TY - JOUR
T1 - Efficacy of Low-Dose Cholesterol-Lowering Drug Therapy in Men With Moderate Hypercholesterolemia
AU - Denke, Margo A.
AU - Grundy, Scott M
N1 - Funding Information:
Thisworkwas supported by the Department of Vet¬ eransAffairs,NationalInstitutesofHealthgrantsHL- 29252 andM01-RR-00633,PublicHealthServicegrant 5-MO1-RR00633,theSouthwesternMedicalFoundation, andtheMossHeartFoundationofDallas,Tex.DrDenke is therecipientofNationalInstitutesofHealth-National Heart, Lung, and Blood Institute Clinical Investigator Award NIH5-K08-HL02456. Reprint requests to CenterforHuman Nutrition, The University ofTexasSouthwesternMedicalCenter,5323 HarryHinesBlvd,Dallas,TX75235-9052(DrDenke).
Copyright:
Copyright 2015 Elsevier B.V., All rights reserved.
PY - 1995/2/27
Y1 - 1995/2/27
N2 - Objective: To test the potency of low-dose cholesterol-lowering drug therapy in patients with moderate hypercholesterolemia and to evaluate the effectiveness for cholesterol lowering of a safe regimen to be used in primary prevention of coronary heart disease. Design: The efficacy of three drug regimens (cholestyramine resin, 8 g/d; cholestyramine resin, 8 g/d, plus lovastatin, 5 mg/d; and lovastatin, 20 mg/d) was tested in 26 men aged 31 to 70 years with moderate hypercholesterolemia after a Step-One cholesterol-lowering diet. Each drug period was 3 months in duration, interspersed by a 1-month period of the Step-One diet only. Blood for lipid and lipoprotein measurements was obtained on 5 different days during the last 2 weeks of each drug and diet-only period. Results: Cholestyramine resin therapy at 8 g/d achieved a significant reduction in low-density lipoprotein cholesterol levels from 4.47 mmol/L (173 mg/dL) to 3.90 mmol/L (151 mg/dL) (P<.005). The addition of 5 mg of lovastatin to cholestyramine therapy achieved even lower levels, averaging 3.39 mmol/L (131 mg/dL) (P<.005). Lovastatin therapy at 20 mg/d produced lowering of low-density lipoprotein cholesterol levels similar to that of the low-dose combination. Conclusions: Low-dose combination drug therapy for the management of hypercholesterolemia appears to be an effective means of lowering cholesterol levels that remain persistently elevated after dietary therapy; at the same time, it should carry a low risk of toxic effects.
AB - Objective: To test the potency of low-dose cholesterol-lowering drug therapy in patients with moderate hypercholesterolemia and to evaluate the effectiveness for cholesterol lowering of a safe regimen to be used in primary prevention of coronary heart disease. Design: The efficacy of three drug regimens (cholestyramine resin, 8 g/d; cholestyramine resin, 8 g/d, plus lovastatin, 5 mg/d; and lovastatin, 20 mg/d) was tested in 26 men aged 31 to 70 years with moderate hypercholesterolemia after a Step-One cholesterol-lowering diet. Each drug period was 3 months in duration, interspersed by a 1-month period of the Step-One diet only. Blood for lipid and lipoprotein measurements was obtained on 5 different days during the last 2 weeks of each drug and diet-only period. Results: Cholestyramine resin therapy at 8 g/d achieved a significant reduction in low-density lipoprotein cholesterol levels from 4.47 mmol/L (173 mg/dL) to 3.90 mmol/L (151 mg/dL) (P<.005). The addition of 5 mg of lovastatin to cholestyramine therapy achieved even lower levels, averaging 3.39 mmol/L (131 mg/dL) (P<.005). Lovastatin therapy at 20 mg/d produced lowering of low-density lipoprotein cholesterol levels similar to that of the low-dose combination. Conclusions: Low-dose combination drug therapy for the management of hypercholesterolemia appears to be an effective means of lowering cholesterol levels that remain persistently elevated after dietary therapy; at the same time, it should carry a low risk of toxic effects.
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U2 - 10.1001/archinte.1995.00430040067008
DO - 10.1001/archinte.1995.00430040067008
M3 - Article
C2 - 7848022
AN - SCOPUS:0028938873
SN - 2168-6106
VL - 155
SP - 393
EP - 399
JO - Archives of internal medicine (Chicago, Ill. : 1908)
JF - Archives of internal medicine (Chicago, Ill. : 1908)
IS - 4
ER -