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微生物组与不同危险因素在心肌梗死发展中的相互作用。

Microbiome interactions with different risk factors in development of myocardial infarction.

机构信息

Department of Biotechnology, Guru Nanak Dev University, Amritsar, India.

Department of Zoology, Swami Shraddhanand College, Delhi University, India.

出版信息

Exp Gerontol. 2024 May;189:112409. doi: 10.1016/j.exger.2024.112409. Epub 2024 Mar 27.

Abstract

Among all non-communicable diseases, Cardiovascular Diseases (CVDs) stand as the leading global cause of mortality. Within this spectrum, Myocardial Infarction (MI) strikingly accounts for over 15 % of all deaths. The intricate web of risk factors for MI, comprising family history, tobacco use, oral health, hypertension, nutritional pattern, and microbial infections, is firmly influenced by the human gut and oral microbiota, their diversity, richness, and dysbiosis, along with their respective metabolites. Host genetic factors, especially allelic variations in signaling and inflammatory markers, greatly affect the progression or severity of the disease. Despite the established significance of the human microbiome-nutrient-metabolite interplay in associations with CVDs, the unexplored terrain of the gut-heart-oral axis has risen as a critical knowledge gap. Moreover, the pivotal role of the microbiome and the complex interplay with host genetics, compounded by age-related changes, emerges as an area of vital importance in the development of MI. In addition, a distinctive disease susceptibility and severity influenced by gender-based or ancestral differences, adds a crucial insights to the association with increased mortality. Here, we aimed to provide an overview on interactions of microbiome (oral and gut) with major risk factors (tobacco use, alcohol consumption, diet, hypertension host genetics, gender, and aging) in the development of MI and therapeutic regulation.

摘要

在所有非传染性疾病中,心血管疾病(CVDs)是全球主要的死亡原因。在这一范畴内,心肌梗死(MI)惊人地占所有死亡人数的 15%以上。MI 的复杂风险因素网络,包括家族史、烟草使用、口腔健康、高血压、营养模式和微生物感染,受到人类肠道和口腔微生物群及其多样性、丰富度和失调以及它们各自的代谢物的强烈影响。宿主遗传因素,特别是信号和炎症标志物的等位基因变异,极大地影响疾病的进展或严重程度。尽管人类微生物组-营养-代谢物相互作用与 CVDs 的关联已得到充分证实,但肠道-心脏-口腔轴这一尚未探索的领域已成为一个关键的知识空白。此外,微生物组的关键作用及其与宿主遗传的复杂相互作用,加上与年龄相关的变化,在 MI 的发展中成为一个至关重要的领域。此外,性别或祖先差异影响疾病易感性和严重程度,这为死亡率增加的关联提供了重要的见解。在这里,我们旨在概述微生物组(口腔和肠道)与主要风险因素(烟草使用、饮酒、饮食、高血压、宿主遗传、性别和衰老)在 MI 发展中的相互作用以及治疗调节。

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