4.7 Article

The association between eicosanoids and incident atrial fibrillation in the Framingham Heart Study

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SCIENTIFIC REPORTS
卷 12, 期 1, 页码 -

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NATURE PORTFOLIO
DOI: 10.1038/s41598-022-21786-0

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资金

  1. National Heart, Lung and Blood Institute [NO1-HC-25195, HHSN268201500001I, 75N92019D00031]
  2. Marie Sklodowska-Curie Actions under the European Union's Horizon 2020 research and innovation programme [838259]
  3. American Heart Association [18SFRN34170442, 18SFRN34150007, AHA_18SFRN34110082]
  4. NIH [R01 HL111314, 5R01HL128914-04, 5R01ES027595, 5K01DK116917, 2R01 HL092577, 2U54HL120163, 1R01AG066010, R01 AG028321, R01HL131532, R01HL151828]
  5. American College of Cardiology Foundation/Merck Research Fellowship in Cardiovascular Diseases and Cardiometabolic Disorders
  6. European Commission Grant [847770]

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This study found an association between chronic inflammation and atrial fibrillation (AF). Using liquid chromatography-mass spectrometry, researchers measured 161 eicosanoids and found that six of them were associated with incident AF. A joint score weighted by the effect sizes of these eicosanoids was also found to be associated with incident AF.
Chronic inflammation is a continuous low-grade activation of the systemic immune response. Whereas downstream inflammatory markers are associated with atrial fibrillation (AF), upstream inflammatory effectors including eicosanoids are less studied. To examine the association between eicosanoids and incident AF. We used a liquid chromatography-mass spectrometry for the non-targeted measurement of 161 eicosanoids and eicosanoid-related metabolites in the Framingham Heart Study. The association of each eicosanoid and incident AF was assessed using Cox proportional hazards models and adjusted for AF risk factors, including age, sex, height, weight, systolic/diastolic blood pressure, current smoking, antihypertensive medication, diabetes, history of myocardial infarction and heart failure. False discovery rate (FDR) was used to adjust for multiple testing. Eicosanoids with FDR < 0.05 were considered significant. In total, 2676 AF-free individuals (mean age 66 +/- 9 years, 56% females) were followed for mean 10.8 +/- 3.4 years; 351 participants developed incident AF. Six eicosanoids were associated with incident AF after adjusting for multiple testing (FDR < 0.05). A joint score was built from the top eicosanoids weighted by their effect sizes, which was associated with incident AF (HR = 2.72, CI = 1.71-4.31, P = 2.1 x 10(-5)). In conclusion, six eicosanoids were associated with incident AF after adjusting for clinical risk factors for AF.

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