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Time-course analysis of flow mediated dilation for the evaluation of endothelial function after a high-fat meal in African Americans
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نویسنده
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marinos a. ,celedonio j.e. ,ramirez c.e. ,gottlieb j. ,gamboa a. ,hui n. ,yu c. ,stein c.m. ,biaggioni i. ,shibao c.a.
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منبع
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journal of the american heart association - 2015 - دوره : 4 - شماره : 11
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چکیده
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Background-flow-mediated dilation (fmd) is used to assess endothelial function through changes in vascular diameter after hyperemia. high-fat meal (hfm) has been shown to induce endothelial dysfunction; recent studies,however,reported conflicting results in obese african american women (aaw). differences in the method used to analyze fmd may explain these discrepancies. methods and results-in protocol 1,we assessed the time course of fmd and compared the repeatability of fmd using the individual maximum peak dilation (fmdpeak) and the dilation at 60 seconds (fmd60). sixteen aaw (age,42±10.4 years; body mass index [bmi],39±5.8 kg/m2) were studied on 2 occasions,4 weeks apart,under fasting conditions (study 1 and study 2). in protocol 2,we used the most repeatable measurement from protocol 1 to assess changes in endothelial function after an hfm in 17 aaw (agen 42±11.1 years; bmin 38±5.6 kg/m2). we found that fmdpeak was the most repeatable measurement (n=16; study 1,5.31±3.12% and study 2,5.80±2.91%; r=0.94). after an hfm,the baseline brachial artery diameter significantly increased at 2 hours (0.10 mm; 95% confidence interval [ci],0.01-0.18; p=0.03) and at 4 hours (0.17 mm; 95% ci,0.09-0.25; p < 0.001). at 2 hours,the fmdpeak decreased compared with pre-hfm (-1.76; 95% ci,-3.55-0.02; p≤0.05). conclusions-the individual's maximum peak dilation after hyperemia is the most consistent measure to assess the effect of an hfm on endothelial function. endothelial dysfunction occurred at 2 hours after an hfm in aaw. © 2015 the authors.
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کلیدواژه
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African American; Endothelial dysfunction; High fat diet; Obesity
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آدرس
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department of internal medicine,william beaumont hospital internal medicine,royal oak,mi, United States, department of medicine,division of clinical pharmacology and the autonomic dysfunction center,vanderbilt university school of medicine,nashville,tn, United States, department of medicine,division of clinical pharmacology and the autonomic dysfunction center,vanderbilt university school of medicine,nashville,tn, United States, clinical research center,vanderbilt university school of medicine,nashville,tn, United States, department of medicine,division of clinical pharmacology and the autonomic dysfunction center,vanderbilt university school of medicine,nashville,tn, United States, department of biostatistics,vanderbilt university school of medicine,nashville,tn, United States, department of biostatistics,vanderbilt university school of medicine,nashville,tn, United States, department of medicine,division of clinical pharmacology and the autonomic dysfunction center,vanderbilt university school of medicine,nashville,tn, United States, department of medicine,division of clinical pharmacology and the autonomic dysfunction center,vanderbilt university school of medicine,nashville,tn, United States, department of medicine,division of clinical pharmacology and the autonomic dysfunction center,vanderbilt university school of medicine,nashville,tn, United States
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Authors
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