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宏基因组学对急性冠状动脉综合征治疗相关肠道微生物群的见解。

Insights from metagenomics into gut microbiome associated with acute coronary syndrome therapy.

作者信息

Guan Yuee, Zhao Shuru, Li Jing, Zhang Wenqian, Guo Zhonghao, Luo Yi, Jiang Xiaofei, Li Jun, Liu Jianxiong, Chen Xi, Zhao Zicheng, Zhang Zhe

机构信息

Department of Cardiology, Zhuhai People's Hospital (Zhuhai Clinical Medical College of Jinan University), Zhuhai, China.

Shenzhen Byoryn Technology Co., Ltd., Shenzhen, China.

出版信息

Front Microbiol. 2024 Jul 5;15:1369478. doi: 10.3389/fmicb.2024.1369478. eCollection 2024.

DOI:10.3389/fmicb.2024.1369478
PMID:39035441
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11258018/
Abstract

Acute coronary syndrome (ACS) is a predominant cause of mortality, and the prompt and precise identification of this condition is crucial to minimize its impact. Recent research indicates that gut microbiota is associated with the onset, progression, and treatment of ACS. To investigate its role, we sequenced the gut microbiota of 38 ACS patients before and after percutaneous coronary intervention and statin therapy at three time points, examining differential species and metabolic pathways. We observed a decrease in the abundance of , , and in patients after treatment and an increase in the abundance of , , , and others. Two pathways related to sugar degradation were more abundant in patients before treatment, possibly correlated with disorders of sugar metabolism and risk factors, such as hyperglycemia, insulin resistance, and insufficient insulin secretion. Additionally, seven pathways related to the biosynthesis of vitamin K2 and its homolog were reduced after treatment, suggesting that ACS patients may gradually recover after therapy. The gut microbiota of patients treated with different statins exhibited notable differences after treatment. Rosuvastatin appeared to promote the growth of anti-inflammatory bacteria while reducing pro-inflammatory bacteria, whereas atorvastatin may have mixed effects on pro-inflammatory and anti-inflammatory bacteria while increasing the abundance of . Our research will provide valuable insights and enhance comprehension of ACS, leading to better patient diagnosis and therapy.

摘要

急性冠状动脉综合征(ACS)是主要的死亡原因,迅速而准确地识别这种病症对于将其影响降至最低至关重要。最近的研究表明,肠道微生物群与ACS的发生、发展及治疗有关。为了研究其作用,我们在三个时间点对38例接受经皮冠状动脉介入治疗和他汀类药物治疗前后的ACS患者的肠道微生物群进行了测序,检测差异物种和代谢途径。我们观察到治疗后患者体内 、 和 的丰度下降,而 、 、 和其他一些物种的丰度增加。治疗前患者体内两条与糖降解相关的途径更为丰富,这可能与糖代谢紊乱及危险因素如高血糖、胰岛素抵抗和胰岛素分泌不足有关。此外,治疗后与维生素K2及其同系物生物合成相关的七条途径减少,这表明ACS患者在治疗后可能会逐渐康复。接受不同他汀类药物治疗的患者的肠道微生物群在治疗后表现出显著差异。瑞舒伐他汀似乎促进抗炎细菌的生长,同时减少促炎细菌,而阿托伐他汀可能对促炎和抗炎细菌有混合作用,同时增加 的丰度。我们的研究将为理解ACS提供有价值的见解,提高对ACS的认识,从而实现更好的患者诊断和治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae85/11258018/feced63628cb/fmicb-15-1369478-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae85/11258018/17c811a89530/fmicb-15-1369478-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae85/11258018/45c2a723949f/fmicb-15-1369478-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae85/11258018/500bde5226a1/fmicb-15-1369478-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae85/11258018/feced63628cb/fmicb-15-1369478-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae85/11258018/17c811a89530/fmicb-15-1369478-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae85/11258018/45c2a723949f/fmicb-15-1369478-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae85/11258018/500bde5226a1/fmicb-15-1369478-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae85/11258018/feced63628cb/fmicb-15-1369478-g004.jpg

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