Source:http://linkedlifedata.com/resource/pubmed/id/19067673
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3
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pubmed:dateCreated |
2009-2-25
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pubmed:abstractText |
3-Hydroxy-3-methylglutaryl-coenzyme A reductase inhibitors have been used clinically for lowering total and low-density lipoprotein cholesterol. Interindividual pharmacological differences observed with this treatment have been attributed to genetic differences. The aim of this study was to assess the association in the low-density lipoprotein cholesterol reduction by atorvastatin and (TTA)n polymorphism in the 3-hydroxy-3-methylglutaryl-coenzyme A reductase gene in patients with coronary artery disease. Changes in total cholesterol levels, triglycerides, high-sensitivity C-reactive protein and free F(2)-isoprostanes were also evaluated. In an open study, patients received 40 mg atorvastatin daily for 8 weeks. Genotyping was done through polymerase chain reaction. The genotype distribution of the 3-hydroxy-3-methylglutaryl-coenzyme A reductase (TTA)n polymorphism was: >10/>10 in 22 out of 64 patients (34%), >10/10 in 14 out of 64 patients (22%) and 10/10 in 28 out of 64 patients (44%). The reduction of low-density lipoprotein cholesterol levels by atorvastatin was not different between allelic variants (TTA)n repeat polymorphism. Reductions in high-sensitivity C-reactive protein were observed in atorvastatin-treated patients with alleles >10/>10 and 10/10. Free F(2)-isoprostanes and total cholesterol were also significantly lower after treatment for all alleles, irrespective of type of polymorphism. In conclusion, the changes induced by atorvastatin treatment on low-density lipoprotein cholesterol, total cholesterol, triglycerides, high-sensitivity C-reactive protein and free F(2)-isoprostane concentrations were not related to the presence of 3-hydroxy-3-methylglutaryl-coenzyme A reductase polymorphism (TTA)n.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/C-Reactive Protein,
http://linkedlifedata.com/resource/pubmed/chemical/Cholesterol,
http://linkedlifedata.com/resource/pubmed/chemical/Cholesterol, LDL,
http://linkedlifedata.com/resource/pubmed/chemical/Heptanoic Acids,
http://linkedlifedata.com/resource/pubmed/chemical/Hydroxymethylglutaryl CoA Reductases,
http://linkedlifedata.com/resource/pubmed/chemical/Hydroxymethylglutaryl-CoA...,
http://linkedlifedata.com/resource/pubmed/chemical/Pyrroles,
http://linkedlifedata.com/resource/pubmed/chemical/Triglycerides,
http://linkedlifedata.com/resource/pubmed/chemical/atorvastatin
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pubmed:status |
MEDLINE
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pubmed:month |
Mar
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pubmed:issn |
1742-7843
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:volume |
104
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
211-5
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pubmed:meshHeading |
pubmed-meshheading:19067673-Aged,
pubmed-meshheading:19067673-Alleles,
pubmed-meshheading:19067673-C-Reactive Protein,
pubmed-meshheading:19067673-Cholesterol,
pubmed-meshheading:19067673-Cholesterol, LDL,
pubmed-meshheading:19067673-Coronary Artery Disease,
pubmed-meshheading:19067673-Female,
pubmed-meshheading:19067673-Follow-Up Studies,
pubmed-meshheading:19067673-Heptanoic Acids,
pubmed-meshheading:19067673-Humans,
pubmed-meshheading:19067673-Hydroxymethylglutaryl CoA Reductases,
pubmed-meshheading:19067673-Hydroxymethylglutaryl-CoA Reductase Inhibitors,
pubmed-meshheading:19067673-Male,
pubmed-meshheading:19067673-Middle Aged,
pubmed-meshheading:19067673-Polymerase Chain Reaction,
pubmed-meshheading:19067673-Polymorphism, Genetic,
pubmed-meshheading:19067673-Pyrroles,
pubmed-meshheading:19067673-Triglycerides,
pubmed-meshheading:19067673-Trinucleotide Repeats
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pubmed:year |
2009
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pubmed:articleTitle |
(TTA)n polymorphism in 3-hydroxy-3-methylglutaryl-coenzyme A and response to atorvastatin in coronary artery disease patients.
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pubmed:affiliation |
FONDAP Center for Molecular Cell Studies, Clinical Hospital, University of Chile, Santiago, Chile.
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pubmed:publicationType |
Journal Article,
Controlled Clinical Trial,
Research Support, Non-U.S. Gov't
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