated the risk of follow-up mortality and coronary events according to the 6-month mortality GRACE score&#46;<a class="elsevierStyleCrossRef" href="#bib0030"><span class="elsevierStyleSup">6</span></a> Complete clinical data and blood samples for laboratory measurements were collected on admission&#46; We performed an echocardiographic evaluation of left ventricular ejection fraction &#40;LVEF&#41; in all subjects within 24<span class="elsevierStyleHsp" style=""></span>hours of admission&#46; Serum hsCRP levels were measured on admission&#46;</p></span><span id="sec0025" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Definitions and endpoints</span><p id="par0055" class="elsevierStylePara elsevierViewall">The ACS diagnosis was validated if the patient met any of the following criteria&#58; new-onset angina with cardiac biomarkers above the highest normal laboratory limit&#44; ST-segment deviation on the electrocardiogram&#44; in-hospital stress testing showing ischemia&#44; or a known history of coronary disease&#46; Patients were classified as having myocardial infarction with ST-segment elevation &#40;STEMI&#41; or non-ST-segment elevation ACS &#40;NSTE-ACS&#41; &#40;unstable angina or non-ST elevation myocardial infarction&#41;&#46; Diabetes was defined as increased fasting plasma glucose concentration of &#8805;126<span class="elsevierStyleHsp" style=""></span>mg&#47;dl&#44; HbA1c of &#8805;6&#46;5&#37;&#44; or treatment with insulin or hypoglycemic agents&#46; Hypertension was defined as systolic&#47;diastolic blood pressure<span class="elsevierStyleHsp" style=""></span>&#62;<span class="elsevierStyleHsp" style=""></span>140&#47;90<span class="elsevierStyleHsp" style=""></span>mmHg or current use of any antihypertensive medication&#46; LVEF<span class="elsevierStyleHsp" style=""></span>&#60;45&#37; was considered to be depressed&#46;</p><p id="par0060" class="elsevierStylePara elsevierViewall">The primary endpoint was the combination of cardiac death and myocardial reinfarction during the follow-up period &#40;median 19&#46;8 months&#44; interquartile range 16&#46;3&#8211;23&#46;7 months&#41;&#46; Reinfarction was defined as the appearance of new symptoms of myocardial ischemia or electrocardiographic ischemic changes accompanied by re-elevation of cardiac biomarkers &#40;high-sensitivity troponin I&#41;&#46;</p></span><span id="sec0030" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Determination of CRP</span><p id="par0065" class="elsevierStylePara elsevierViewall">Blood samples were stored in evacuated tubes at &#8722;20<span class="elsevierStyleHsp" style=""></span>&#176;C and were processed within 24<span class="elsevierStyleHsp" style=""></span>hours by automated microparticle immunoassay &#40;ELISA&#41;&#46; The CRP detection range corresponds to values of 0&#46;1&#8211;12&#46;0<span class="elsevierStyleHsp" style=""></span>mg&#47;dl&#44; with an interassay variation coefficient of &#60;5&#37; &#40;normal values<span class="elsevierStyleHsp" style=""></span>&#60;0&#46;3<span class="elsevierStyleHsp" style=""></span>mg&#47;dl&#41;&#46;</p></span><span id="sec0035" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Statistical analysis</span><p id="par0070" class="elsevierStylePara elsevierViewall">All information was prospectively recorded in a database created with Microsoft Office Access 2007&#46; The statistical analyses were performed with SPSS &#40;Statistical Package for the Social Sciences&#41; version 17&#46;0&#46; Categorical or dichotomous variables are expressed as absolute values and percentages&#44; and were compared with Pearson&#39;s chi-square test&#46; Continuous variables with a normal distribution are expressed as mean<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>standard deviation&#44; and the Student&#39;s <span class="elsevierStyleItalic">t</span> test was used for comparisons between groups&#46; Continuous variables without normal distribution are expressed as median and interquartile range&#46; Pearson&#39;s test was used to study the correlation between