Vaiomer Labège France.
Department of Therapeutics Rangueil Hospital CHU Toulouse Toulouse France.
J Am Heart Assoc. 2019 Oct;8(19):e011797. doi: 10.1161/JAHA.118.011797. Epub 2019 Sep 28.
Background The role of bacteria on the onset of cardiovascular disease has been suggested. Reciprocally, increased intestinal bacterial translocation and bloodstream infection are common comorbidities associated with heart failure and myocardial infarction (MI). In this context, the aim of this study was to analyze the blood microbiome in patients shortly after acute myocardial infarction. Methods and Results We carried out a case control study comparing 103 patients at high cardiovascular risk but free of coronary disease and 99 patients who had an MI. The blood microbiome was analyzed both quantitatively by 16S quantitative polymerase chain reaction and qualitatively by 16S targeted metagenomic sequencing specifically optimized for blood samples. A significant increase in blood bacterial 16S rDNA concentration was observed in patients admitted for MI. This increase in blood bacterial DNA concentration was independent of post-MI left ventricular function and was more marked in patients with low-density lipoprotein cholesterol ≥1 g/L. In addition, differences in the proportion of numerous bacterial taxa in blood were significantly modified with the onset of MI, thus defining a blood microbiota signature of MI. Among the bacterial taxa whose proportions are decreased in patients with MI, at least 6 are known to include species able to metabolize cholesterol. Conclusions These results could provide the basis for the identification of blood microbiome-based biomarkers for the stratification of MI patients. Furthermore, these findings should provide insight into the mechanism underlying the negative correlation reported between low-density lipoprotein cholesterol concentration and the prognosis at the acute onset of MI and mortality. Clinical Trial Registration URL: http://www.clinicaltrials.gov. Unique identifier: NCT02405468.
已有研究提示细菌在心血管疾病发病中的作用。相反,肠道细菌易位和血流感染增加是心力衰竭和心肌梗死(MI)常见的合并症。在此背景下,本研究旨在分析急性心肌梗死后患者的血液微生物组。
我们进行了一项病例对照研究,比较了 103 名高心血管风险但无冠状动脉疾病的患者和 99 名 MI 患者。通过 16S 定量聚合酶链反应对血液微生物组进行定量分析,通过专门针对血液样本优化的 16S 靶向宏基因组测序进行定性分析。发现 MI 患者的血液细菌 16S rDNA 浓度显著增加。这种血液细菌 DNA 浓度的增加与 MI 后左心室功能无关,在低密度脂蛋白胆固醇≥1g/L 的患者中更为明显。此外,MI 发生后,血液中许多细菌分类群的比例差异明显改变,从而定义了 MI 的血液微生物组特征。在 MI 患者中比例降低的细菌分类群中,至少有 6 种被认为包括能够代谢胆固醇的物种。
这些结果可为 MI 患者分层的血液微生物组标志物的识别提供依据。此外,这些发现应该为报告的低密度脂蛋白胆固醇浓度与急性 MI 发病和死亡率之间的负相关的机制提供深入了解。