Untargeted Metabolomics Provides Insight into the Mechanisms Underlying Resistant Hypertension
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Published:2019-03-14
Issue:1
Volume:26
Page:232-243
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ISSN:0929-8673
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Container-title:Current Medicinal Chemistry
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language:en
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Short-container-title:CMC
Author:
Wawrzyniak Renata1, Mpanga Arlette Yumba1, Struck-Lewicka Wiktoria1, Kordalewska Marta1, Polonis Katarzyna2, Patejko Małgorzata1, Mironiuk Monika1, Szyndler Anna2, Chrostowska Marzena2, Hoffmann Michał2, Smoleński Ryszard T.3, Kaliszan Roman1, Narkiewicz Krzysztof2, Markuszewski Michał J.1
Affiliation:
1. Department of Biopharmaceutics and Pharmacodynamics, Medical University of Gdansk, Al. Gen. J. Hallera 107, 80-416, Gdansk, Poland 2. Department of Hypertension and Diabetology, Medical University of Gdansk, Debinki 7c, 80-211 Gdansk, Poland 3. Department of Biochemistry, Medical University of Gdansk, Debinki 1, 80-211 Gdansk, Poland
Abstract
Background:
Resistant hypertension (RH) affects about 15-20% of treated hypertensive
patients worldwide. RH increases the risk of cardiovascular events such as myocardial
infarction and stroke by 50%. The pathological mechanisms underlying resistance to treatment
are still poorly understood.
Objective:
The main goal of this pilot study was to determine and compare plasma metabolomic
profiles in resistant and non-resistant hypertensive patients.
Methods:
We applied untargeted metabolomic profiling in plasma samples collected from 69
subjects with RH and 81 subjects with controlled hypertension. To confirm patients’ compliance
to antihypertensive treatment, levels of selected drugs and their metabolites were determined
in plasma samples with the LC-ESI-TOF/MS technique.
Results:
The results showed no statistically significant differences in the administration of
antihypertensive drug in the compared groups. We identified 19 up-regulated and 13 downregulated
metabolites in the RH.
Conclusion:
The metabolites altered in RH are linked to oxidative stress and inflammation,
endothelium dysfunction, vasoconstriction and cell proliferation. Our results may generate
new hypothesis about RH development and progression.
Funder
The Polish-Norwegian Research Fund European Union - project ICRC-ERA-HumanBridge European Regional Development Fund - Project FNUSA-ICRC Ministry of Science and Higher Education, Warsaw, Poland National Science Centre, Poland
Publisher
Bentham Science Publishers Ltd.
Subject
Pharmacology,Molecular Medicine,Drug Discovery,Biochemistry,Organic Chemistry
Reference32 articles.
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