quantitative variables&#46; A multivariate logistic regression model was used to evaluate the independent contribution of hsCRP levels to the risk of new events during follow-up&#46; Univariate predictors of potential significance and hsCRP values were included in multivariate analysis &#40;backward stepwise Cox proportional hazard analysis&#41;&#46; Adjusted hazard ratios and 95&#37; confidence intervals &#40;CI&#41; are presented&#46; Kaplan&#8211;Meier curves were constructed to evaluate the prognostic value of hsCRP during follow-up&#46; A p value<span class="elsevierStyleHsp" style=""></span>&#60;0&#46;05 was considered statistically significant&#46;</p></span></span><span id="sec0040" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Results</span><span id="sec0045" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Baseline characteristics</span><p id="par0075" class="elsevierStylePara elsevierViewall"><a class="elsevierStyleCrossRef" href="#tbl0005">Table 1</a> describes the baseline characteristics of the population&#46; CRP values &#40;median and 25&#8211;75&#37; interquartile range&#41; on admission were 0&#46;9 &#40;0&#46;3&#8211;1&#46;9&#41;<span class="elsevierStyleHsp" style=""></span>mg&#47;dl&#46; Of the patients recruited&#44; 80 had STEMI&#46; Although hsCRP values were higher in patients with STEMI &#40;2&#46;6<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>4&#46;2<span class="elsevierStyleHsp" style=""></span>mg&#47;dl&#41;&#44; there was no statistically significant difference compared with NSTE-ACS patients &#40;1&#46;8<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>2&#46;9<span class="elsevierStyleHsp" style=""></span>mg&#47;dl&#44; p&#61;0&#46;161&#41;&#46;</p><elsevierMultimedia ident="tbl0005"></elsevierMultimedia></span><span id="sec0050" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Correlation with in-hospital events</span><p id="par0080" class="elsevierStylePara elsevierViewall">During the follow-up period&#44; 18 &#40;11&#46;9&#37;&#41; patients presented cardiac events &#40;six cardiac deaths&#44; 11 re-infarctions&#41;&#46; These patients had a higher percentage of diabetes&#44; higher Killip functional class&#44; greater proportion of depressed LVEF and higher GRACE risk score&#46; The occurrence of follow-up events was significantly related to admission hsCRP level&#44; which was an excellent predictor of cardiac death and re-infarction during follow-up &#40;HR 1&#46;091&#44; 95&#37; CI 1&#46;014&#8211;1&#46;174&#59; p&#61;0&#46;019&#41;&#46; Stratifying the population based on type of ACS&#44; we found that hsCRP predicted outcome only in the NSTE-ACS group &#40;HR 1&#46;174&#44; 95&#37; CI 1&#46;076&#8211;1&#46;280&#59; p&#61;0&#46;004&#41;&#44; not in patients with STEMI &#40;HR 0&#46;999&#44; 95&#37; CI 0&#46;859&#8211;1&#46;163&#59; p&#61;0&#46;990&#41;&#46; Likewise hsCRP and GRACE risk score at discharge showed a significant positive correlation &#40;r&#61;0&#46;226&#44; p&#61;0&#46;005&#41; &#40;<a class="elsevierStyleCrossRef" href="#fig0005">Figure 1</a>&#41;&#46;</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia><p id="par0085" class="elsevierStylePara elsevierViewall">In ROC analysis&#44; the area under the curve for hsCRP in predicting follow-up outcomes was 0&#46;75<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>0&#46;05&#46; The best cutoff level of hsCRP was 1&#46;1<span class="elsevierStyleHsp" style=""></span>mg&#47;dl&#44; with sensitivity of 77&#46;8&#37; and specificity of 63&#46;2&#37; &#40;<a class="elsevierStyleCrossRef" href="#fig0010">Figure 2</a>&#41;&#46; <a class="elsevierStyleCrossRef" href="#fig0015">Figure 3</a> shows the Kaplan&#8211;Meier survival curves according to hsCRP levels above and below this cutoff &#40;1&#46;1<span class="elsevierStyleHsp" style=""></span>mg&#47;dl&#41;&#46;</p><elsevierMultimedia ident="fig0010"></elsevierMultimedia><elsevierMultimedia ident="fig0015"></elsevierMultimedia></span><span id="sec0055" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Multivariate analysis</span><p