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Relationship of Abdominal Visceral and Subcutaneous Adipose Tissue With Lipoprotein Particle Number and Size in Type 2 Diabetes

  1. Susan Sam1,
  2. Steven Haffner2,
  3. Michael H. Davidson3,
  4. Ralph B. D'Agostino, Sr.4,
  5. Steven Feinstein5,
  6. George Kondos6,
  7. Alfonso Perez7 and
  8. Theodore Mazzone1
  1. 1Department of Medicine, Section of Endocrinology, Diabetes and Metabolism, Chicago, Illinois
  2. 2Department of Medicine, University of Texas Health Science Center, San Antonio, Texas
  3. 3Pritzker School of Medicine, The University of Chicago, Chicago, Illinois
  4. 4Department of Mathematics, Statistics and Consulting Unit, Boston University, Boston, Massachusetts
  5. 5Department of Medicine, Section of Cardiology, Rush University Medical Center, Chicago, Illinois
  6. 6Department of Medicine, Section of Cardiology, University of Illinois College of Medicine, Chicago, Illinois
  7. 7Takeda Global Research and Development, Deerfield, Illinois
  1. Corresponding author: Theodore Mazzone, tmazzone{at}uic.edu

Abstract

OBJECTIVE—Insulin resistance and type 2 diabetes are associated with an atherogenic lipoprotein profile. We examined the role of visceral and subcutaneous fat depots, independent of BMI, on the dyslipidemia associated with type 2 diabetes.

RESEARCH DESIGN AND METHODS— A total of 382 subjects with type 2 diabetes underwent abdominal computed tomography to evaluate subcutaneous (SAT) and visceral adipose tissue (VAT) distribution and had anthropometric measurements to determine BMI and waist and hip circumference. Fasting blood was obtained for lipoprotein particle number and size using nuclear magnetic resonance spectroscopy. The relationship of lipoprotein particle number and size with BMI, SAT, and VAT was examined using multivariable regression models adjusted for age, sex, diabetes therapy, duration of diabetes, smoking, statin use, and A1C levels. The relation of VAT to lipoprotein particle number and size was further evaluated after the addition of BMI, BMI plus SAT, or BMI plus homeostatis is model assessment of insulin resistance (HOMA-IR) to the model.

RESULTS—VAT was positively related to VLDL particle number (P < 0.0001), LDL particle number (P < 0.01), and VLDL size (P < 0.0001) and negatively related to LDL size (P < 0.0001) and HDL size (P < 0.0001). These relationships remained unchanged after addition of BMI and SAT to the model. After addition of HOMA-IR, VAT remained positively related to VLDL particle number (P < 0.0001) and size (P < 0.01) and negatively related to LDL and HDL particle size (P < 0.0001 for both comparisons). Neither BMI nor SAT was independently related to lipoprotein parameters.

CONCLUSIONS—In patients with type 2 diabetes, higher VAT independent of BMI was associated with higher VLDL and LDL particle number, larger VLDL particles, and smaller LDL and HDL particles. This lipoprotein pattern has been associated with increased risk for atherosclerosis and cardiovascular disease.

Footnotes

  • Published ahead of print at http://diabetes.diabetesjournals.org on 9 May 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 May 4, 2008.
    • Received February 4, 2008.
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This Article

  1. Diabetes vol. 57 no. 8 2022-2027
  1. All Versions of this Article:
    1. db08-0157v1
    2. 57/8/2022 most recent
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