M. Tawata et al., CLINICAL EFFICACY OF PRAVASTATIN FOR HYPERLIPIDEMIA IN PATIENTS WITH TYPE-2 DIABETES-MELLITUS, Arzneimittel-Forschung, 45-1(6), 1995, pp. 704-708
The efficacy of pravastatin (GAS 81131-70-6) on serum lipid levels in
91 type 2 diabetic patients with mean glycosylated hemoglobin of 8.5 %
was investigated up to 12 weeks OI al administration of 10 to 20 mg/d
of pravastatin significantly decreased total cholesterol by 18.4 +/-
1.5 % after 4 weeks. When analyzed separately in type IIa and IIb hype
rlipidemia, the reduction of total cholesterol by pravastatin was more
prominent in the former. Low-density lipoprotein cholesterol were als
o significantly decreased 22.2 +/- 2.7 % after 4 weeks. The effect of
pravastatin in reducing trigylceride was more prominent in patients wi
th higher triglyceride ide compared to those with lower triglyceride b
efore the administration of the drug. High-density lipoprotein cholest
erol showed a slight but significant increase by 4.2 +/- 1.9% after 4
weeks. Among the apolipoproteins examined apolipoprotein B was signifi
cantly decreased after 4 weeks. Atherogenic index and apolipoprotein B
/ apolipoprotein A-I ratio were also significantly decreased after 4
weeks. The efficacy of pravastatin was also observed after 12 weeks to
the same extent as after 4 weeks No major side effects or abnormaliti
es of laboratory parameters have been observed. These data lean to the
conclusion that pravastatin is useful for the treatment of hyperlipid
emia in type 2 diabetic patients with poor glycemic control without ma
jor adverse effects.