Abstract

BackgroundInflammation is involved in the progression of degenerative valvular heart disease (DVHD). microRNA-222 (miR-222) contributes to inflammation-mediated vascular remodeling, but its involvement in DVHD in relation to atrial fibrillation (AF) is unknown. This study aimed to investigate the changes in miR-222, interleukin (IL)-6, high-sensitivity C-reactive protein (hs-CRP), and N-terminal pro-brain natriuretic peptide (NT-proBNP) in patients with DVHD complicated with AF.MethodsThis was a case control study of patients with DVHD who were hospitalized at the Geriatrics Department of the Affiliated Huai’an Hospital of Xuzhou Medical University between 01/2017 and 08/2018. The participants were grouped according to the presence of AF, and serum miR-222, IL-6, hs-CRP, and NT-proBNP levels were compared.ResultsThere were fifty-two participants (28 males) in the DVHD with AF group, aged 60–80 years (73.0 ± 5.9 years). Sixty participants (31 males) were included in the DVHD without AF group, aged 60–80 years (71.9 ± 6.92 years). There were no significant differences in age, sex, body mass index, fasting blood glucose, triglycerides, cholesterol, and blood pressure between the two groups. The serum levels of miRNA-222, IL-6, hs-CRP, and NT-proBNP in DVHD patients were significantly higher in those with AF compared with the non-AF group (all P < 0.05). Correlation analyses revealed that IL-6, hs-CRP, and NT-proBNP levels were positively correlated with miR-222 levels in all patients (IL-6: r = 0.507, P < 0.01; hs-CRP: r = 0.390, P < 0.01; NT-proBNP: r = 0.509, P < 0.01).ConclusionsSerum miR-222 was independently associated with AF in patients with DVHD.

Highlights

  • Inflammation is involved in the progression of degenerative valvular heart disease (DVHD). microRNA-222 contributes to inflammation-mediated vascular remodeling, but its involvement in DVHD in relation to atrial fibrillation (AF) is unknown

  • The present study aimed to investigate the differences of miR-222, IL-6, high-sensitivity C-reactive protein, and N-terminal pro-brain natriuretic peptide (NTproBNP) levels in patients with DVHD with or without AF

  • There were no significant differences in age, sex, body mass index (BMI), fasting blood glucose, TG, total cholesterol (TC), systolic blood pressure (SBP), and diastolic blood pressure (DBP) between the two groups

Read more

Summary

Introduction

Inflammation is involved in the progression of degenerative valvular heart disease (DVHD). microRNA-222 (miR-222) contributes to inflammation-mediated vascular remodeling, but its involvement in DVHD in relation to atrial fibrillation (AF) is unknown. Inflammation is involved in the progression of degenerative valvular heart disease (DVHD). MicroRNA-222 (miR-222) contributes to inflammation-mediated vascular remodeling, but its involvement in DVHD in relation to atrial fibrillation (AF) is unknown. Degenerative valvular heart disease (DVHD), known as calcific aortic valve disease, represents a common heart disease in the elderly and is characterized by the deposition of a large amount of calcium in a cardiac valve. DVHD can lead to heart failure, Atrial fibrillation (AF) is a common supraventricular tachyarrhythmia caused by uncoordinated atrial activation and associated with an irregularly irregular ventricular response [6, 7]. Causes of atrial fibrillation include an underlying structural heart disease, metabolic disorders, endocrine diseases, and certain medications [6, 7]. AF is an independent risk factor in patients with valve calcification [8]

Objectives
Methods
Results
Discussion
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call