997 resultados para C template metaprogramming


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Fundamento: Em pacientes com hipertens&#227;o arterial sist&#234;mica, a microalbumin&#250;ria &#233; um marcador de les&#227;o endotelial e est&#225; associada a um risco aumentado de doen&#231;a cardiovascular. Objetivo: O objetivo do presente estudo foi determinar os fatores que influenciam a ocorr&#234;ncia de microalbumi&#250;ria em pacientes hipertensos com creatinina s&#233;rica menor que 1,5 mg/dL. M&#233;todos: Foram inclu&#237;dos no estudo 133 pacientes brasileiros atendidos em um ambulat&#243;rio multidisciplinar para hipertensos. Pacientes com creatinina s&#233;rica maior do que 1,5 mg/dL e aqueles com diabete mellitus foram exclu&#237;dos do estudo. A press&#227;o arterial sist&#243;lica e diast&#243;lica foi aferida. O &#237;ndice de massa corporal (IMC) e a taxa de filtra&#231;&#227;o glomerular estimada pela f&#243;rmula CKD-EPI foram calculados. Em um estudo transversal, creatinina, cistatina C, colesterol total, HDL colesterol, LDL colesterol, triglicer&#237;deos, prote&#237;na C-reativa (PCR) e glicose foram mensurados em amostra de sangue. A microalbumin&#250;ria foi determinada na urina colhida em 24 horas. Os hipertensos foram classificados pela presen&#231;a de um ou mais crit&#233;rios para s&#237;ndrome metab&#243;lica. Resultados: Em an&#225;lise de regress&#227;o m&#250;ltipla, os n&#237;veis s&#233;ricos de cistatina C, PCR, o &#237;ndice aterog&#234;nico log TG/HDLc e a presen&#231;a de tr&#234;s ou mais crit&#233;rios para s&#237;ndrome metab&#243;lica foram positivamente correlacionados com a microalbuminuria (r2: 0,277; p < 0,05). Conclus&#227;o: Cistatina C, PCR, log TG/HDLc e presen&#231;a de tr&#234;s ou mais crit&#233;rios para s&#237;ndrome metab&#243;lica, independentemente da creatinina s&#233;rica, foram associados com a microalbumin&#250;ria, um marcador precoce de les&#227;o renal e de risco cardiovascular em pacientes com hipertens&#227;o arterial essencial.

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Fundamento: O valor progn&#243;stico incremental da dosagem plasm&#225;tica de Prote&#237;na C-reativa (PCR) em rela&#231;&#227;o ao Escore GRACE n&#227;o est&#225; estabelecido em pacientes com s&#237;ndromes coronarianas agudas sem supradesnivelamento do segmento ST (SCA). Objetivo: Testar a hip&#243;tese de que a medida de PCR na admiss&#227;o incrementa o valor progn&#243;stico do escore GRACE em pacientes com SCA. M&#233;todos: Foram estudados 290 indiv&#237;duos, internados consecutivamente por SCA, os quais tiveram material plasm&#225;tico colhido na admiss&#227;o para dosagem de PCR por m&#233;todo de alta sensibilidade (nefelometria). Desfechos cardiovasculares durante hospitaliza&#231;&#227;o foram definidos pela combina&#231;&#227;o de &#243;bito, infarto n&#227;o fatal ou angina refrat&#225;ria n&#227;o fatal. Resultados: A incid&#234;ncia de eventos cardiovasculares durante hospitaliza&#231;&#227;o foi 15% (18 &#243;bitos, 11 infartos, 13 anginas), tendo a PCR apresentado estat&#237;stica-C de 0,60 (95% IC = 0,51 - 0,70; p = 0,034) na predi&#231;&#227;o desses desfechos. Ap&#243;s ajuste para o Escore GRACE, PCR elevada (definida pelo melhor ponto de corte) apresentou tend&#234;ncia a associa&#231;&#227;o com eventos hospitalares (OR = 1,89; 95% IC = 0,92 - 3,88; p = 0,08). No entanto, a adi&#231;&#227;o da vari&#225;vel PCR elevada no modelo GRACE n&#227;o promoveu incremento significativo na estat&#237;stica-C, a qual variou de 0,705 para 0,718 (p = 0,46). Da mesma forma, n&#227;o houve reclassifica&#231;&#227;o de risco significativa com a adi&#231;&#227;o da PCR no modelo preditor (reclassifica&#231;&#227;o l&#237;quida = 5,7%; p = 0,15). Conclus&#227;o Embora PCR possua associa&#231;&#227;o com desfechos hospitalares, esse marcador inflamat&#243;rio n&#227;o incrementa o valor progn&#243;stico do Escore GRACE.

