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Apolipoprotein E Polymorphism as a Risk Factor for Vascular Disease in Diabetic Patients

  1. Massimo Boemi, MD,
  2. Cristina Sirolla, MSC,
  3. Loredana Amadio, MSC,
  4. Paolo Fumelli, MD,
  5. Daniel Pometta, MD and
  6. Richard W James, PHD
  1. Division of Diabetology, Instituto Nationale Riposa Cura per Anziani Ancona, Italy
  2. Department of Demographic and Statistical Studies, Instituto Nationale Riposa Cura per Anziani Ancona, Italy
  3. Division of Diabetology, University Hospital Geneva, Switzerland
  1. Address correspondence and reprint requests to Richard W. James, PhD, Division of Diabetology, Department of Medicine, University Hospital, 24 Rue Micheli-du-Crest, 1211 Geneva 14, Switzerland.

Abstract

OBJECTIVE To examine the prevalence of cardiovascular disease in diabetic patients as a function of apolipoprotein (apo) E polymorphism.

RESEARCH DESIGN AND METHODS The apo E phenotypes and plasma lipid, lipoprotein, and apo levels were determined for 517 Italian diabetic patients. The prevalence of cardiovascular disease (defined as ischemic heart disease [IHD] and/or peripheral vascular disease and/or cerebrovascular disease) was assessed as a function of apo E polymorphism at entry and after 4 years.

RESULTS The occurrence of vascular disease did not differ significantly between diabetic patients in the various categories of apo E phenotype either at entry into the study or after 4 years. When expressed as a percentage of patients with disease, we observed—for E2, E3, and E4 carriers, respectively—at entry: IHD, 20.0% (n = 14), 21.0% (n = 79), and 21.5% (n = 14); and macroangiopathy, 24.3% (n = 17), 29.3% (n = 110), and 24.6% (n = 16). Apo E polymorphism did not make a significant contribution to multiple logistic regression models designed to identify the factors associated with the occurrence of vascular disease in diabetic patients.

CONCLUSION Apo E polymorphism and, notably, the apo E4 allele cannot be universally considered as a particular risk factor for cardiovascular disease in diabetic patients.

  • Received May 31, 1994.
  • Revision received October 6, 1994.
  • Accepted October 6, 1994.
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