SCAPIS研究中肠道微生物组与24小时血压测量之间的关系。

IF 5.4 Q1 MEDICINE, RESEARCH & EXPERIMENTAL
Yi-Ting Lin, Sergi Sayols-Baixeras, Gabriel Baldanzi, Koen F Dekkers, Ulf Hammar, Diem Nguyen, Nynne Nielsen, Aron C Eklund, Georgios Varotsis, Jacob B Holm, H Bjørn Nielsen, Lars Lind, Göran Bergström, J Gustav Smith, Gunnar Engström, Johan Ärnlöv, Johan Sundström, Marju Orho-Melander, Tove Fall
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引用次数: 0

摘要

背景:越来越多的证据支持微生物群在高血压中的作用,这些证据来自实验研究和基于人群的研究。我们的目的是研究肠道微生物组的特定特征与24小时动态血压测量之间的关系。方法:通过粪便样本的鸟枪宏基因组测序确定肠道微生物种类和微生物功能与3695名参与者的24小时动态血压测量和来自瑞典心肺生物图像研究的2770名未服用抗高血压药物的参与者的多变量调整模型评估办公室血压的关系。结果:肠道微生物组α多样性与舒张压变异性呈负相关。此外,四种微生物与24小时血压特征中的至少一种有关。链球菌sp001556435与较高的收缩压相关,马氏无肠单胞菌和sp001916835与较低的收缩压相关,sp001916835与较低的舒张压相关,ER4 sp900317525与较低的收缩压变异性相关。此外,没有动态血压测量的亚样本的办公室血压数据重复了马西利肠单胞菌与收缩压和呼吸困难菌sp001916835与舒张压的关联。与24小时血压相关的物种与类似的代谢物模式有关。结论:在这项大型横断面分析中,肠道微生物组α多样性与舒张压变异性呈负相关,四种肠道微生物物种与24小时血压特征相关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The association between the gut microbiome and 24-h blood pressure measurements in the SCAPIS study.

Background: There is mounting evidence supporting the role of the microbiota in hypertension from experimental studies and population-based studies. We aimed to investigate the relationship between specific characteristics of the gut microbiome and 24-h ambulatory blood pressure measurements.

Methods: The association of gut microbial species and microbial functions, determined by shotgun metagenomic sequencing of fecal samples, with 24-h ambulatory blood pressure measurements in 3695 participants and office blood pressure was assessed in multivariable-adjusted models in 2770 participants without antihypertensive medication from the Swedish CArdioPulmonary bioImage Study.

Results: Gut microbiome alpha diversity was negatively associated with diastolic blood pressure variability. Additionally, four microbial species were associated with at least one of the 24-h blood pressure traits. Streptococcus sp001556435 was associated with higher systolic blood pressure, Intestinimonas massiliensis and Dysosmobacter sp001916835 with lower systolic blood pressure, Dysosmobacter sp001916835 with lower diastolic blood pressure, and ER4 sp900317525 with lower systolic blood pressure variability. Moreover, office blood pressure data from a subsample without ambulatory blood pressure measurements replicated the association of Intestinimonas massiliensis with systolic blood pressure and Dysosmobacter sp001916835 with diastolic blood pressure. Species associated with 24-h blood pressure were linked to a similar pattern of metabolites.

Conclusions: In this large cross-sectional analysis, gut microbiome alpha diversity negatively associates with diastolic blood pressure variability, and four gut microbial species associate with 24-h blood pressure traits.

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