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Background: The association between high-sensitivity C-reactive protein and recurrent major adverse cardiovascular events (MACE) in patients with ST-elevation myocardial infarction who undergo primary percutaneous coronary intervention remains controversial. Objective: To investigate the potential association between high-sensitivity C-reactive protein and an increased risk of MACE such as death, heart failure, reinfarction, and new revascularization in patients with ST-elevation myocardial infarction treated with primary percutaneous coronary intervention. Methods: This prospective cohort study included 300 individuals aged >18 years who were diagnosed with ST-elevation myocardial infarction and underwent primary percutaneous coronary intervention at a tertiary health center. An instrument evaluating clinical variables and the Thrombolysis in Myocardial Infarction (TIMI) and Global Registry of Acute Coronary Events (GRACE) risk scores was used. High-sensitivity C-reactive protein was determined by nephelometry. The patients were followed-up during hospitalization and up to 30 days after infarction for the occurrence of MACE. Student's t, Mann-Whitney, chi-square, and logistic regression tests were used for statistical analyses. P values of &#8804;0.05 were considered statistically significant. Results: The mean age was 59.76 years, and 69.3% of patients were male. No statistically significant association was observed between high-sensitivity C-reactive protein and recurrent MACE (p = 0.11). However, high-sensitivity C-reactive protein was independently associated with 30-day mortality when adjusted for TIMI [odds ratio (OR), 1.27; 95% confidence interval (CI), 1.07-1.51; p = 0.005] and GRACE (OR, 1.26; 95% CI, 1.06-1.49; p = 0.007) risk scores. Conclusion: Although high-sensitivity C-reactive protein was not predictive of combined major cardiovascular events within 30 days after ST-elevation myocardial infarction in patients who underwent primary angioplasty and stent implantation, it was an independent predictor of 30-day mortality.

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Chiral auxiliaries, cyclizations, Lewis acids, Sakurai reaction, annulations, asymmetric induction, azepines, radical cyclization, spiro compounds

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Background: High sensitivity C-reactive protein (hs-CRP) is commonly used in clinical practice to assess cardiovascular risk. However, a correlation has not yet been established between the absolute levels of peripheral and central hs-CRP. Objective: To assess the correlation between serum hs-CRP levels (mg/L) in a peripheral vein in the left forearm (LFPV) with those in the coronary sinus (CS) of patients with coronary artery disease (CAD) and a diagnosis of stable angina (SA) or unstable angina (UA). Methods: This observational, descriptive, and cross-sectional study was conducted at the Instituto do Cora&#231;&#227;o, Hospital das Clinicas, Faculdade de Medicina, Universidade de S&#227;o Paulo, and at the Hospital Benefic&#234;ncia Portuguesa de Sao Paulo, where CAD patients referred to the hospital for coronary angiography were evaluated. Results: Forty patients with CAD (20 with SA and 20 with UA) were included in the study. Blood samples from LFPV and CS were collected before coronary angiography. Furthermore, analysis of the correlation between serum levels of hs-CRP in LFPV versus CS showed a strong linear correlation for both SA (r = 0.993, p < 0.001) and UA (r = 0.976, p < 0.001) and for the entire sample (r = 0.985, p < 0.001). Conclusion: Our data suggest a strong linear correlation between hs-CRP levels in LFPV versus CS in patients with SA and UA.

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Background:Previous reports have inferred a linear relationship between LDL-C and changes in coronary plaque volume (CPV) measured by intravascular ultrasound. However, these publications included a small number of studies and did not explore other lipid markers.Objective:To assess the association between changes in lipid markers and regression of CPV using published data.Methods:We collected data from the control, placebo and intervention arms in studies that compared the effect of lipidlowering treatments on CPV, and from the placebo and control arms in studies that tested drugs that did not affect lipids. Baseline and final measurements of plaque volume, expressed in mm3, were extracted and the percentage changes after the interventions were calculated. Performing three linear regression analyses, we assessed the relationship between percentage and absolute changes in lipid markers and percentage variations in CPV.Results:Twenty-seven studies were selected. Correlations between percentage changes in LDL-C, non-HDL-C, and apolipoprotein B (ApoB) and percentage changes in CPV were moderate (r = 0.48, r = 0.47, and r = 0.44, respectively). Correlations between absolute differences in LDL-C, non&#8209;HDL-C, and ApoB with percentage differences in CPV were stronger (r = 0.57, r = 0.52, and r = 0.79). The linear regression model showed a statistically significant association between a reduction in lipid markers and regression of plaque volume.Conclusion:A significant association between changes in different atherogenic particles and regression of CPV was observed. The absolute reduction in ApoB showed the strongest correlation with coronary plaque regression.