Abstract

BackgroundA high-fat diet promotes postprandial systemic inflammation and metabolic endotoxemia. We investigated the effects of three consecutive high-fat meals on endotoxemia, inflammation, vascular function, and postprandial lipid metabolism in patients with type 1 diabetes.MethodsNon-diabetic controls (n = 34) and patients with type 1 diabetes (n = 37) were given three high-caloric, fat-containing meals during one day. Blood samples were drawn at fasting (8:00) and every two hours thereafter until 18:00. Applanation tonometry was used to assess changes in the augmentation index during the investigation day.ResultsThree consecutive high-fat meals had only a modest effect on serum LPS-activity levels and inflammatory markers throughout the day in both groups. Of note, patients with type 1 diabetes were unable to decrease the augmentation index in response to the high-fat meals. The most profound effects of the consecutive fat loads were seen in chylomicron and HDL-metabolism. The triglyceride-rich lipoprotein remnant marker, apoB-48, was elevated in patients compared to controls both at fasting (p = 0.014) and postprandially (p = 0.035). The activities of the HDL-associated enzymes PLTP (p < 0.001), and CETP (p = 0.007) were higher and paraoxonase (PON-1) activity, an anti-oxidative enzyme bound to HDL, decreased in patients with type 1 diabetes (p = 0.027).ConclusionsIn response to high-fat meals, early signs of vascular dysfunction alongside accumulation of chylomicron remnants, higher augmentation index, and decreased PON-1 activity were observed in patients with type 1 diabetes. The high-fat meals had no significant impact on postprandial LPS-activity in non-diabetic subjects or patients with type 1 diabetes suggesting that metabolic endotoxemia may be more central in patients with chronic metabolic disturbances such as obesity, type 2 diabetes, or diabetic kidney disease.

Highlights

  • A high-fat diet promotes postprandial systemic inflammation and metabolic endotoxemia

  • Endotoxins are primarily associated with circulating LPS-binding proteins (LBP), the endothelium of blood vessels, and lipoprotein particles

  • Type 1 diabetes was defined as age at onset below 40 years and permanent insulin treatment initiated within one year of diagnosis

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Summary

Introduction

A high-fat diet promotes postprandial systemic inflammation and metabolic endotoxemia. We investigated the effects of three consecutive high-fat meals on endotoxemia, inflammation, vascular function, and postprandial lipid metabolism in patients with type 1 diabetes. Postprandial lipid accumulation, in the form of triglyceride-rich lipoprotein (TRL) particles, is linked to high-fat meal induced inflammation [1]. Absorption of bacterial endotoxin/lipopolysaccharide (LPS) from the gut is postulated to contribute to the development of chronic inflammation in mammals after a high-fat diet [2,3]. Endotoxins are primarily associated with circulating LPS-binding proteins (LBP), the endothelium of blood vessels, and lipoprotein particles. High LPS-activity is further a risk factor for incident type 2 diabetes and associated with obesity, features of the metabolic syndrome, and the development of kidney disease in patients with type 1 diabetes [6,7,8]

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