id="par0090" class="elsevierStylePara elsevierViewall">In our model &#40;<a class="elsevierStyleCrossRef" href="#tbl0010">Table 2</a>&#41;&#44; adjusted by variables associated with cardiac events &#40;hsCRP&#44; diabetes&#44; depressed LVEF and GRACE risk score&#41;&#44; hsCRP &#40;as a continuous variable&#41; was an independent predictor of follow-up outcomes only in NSTE-ACS patients &#40;HR 1&#46;217&#44; 95&#37; CI&#58; 1&#46;093&#8211;1&#46;356&#44; p&#60;0&#46;001&#41;&#46;</p><elsevierMultimedia ident="tbl0010"></elsevierMultimedia></span></span><span id="sec0060" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Discussion</span><p id="par0095" class="elsevierStylePara elsevierViewall">In this single-center study we showed that hsCRP was significantly associated with adverse follow-up outcomes in patients with NSTE-ACS&#44; independently of GRACE risk score&#44; but not in patients with STEMI&#46;</p><p id="par0100" class="elsevierStylePara elsevierViewall">Many studies have assessed the prognostic value of CRP in the hospital phase of ACS&#46;<a class="elsevierStyleCrossRefs" href="#bib0045"><span class="elsevierStyleSup">9&#8211;12</span></a> However&#44; fewer studies have examined its prognostic value in follow-up&#44; and very few have investigated its prognostic role over the entire spectrum of ACS patients&#44; classified as NSTE-ACS or non-STEMI&#46;</p><p id="par0105" class="elsevierStylePara elsevierViewall">The hypothesis that inflammatory reactions promote plaque fissuring&#44; erosion&#44; ulceration&#44; and rupture of the plaque surface should in most cases be applicable to both settings of ACS&#46;<a class="elsevierStyleCrossRefs" href="#bib0105"><span class="elsevierStyleSup">13&#44;14</span></a> They may share the same underlying pathophysiologic processes&#44; with coronary plaque disruption and consequent platelet aggregation and thrombosis&#46; However&#44; the differences found in our study between the two types of ACS were in agreement with previous studies in which hsCRP was a predictor of negative outcome&#44; especially in patients with unstable angina and non-STEMI&#46; Kuch et al&#46;<a class="elsevierStyleCrossRef" href="#bib0065"><span class="elsevierStyleSup">15</span></a> reported data on an unselected sample of patients with myocardial infarction admitted to a community hospital&#44; showing that CRP was significantly associated with adverse short-term outcome&#46; Their multivariate analysis showed that both troponin positivity and CRP positivity were associated with a 2-fold increased risk of dying within 28 days after the acute event for all patients with myocardial infarction&#46; Stratifying by myocardial infarction type showed that in patients with STEMI&#44; troponin positivity&#44; but not CRP positivity&#44; independently predicted 28-day case fatality&#44; while in patients with non-STEMI&#44; CRP positivity&#44; but not troponin positivity&#44; predicted outcome&#46; They concluded that admission CRP is a powerful parameter for risk stratification of patients with myocardial infraction&#44; with better stratification in patients with non-STEMI&#46;</p><p id="par0110" class="elsevierStylePara elsevierViewall">Morrow et al&#46;&#44; using a cutoff of 1&#46;5<span class="elsevierStyleHsp" style=""></span>mg&#47;dl &#40;similar to ours&#41;&#44; observed that elevated CRP at admission was associated with higher mortality at 14 days&#46; Schoos et al&#46;<a class="elsevierStyleCrossRef" href="#bib0080"><span class="elsevierStyleSup">16</span></a> demonstrated that preprocedure hsCRP is an independent and strong predictor of a composite endpoint of death&#44; nonfatal recurrent myocardial infarction&#44; and stent thrombosis after percutaneous intervention with coronary stent implantation&#46; Abbate et al&#46; confirmed the prognostic value of CRP in predicting short- and long-term outcomes after ACS&#46; Our group has shown that hsCRP was a predictor of adverse outcomes in the in-hospital phase of ACS independently of GRACE risk score&#46; However&#44; to date&#44; no