World-Class Research Center "Digital Biodesign and Personalized Healthcare", I. M. Sechenov First Moscow State Medical University, 119991 Moscow, Russia.
Department of Normal Physiology, N.V. Sklifosovsky Institute of Clinical Medicine, I. M. Sechenov First Moscow State Medical University, 119991 Moscow, Russia.
Int J Mol Sci. 2023 Sep 24;24(19):14498. doi: 10.3390/ijms241914498.
Along with the known risk factors of cardiovascular diseases (CVDs) constituting metabolic syndrome (MS), the gut microbiome and some of its metabolites, in particular trimethylamine-N-oxide (TMAO), are actively discussed. A prolonged stay under natural hypoxic conditions significantly and multi-directionally changes the ratio of gut microbiome strains and their metabolites in feces and blood, which is the basis for using hypoxia preconditioning for targeted effects on potential risk factors of CVD. A prospective randomized study included 65 patients (32 females) with MS and optimal medical therapy. Thirty-three patients underwent a course of 15 intermittent hypoxic-hyperoxic exposures (IHHE group). The other 32 patients underwent sham procedures (placebo group). Before and after the IHHE course, patients underwent liver elastometry, biochemical blood tests, and blood and fecal sampling for TMAO analysis (tandem mass spectrometry). No significant dynamics of TMAO were detected in both the IHHE and sham groups. In the subgroup of IHHE patients with baseline TMAO values above the reference (TMAO ≥ 5 μmol/l), there was a significant reduction in TMAO plasma levels. But the degree of reduction in total cholesterol (TCh), low-density lipoprotein (LDL), and regression of liver steatosis index was more pronounced in patients with initially normal TMAO values. Despite significant interindividual variations, in the subgroup of IHHE patients with MS and high baseline TMAO values, there were more significant reductions in cardiometabolic and hepatic indicators of MS than in controls. More research is needed to objectify the prognostic role of TMAO and the possibilities of its correction using hypoxia adaptation techniques.
除了心血管疾病(CVDs)的已知风险因素构成代谢综合征(MS)之外,肠道微生物组及其某些代谢产物,特别是三甲胺 N-氧化物(TMAO),也在积极讨论中。在自然低氧条件下长时间停留会显著且多方向地改变粪便和血液中肠道微生物组菌株及其代谢物的比例,这是利用低氧预处理对 CVD 潜在风险因素进行靶向治疗的基础。一项前瞻性随机研究纳入了 65 名(32 名女性)患有 MS 和最佳药物治疗的患者。33 名患者接受了 15 次间歇性低氧-高氧暴露(IHHE 组)疗程。另外 32 名患者接受了假处理(安慰剂组)。在 IHHE 疗程前后,患者接受了肝脏弹性测量、生化血液检查以及血液和粪便取样以进行 TMAO 分析(串联质谱法)。在 IHHE 和安慰剂组中均未检测到 TMAO 的显著动态变化。在基线 TMAO 值高于参考值(TMAO≥5μmol/l)的 IHHE 患者亚组中,血浆 TMAO 水平显著降低。但是,在 TMAO 初始值正常的患者中,总胆固醇(TCh)、低密度脂蛋白(LDL)的降低程度以及肝脏脂肪变性指数的消退更为明显。尽管存在显著的个体间差异,但在基线 TMAO 值较高的 IHHE 患者亚组中,MS 的心脏代谢和肝脏指标的降低程度比对照组更为显著。需要进一步的研究来客观化 TMAO 的预后作用以及使用低氧适应技术纠正 TMAO 的可能性。