Department of Medical Sciences Uppsala University Uppsala Sweden.
Department of Medical Sciences Molecular Epidemiology and Science for Life Laboratory Uppsala University Uppsala Sweden.
J Am Heart Assoc. 2021 Jan 19;10(2):e017579. doi: 10.1161/JAHA.120.017579. Epub 2021 Jan 5.
Background The molecular mechanisms involved in atrial fibrillation are not well known. We used plasma metabolomics to investigate if we could identify novel biomarkers and pathophysiological pathways of incident atrial fibrillation. Methods and Results We identified 200 endogenous metabolites in plasma/serum by nontargeted ultra-performance liquid chromatography coupled to time-of-flight mass spectrometry in 3 independent population-based samples (TwinGene, n=1935, mean age 68, 43% females; PIVUS [Prospective Investigation of the Vasculature in Uppsala Seniors], n=897, mean age 70, 51% females; and ULSAM [Uppsala Longitudinal Study of Adult Men], n=1118, mean age 71, all males), with available data on incident atrial fibrillation during 10 to 12 years of follow-up. A meta-analysis of ULSAM and PIVUS was used as a discovery sample and TwinGene was used for validation. In PIVUS, we also investigated associations between metabolites of interest and echocardiographic indices of myocardial geometry and function. Genome-wide association studies were performed in all 3 cohorts for metabolites of interest. In the meta-analysis of PIVUS and ULSAM with 430 incident cases, 4 metabolites were associated with incident atrial fibrillation at a false discovery rate <5%. Of those, only 9-decenoylcarnitine was associated with incident atrial fibrillation and replicated in the TwinGene sample (288 cases) following adjustment for traditional risk factors (hazard ratio, 1.24 per unit; 95% CI, 1.06-1.45, =0.0061). A meta-analysis of all 3 cohorts disclosed another 4 significant metabolites. In PIVUS, 9-decenoylcarnitine was related to left atrium size and left ventricular mass. A Mendelian randomization analysis did not suggest a causal role of 9-decenoylcarnitine in atrial fibrillation. Conclusions A nontargeted metabolomics analysis disclosed 1 novel replicated biomarker for atrial fibrillation, 9-Decenoylcarnitine, but this acetylcarnitine is likely not causally related to atrial fibrillation.
背景 心房颤动的分子机制尚不清楚。我们使用血浆代谢组学来研究是否可以鉴定出心房颤动的新生物标志物和病理生理途径。
方法和结果 我们通过靶向超高效液相色谱与飞行时间质谱在 3 个独立的基于人群的样本(TwinGene,n=1935,平均年龄 68 岁,女性占 43%;PIVUS[乌普萨拉老年人血管前瞻性研究],n=897,平均年龄 70 岁,女性占 51%;ULSAM[乌普萨拉男性成人纵向研究],n=1118,平均年龄 71 岁,均为男性)中鉴定了 200 种内源性代谢物,这些样本均有 10 至 12 年的心房颤动随访数据。对 ULSAM 和 PIVUS 的荟萃分析用作发现样本,TwinGene 用作验证样本。在 PIVUS 中,我们还研究了感兴趣的代谢物与心肌几何和功能的超声心动图指标之间的关系。对所有 3 个队列的感兴趣代谢物进行了全基因组关联研究。在 PIVUS 和 ULSAM 的荟萃分析中,有 430 例新发心房颤动病例,有 4 种代谢物在错误发现率<5%的情况下与新发心房颤动相关。其中,只有 9-癸烯酰肉碱与心房颤动相关,并在经过传统危险因素调整后在 TwinGene 样本(288 例)中得到复制(风险比,每单位 1.24;95%CI,1.06-1.45,=0.0061)。对所有 3 个队列的荟萃分析显示了另外 4 种有意义的代谢物。在 PIVUS 中,9-癸烯酰肉碱与左心房大小和左心室质量有关。孟德尔随机分析表明 9-癸烯酰肉碱与心房颤动之间没有因果关系。
结论 非靶向代谢组学分析揭示了 1 种新的、可复制的心房颤动生物标志物 9-癸烯酰肉碱,但这种乙酰肉碱可能与心房颤动没有因果关系。