Dyslipidemic drugs in metabolic syndrome

Introduction: Metabolic syndrome predisposes to diabetes and atherosclerotic vascular disease. Statins reduce cardiovascular events, so all metabolic syndrome patients should be evaluated for dyslipidemia. Many patients fail to achieve lipid goals with statin monotherapy. Co-administration of ezetim...

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Main Authors: Sheelu S Siddiqi, Misbahuddin, Farida Ahmad, Syed Z Rahman, Asad U Khan
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2013-01-01
Series:Indian Journal of Endocrinology and Metabolism
Subjects:
Online Access:http://www.ijem.in/article.asp?issn=2230-8210;year=2013;volume=17;issue=3;spage=472;epage=479;aulast=Siddiqi
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spelling doaj-69a4d3f494fd4407a6f828186c0e55c02020-11-24T22:43:59ZengWolters Kluwer Medknow PublicationsIndian Journal of Endocrinology and Metabolism2230-82102230-95002013-01-0117347247910.4103/2230-8210.111644Dyslipidemic drugs in metabolic syndromeSheelu S SiddiqiMisbahuddinFarida AhmadSyed Z RahmanAsad U KhanIntroduction: Metabolic syndrome predisposes to diabetes and atherosclerotic vascular disease. Statins reduce cardiovascular events, so all metabolic syndrome patients should be evaluated for dyslipidemia. Many patients fail to achieve lipid goals with statin monotherapy. Co-administration of ezetimibe (EZE) and atorvastatin (ATV) may enable more patients to achievelow-density lipoproteincholesterol (LDL-C) goal while avoiding risks of high-dose statin monotherapy. Materials and Methods: The present study compares rosuvastatin (Rsv) with a combination of (Atv) and (Eze). Metabolic syndrome patients, 30-70 years with LDL-C ≥130 mg/dl and a 10-year CHD risk score of 10% were randomized to double-blind treatment with (Rsv) 5 mg (n = 67) or (Atv) 10 mg+(Eze) 10 mg (n = 68) for 12 weeks. Results: LDL-C reduced significantly; (32.3% and 30.3%, P < 0.001) in (Atv)+(Eze) and (Rsv), respectively, but there was no significant difference between two arms. More patients achieved LDL-C goal of ≤100 mg/dl with (Atv)+(Eze) compared to (Rsv) (65% vs. 58%, P < 0.05). Triglycerides (TG) were reduced more with (Atv)+(Eze) compared to (Rsv) (28.1% and 21.4%, P < 0.001). Greater increase in high-density lipoprotein cholesterol (HDL-C) was observed with (Atv)+(Eze). Both treatments were well tolerated. Conclusion: This study shows that the combination of (Atv)+(Eze) has more efficacy and comparable safety to that of (Rsv).http://www.ijem.in/article.asp?issn=2230-8210;year=2013;volume=17;issue=3;spage=472;epage=479;aulast=Siddiqi3-hydroxy-3-methyglutaryl-CoAreductaseinsulin resistance syndromelow-density lipoproteincholesterolstatins
collection DOAJ
language English
format Article
sources DOAJ
author Sheelu S Siddiqi
Misbahuddin
Farida Ahmad
Syed Z Rahman
Asad U Khan
spellingShingle Sheelu S Siddiqi
Misbahuddin
Farida Ahmad
Syed Z Rahman
Asad U Khan
Dyslipidemic drugs in metabolic syndrome
Indian Journal of Endocrinology and Metabolism
3-hydroxy-3-methyglutaryl-CoA
reductase
insulin resistance syndrome
low-density lipoproteincholesterol
statins
author_facet Sheelu S Siddiqi
Misbahuddin
Farida Ahmad
Syed Z Rahman
Asad U Khan
author_sort Sheelu S Siddiqi
title Dyslipidemic drugs in metabolic syndrome
title_short Dyslipidemic drugs in metabolic syndrome
title_full Dyslipidemic drugs in metabolic syndrome
title_fullStr Dyslipidemic drugs in metabolic syndrome
title_full_unstemmed Dyslipidemic drugs in metabolic syndrome
title_sort dyslipidemic drugs in metabolic syndrome
publisher Wolters Kluwer Medknow Publications
series Indian Journal of Endocrinology and Metabolism
issn 2230-8210
2230-9500
publishDate 2013-01-01
description Introduction: Metabolic syndrome predisposes to diabetes and atherosclerotic vascular disease. Statins reduce cardiovascular events, so all metabolic syndrome patients should be evaluated for dyslipidemia. Many patients fail to achieve lipid goals with statin monotherapy. Co-administration of ezetimibe (EZE) and atorvastatin (ATV) may enable more patients to achievelow-density lipoproteincholesterol (LDL-C) goal while avoiding risks of high-dose statin monotherapy. Materials and Methods: The present study compares rosuvastatin (Rsv) with a combination of (Atv) and (Eze). Metabolic syndrome patients, 30-70 years with LDL-C ≥130 mg/dl and a 10-year CHD risk score of 10% were randomized to double-blind treatment with (Rsv) 5 mg (n = 67) or (Atv) 10 mg+(Eze) 10 mg (n = 68) for 12 weeks. Results: LDL-C reduced significantly; (32.3% and 30.3%, P < 0.001) in (Atv)+(Eze) and (Rsv), respectively, but there was no significant difference between two arms. More patients achieved LDL-C goal of ≤100 mg/dl with (Atv)+(Eze) compared to (Rsv) (65% vs. 58%, P < 0.05). Triglycerides (TG) were reduced more with (Atv)+(Eze) compared to (Rsv) (28.1% and 21.4%, P < 0.001). Greater increase in high-density lipoprotein cholesterol (HDL-C) was observed with (Atv)+(Eze). Both treatments were well tolerated. Conclusion: This study shows that the combination of (Atv)+(Eze) has more efficacy and comparable safety to that of (Rsv).
topic 3-hydroxy-3-methyglutaryl-CoA
reductase
insulin resistance syndrome
low-density lipoproteincholesterol
statins
url http://www.ijem.in/article.asp?issn=2230-8210;year=2013;volume=17;issue=3;spage=472;epage=479;aulast=Siddiqi
work_keys_str_mv AT sheelussiddiqi dyslipidemicdrugsinmetabolicsyndrome
AT misbahuddin dyslipidemicdrugsinmetabolicsyndrome
AT faridaahmad dyslipidemicdrugsinmetabolicsyndrome
AT syedzrahman dyslipidemicdrugsinmetabolicsyndrome
AT asadukhan dyslipidemicdrugsinmetabolicsyndrome
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