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Long-term efficacy and tolerability of simvastatin in a large cohort of elderly hypercholesterolemic patients

Identifieur interne : 002F45 ( Istex/Corpus ); précédent : 002F44; suivant : 002F46

Long-term efficacy and tolerability of simvastatin in a large cohort of elderly hypercholesterolemic patients

Auteurs : P. J. Lansberg ; Y. B. Mitchel ; D. Shapiro ; J. J. P. Kastelein ; R. Altman ; G. Jerums ; K. Bolzano ; S. Giannini ; J. Davignon ; P. Dewailly ; R. Darioli ; M. Mancini ; R. Scott ; M. R. Hayden

Source :

RBID : ISTEX:FB716334D080597D1ED6A7D941FDF7754701CAFD

English descriptors

Abstract

Abstract: The long-term efficacy and tolerability of simvastatin, a 3-hydroxy-3-methylglutaryl-co-enzyme A (HMG-CoA) reductase inhibitor, was assessed during a 24-month follow-up period in 168 elderly hypercholesterolemic patients. After completing a 4 week double blind dose ranging study with simvastatin 47 males and 122 females over 62 years of age with type II hyperlipidemia, a total cholesterol level above 6.5 mmol/l and clinically manifest cardiovascular disease were included in this extended study. A total of 159 patients completed the 12-month follow-up period and 141 patients were monitored over the full 24 months. All patients were started on 10 mg simvastatin once daily and the dosage was increased until the target levels of low density lipoprotein (LDL) cholesterol between 2.3 mmol/l (90 mg/dl) and 3.6 mmol/l (140 mg/dl) were reached. Fifty percent of patients reached the targeted LDL cholesterol goal of < 3.6 mmol/l (140 mg/dl) during the study. At study completion, 65 patients (39%) were taking 40 mg simvastatin per day, 56 patients (33%) 20 mg, 42 patients (25%) 10 mg and 5 patients (3%) only used 5 mg per day. Sixteen patients (9%) received concomitant lipid lowering therapy. Over 2 years, the mean decrease in LDL cholesterol ranged from 36% to 38%, the median decrease in triglycerides was 12% to 19% and the mean increase in high density lipoprotein (HDL) cholesterol ranged from 9% to 10%, respectively. Seven patients discontinued simvastatin because of adverse clinical or laboratory events, but only in two (1.1%) was this considered to be drug-related. Side-effects were mild and most frequently gastrointestinal in nature. Mean changes in asparate aminotransferase (AST) were not significantly different from zero and mean changes in alanine aminotransferase (ALT) and creatine phosphokinase (CPK) showed a small increase. We conclude that simvastatin is an efficacious and well-tolerated treatment for hypercholesterolemia in elderly individuals for extended periods.

