Your browser doesn't support javascript.
loading
Efeitos da pravastatina nas lipoproteínas, Lp(a), apo B e apo A-I em pacientes com hipercolesterolemia primária / Effects of Pravastatin on Lipoproteins, Lp(a), apo B and apo A-I in Patients with Primary Hypercholesterolemia
Novazzi, José Paulo; Fonseca, Francisco Antonio Helfenstein; Feres, Marcia Cristina; Silva, Regina Correa da; Lima, José Carlos Carneiro; Martinez, Tania Leme da Rocha.
  • Novazzi, José Paulo; s.af
  • Fonseca, Francisco Antonio Helfenstein; s.af
  • Feres, Marcia Cristina; s.af
  • Silva, Regina Correa da; s.af
  • Lima, José Carlos Carneiro; s.af
  • Martinez, Tania Leme da Rocha; s.af
Arq. bras. cardiol ; 62(6): 395-398, jun. 1994. tab, graf
Article in Portuguese | LILACS | ID: lil-159855
RESUMO
PURPOSE--To evaluate the effects of pravastatin on lipoproteins, Lp (a), apo B and apo A-I and its tolerability in primary hypercholesterolemic patients in our outpatient lipid clinic. METHODS--Twenty-two primary hypercholesterolemic patients were evaluated. They had all been treated previously with other hypocholesterolemic drugs, including the statins, forming a specific and homogeneous group with hypercholesterolemia and definite coronary risk. After 7 weeks with American Heart Association phase I diet and placebo drug, pravastatin was administered during 12 weeks. All patients received an initial daily dose of 10 mg for six weeks. After this period, this dose was increased to 20 mg. The levels of cholesterol, triglycerides, high-density lipoprotein, lipoprotein (a) and apolipoproteins A-1 and B were determined. RESULTS--No changes occurred with diet and placebo, but pravastatin at a daily dose of 10 mg, reduced significantly cholesterol level (7.22 per cent) LDL-cholesterol (13.08 per cent) and increased HDL-cholesterol (7.8 per cent). The results were better with 20 mg, achieving a reduction of (28.21 per cent) in cholesterol, (36.88 per cent) in LDL-cholesterol, (17.06 per cent) in apo B level and an increase of (10.06 per cent) in HDL-cholesterol. The smaller effect observed with the more commonly used dosage (10 mg/day) was most probably due to the characteristics of the sample with already established hypercholesterolemia, being thus dependent of higher concentrations of medications, as observed in previous treatments in our outpatient clinic. Side affects with this drug were rare. No biochemical changes were observed that would interrupt the continuation of therapy. CONCLUSION--Pravastatin was well tolerated and promoted favorable changes in the total cholesterol, LDL, apo B and cholesterol/HDL and LDL/HDL ratios of primary hypercholesterolemic patients
Subject(s)

Full text: Available Index: LILACS (Americas) Main subject: Pravastatin / Hypercholesterolemia / Lipoproteins Type of study: Controlled clinical trial Limits: Adult / Female / Humans / Male Language: Portuguese Journal: Arq. bras. cardiol Journal subject: Cardiology Year: 1994 Type: Article

Similar

MEDLINE

...
LILACS

LIS

Full text: Available Index: LILACS (Americas) Main subject: Pravastatin / Hypercholesterolemia / Lipoproteins Type of study: Controlled clinical trial Limits: Adult / Female / Humans / Male Language: Portuguese Journal: Arq. bras. cardiol Journal subject: Cardiology Year: 1994 Type: Article