Semporé Wendsèndaté Yves, Chao De La Barca Juan Manuel, Hersant Jeanne, Ouédraogo Nafi, Yaméogo Téné Marceline, Henni Samir, Reynier Pascal, Abraham Pierre
Centre MURAZ, National Institute of Public Health, Bobo Dioulasso, Burkina Faso.
Sports Medicine Department, University Hospital of Angers, Angers, France.
Front Physiol. 2021 Nov 18;12:758085. doi: 10.3389/fphys.2021.758085. eCollection 2021.
A better knowledge of the biological consequences in the blood of these exercise-induced ischemic events in lower extremity artery disease (LEAD) may improve the prospects of disease management. We explored the preminus postexercise metabolomic difference in 39 patients with LEAD referred for a treadmill oximetry test [transcutaneous oximetry (TcPO)]. Ischemia was estimated through the sum of decrease from rest of oxygen pressure (DROPs) (limb TcPO changes minus chest TcPO changes) at buttocks, thighs, and calves regions. Targeted metabolomic analyses measuring 188 metabolites were performed on a few microliters blood samples taken at the earlobe at rest and 3 min after exercise. Maximum walking distance (MWD) was 290 m (120-652 m) and ankle brachial index (ABI) was 0.67 ± 0.17. Supervised paired partial least squares discriminant analysis based on 23,345 models showed good predictive performance for test sets with a median area under the receiver operating characteristic (AUROC) curve value of 0.99 and a -value of 0.00049. The best discriminant metabolites contributing to the model included a subset of 71 (47%) of the 150 accurately measured metabolites in the plasma, comprising 3 acylcarnitines, 3 amino acids, 5 biogenic amines, 9 sphingomyelin, 7 lysophosphatidylcholines, and 44 phosphatidylcholines. In addition, 16 of these metabolites were found to correlate with one or more severity scores of the LEAD. Our results provide new insights into the biological changes that accompany exercise in LEAD and contribute to a better understanding of walking impairment pathophysiology in LEAD, highlighting new candidate biomarkers.
更好地了解这些运动诱发的缺血事件在下肢动脉疾病(LEAD)患者血液中的生物学后果,可能会改善疾病管理的前景。我们探讨了39例因跑步机血氧饱和度测试[经皮血氧饱和度(TcPO)]而转诊的LEAD患者运动前后的代谢组学差异。通过测量臀部、大腿和小腿区域静息时氧分压下降总和(DROPs)(肢体TcPO变化减去胸部TcPO变化)来评估缺血情况。对在耳垂处采集的微量血液样本进行靶向代谢组学分析,测量188种代谢物,分别在静息时和运动后3分钟采集。最大步行距离(MWD)为290米(120 - 652米),踝肱指数(ABI)为0.67±0.17。基于23345个模型的监督配对偏最小二乘判别分析对测试集显示出良好的预测性能,受试者工作特征(AUROC)曲线下面积的中位数为0.99,P值为0.00049。对模型贡献最大的判别代谢物包括血浆中150种精确测量代谢物中的71种(47%),其中包括3种酰基肉碱、3种氨基酸、5种生物胺、9种鞘磷脂、7种溶血磷脂酰胆碱和44种磷脂酰胆碱。此外,发现其中16种代谢物与LEAD的一种或多种严重程度评分相关。我们的研究结果为LEAD运动时伴随的生物学变化提供了新的见解,有助于更好地理解LEAD行走障碍的病理生理学,突出了新的候选生物标志物。