Horm Metab Res 1995; 27(5): 239-243
DOI: 10.1055/s-2007-979948
Originals Clinical

© Georg Thieme Verlag Stuttgart · New York

Long-Term Effects of Simvastatin in Hypercholesterolemic Patients with NIDDM and Additional Atherosclerotic Risk Factors

T. Kazumi1 , G. Yoshino2 , A. Ohki3 , K. Matsuba4 , T. Ino5 , M. Amono6 , M. Kosugo2 , the Hyogo Simvastotin Study Group*
  • 1Department of Medicine, Division of Endocrinology and Metabolism, Hyogo Medical Center for Adults, Akashi
  • 2Second Department of Internal Medicine, Kobe University School of Medicine, Kobe
  • 3Itami City Hospital, Itami
  • 4Himeji Cardiovascular Center, Himeji
  • 5Ino Hospital, Himeji
  • 6Nishiwaki Municipal Hospital, Nishiwaki, Japan
Further Information

Publication History

1994

1995

Publication Date:
23 April 2007 (online)

Abstract

Effects of 12 months of simvastatin treatment were examined in 48 NIDDM patients with total serum cholesterol levels exceeding 220 mg/dl and were compared with those in 35 nondiabetic patients with hypercholesterolemia. In the diabetic group, 5 ∼ 10 mg of simvastatin given once daily at bedtime significantly lowered total cholesterol (21%), LDL cholesterol (28%), apoB (15%) and triglycerides (8%) levels. These changes were identical to those in the nondiabetic group, except for triglycerides which did not change significantly. HDL cholesterol increased significantly in the nondiabetic group but not in the diabetic group. The reductions in LDL cholesterol and apoB in hypercholesterolemic patients with NIDDM were not influenced by gender, age, glycemic control, the presence or absence of systemic hypertension, obesity and overt proteinuria. In addition, the decrease in LDL cholesterol was not affected by the number of risk factors per patient. Simvastatin did not significantly alter hemoglobin A1c or fasting plasma glucose and was well tolerated in both groups. Simvastatin produced beneficial effects on serum lipids and apolipoproteins and neutral effects on glycemic control in hypercholesterolemic patients with NIDDM, whether or not they had an additional atherosclerotic risk factor.