studies have analyzed the follow-up prognostic value of hsCRP regardless of GRACE risk score at discharge&#46;</p><p id="par0115" class="elsevierStylePara elsevierViewall">There is an intracardiac inflammatory response in ACS that appears to be the result of the evolution of myocardial necrosis&#44; as shown by higher CRP&#44; TNF&#945; and IL-6 levels in patients with major adverse cardiac events&#46; Patients with ACS and higher CRP may represent a group with hyperresponsiveness of the inflammatory system&#44; which might exaggerate the acute-phase reaction and increase immune system activation&#44; which may in turn mediate myocardial damage and promote cardiac complications&#46;<a class="elsevierStyleCrossRefs" href="#bib0085"><span class="elsevierStyleSup">17&#8211;20</span></a> This may be more pronounced in patients with NSTE-ACS than in those with STEMI&#44; due to a higher atherosclerotic burden&#46;</p><p id="par0120" class="elsevierStylePara elsevierViewall">hsCRP measurement&#44; as a marker of inflammatory activity&#44; has several advantages&#46; Firstly&#44; it is a stable compound and secondly&#44; it can be measured at any time of day without regard for the biological clock&#44; since unlike measurements of cytokines such as IL-6&#44; no circadian variation appears to exist for hsCRP&#46;</p></span><span id="sec0065" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Conclusions</span><p id="par0125" class="elsevierStylePara elsevierViewall">Although the GRACE risk score is routinely used for stratification of patients with acute coronary syndrome&#44; assessment of hsCRP may provide additional prognostic value&#46; High hsCRP values were an independent and strong predictor of a composite endpoint of death and nonfatal recurrent myocardial infarction&#46; These findings highlight the importance of determining levels of this biomarker for risk stratification of these patients during follow-up&#46;</p></span><span id="sec0070" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Ethical disclosures</span><span id="sec0075" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Protection of human and animal subjects</span><p id="par0130" class="elsevierStylePara elsevierViewall">The authors declare that no experiments were performed on humans or animals for this study&#46;</p></span><span id="sec0080" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Confidentiality of data</span><p id="par0135" class="elsevierStylePara elsevierViewall">The authors declare that no patient data appear in this article&#46;</p></span><span id="sec0085" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Right to privacy and informed consent</span><p id="par0140" class="elsevierStylePara elsevierViewall">The authors declare that no patient data appear in this article&#46;</p></span></span><span id="sec0090" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Conflict of interest</span><p id="par0145" class="elsevierStylePara elsevierViewall">The authors have no conflicts of interest to declare&#46;</p></span></span>"
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            0 => "Elevada sensibilidade de prote&#237;na C-reativa"
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        "titulo" => "Abstract"
        "resumen" => "<span class="elsevierStyleSectionTitle">Introduction</span><p id="spar0005" class="elsevierStyleSimplePara elsevierViewall">Atherosclerosis is an active process and the inflammatory component appears to be particularly correlated with the development of acute coronary syndromes &#40;ACS&#41;&#46; C-reactive protein &#40;CRP&#41; is an acute phase protein that appears in the circulation in response to inflammatory cytokines&#46; The present study investigated the association between high-sensitivity C-reactive protein &#40;hsCRP&#41; on admission and follow-up prognosis after an ACS&#46;</p> <span class="elsevierStyleSectionTitle">Methods</span><p id="spar0010" class="elsevierStyleSimplePara elsevierViewall">We included 151 consecutive patients admitted to the coronary care unit with