Relation of multiple inflammatory biomarkers to incident atrial fibrillation.

Relation of multiple inflammatory biomarkers to incident atrial fibrillation.
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DOI:
10.1016/j.amjcard.2009.02.053
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发表时间:
2009-07-01
影响因子:
2.8
通讯作者:
Benjamin, Emelia J.
Benjamin, Emelia J.
中科院分区:
医学3区
文献类型:
--
作者:
Schnabel, Renate B.;Larson, Martin G.;Yamamoto, Jennifer F.;Kathiresan, Sekar;Rong, Jian;Levy, Daniel;Keaney, John F., Jr.;Wang, Thomas J.;Vasan, Ramachandran S.;Benjamin, Emelia J.

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Basic and clinical studies suggest that inflammation predisposes to atrial fibrillation (AF). We assessed the association of 12 circulating inflammatory biomarkers [C-reactive protein, fibrinogen, interleukin-6, intercellular adhesion molecule-1, lipoprotein-associated phospholipase A2 (mass and activity), monocyte chemoattractant protein-1, myeloperoxidase, CD40 ligand, osteoprotegerin, P-selectin, tumor necrosis factor receptor II] with incident AF in 2863 Framingham Offspring Study participants (mean age 60.7 years, SD=9.4, 55% women). During follow-up (median 6 years), 148 participants (43% women) developed incident AF. In multivariable proportional-hazards models, the inflammatory biomarker panel was associated with incident AF (p=0.03). With stepwise selection (p<0.01 for entry and retention), log-transformed osteoprotegerin was associated with incident AF (hazard ratio [HR] per standard deviation 1.30, 95% confidence interval [CI] 1.08–1.56, p=0.006). Adjusting for interim myocardial infarction or heart failure attenuated the association between osteoprotegerin and incident AF (HR 1.18, 95% CI 0.98–1.43, p=0.09). In conclusion, circulating osteoprotegerin concentration was significantly associated with incident AF in our community-based sample, possibly mediated by interim cardiovascular events.
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