Lipid and Lipoprotein Profiles in Youth With and Without Type 1 Diabetes

The SEARCH for Diabetes in Youth Case-Control Study

  1. John Guy, MPH1,
  2. Lorraine Ogden, PHD2,
  3. R. Paul Wadwa, MD3,
  4. Richard F. Hamman, MD, DRPH1,
  5. Elizabeth J. Mayer-Davis, PHD4,
  6. Angela D. Liese, PHD5,
  7. Ralph D'Agostino, Jr., PHD6,
  8. Santica Marcovina, PHD7 and
  9. Dana Dabelea, MD, PHD1
  1. 1Department of Epidemiology, Colorado School of Public Health, University of Colorado, Denver, Colorado
  2. 2Department of Biostatistics and Informatics, Colorado School of Public Health, University of Colorado, Denver, Colorado
  3. 3Barbara Davis Center, University of Colorado, Denver, Colorado
  4. 4Nutrition Department, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina
  5. 5Department of Epidemiology and Biostatistics and Center for Research in Nutrition and Health Disparities, University of South Carolina, Columbia, South Carolina
  6. 6Department of Public Health Sciences, Wake Forest University School of Medicine, Winston-Salem, North Carolina
  7. 7Northwest Lipid Metabolism and Diabetes Research Laboratories, University of Washington, Seattle, Washington
  1. Corresponding author: Dana Dabelea, dana.dabelea{at}ucdenver.edu

Abstract

OBJECTIVE—The purpose of this study was to compare the lipid profile and the prevalence of lipid abnormalities in youth with and without type 1 diabetes and explore the role of glycemic control on the hypothesized altered lipid profile in youth with type 1 diabetes.

RESEARCH DESIGN AND METHODS—We conducted a cross-sectional analysis of 512 youth with type 1 diabetes (mean duration 4.22 years) and 188 healthy control subjects aged 10–22 years in Colorado and South Carolina. SEARCH for Diabetes in Youth (SEARCH) participants with type 1 diabetes and healthy control subjects recruited from primary care offices in the same geographic regions were invited to attend a research visit. Fasting lipid profiles were compared between youth with type 1 diabetes (stratified according to categories of optimal [A1C <7.5%] and suboptimal [A1C ≥7.5%] glycemic control) and healthy nondiabetic youth, using multiple linear and logistic regression.

RESULTS—Youth with type 1 diabetes and optimal A1C had lipid concentrations that were similar (total cholesterol, LDL cholesterol, and LDL particle size) or even less atherogenic (HDL cholesterol, non-HDL cholesterol, triglyceride, and triglyceride–to–HDL cholesterol ratio) than those observed in nondiabetic youth, whereas youth with suboptimal glycemic control had elevated standard lipid levels (total cholesterol, LDL cholesterol, and non-HDL cholesterol). Youth with type 1 diabetes also had significantly elevated apolipoprotein B levels and more small, dense LDL particles than nondiabetic youth, regardless of glycemic control.

CONCLUSIONS—Youth with type 1 diabetes have abnormal lipid levels and atherogenic changes in lipoprotein composition, even after a relatively short disease duration. As in adults, glycemic control is an important mediator of these abnormalities.

Footnotes

  • Published ahead of print at http://care.diabetesjournals.org on 17 December 2008.

    Readers may use this article as long as the work is properly cited, the use is educational and not for profit, and the work is not altered. See http://creativecommons.org/licenses/by-nc-nd/3.0/ for details.

    The costs of publication of this article were defrayed in part by the payment of page charges. This article must therefore be hereby marked “advertisement” in accordance with 18 U.S.C Section 1734 solely to indicate this fact.

    • Accepted December 9, 2008.
    • Received September 26, 2008.
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