Zhou Zhihong, Sun Lizhe, Zhou Wei, Gao Wen, Yuan Xiao, Zhou Huijuan, Ren Yuzhen, Li Bihua, Wu Yue, She Jianqing
Department of Cardiology, Bayannur Hospital, Bayannur, Inner Mongolia Autonomous Region, China.
Department of Cardiovascular Medicine, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, Shaanxi, China.
Liver Res. 2025 Feb 19;9(1):57-65. doi: 10.1016/j.livres.2025.02.001. eCollection 2025 Mar.
Studies indicate that the gut microbiota and its metabolites are involved in the progression of cardiovascular diseases, and enterohepatic circulation plays an important role in this progression. This study aims to identify potential probiotics for the treatment of unstable angina (UA) and elucidate their mechanisms of action.
Initially, the gut microbiota from patients with UA and control was analyzed. To directly assess the effects of supplementation, 10 patients with UA were enrolled and administered (630 mg per intake twice a day for 1 month). The fecal metagenome, serum trimethylamine N-oxide (TMAO) levels, and other laboratory parameters were evaluated before and after supplementation.
After supplementing with for 1 month, there were statistically significant differences ( < 0.05) in TMAO, aspartate aminotransferase, total cholesterol, and low-density lipoprotein compared to before. Additionally, the abundance of increased significantly, although the overall abundance of did not reach statistical significance. The gut microbiota, metabolites, and gut-liver axis are involved in the progression of UA, and potential mechanisms should be further studied.
Metagenomic analysis demonstrated a reduced abundance of in patients with UA. Supplementation with restored gut dysbiosis and decreased circulating TMAO levels in patients with UA. This study provides evidence that may exert cardiovascular-protective effects through the gut-liver-heart axis.
ChiCTR2400093946.
研究表明,肠道微生物群及其代谢产物参与心血管疾病的进展,而肠肝循环在这一进展中起重要作用。本研究旨在确定治疗不稳定型心绞痛(UA)的潜在益生菌,并阐明其作用机制。
首先,分析UA患者和对照组的肠道微生物群。为了直接评估补充剂的效果,招募了10例UA患者并给予补充剂(每次摄入630mg,每天两次,持续1个月)。在补充剂前后评估粪便宏基因组、血清三甲胺N-氧化物(TMAO)水平和其他实验室参数。
补充剂1个月后,与之前相比,TMAO、天冬氨酸转氨酶、总胆固醇和低密度脂蛋白有统计学显著差异(P<0.05)。此外,尽管的总体丰度未达到统计学显著差异,但的丰度显著增加。肠道微生物群、代谢产物和肠肝轴参与UA的进展,潜在机制应进一步研究。
宏基因组分析表明UA患者中的丰度降低。补充剂可恢复UA患者的肠道生态失调并降低循环TMAO水平。本研究提供了证据表明可能通过肠-肝-心轴发挥心血管保护作用。
ChiCTR2400093946。