a diagnosis of ACS &#40;47&#37; ST-segment elevation myocardial infarction &#91;STEMI&#93;&#41;&#46; The primary endpoint was the combination of cardiac death and myocardial reinfarction during the follow-up period &#40;median 19&#46;8 months&#44; interquartile range 16&#46;3&#8211;23&#46;7 months&#41;&#46;</p> <span class="elsevierStyleSectionTitle">Results</span><p id="spar0015" class="elsevierStyleSimplePara elsevierViewall">The occurrence of follow-up events was significantly related to admission hsCRP level&#44; which was an excellent predictor of cardiac death and reinfarction during follow-up &#40;HR 1&#46;091&#44; 95&#37; CI 1&#46;014&#8211;1&#46;174&#59; p&#61;0&#46;019&#41;&#46; Stratifying the population based on type of ACS&#44; adjusted by variables associated with cardiac events in univariate analysis &#40;hsCRP&#44; diabetes&#44; depressed ejection fraction and GRACE risk score&#41;&#44; hsCRP proved to be an independent predictor of follow-up outcomes only in non-STEMI patients &#40;HR 1&#46;217&#44; 95&#37; CI&#58; 1&#46;093&#8211;1&#46;356&#44; p&#60;0&#46;001&#41;&#44; not in STEMI patients&#46; The best cutoff level of hsCRP to predict follow-up outcomes was 1&#46;1<span class="elsevierStyleHsp" style=""></span>mg&#47;dl&#44; with sensitivity of 77&#46;8&#37; and specificity of 63&#46;2&#37;&#46;</p> <span class="elsevierStyleSectionTitle">Conclusion</span><p id="spar0020" class="elsevierStyleSimplePara elsevierViewall">Although the GRACE risk score is routinely used for stratification of patients with ACS&#44; assessment of hsCRP may provide additional prognostic value in the follow-up of non-STEMI patients&#46;</p>"
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        "resumen" => "<span class="elsevierStyleSectionTitle">Introdu&#231;&#227;o</span><p id="spar0025" class="elsevierStyleSimplePara elsevierViewall">A aterosclerose &#233; um processo ativo e a sua componente inflamat&#243;ria parece estar particularmente relacionada com o desenvolvimento de s&#237;ndromes coron&#225;rias agudas &#40;SCA&#41;&#46; A prote&#237;na C-reativa &#40;PCR&#41; &#233; uma prote&#237;na que aparece na circula&#231;&#227;o&#44; na fase aguda do processo inflamat&#243;rio&#46; O presente estudo teve como objetivo analisar a associa&#231;&#227;o entre o valor do teste de alta sensibilidade da prote&#237;na C-reativa &#40;PCR-as&#41; na admiss&#227;o&#44; com o progn&#243;stico no seguimento&#44; em doentes p&#243;s-SCA&#46;</p> <span class="elsevierStyleSectionTitle">M&#233;todos</span><p id="spar0035" class="elsevierStyleSimplePara elsevierViewall">Foram inclu&#237;dos 151 doentes consecutivos&#44; internados na unidade de cuidados coron&#225;rios&#44; com diagn&#243;stico de SCA &#40;47&#37; com enfarte agudo do mioc&#225;rdio com eleva&#231;&#227;o do segmento ST &#8211; STEMI&#41;&#46; O <span class="elsevierStyleItalic">end-point</span> estudado foi a vari&#225;vel composta pela morte associada a patologia card&#237;aca e re-enfarte mioc&#225;rdio durante o per&#237;odo de seguimento &#40;mediana de 19&#44;8 meses&#44; intervalo interquartil 16&#44;3-23&#44;7 meses&#41;&#46;</p> <span class="elsevierStyleSectionTitle">Resultados</span><p id="spar0040" class="elsevierStyleSimplePara elsevierViewall">A ocorr&#234;ncia de eventos apresentou uma forte rela&#231;&#227;o com o valor de CPR-as registado na admiss&#227;o&#44; sendo por isso considerado como um bom preditor para a ocorr&#234;ncia de morte associada a patologia card&#237;aca e a re-enfarte no per&#237;odo de seguimento de doentes p&#243;s-SCA &#40;HR 1&#44;091&#44; CI 95&#37; 1&#44;014-1&#44;174&#59; p<span class="elsevierStyleHsp" style=""></span>&#61;<span class="elsevierStyleHsp" style=""></span>0&#44;019&#41;&#46; Ap&#243;s estratifica&#231;&#227;o da popula&#231;&#227;o pelo tipo de SCA e ajustando as vari&#225;veis associadas &#224; ocorr&#234;ncia de eventos card&#237;acos &#40;an&#225;lise univariada das vari&#225;veis valor de PCR-as&#44; diabetes <span class="elsevierStyleItalic">mellitus</span>&#44; fra&#231;&#227;o de