Postprandial Hypertriglyceridemia and Insulin Resistance in Normoglycemic First-Degree Relatives of Patients with Type 2 Diabetes
- Mette Axelsen, PhD;
- Ulf Smith, MD, PhD;
- Jan W. Eriksson, MD, PhD;
- Marja-Riitta Taskinen, MD, PhD; and
- Per-Anders Jansson, MD, PhD
- From the Lundberg Laboratory for Diabetes Research, Sahlgrenska University Hospital, Göteborg University, Göteborg, Sweden; Norrland University Hospital, Umeå, Sweden; and the University of Helsinki, Helsinki, Finland.
Abstract
Background: Impaired ability to eliminate lipids in the postprandial state is an atherogenic trait associated with insulin resistance.
Objective: To assess insulin sensitivity and postprandial triglyceride metabolism in prediabetic persons.
Design: Cross-sectional study.
Setting: Sahlgrenska University Hospital, Göteborg, Sweden.
Participants: 13 healthy, normotriglyceridemic men with two first-degree relatives with type 2 diabetes and 13 carefully matched controls without known diabetes heredity.
Measurements: Oral glucose tolerance test, insulin sensitivity (euglycemic clamp technique), and fasting and postprandial triglyceride levels after a mixed meal.
Results: Relatives of persons with type 2 diabetes were insulin resistant but had normal glucose tolerance. They exhibited postprandial hypertriglyceridemia; the 6-hour triglyceride incremental area under the curve was 50% higher than that of the control group (P = 0.037).
Conclusions: These healthy male first-degree relatives of patients with type 2 diabetes are insulin resistant and exhibit postprandial lipid intolerance despite having normal fasting triglyceride levels. These characteristics, which occur in the absence of glucose intolerance, are associated with an increased risk for macroangiopathy.
- Diabetes mellitus, non-insulin-dependent
- Insulin resistance
- Prediabetic state
- Hypertriglyceridemia
- Postprandial period
Article and Author Information
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Acknowledgment: The authors thank Ms. Margareta Landén for technical assistance.
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Grant Support: By the Swedish Medical Research Council (project B-3506), the IngaBritt and Arne Lundberg Foundation, the Swedish Diabetes Association, the European Community (BMH4-CT96-0751), the Å ke Wiberg Foundation, the Magnus Bergvall Foundation, and the Regional Health Care Authority of West Sweden.
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Requests for Reprints: Mette Axelsen, PhD, The Lundberg Laboratory for Diabetes Research, Department of Internal Medicine, Sahlgrenska University Hospital/SS, S-413 45 Göteborg, Sweden.
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Current Author Addresses: Drs. Axelsen, Smith, and Jansson: The Lundberg Laboratory for Diabetes Research, Department of Internal Medicine, Sahlgrenska University Hospital/SS, S-413 45 Göteborg, Sweden.
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Dr. Eriksson: Department of Medicine, Norrland University Hospital, S-901 85 Umeå, Sweden.
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Dr. Taskinen: Department of Medicine, University Central Hospital, 002 90 Helsinki 29, Finland.
- Copyright ©2004 by the American College of Physicians
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