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13 May 2026 : Clinical Research  

[In Press] Association of miR-133a With Microalbuminuria in Patients With Resistant Arterial Hypertension and Chronic Kidney Disease

Robert Tomasz Błaszczyk ORCID logo1ABCDEF, Alicja Petniak ORCID logo2AC, Jacek Bogucki ORCID logo3CD, Janusz Kocki ORCID logo2AC, Łukasz Wiśniowski1AD, Andrzej Głowniak ORCID logo1ADG

DOI: 10.12659/MSM.952860

Med Sci Monit In Press; DOI: 10.12659/MSM.952860  

Available online: 2026-05-13, In Press, Corrected Proof

Publication in the "In-Press" formula aims at speeding up the public availability of the pending manuscript while waiting for the final publication. The assigned DOI number is active and citable. The availability of the article in the Medline, PubMed and PMC databases as well as Web of Science will be obtained after the final publication according to the journal schedule

Abstract

BACKGROUND
MicroRNAs (miRNAs) are important post-transcriptional regulators of gene expression and have emerged as potential biomarkers of cardiovascular and renal diseases. Resistant arterial hypertension (RAH) is frequently associated with chronic kidney disease (CKD) and microalbuminuria, reflecting early microvascular damage. However, the relationship between microRNA expression and microalbuminuria in patients with RAH remains insufficiently researched. This study aimed to evaluate the expression of selected miRNAs in patients with RAH, with and without CKD, and to assess their association with urinary albumin excretion.
MATERIAL AND METHODS
This cross-sectional study included 115 patients with RAH, of whom 42 (36.5%) had coexisting CKD. The expression levels of 11 selected miRNAs were assessed in peripheral blood mononuclear cells using quantitative real-time polymerase chain reaction. Urinary albumin-to-creatinine ratio (UACR) was used to assess albuminuria. Correlations between microRNA expression and UACR were analyzed using Spearman’s rank correlation.
RESULTS
In patients with RAH and microalbuminuria, a statistically significant positive correlation was observed between hsa-miR-133a expression and UACR (Spearman’s r=0.38, P=0.024, n=35). No significant correlations were found between urinary albumin excretion and other analyzed microRNAs or in patients without microalbuminuria.
CONCLUSIONS
Expression of hsa-miR-133a was associated with urinary albumin excretion in patients with RAH and microalbuminuria. The findings suggest that hsa-miR-133a may be a potential noninvasive biomarker of microalbuminuria and early renal microvascular injury in a high-risk hypertensive population; however, further longitudinal studies are required to clarify the prognostic value and clinical utility of miR-133a in this patient population.

Keywords: Hypertension; MicroRNAs; Kidney Failure, Chronic

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Dinah V. Parums ORCID logo

DOI: 10.12659/MSM.952454

Med Sci Monit 2026; 32:e952454

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Medical Science Monitor eISSN: 1643-3750
Medical Science Monitor eISSN: 1643-3750