Implications of Lipid Profile Dosages in Fasting and Postprandial Status
Implications of Lipid Profile Dosages in Fasting and Postprandial Status
Atherosclerosis: Open Access (Omics Publishing S.L) has announced almost 50 % discount on article processing charge to commemorate its 10th Anniversary.
Atherosclerosis: Open Access is an open access, peer-reviewed journal that focuses and welcomes submissions on all aspects of Coronary Heart disease, Stroke, Peripheral Arterial Disease, Chronic Kidney Disease, arteriosclerosis, Coronary Atherosclerosis, intracranial atherosclerosis etc.
It gives us great pleasure to announce the call for paper on the occasion of 10th Anniversary of the Journal at special and hefty discount of up to 50 % on one-time article processing charge. Prospective academicians and scientists are encouraged to utilize this opportunity to get their articles reviewed, processed and published at relatively faster pace and at lower charges. In addition to this, the authors who publish with us during the year-long celebrations will also be eligible for academic awards recommended by the editorial panel.
The Archive page contains wide variety of articles such as Research / Review / Case reports / short communication / Mini review / Prospective / Letter to Editors Etc. We would like introduce a Research article which has been spread to the widest audience of experts; and thus increased in readership, citations and altimetry score.
Title: “Implications of Lipid Profile Dosages in Fasting and Postprandial Status”
Abstract: 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. 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 4h 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. 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). : 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.
To have a glance at the full length manuscript, you can visit us at our archive page and Currently, Journal’s Archive is holding not only normal issues but also focusing on special issues. The purpose of special issues is to publish the most exciting research with respect to the subjects of Atherosclerosis / Cardiovascular Diseases and to provide a rapid turn-around time regarding reviewing and publishing, and to publicize the articles freely for research, teaching and reference purposes. Submit manuscript of your research articles or special issue articles online through manuscript submission or forwarded to the Editorial Office at atherosclerosis@oajournal.org
Media Contact:
Steven Edwards
Editorial Assistant
Atherosclerosis: Open Access