Insulin deficiency and hyperglycaemia in type 1 (insulin-dependent) diabete
s mellitus produce lipid abnormalities, which can be corrected by appropria
te insulin therapy. Diabetic nephropathy, which is the main risk factor for
coronary heart disease (CHD) in type 1 diabetes, causes pro-atheroscleroti
c changes in lipid metabolism. Detection and treatment of elevated choleste
rol levels is likely to be of benefit in these patients.
Type 2 (noninsulin-dependent) diabetes mellitus is associated with abnormal
lipid metabolism, even when glycaemic control is good and nephropathy abse
nt. Elevated triglyceride levels, reduced high density lipoprotein (HDL) ch
olesterol and a preponderance of small, dense low density lipoprotein (LDL)
particles are the key abnormalities that constitute diabetic dyslipidaemia
. The prevalence of hypercholesterolaemia is the same as for the nondiabeti
c population, but the relative risk of CHD is greatly increased at every le
vel of cholesterol. Based on effectiveness, tolerability and clinical trial
results, treatment with HMG-CoA reductase inhibitors to lower LDL choleste
rol is recommended as primary therapy. These agents are also moderately eff
ective at reducing triglyceride and increasing HDL cholesterol levels. If h
ypertriglyceridaemia predominates, treatment with fibric acid derivatives i
s appropriate, although there is currently only limited clinical trial evid
ence that the risk of CHD will be reduced.
In type I diabetes, but particularly in type 2 diabetes, lipid disorders ar
e likely to contribute significantly to the increased risk of macrovascular
complications, especially CHD. Management of the disordered lipid metaboli
sm should be given a high priority in the clinical care of all patients wit
h diabetes.