Url:
DOI: 10.1016/0021-9150(95)05523-Y

Links to Exploration step

ISTEX:FB716334D080597D1ED6A7D941FDF7754701CAFD

Le document en format XML

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<term>Baseline values</term>
<term>Blood samples</term>
<term>Cardiovascular disease</term>
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<term>Congestive heart failure</term>
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<term>Elderly individuals</term>
<term>Elderly patients</term>
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<div type="abstract" xml:lang="en">Abstract: The long-term efficacy and tolerability of simvastatin, a 3-hydroxy-3-methylglutaryl-co-enzyme A (HMG-CoA) reductase inhibitor, was assessed during a 24-month follow-up period in 168 elderly hypercholesterolemic patients. After completing a 4 week double blind dose ranging study with simvastatin 47 males and 122 females over 62 years of age with type II hyperlipidemia, a total cholesterol level above 6.5 mmol/l and clinically manifest cardiovascular disease were included in this extended study. A total of 159 patients completed the 12-month follow-up period and 141 patients were monitored over the full 24 months. All patients were started on 10 mg simvastatin once daily and the dosage was increased until the target levels of low density lipoprotein (LDL) cholesterol between 2.3 mmol/l (90 mg/dl) and 3.6 mmol/l (140 mg/dl) were reached. Fifty percent of patients reached the targeted LDL cholesterol goal of < 3.6 mmol/l (140 mg/dl) during the study. At study completion, 65 patients (39%) were taking 40 mg simvastatin per day, 56 patients (33%) 20 mg, 42 patients (25%) 10 mg and 5 patients (3%) only used 5 mg per day. Sixteen patients (9%) received concomitant lipid lowering therapy. Over 2 years, the mean decrease in LDL cholesterol ranged from 36% to 38%, the median decrease in triglycerides was 12% to 19% and the mean increase in high density lipoprotein (HDL) cholesterol ranged from 9% to 10%, respectively. Seven patients discontinued simvastatin because of adverse clinical or laboratory events, but only in two (1.1%) was this considered to be drug-related. Side-effects were mild and most frequently gastrointestinal in nature. Mean changes in asparate aminotransferase (AST) were not significantly different from zero and mean changes in alanine aminotransferase (ALT) and creatine phosphokinase (CPK) showed a small increase. We conclude that simvastatin is an efficacious and well-tolerated treatment for hypercholesterolemia in elderly individuals for extended periods.</div>
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<ce:textfn>Department of Medical Genetics, University of British Columbia, 416-2125 East Mall, Vancouver, B.C. V6T 1Z4, Canada</ce:textfn>
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<ce:correspondence id="COR1">
<ce:label></ce:label>
<ce:text>Corresponding author. Tel.: (604) 822 9240; Fax: (604) 822 9238.</ce:text>
</ce:correspondence>
</ce:author-group>
<ce:date-received day="31" month="10" year="1994"></ce:date-received>
<ce:date-revised day="17" month="1" year="1995"></ce:date-revised>
<ce:date-accepted day="19" month="1" year="1995"></ce:date-accepted>
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<ce:section-title>Abstract</ce:section-title>
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<ce:simple-para>The long-term efficacy and tolerability of simvastatin, a 3-hydroxy-3-methylglutaryl-co-enzyme A (HMG-CoA) reductase inhibitor, was assessed during a 24-month follow-up period in 168 elderly hypercholesterolemic patients. After completing a 4 week double blind dose ranging study with simvastatin 47 males and 122 females over 62 years of age with type II hyperlipidemia, a total cholesterol level above 6.5 mmol/l and clinically manifest cardiovascular disease were included in this extended study. A total of 159 patients completed the 12-month follow-up period and 141 patients were monitored over the full 24 months. All patients were started on 10 mg simvastatin once daily and the dosage was increased until the target levels of low density lipoprotein (LDL) cholesterol between 2.3 mmol/l (90 mg/dl) and 3.6 mmol/l (140 mg/dl) were reached. Fifty percent of patients reached the targeted LDL cholesterol goal of < 3.6 mmol/l (140 mg/dl) during the study. At study completion, 65 patients (39%) were taking 40 mg simvastatin per day, 56 patients (33%) 20 mg, 42 patients (25%) 10 mg and 5 patients (3%) only used 5 mg per day. Sixteen patients (9%) received concomitant lipid lowering therapy. Over 2 years, the mean decrease in LDL cholesterol ranged from 36% to 38%, the median decrease in triglycerides was 12% to 19% and the mean increase in high density lipoprotein (HDL) cholesterol ranged from 9% to 10%, respectively. Seven patients discontinued simvastatin because of adverse clinical or laboratory events, but only in two (1.1%) was this considered to be drug-related. Side-effects were mild and most frequently gastrointestinal in nature. Mean changes in asparate aminotransferase (AST) were not significantly different from zero and mean changes in alanine aminotransferase (ALT) and creatine phosphokinase (CPK) showed a small increase. We conclude that simvastatin is an efficacious and well-tolerated treatment for hypercholesterolemia in elderly individuals for extended periods.</ce:simple-para>
