Effects of prandial challenge on triglyceridemia, glycemia, and pro-inflammatory activity in persons with chronic paraplegia

被引:20
作者
Ellenbroek, Dennis [1 ]
Kressler, Jochen [2 ]
Cowan, Rachel E. [2 ,3 ]
Burns, Patricia A. [2 ]
Mendez, Armando J. [4 ,5 ]
Nash, Mark S. [2 ,3 ,6 ]
机构
[1] Radboud Univ Nijmegen, Med Ctr, Dept Physiol, NL-6525 ED Nijmegen, Netherlands
[2] Univ Miami, Miami Project Cure Paralysis, Miami, FL 33136 USA
[3] Univ Miami, Dept Neurol Surg, Miami, FL 33136 USA
[4] Univ Miami, Dept Med, Miami, FL 33136 USA
[5] Univ Miami, Diabet Res Inst, Miami, FL 33136 USA
[6] Univ Miami, Miller Sch Med, Dept Rehabil Med, Miami, FL 33136 USA
关键词
Feeding; Meal challenge; Glucose; Lipids; C-REACTIVE PROTEIN; SPINAL-CORD-INJURY; INSULIN-RESISTANCE; POSTPRANDIAL LIPEMIA; METABOLIC SYNDROME; ENDOTHELIAL ACTIVATION; OXIDATIVE STRESS; HIGH-FAT; MEN; RISK;
D O I
10.1179/2045772314Y.0000000199
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Context/Objective: Exaggerated postprandial lipemia has been reported after spinal cord injury (SCI). We examined metabolite and accompanying pro-inflammatory biomarker responses to repeat feeding of typical high-fat meals in individuals with chronic paraplegia. Design: Descriptive trial. Methods: Metabolites (triglycerides, glucose, and insulin) and inflammatory biomarkers (interleukin-6 and highsensitivity C-reactive protein (hsCRP)) were measured under fasting conditions in 11 recreationally active individuals with chronic (> 1 year) paraplegia. Subjects received high-fat meals at time point 0 and again at minute 240. Antecubital venous blood was obtained at time points -30 (fasting), 0 (first meal), 30, 60, 90, 120, 240 (second meal), 360, and 480 minutes. Correlations were examined among the study variables. Exploratory subgroup analysis was performed for subjects with levels of postprandial glucose greater than > 200 mg/dl. Results: Triglycerides showed a significant rise 4 hours after eating. Basal inflammatory markers were elevated, and did not undergo additional change during the testing. Additionally, subjects with excessive postprandial glucose responses showed higher hsCRP levels than those having typical glucose responses both for fasting (11.8 +/- 6.5 vs. 2.9 +/- 2.7 mg/l, P=0.064) and postprandial (11.1 +/- 4.9 vs. 3.7 +/- 3.8 mg/l, P=0.018) values. Conclusions: Despite elevations in metabolic response markers, inflammatory markers did not change significantly after consumption of population-representative (i.e. hypercaloric) mixed-nutrient meals. Levels of fasting CRP in the high-risk range are consistent with other reports in persons with SCI and continue to pose concern for their cardiovascular disease risk. The possible association between postprandial metabolic responses and inflammatory states warrants further investigation to identify individual component risks for this secondary health hazard.
引用
收藏
页码:468 / 475
页数:8
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