Volume 20, Issue 2 , Pages 101-109, February 2010
Acute effects of casein on postprandial lipemia and incretin responses in type 2 diabetic subjects☆
Abstract
Background and aims
Exaggerated and prolonged postprandial lipemia is potentially atherogenic and associated with type 2 diabetes. Limited data exist regarding the influence of dietary protein on postprandial lipemia in type 2 diabetes. We investigated, over 8-h, the acute effects of casein alone or in combination with carbohydrate on postprandial lipid and incretin responses to a fat-rich meal in type 2 diabetes.
Methods and results
Eleven type 2 diabetic subjects ingested four test meals in random order: an energy-free soup plus 80
g of fat (control-meal); control-meal plus 45
g carbohydrates (CHO-meal); control-meal plus 45
g of casein (PRO-meal); and PRO-meal plus 45
g carbohydrates (CHO
+
PRO-meal). Triglyceride and retinyl palmitate responses were measured in plasma and in a chylomicron-rich and chylomicron-poor fraction. We found no significant differences in triglyceride responses to PRO- and CHO
+
PRO-meal compared to the control-meal. However, the addition of casein to the CHO-meal reduced the raised triglyceride response in the chylomicron-rich fraction. Retinyl palmitate responses did not differ significantly between meals in the chylomicron-rich fraction, whereas the PRO-meal increased retinyl palmitate in the chylomicron-poor fraction. PRO- and PRO
+
CHO-meal increased insulin and glucagon compared to the control-meal. PRO
+
CHO-meal increased the glucose-dependent insulinotropic peptide response while no change in glucagon-like peptide-1 responses was detected.
Conclusions
The data presented suggest that casein per se did not modulate the postprandial triglyceride response in type 2 diabetes. When added to carbohydrate, casein suppressed the triglyceride response in the chylomicron-rich fraction, increased insulin and glucagon but did not affect the incretin responses.
Keywords: Type 2 diabetes, Casein, Triglyceride, Postprandial period, Incretins, Islet hormones
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☆ Sponsorship: this work is carried out as part of the research program of the Danish Obesity Research Centre (DanORC, see www.danorc.dk). It is furthermore supported by the Nordic Centre of Excellence (NCoE) programme (Systems biology in controlled dietary interventions and cohort studies – SYSDIET, P No., 070014) and the Danish Diabetes Association.
PII: S0939-4753(09)00062-3
doi:10.1016/j.numecd.2009.03.019
© 2009 Elsevier B.V. All rights reserved.
Volume 20, Issue 2 , Pages 101-109, February 2010
