एथेरोस्क्लेरोसिस: ओपन एक्सेस

खुला एक्सेस

हमारा समूह 1000 से अधिक वैज्ञानिक सोसायटी के सहयोग से हर साल संयुक्त राज्य अमेरिका, यूरोप और एशिया में 3000+ वैश्विक सम्मेलन श्रृंखला कार्यक्रम आयोजित करता है और 700+ ओपन एक्सेस जर्नल प्रकाशित करता है जिसमें 50000 से अधिक प्रतिष्ठित व्यक्तित्व, प्रतिष्ठित वैज्ञानिक संपादकीय बोर्ड के सदस्यों के रूप में शामिल होते हैं।

ओपन एक्सेस जर्नल्स को अधिक पाठक और उद्धरण मिल रहे हैं
700 जर्नल और 15,000,000 पाठक प्रत्येक जर्नल को 25,000+ पाठक मिल रहे हैं

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अमूर्त

Implications of Lipid Profile Dosages in Fasting and Postprandial Status

Marcia C Feres, Bruna B Perez, Julia T. M Thorrecilha, Rolando Bini Jr, Newton A Raphael, Maria Cristina De Martino, Debora R.R. Boscolo, Altay A Lino de Souza and Sergio Tufik

Introduction: To improve patient adherence to lipid tests, many laboratories around the world perform these tests without the need for a 12 h fast at random times during the day.
Methods: The study consisted of 51 volunteers and venous blood was collected in a 12 h fast and after a meal the next day. The volunteer returns to the laboratory after having his usual breakfast to be collected blood 2, 3 and 4 h after that meal. The following tests will be performed: cholesterol, triglycerides, C-LDL, C-HDL and VLDL with the Enzyme/Colorimetric method on Beckman-Coulter®AU5800 equipment and Beckman-Coulter reagent. In addition to the dosage, C-LDL was calculated by Friedewald Equation.
Results: In the comparison of the fasting lipid profile versus 2, 3 and 4 h after the meal, it was observed that there was no significant difference for the parameters of TC and C-HDL and for the calculated C-LDL, with average TC (p=0.237), C-HDL (p=0.130) and for C-LDL (p=0.089). However, for the dosed C-LDL, TG and VLDL showed significant differences with the respective mean concentrations and standard deviation for each hour after 2 h C-LDL (112.1 ± 33.6 mg/dL, p=0.008), 3 h (111.7 ± 35.0 mg/dL, p=0.019) and 4 h (115.0 ± 34.9 mg/dL, p=0.017) for TG 2 h (156.0 ± 86.4 mg/dL, p=0.000), 3 h (148.5 ± 92.0 mg/dL, p=0.000) and 4 h (143.4 ± 93.0 mg/dL, p=0.000) and for VLDL calculated: 2, 3 and 4 h (35.9 ± 53.5 mg/dL, p=0.000, 35.2 ± 53.6 mg/dL, p=0.001, and 34.0 ± 53.6 mg/dL, p=0.000).
Conclusion: Our data confirmed that the meal did not influence the TC, C-HDL and C-LDL calculate data, but for TG, VLDL and C-LDL doses a significant difference was observed at post-meal concentrations. Although disturbing the C-LDL for methodological reasons, did not affect the clinic. Analyzing our data, we observed that the best blood collection time could be between 2 and 3 h after the meal, where the degree of lipemia would have less influence in most individuals.