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J Nephropathol. 2023;12(2): e18393.
doi: 10.34172/jnp.2022.18393

Scopus ID: 85151365626
  Abstract View: 1186
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Original Article

Determinants of left ventricular diastolic dysfunction in hemodialysis patients

Dorin Dragoş 1,2 ORCID logo, Delia Timofte 3 ORCID logo, Dorin Ionescu 1,4* ORCID logo, Andra-Elena Balcangiu-Stroescu 3,5 ORCID logo, Maria Iuliana Ghenu 1,2 ORCID logo, Ileana Adela Vacaroiu 6,7 ORCID logo, Maria Mirabela Manea 8,9 ORCID logo

1 Medical Semiology and Nephrology Discipline, Bucharest Emergency University Hospital, Faculty of Medicine, “Carol Davila” University of Medicine and Pharmacy, Bucharest, Romania
2 1st Internal Medicine Clinic, Bucharest University Emergency Hospital, Bucharest, Romania
3 Dialysis Department, Bucharest University Emergency Hospital, Bucharest, Romania
4 Nephrology Clinic, University Emergency Hospital Bucharest, Romania
5 Discipline of Physiology, Faculty of Dental Medicine, “Carol Davila” University of Medicine and Pharmacy, Bucharest, Romania
6 Nephrology Discipline, Emergency Clinical Hospital “Sf.Ioan”, Faculty of Medicine, “Carol Davila” University of Medicine and Pharmacy, Bucharest, Romania
7 Nephrology and Dialysis Clinic, “Sf.Ioan” Emergency Clinical Hospital, Bucharest, Romania
8 Neurology Discipline, National Institute of Neurology and Neurovascular Diseases, Faculty of Medicine, “Carol Davila” University of Medicine and Pharmacy, Bucharest, Romania
9 National Institute of Neurology and Neurovascular Diseases, Bucharest, Romania
*Corresponding Author: Corresponding author: Dorin Ionescu, Email: , Email: dorin.ionescu@umfcd.ro

Abstract

Introduction: Chronic kidney disease (CKD) induces changes in the myocardium known to influence morbidity and mortality, most severe in patients with end stage renal disease.

Objectives: The working hypothesis was that in patients on chronic hemodialysis the prevalence of left ventricular diastolic dysfunction is correlated with the inflammatory, oxidative, metabolic, nutritional, and atherosclerotic status.

Patients and Methods: An observational study was performed on 51 patients (age 59.76 ± 13.24 years) on hemodialysis treatment. Transthoracic cardiac ultrasound was conducted to evaluate LVDD. The burden of cardiac and arterial atherosclerosis was evaluated by cardiac ultrasound (aortic and mitral valve calcifications), vascular ultrasound (carotid and femoral atheroma plaques, common carotid intima-media thickness), and by abdominal radiography (aortic calcification score). Demographic and anthropometric parameters were determined. Blood samples were used to determine laboratory parameters reflecting the inflammatory, oxidative, and metabolic/nutrition status.

Results: LVDD is positively correlated with the serum level of C-reactive protein (CRP) (P=0.04), the total antioxidant capacity of the serum (P=0.04), the presence (P=0.022) and number (P=0.04) of femoral plaques, the aortic calcification score (P=0.02), aortic valve stenosis (P=0.037), aortic annulus calcifications (P=0.02) and mitral valve calcifications (P=0.041). After the removal of the main confounder, degenerative aortic stenosis, only the associations with serum total antioxidant capacity (P=0.04) and aortic calcification score (P= 0.02) maintain their statistical significance.

Conclusion: LVDD is positively correlated with inflammation and oxidative stress markers and with the severity of aortic calcification.


Implication for health policy/practice/research/medical education:

In patients on chronic hemodialysis, the prevalence of LVDD is positively correlated with inflammation and oxidative stress markers and with the severity of aortic calcification. The purpose of designing therapeutic strategies is to prevent or slow the course of LVDD, thereby influencing the cardiovascular and general outcomes of these patients.

Please cite this paper as: Dragoş D, Timofte D, Ionescu D, Balcangiu-Stroescu AE, Ghenu MI, Vacaroiu IA, Manea MM. Determinants of left ventricular diastolic dysfunction in hemodialysis patients. J Nephropathol. 2023;12(2):e18393. DOI: 10.34172/jnp.2022.18393.

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Submitted: 04 Jul 2022
Accepted: 23 Aug 2022
ePublished: 03 Sep 2022
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