Gl. Vega et Sm. Grundy, LIPOPROTEIN RESPONSES TO TREATMENT WITH LOVASTATIN, GEMFIBROZIL, AND NICOTINIC-ACID IN NORMOLIPIDEMIC PATIENTS WITH HYPOALPHALIPOPROTEINEMIA, Archives of internal medicine, 154(1), 1994, pp. 73-82
Background: The lipoprotein responses to conventional lipid-modifying
drugs have not been adequately evaluated in normolipidemic patients wi
th hypoalphalipoproteinemia (low levels of high-density lipoproteins).
The purpose of this study was to compare responses to lovastatin, gem
fibrozil, and nicotinic acid in such patients. Methods: The first phas
e of the study compared lipoprotein responses to lovastatin and gemfib
rozil in 61 middle-aged men with low levels of high-density lipoprotei
ns. In the second phase, 37 patients agreed to take nicotinic acid; 27
patients finished this phase at a dose of 4.5 g/d. Nicotinic acid res
ults were compared with those with lovastatin and gemfibrozil in the s
ame patients. Results: In the first phase, both drugs effectively lowe
red triglyceride levels. Gemfibrozil therapy increased high-density li
poprotein cholesterol levels by 10% and lovastatin by 6%, but lovastat
in was much more effective for reducing low-density lipoprotein levels
. Nicotinic acid did not significantly lower low-density lipoprotein l
evels in the second phase, but it raised high-density lipoprotein leve
ls by 30%. Conclusions: Gemfibrozil therapy produced the least favorab
le response of the three drugs. Lovastatin markedly lowered low-densit
y lipoprotein levels but only modestly raised levels of high-density l
ipoprotein, whereas nicotinic acid had the opposite effect. Consequent
ly, the latter two drugs similarly reduced low-density lipoprotein-hig
h-density lipoprotein ratios, although these effects were obtained in
different ways. Between these two drugs, lovastatin therapy was more l
ikely to reduce low-density lipoprotein cholesterol levels to below 2.
6 mmol/L (100 mg/dL), and in view of recent recommendations, it may be
preferable to nicotinic acid for many normolipidemic patients with es
tablished coronary heart disease.