Source:http://linkedlifedata.com/resource/pubmed/id/21028996
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
6
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pubmed:dateCreated |
2010-10-29
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pubmed:abstractText |
Lipid-lowering therapy with a statin not only powerfully lowers cholesterol but also exerts anti-inflammatory effects by decreasing serum C-reactive protein (CRP). Since an angiotensin II, type-1 receptor antagonist (ARB) also decreases CRP levels, the add-on effect of statins on CRP may be worth exploring. We determined the effect of pitavastatin on serum levels of highly sensitive CRP (hs-CRP) in 30 patients with hypercholesterolemia undergoing treatment with anti-hypertensive medication including ARBs. Pitavastatin, 2 mg daily, was given. The control group consisted of hypertensive patients without hyperlipidemia. The low-density lipoprotein cholesterol (LDL-C), high-density lipoprotein cholesterol (HDL-C), and hs-CRP were measured at baseline, 1, 3, 6, and 12 months after treatment. For the atherosclerotic index, LDL-C/HDL-C ratios at 12 months were calculated. The LDL-C level was markedly reduced at 1 month and thereafter. The baseline level of hs-CRP in the hyperlipidemia group was significantly higher than that in the control group (1.647 ± 0.210 mg/L vs. 0.666 ± 0.097 mg/L p < 0.0001). After 3 months, the percentage of reduction of hs-CRP was significantly higher than that in the control group. The absolute values of hs-CRP were significantly decreased to a level similar to the control group, and the hs-CRP in both groups was remained at the same level for 12 months. Although the LDL-C/HDL-C ratios of the pitavastatin group was significantly reduced from 3.3 to 1.8, those of the control group were not changed. In conclusion, pitavastatin was found to have powerful anti-inflammatory, add-on effects over the similar effects of ARB as assessed by hs-CRP.
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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/Angiotensin II Type 1 Receptor...,
http://linkedlifedata.com/resource/pubmed/chemical/C-Reactive Protein,
http://linkedlifedata.com/resource/pubmed/chemical/Hydroxymethylglutaryl-CoA...,
http://linkedlifedata.com/resource/pubmed/chemical/Quinolines,
http://linkedlifedata.com/resource/pubmed/chemical/pitavastatin
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pubmed:status |
MEDLINE
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pubmed:issn |
1525-6006
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:volume |
32
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
341-6
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pubmed:meshHeading |
pubmed-meshheading:21028996-Aged,
pubmed-meshheading:21028996-Angiotensin II Type 1 Receptor Blockers,
pubmed-meshheading:21028996-C-Reactive Protein,
pubmed-meshheading:21028996-Female,
pubmed-meshheading:21028996-Humans,
pubmed-meshheading:21028996-Hydroxymethylglutaryl-CoA Reductase Inhibitors,
pubmed-meshheading:21028996-Hypercholesterolemia,
pubmed-meshheading:21028996-Hypertension,
pubmed-meshheading:21028996-Male,
pubmed-meshheading:21028996-Middle Aged,
pubmed-meshheading:21028996-Quinolines,
pubmed-meshheading:21028996-Treatment Outcome
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pubmed:year |
2010
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pubmed:articleTitle |
Pitavastatin further decreases serum high-sensitive C-reactive protein levels in hypertensive patients with hypercholesterolemia treated with angiotensin II, type-1 receptor antagonists.
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pubmed:affiliation |
Department of Clinical Sciences and Laboratory Medicine, Kansai Medical University, Moriguchi, Japan.
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pubmed:publicationType |
Journal Article,
Clinical Trial
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