Circulating microrna-133a in Patients With Arterial Hypertension, Hypertensive Heart Disease, and Left Ventricular Diastolic Dysfunction

dc.contributor.authorKoval, S. M.
dc.contributor.authorSnihurska, I. O.
dc.contributor.authorYushko, K. O.
dc.contributor.authorMysnychenko, O. V.
dc.contributor.authorPenkova, M. Y.
dc.contributor.authorLytvynova, O. M.
dc.contributor.authorBerezin, A. E.
dc.contributor.authorLytvynov, V. S.
dc.contributor.authorКоваль, С. М.
dc.contributor.authorСнігурська, І. О.
dc.contributor.authorЮшко, К. О.
dc.contributor.authorМисниченко, О. В.
dc.contributor.authorПенькова, М. Ю.
dc.contributor.authorЛитвинова, О. М.
dc.contributor.authorБерезін, Олександр Євгенійович
dc.contributor.authorЛитвинов, В. С.
dc.date.accessioned2021-06-29T08:46:22Z
dc.date.available2021-06-29T08:46:22Z
dc.date.issued2020
dc.description.abstractThe aim of the work was to study the circulating microRNA-133a levels in blood plasma of patients with arterial hypertension (AH), hypertensive heart disease (HHD), and left ventricular (LV) diastolic dysfunction (DD). Materials and Methods: A total of 48 patients with grade 2–3 AH and HHD at the age of 52.23 ± 7.26 (23 patients had LV DD [main group] and 25 patients had normal LV diastolic function [comparison group]) and 21 practically healthy individuals of comparable gender and age were examined. Diagnosis of AH and HHD was carried out according to the 2018 ESC/ESH recommendations. LV DD was determined according to the 2016 ASE/EACVI recommendations. Plasma microRNA-133a level was obtained by polymerase chain reaction using the CFX96 Touch System (BioRad), ≪TaqMan microRNA Assay≫ and ≪TaqMan® Universal PCR Master Mix≫ reagent kits (Thermo Fisher Scientific, USA). Results: We have found that in patients from the main and comparison groups plasma microRNA-133a levels were significantly lower than in practically healthy individuals (0.094 [0.067, 0.147]) and (0.182 [0.102, 0.301]) vs. (0.382 [0.198,0.474]), p = 0.002 and p = 0.04, respectively. In all this among patients with AH, HHD, and LV DD, plasma microRNA-133a levels were significantly lower than in patients with AH, HHD, and normal diastolic function (p = 0.03). In the main and comparison groups there was a statistically significant negative relationship between plasma microRNA-133a level and left ventricular mass index (LVMI) (R = −0.40, p = 0.003 and R = −0.35, p = 0.04, respectively). Conclusions: The findings suggest the significant role of decreased microRNA-133a levels in blood plasma of patients with AH in the pathogenesis and development of both HHD and LV DD.uk_UK
dc.identifier.citationCirculating microrna-133a in Patients With Arterial Hypertension, Hypertensive Heart Disease, and Left Ventricular Diastolic Dysfunction / S. M. Koval, I. O. Snihurska, K. O. Yushko [et al.] // Frontiers in Cardiovascular Medicine. - 2020. - Vol. 7. - Ст. Article 104. - https://doi.org/10.3389/fcvm.2020.00104uk_UK
dc.identifier.urihttps://zsmu.rosbai.com/handle/123456789/14201
dc.language.isoenuk_UK
dc.subjectarterial hypertensionuk_UK
dc.subjecthypertensive heart diseaseuk_UK
dc.subjectmicroRNA-133auk_UK
dc.subjectleft ventricular diastolic dysfunctionuk_UK
dc.subjectepigeneticsuk_UK
dc.titleCirculating microrna-133a in Patients With Arterial Hypertension, Hypertensive Heart Disease, and Left Ventricular Diastolic Dysfunctionuk_UK
dc.typeArticleuk_UK

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