共 37 条
Improved neurocognitive functions correlate with reduced inflammatory burden in atrial fibrillation patients treated with intensive cholesterol lowering therapy
被引:35
作者:
Lappegard, Knut Tore
[1
,2
]
Pop-Purceleanu, Monica
[3
]
van Heerde, Waander
[4
]
Sexton, Joe
[5
]
Tendolkar, Indira
[3
,6
]
Pop, Gheorghe
[7
]
机构:
[1] Nordland Hosp, Div Internal Med, Trondheim, Norway
[2] Univ Tromso, Bodo, Norway
[3] Radboud Univ Nijmegen, Med Ctr, Dept Psychiat, NL-6525 ED Nijmegen, Netherlands
[4] Radboud Univ Nijmegen, Med Ctr, Dept Lab Med, Hematol Lab, NL-6525 ED Nijmegen, Netherlands
[5] Univ Oslo, Dept Biostat, N-0372 Oslo, Norway
[6] Ctr Cognit Neuroimaging, Donders Inst Brain,Cognit & Behav, Nijmegen, Netherlands
[7] Radboud Univ Nijmegen, Med Ctr, Dept Cardiol, NL-6525 ED Nijmegen, Netherlands
来源:
JOURNAL OF NEUROINFLAMMATION
|
2013年
/
10卷
关键词:
Atrial Fibrillation;
Inflammation;
Neurocognitive Function;
Cerebral MRI;
Statins;
STATIN THERAPY;
PREVENTION;
DEMENTIA;
SURGERY;
METAANALYSIS;
REDUCTION;
RECEPTOR;
RISK;
D O I:
10.1186/1742-2094-10-78
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
Background: Atrial fibrillation (AF) is associated with increased mortality and morbidity, including risk for cerebral macro-and microinfarctions and cognitive decline, even in the presence of adequate oral anticoagulation. AF is strongly related to increased inflammatory activity whereby anti-inflammatory agents can reduce the risk of new or recurrent AF. However, it is not known whether anti-inflammatory therapy can also modify the deterioration of neurocognitive function in older patients with AF. In the present study, older patients with AF were treated with intensive lipid-lowering therapy with atorvastatin 40 mg and ezetimibe 10 mg, or placebo. We examined the relationship between neurocognitive functions and inflammatory burden. Findings: Analysis of inflammatory markers revealed significant reductions in high sensitivity C-reactive protein (hs-CRP), fibroblast growth factor (FGF), granulocyte colony-stimulating factor (G-CSF), granulocyte-macrophage colony-stimulating factor (GM-CSF), interleukin-1 receptor antagonist (IL-1RA), interleukin (IL)-9, IL-13 and IL-17, and interferon-gamma (IFN gamma) in the treatment group compared to placebo. Reduction in plasma concentration of IL-1RA, IL-2, IL-9 and IL-12, and macrophage inflammatory protein-1 beta (MIP-1 beta) correlated significantly with improvement in the neurocognitive functions memory and speed. Loss of volume in amygdala and hippocampus, as determined by magnetic resonance imaging (MRI), was reduced in the treatment arm, statistically significant for left amygdala. Conclusions: Anti-inflammatory therapy through intensive lipid-lowering treatment with atorvastatin 40 mg and ezetimibe 10 mg can modify the deterioration of neurocognitive function, and the loss of volume in certain cerebral areas in older patients with AF. Trial registration Clinical Trials.gov: NCT00449410
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