</ce:abstract-sec>
</ce:abstract>
<ce:keywords>
<ce:section-title>Keywords</ce:section-title>
<ce:keyword>
<ce:text>Elderly</ce:text>
</ce:keyword>
<ce:keyword>
<ce:text>Hypercholesterolemia</ce:text>
</ce:keyword>
<ce:keyword>
<ce:text>Treatment</ce:text>
</ce:keyword>
<ce:keyword>
<ce:text>HMG-CoA reductase inhibitors</ce:text>
</ce:keyword>
<ce:keyword>
<ce:text>Simvastatin</ce:text>
</ce:keyword>
</ce:keywords>
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<affiliation>Center for Hemostasis, Thrombosis, Atherosclerosis and Inflammation, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands</affiliation>
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<affiliation>Center for Hemostasis, Thrombosis, Atherosclerosis and Inflammation, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands</affiliation>
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<affiliation>Endocrine Unit, Department of Medicine Austin Hospital, Heidelberg, Victoria, Australia</affiliation>
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<namePart type="given">K.</namePart>
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<affiliation>Landeskrankenhaus Salzburg, Innere Medizin Abteilung, Salzburg, Austria</affiliation>
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<affiliation>Policlinique Medicale Universitaire Lausanne, Lausanne, Switzerland</affiliation>
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<name type="personal">
<namePart type="given">R.</namePart>
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<affiliation>The Princess Margaret Hospital Christchurch, Christchurch, New Zealand</affiliation>
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<namePart type="given">M.R.</namePart>
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<affiliation>Corresponding author. Tel.: (604) 822 9240; Fax: (604) 822 9238.</affiliation>
<affiliation>Department of Medical Genetics, University of British Columbia, 416-2125 East Mall, Vancouver, B.C. V6T 1Z4, Canada</affiliation>
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<abstract lang="en">Abstract: The long-term efficacy and tolerability of simvastatin, a 3-hydroxy-3-methylglutaryl-co-enzyme A (HMG-CoA) reductase inhibitor, was assessed during a 24-month follow-up period in 168 elderly hypercholesterolemic patients. After completing a 4 week double blind dose ranging study with simvastatin 47 males and 122 females over 62 years of age with type II hyperlipidemia, a total cholesterol level above 6.5 mmol/l and clinically manifest cardiovascular disease were included in this extended study. A total of 159 patients completed the 12-month follow-up period and 141 patients were monitored over the full 24 months. All patients were started on 10 mg simvastatin once daily and the dosage was increased until the target levels of low density lipoprotein (LDL) cholesterol between 2.3 mmol/l (90 mg/dl) and 3.6 mmol/l (140 mg/dl) were reached. Fifty percent of patients reached the targeted LDL cholesterol goal of < 3.6 mmol/l (140 mg/dl) during the study. At study completion, 65 patients (39%) were taking 40 mg simvastatin per day, 56 patients (33%) 20 mg, 42 patients (25%) 10 mg and 5 patients (3%) only used 5 mg per day. Sixteen patients (9%) received concomitant lipid lowering therapy. Over 2 years, the mean decrease in LDL cholesterol ranged from 36% to 38%, the median decrease in triglycerides was 12% to 19% and the mean increase in high density lipoprotein (HDL) cholesterol ranged from 9% to 10%, respectively. Seven patients discontinued simvastatin because of adverse clinical or laboratory events, but only in two (1.1%) was this considered to be drug-related. Side-effects were mild and most frequently gastrointestinal in nature. Mean changes in asparate aminotransferase (AST) were not significantly different from zero and mean changes in alanine aminotransferase (ALT) and creatine phosphokinase (CPK) showed a small increase. We conclude that simvastatin is an efficacious and well-tolerated treatment for hypercholesterolemia in elderly individuals for extended periods.</abstract>
<note type="content">Section title: Research report</note>
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<genre>Keywords</genre>
<topic>Elderly</topic>
<topic>Hypercholesterolemia</topic>
<topic>Treatment</topic>
<topic>HMG-CoA reductase inhibitors</topic>
<topic>Simvastatin</topic>
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