Metabolomic Profiling in Relation to New-Onset Atrial Fibrillation (from the Framingham Heart Study)

被引:27
|
作者
Ko, Darae [1 ,5 ,6 ]
Riles, Eric M. [2 ]
Marcos, Ernaldo G. [7 ]
Magnani, Jared W. [2 ]
Lubitz, Steven A. [8 ,9 ]
Lin, Honghuang
Long, Michelle T. [3 ]
Schnabel, Renate B. [12 ]
McManus, David D. [13 ]
Ellinor, Patrick T. [8 ,9 ]
Ramachandran, Vasan S. [2 ,4 ,5 ,10 ,11 ,14 ]
Wang, Thomas J. [15 ]
Gerszten, Robert E. [8 ]
Benjamin, Emelia J. [2 ,4 ,5 ,10 ,11 ,14 ]
Yin, Xiaoyan [16 ]
Rienstra, Michiel [7 ]
机构
[1] Boston Univ, Sch Med, Boston Med Ctr, Dept Internal Med,Gen Internal Med Sect, Boston, MA 02118 USA
[2] Boston Univ, Sch Med, Boston Med Ctr, Dept Internal Med,Sect Cardiovasc Med, Boston, MA 02118 USA
[3] Boston Univ, Sch Med, Boston Med Ctr, Dept Internal Med,Gastroenterol Sect, Boston, MA 02118 USA
[4] Boston Univ, Sch Med, Boston Med Ctr, Dept Internal Med,Sect Prevent Med, Boston, MA 02118 USA
[5] Boston Univ, Sch Med, Whitaker Cardiovasc Inst, Boston, MA 02118 USA
[6] Boston Univ, Sch Med, Clin & Translat Sci Inst, Boston, MA 02118 USA
[7] Univ Groningen, Univ Med Ctr Groningen, Dept Cardiol, Groningen, Netherlands
[8] Harvard Med Sch, Massachusetts Gen Hosp, Cardiovasc Res Ctr, Boston, MA USA
[9] Harvard Med Sch, Massachusetts Gen Hosp, Cardiac Arrhythmia Serv, Boston, MA USA
[10] Boston Univ, Framingham, MA USA
[11] Natl Heart Lung & Blood Inst Framingham Heart Stu, Framingham, MA USA
[12] Univ Hamburg, Heart Ctr Hamburg Eppendorf, Dept Gen & Intervent Cardiol, Hamburg, Germany
[13] Univ Massachusetts, Sch Med, Div Cardiovasc Med, Worcester, MA USA
[14] Boston Univ, Sch Publ Hlth, Dept Epidemiol, Boston, MA USA
[15] Vanderbilt Univ, Div Cardiovasc Med, 221 Kirkland Hall, Nashville, TN 37235 USA
[16] Boston Univ, Sch Publ Hlth, Dept Biostat, Boston, MA USA
来源
AMERICAN JOURNAL OF CARDIOLOGY | 2016年 / 118卷 / 10期
基金
美国国家卫生研究院; 欧洲研究理事会;
关键词
SERUM URIC-ACID; OXIDATIVE STRESS; RISK; BIOMARKER; FAILURE;
D O I
10.1016/j.amjcard.2016.08.010
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Previous studies have shown several metabolic biomarkers to be associated with prevalent and incident atrial fibrillation (AF), but the results have not been replicated.. We investigated metabolite profiles of 2,458 European ancestry participants from the Framingham Heart Study without AF at the index examination and followed them for 10 years for new onset AF. Amino acids, organic acids, lipids, and other plasma metabolites were profiled by liquid chromatography tandem mass spectrometry using fasting plasma samples. We conducted Cox proportional hazard analyses for association between metabolites and new onset AF. We performed hypothesis-generating analysis to identify novel metabolites and hypothesis-testing analysis to confirm the previously reported associations between metabolites and AF. Mean age was 55.1 +/- 9.9 years, and 53% were women. Incident AF developed in 156 participants (6.3%) in 10 years of follow-up. A total of 217 metabolites were examined, consisting of 54 positively charged metabolites, 59 negatively charged metabolites, and 104 lipids. None of the 217 metabolites met our a priori specified Bonferroni corrected level of significance in the multivariate analyses. We were unable to replicate previous results demonstrating associations between metabolites that we had measured and AF. In conclusion, in our metabolomics approach, none of the metabolites we tested were significantly associated with the risk of future AF. (C) 2016 Elsevier Inc. All rights reserved.
引用
收藏
页码:1493 / 1496
页数:4
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