eje&#231;&#227;o deprimida e <span class="elsevierStyleItalic">score</span> de risco GRACE&#41;&#44; o valor de PCR-as destacou-se como preditor independente no seguimento dos doentes com EAM sem eleva&#231;&#227;o ST &#40;HR 1&#44;217&#44; IC 95&#37;&#58; 1&#44;093-1&#44;356&#44; p<span class="elsevierStyleHsp" style=""></span>&#60;<span class="elsevierStyleHsp" style=""></span>0&#44;001&#41;&#46; O valor de <span class="elsevierStyleItalic">cut-off</span> para o n&#237;vel de PCR-as preditor foi de 1&#44;1<span class="elsevierStyleHsp" style=""></span>mg&#47;dl&#44; com uma sensibilidade de 77&#44;8&#37; e uma especificidade de 63&#44;2&#37;&#46;</p> <span class="elsevierStyleSectionTitle">Conclus&#227;o</span><p id="spar0055" class="elsevierStyleSimplePara elsevierViewall">Apesar de o <span class="elsevierStyleItalic">score</span> de risco GRACE ser utilizado&#44; por rotina&#44; para estratificar os doentes com SCA&#44; a medi&#231;&#227;o do valor de PCR-as pode acrescentar valor progn&#243;stico no seguimento de doentes com EAM sem eleva&#231;&#227;o e ST&#46;</p>"
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    "nomenclatura" => array:1 [
      0 => array:2 [
        "titulo" => "<span class="elsevierStyleSectionTitle">Abbreviations</span>"
        "listaDefinicion" => array:1 [
          0 => array:1 [
            "definicion" => array:6 [
              0 => array:2 [
                "termino" => "ACS"
                "descripcion" => "<p id="par0005" class="elsevierStylePara elsevierViewall">acute coronary syndrome</p>"
              ]
              1 => array:2 [
                "termino" => "CRP"
                "descripcion" => "<p id="par0010" class="elsevierStylePara elsevierViewall">C-reactive protein</p>"
              ]
              2 => array:2 [
                "termino" => "hsCRP"
                "descripcion" => "<p id="par0015" class="elsevierStylePara elsevierViewall">high-sensitivity C-reactive protein</p>"
              ]
              3 => array:2 [
                "termino" => "LVEF"
                "descripcion" => "<p id="par0020" class="elsevierStylePara elsevierViewall">left ventricular ejection fraction</p>"
              ]
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                "termino" => "NSTE-ACS"
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                  \t\t\t\t">0&#46;934 &#40;0&#46;806&#8211;1&#46;083&#41;&nbsp;\t\t\t\t\t\t\n
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                  \t\t\t\t">0&#46;166&nbsp;\t\t\t\t\t\t\n
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                  """
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                    0 => array:2 [
                      "titulo" => "Inflammation and atherosclerosis"
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                        0 => array:2 [
                          "etal" => false
                          "autores" => array:3 [
                            0 => "P&#46; Libby"
                            1 => "P&#46;M&#46; Ridker"
                            2 => "A&#46; Maseri"
                          ]
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                            1 => "M&#46;V&#46; Rodr&#237;guez"
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                        "tituloSerie" => "Rev Esp Cardiol"
                        "fecha" => "2006"
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        "identificador" => "xack45566"
        "titulo" => "Acknowledgements"
        "texto" => "<p id="par0155" class="elsevierStylePara elsevierViewall">We thank the medical residents and nurses of the coronary cardiac unit of the University Clinical Hospital of Santiago de Compostela for their assistance in this study&#46;</p>"
      ]
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Article information
ISSN: 21742049
Original language: English
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Idiomas
Revista Portuguesa de Cardiologia (English edition)
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