TY - JOUR
T1 - Untargeted metabolomics provides insight into the mechanisms underlying resistant hypertension
AU - Wawrzyniak, Renata
AU - Mpanga, Arlette Yumba
AU - Struck-Lewicka, Wiktoria
AU - Kordalewska, Marta
AU - Polonis, Katarzyna
AU - Patejko, Małgorzata
AU - Mironiuk, Monika
AU - Szyndler, Anna
AU - Chrostowska, Marzena
AU - Hoffmann, Michał
AU - Smoleński, Ryszard T.
AU - Kaliszan, Roman
AU - Narkiewicz, Krzysztof
AU - Markuszewski, Michał J.
N1 - Funding Information:
The study was funded by the National Science Centre, Poland, allocated on the basis of the decision number 2012/07/E/NZ7/0441. This study was supported by the Ministry of Science and Higher Education, Warsaw, Poland (grant number 0042/IP1/2016/74) from budget resources for years 2016-2018. Krzysztof Narkiewicz is supported by European Regional Development Fund - Project FNUSA-ICRC (No. CZ.1.05/1.1.00/02.0123) and by the European Union - project ICRC-ERA-HumanBridge (No. 316345). The study was funded by The Polish-Norwegian Research Fund (Novel Biomarkers of Cardiovascular Risk Evaluation in Northern Europe — CARE NORTH, PNRF-213-AI-1/07).
Publisher Copyright:
© 2019 Bentham Science Publishers.
PY - 2019
Y1 - 2019
N2 - 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.
AB - 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.
KW - Biomarker candidates
KW - Liquid chromatography
KW - Mass spectrometry
KW - Metabolomics
KW - Multivariate analysis
KW - Resistant hypertension
UR - http://www.scopus.com/inward/record.url?scp=85063692865&partnerID=8YFLogxK
U2 - 10.2174/0929867324666171006122656
DO - 10.2174/0929867324666171006122656
M3 - Article
C2 - 28990522
AN - SCOPUS:85063692865
SN - 0929-8673
VL - 26
SP - 232
EP - 243
JO - Current Medicinal Chemistry
JF - Current Medicinal Chemistry
IS - 1
ER -