Association of ACE gene polymorphism with arterial stiffness in patients with type 2 diabetes

Diabetes Care. 1999 Nov;22(11):1858-64. doi: 10.2337/diacare.22.11.1858.

Abstract

Objective: To assess the relationship between the insertion (I)/deletion (D) polymorphism of the ACE gene and arterial distensibility in patients with type 2 diabetes and healthy control subjects.

Research design and methods: Aortic and carotid arterial distensibility were evaluated by measuring aortic pulse-wave velocity (a-PWV) and carotid stiffness beta using an echo-tracking system in 137 patients with type 2 diabetes and 260 age-matched control subjects.

Results: a-PWV and carotid stiffness beta were significantly higher in patients with type 2 diabetes than in age-matched control subjects (P < 0.05). Both stiffness beta and a-PWV were significantly higher in the patients with the II genotype than in those with the DD genotype (P < 0.001). In the control subjects, multiple regression analysis showed that age and decreased HDL cholesterol were independently associated with increased a-PWV (R2 = 0.244, P < 0.0001) and that age, systolic and diastolic blood pressure, and BMI were independently associated with increased carotid stiffness beta (R2 = 0.454, P < 0.0001). In the patients with type 2 diabetes, age, gene dose of the I allele, and systolic and diastolic blood pressure were independently associated with increased a-PWV (R2 = 0.545, P < 0.0001), and age, gene dose of the I allele, and systolic blood pressure were associated with increases in carotid stiffness beta (R2 = 0.314, P < 0.0001).

Conclusions: These results suggested that ACE polymorphism is associated with the impairment of aortic and carotid distensibility in patients with type 2 diabetes.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetylcholinesterase / genetics*
  • Adolescent
  • Adult
  • Aged
  • Aorta, Abdominal / physiopathology
  • Aorta, Thoracic / physiopathology
  • Carotid Artery, Common / physiopathology
  • Case-Control Studies
  • Compliance
  • Diabetes Mellitus, Type 2 / genetics*
  • Diabetic Angiopathies / genetics*
  • Female
  • Gene Deletion
  • Genotype
  • Humans
  • Male
  • Middle Aged
  • Mutagenesis, Insertional
  • Polymorphism, Genetic*
  • Risk Factors
  • Sclerosis / genetics

Substances

  • Acetylcholinesterase