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Antihypertensive Therapy by ACEI/ARB Is Associated With Intestinal Flora Alterations and Metabolomic Profiles in Hypertensive Patients

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Specialty Cell Biology
Date 2022 Apr 11
PMID 35399511
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Abstract

Angiotensin-converting enzyme inhibitors and angiotensin receptor blockers (ACEI/ARB) are the first-line drugs for the treatment of essential hypertension (HTN), one of the most important risk factors for cardiovascular and cerebrovascular diseases. Intestinal flora and microbial metabolites have been demonstrated to play important roles in blood pressure (BP) regulation and HTN development. However, it remains elusive that intestinal bacteria and metabolites are associated with the protective effects of ACEI/ARB anti-hypertensive drugs against HTN. In this study, we evaluated the effect of ACEI/ARB on gut microbiome and metabolites in patients suffering from HTN. We performed 16S rRNA sequencing and fecal metabolomic analysis of 36 HTN patients placed on ACEI/ARB therapy and 19 newly diagnosed HTN patients with no history of anti-hypertensive treatment. Patients under medication treatment were further classified into well-controlled ( = 24) and poor-controlled ( = 12) groups according to their BP levels. The ACEI/ARB improved the intestinal microbiome of the HTN patients by reducing potentially pathogenic bacteria such as and and increasing beneficial bacteria such as . Moreover, ACEI/ARB therapy was correlated with significant metabolomic changes in the HTN patients, including progressively enhanced inositol from poor-controlled to well-controlled groups. The profiles of gut bacteria were linked to the production of metabolites, and inositol was negatively correlated with , , and . Our study suggests that ACEI/ARB modulates gut microbial composition and functions and alters microbial metabolites in HTN patients.

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References
1.
Hashemi Tari S, Sohouli M, Lari A, Fatahi S, Rahideh S . The effect of inositol supplementation on blood pressure: A systematic review and meta-analysis of randomized-controlled trials. Clin Nutr ESPEN. 2021; 44:78-84. DOI: 10.1016/j.clnesp.2021.06.017. View

2.
Dorman M, Short F . Genome watch: Klebsiella pneumoniae: when a colonizer turns bad. Nat Rev Microbiol. 2017; 15(7):384. DOI: 10.1038/nrmicro.2017.64. View

3.
Hu X, Li H, Zhao X, Zhou R, Liu H, Sun Y . Multi-omics study reveals that statin therapy is associated with restoration of gut microbiota homeostasis and improvement in outcomes in patients with acute coronary syndrome. Theranostics. 2021; 11(12):5778-5793. PMC: 8058718. DOI: 10.7150/thno.55946. View

4.
Pendleton J, Gorman S, Gilmore B . Clinical relevance of the ESKAPE pathogens. Expert Rev Anti Infect Ther. 2013; 11(3):297-308. DOI: 10.1586/eri.13.12. View

5.
Xu R, Wu B, Liang J, He F, Gu W, Li K . Altered gut microbiota and mucosal immunity in patients with schizophrenia. Brain Behav Immun. 2019; 85:120-127. DOI: 10.1016/j.bbi.2019.06.039. View