Gut microbial metabolite trimethylamine N-oxide as a novel predictor for adverse cardiovascular events after PCI: a systematic review and dose-response meta-analysis.

IF 3.8 2区 医学 Q1 NUTRITION & DIETETICS
Chunyu Zhang, Jinyu He, Yujia Huo, Lin Liu, Yong Xie, Yufei Meng, Gang Wei, Li Deng, Yang Jiang, Jian Feng
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引用次数: 0

Abstract

Background: Cardiovascular diseases are the leading cause of mortality worldwide, with acute coronary syndrome (ACS) being particularly fatal. Percutaneous coronary intervention (PCI) is a key treatment for ACS; however, major adverse cardiovascular events (MACE) frequently occur postoperatively. Trimethylamine N-oxide (TMAO), a gut microbiota-derived metabolite, has been proposed as an emerging risk factor for cardiovascular disease. This study aims to systematically evaluate TMAO's predictive value for MACE post-PCI and explore its dose-response relationship.

Methods: A comprehensive literature search was conducted in four databases (PubMed, Web of Science, Embase, and the Cochrane Library), including retrospective or prospective cohort studies involving patients undergoing PCI. The primary outcome was MACE, and the secondary outcome was all-cause mortality. A dose-response analysis was conducted using a restricted cubic spline model to explore potential nonlinear associations between TMAO levels and outcomes. Heterogeneity was assessed using the Cochrane Q test and the I² statistic. Subgroup analysis and meta-regression were performed to identify sources of heterogeneity.

Results: Eleven studies (comprising 13 independent cohorts) with 11,279 participants were included. Pooled analysis showed a significant association between elevated plasma TMAO levels and an increased risk of MACE after PCI (HR: 1.99, 95%CI: 1.68-2.35, 95%PI: 1.64-2.40, I² = 0%, p < 0.00001). Similarly, elevated plasma TMAO levels were significantly associated with an increased risk of all-cause mortality after PCI (HR: 1.76, 95%CI: 1.32-2.35, 95%PI: 0.79-3.90, I² = 65.1%, p < 0.00001). The dose-response analysis did not reveal a nonlinear relationship between TMAO and MACE or all-cause mortality. The linear model showed that each 1 µmol/L increase in plasma TMAO was associated with an 8.95% increased hazard of MACE (HR = 1.0895, 95%CI: 1.03-1.15), while all-cause mortality increased by 4% (HR = 1.04, 95%CI: 0.99-1.09).

Conclusions: This study demonstrates that elevated plasma TMAO levels are significantly associated with an increased risk of MACE and all-cause mortality after PCI, with a dose-dependent effect on MACE risk. As a potential biomarker, TMAO may be used to predict the risk of adverse cardiovascular events after PCI, and future studies should further validate its clinical utility.

Registration: PROSPERO CRD42024557486.

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肠道微生物代谢物三甲胺n -氧化物作为PCI术后不良心血管事件的新预测因子:系统评价和剂量反应荟萃分析
背景:心血管疾病是世界范围内导致死亡的主要原因,其中急性冠脉综合征(ACS)尤为致命。经皮冠状动脉介入治疗(PCI)是ACS的关键治疗方法;然而,主要不良心血管事件(MACE)经常发生在术后。三甲胺n -氧化物(TMAO)是一种肠道微生物衍生的代谢物,已被认为是心血管疾病的新危险因素。本研究旨在系统评价TMAO对pci术后MACE的预测价值,并探讨其剂量-反应关系。方法:在四个数据库(PubMed、Web of Science、Embase和Cochrane Library)中进行全面的文献检索,包括涉及PCI患者的回顾性或前瞻性队列研究。主要终点为MACE,次要终点为全因死亡率。使用受限三次样条模型进行了剂量-反应分析,以探索TMAO水平与预后之间潜在的非线性关联。采用Cochrane Q检验和I²统计量评估异质性。进行亚组分析和meta回归来确定异质性的来源。结果:纳入11项研究(包括13个独立队列),11,279名受试者。合并分析显示血浆TMAO水平升高与PCI术后MACE风险增加之间存在显著相关性(HR: 1.99, 95%CI: 1.68-2.35, 95%PI: 1.64-2.40, I²= 0%,p)。结论:本研究表明血浆TMAO水平升高与PCI术后MACE风险增加和全因死亡率显著相关,且对MACE风险有剂量依赖性。作为一种潜在的生物标志物,TMAO可用于预测PCI术后不良心血管事件的风险,未来的研究应进一步验证其临床应用价值。注册号:PROSPERO CRD42024557486。
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来源期刊
Nutrition Journal
Nutrition Journal NUTRITION & DIETETICS-
CiteScore
9.80
自引率
0.00%
发文量
68
审稿时长
4-8 weeks
期刊介绍: Nutrition Journal publishes surveillance, epidemiologic, and intervention research that sheds light on i) influences (e.g., familial, environmental) on eating patterns; ii) associations between eating patterns and health, and iii) strategies to improve eating patterns among populations. The journal also welcomes manuscripts reporting on the psychometric properties (e.g., validity, reliability) and feasibility of methods (e.g., for assessing dietary intake) for human nutrition research. In addition, study protocols for controlled trials and cohort studies, with an emphasis on methods for assessing dietary exposures and outcomes as well as intervention components, will be considered. Manuscripts that consider eating patterns holistically, as opposed to solely reductionist approaches that focus on specific dietary components in isolation, are encouraged. Also encouraged are papers that take a holistic or systems perspective in attempting to understand possible compensatory and differential effects of nutrition interventions. The journal does not consider animal studies. In addition to the influence of eating patterns for human health, we also invite research providing insights into the environmental sustainability of dietary practices. Again, a holistic perspective is encouraged, for example, through the consideration of how eating patterns might maximize both human and planetary health.
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