Effect of atorvastatin on plasma levels of asymmetric dimethylarginine in patients with non-ischaemic heart failure
被引:33
作者:
Young, Joanna M.
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机构:
Christchurch Hosp, Lipid & Diabet Res Grp, Christchurch, New ZealandChristchurch Hosp, Lipid & Diabet Res Grp, Christchurch, New Zealand
Young, Joanna M.
[1
]
Strey, Christopher H.
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Christchurch Hosp, Lipid & Diabet Res Grp, Christchurch, New ZealandChristchurch Hosp, Lipid & Diabet Res Grp, Christchurch, New Zealand
Strey, Christopher H.
[1
]
George, Peter M.
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机构:
Canterbury Hlth Labs, Clin Biochem Unit, Christchurch, New ZealandChristchurch Hosp, Lipid & Diabet Res Grp, Christchurch, New Zealand
George, Peter M.
[2
]
Florkowski, Christopher M.
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机构:
Christchurch Hosp, Lipid & Diabet Res Grp, Christchurch, New Zealand
Canterbury Hlth Labs, Clin Biochem Unit, Christchurch, New ZealandChristchurch Hosp, Lipid & Diabet Res Grp, Christchurch, New Zealand
Florkowski, Christopher M.
[1
,2
]
Sies, Christiaan W.
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Canterbury Hlth Labs, Clin Biochem Unit, Christchurch, New ZealandChristchurch Hosp, Lipid & Diabet Res Grp, Christchurch, New Zealand
Sies, Christiaan W.
[2
]
Frampton, Christopher M.
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Univ Otago, Dept Med, Christchurch, New ZealandChristchurch Hosp, Lipid & Diabet Res Grp, Christchurch, New Zealand
Frampton, Christopher M.
[3
]
Scott, Russell S.
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Christchurch Hosp, Lipid & Diabet Res Grp, Christchurch, New ZealandChristchurch Hosp, Lipid & Diabet Res Grp, Christchurch, New Zealand
Scott, Russell S.
[1
]
机构:
[1] Christchurch Hosp, Lipid & Diabet Res Grp, Christchurch, New Zealand
[2] Canterbury Hlth Labs, Clin Biochem Unit, Christchurch, New Zealand
[3] Univ Otago, Dept Med, Christchurch, New Zealand
asymmetric dimethylarginine;
left ventricular dysfunction;
chronic heart failure;
Stalin treatment;
endothelial function;
D O I:
10.1016/j.ejheart.2008.03.010
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
Background: Elevated plasma levels of asymmetric dimethylarginine (ADMA), an endothelial nitric oxide synthase (eNOS) inhibitor, may contribute to endothelial dysfunction in chronic heart failure (CHF). Since statins upregulate eNOS and ameliorate endothelial dysfunction in non-ischaemic CHF, we hypothesized that this may be in part through modification of ADMA. Aim: To evaluate the effect of atorvastatin on the relationship between ADMA and endothelial function in non-ischaemic CHF. Methods: Twenty-four patients with CHF (ejection fraction <40%, New York Heart Association Functional Classes II and III) were randomised to atorvastatin treatment (40 mg) or placebo once daily for 6 weeks in a double-blinded, placebo-controlled crossover study. Plasma ADMA and L-arginine levels were measured by HPLC. Endothelial function was assessed by flow-mediated dilatation and invasive forearm plethysmography. Results: Post-statin therapy, endothelial function was improved (p<0.05) independent of LDL-cholesterol reductions, but no changes were observed in ADMA levels or the L-arginine to ADMA ratio. There was a trend for ADMA to inversely correlate with endothelial function at baseline. Conclusions: Short-term atorvastatin treatment in non-ischaemic CHF improves endothelial function but has no effect on ADMA or the L-arginine to ADMA ratio. Our finding suggests that the observed statin-induced improvements in endothelial function are likely mediated via alternative pathways. (C) 2008 European Society of Cardiology. Published by Elsevier B.V. All rights reserved.