Serum miR-222 is independently associated with atrial fibrillation in patients with degenerative valvular heart disease

Degenerative valvular heart disease (DVHD), also 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. In the United States, the prevalence rates of DVHD is 0.86% in the adult population and 2.8% in people ≥ 75 years of age [1]. DVHD can lead to heart failure, arrhythmia, and even sudden death in the elderly [2‐5]. Its risk factors include high levels of von Willebrand factor, congenital abnormality, age, metabolic syndrome, elevated lipoprotein amounts, and the classical risk factors for atherosclerosis [5].

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]. The prevalence of AF is approximately 1–2% in the general population in developed countries [6, 7]. AF may lead to systemic embolization and heart failure [6, 7]. AF is an independent risk factor in patients with valve calcification [8].

Calcific aortic stenosis results from processes similar to atherosclerosis, including lipid accumulation and damage to endothelial cells (e.g., due to stress or radiation) that allows infiltration of lipids into the fibrosa; lipid infiltration and accumulation may recruit inflammatory cells (such as macrophages) into the aortic valve, and bioactive lipid species may be formed due to oxidation, which further promotes inflammation and mineralization of valve leaflets [5]. Inflammation is considered to be involved in the osteogenic processes leading to mineralization and calcification [9]. Matrix metalloproteinases (MMPs) are overexpressed, resulting in remodeling of valve tissue and the accumulation of disorganized fibrous tissue [9]. Various cytokines secreted by inflammatory cells, such as tumor necrosis factor (TNF)-α and interleukin (IL)-6, are involved in molecular pathways leading to mineralization and calcification [9].

Many studies have shown that microRNAs are involved in valve calcification [10, 11]. Studies also revealed that the expression levels of miR-125b and chemokine receptor type 4 (CCR4) are increased in patients with calcific aortic valve disease, suggesting that miRNA and inflammatory responses are important in the development and progression of valvular heart disease [12, 13]. A previous study reported that miR-222 is involved in inflammation-mediated vascular remodeling [14].

Nevertheless, studies assessing the relationship between microRNA-222 (miR-222) and DVHD are rare. The present study aimed to investigate the differences of miR-222, IL-6, high-sensitivity C-reactive protein (hs-CRP), and N-terminal pro-brain natriuretic peptide (NT-proBNP) levels in patients with DVHD with or without AF.

Inflammation is involved in the progression of DVHD. Meanwhile, miR-222 contributes to inflammation-mediated vascular remodeling, but its involvement in DVHD in relation to AF is unknown. Therefore, this study aimed to investigate the changes in miR-222, IL-6, hs-CRP, and NT-proBNP in patients with DVHD complicated with AF. The results suggest that serum miR-222, IL-6, hs-CRP, and NT-proBNP were associated with AF in patients with DVHD.

MiRNAs are endogenous, highly evolutionarily conserved, single-stranded, non-coding small RNAs [18, 19]. By binding to the 3′UTR regions of target mRNAs, miRNAs regulate gene expression to participate in the occurrence and development of various cellular biological processes such as apoptosis, angiogenesis, inflammation, and ischemic preconditioning [18, 19]. The expression levels of miRNAs vary greatly in different health and disease states, and are often tissue-specific. Detection of the levels of different miRNAs in blood, body fluids, and tissues can be used as a marker for the diagnosis of a given disease and/or a therapeutic target [20, 21]. Studies showed that miR-333 is involved in the development of atherosclerosis in acute coronary syndrome [22]. MiR-126 expression is lower in patients with heart failure and AF [23]. Meanwhile, miR-150 is a predictor of heart failure after myocardial infarction [24]. Blood miR-125, miR-126, miR-21, miR-29b, and miR-30b are downregulated in patients with DVHD [25]. The present study showed that the serum levels of miRNA-222, IL-6, hs-CRP, and NT-proBNP in patients with DVHD with AF were significantly higher compared with those of patients with DVHD without AF.

Next, multivariate logistic regression analysis was performed to assess mirNA-222, IL-6, HS-CRP and NT-proBNP levels for independent associations with DVHD complicated with AF. Of these, only mirNA-222 level was independently associated with DVHD complicated with AF. Other reports have demonstrated the roles of miRNAs in DVHD accompanied by AF. For example, the levels of miRNA-146b-5p and miRNA-155, which are known to be correlated with inflammation, are independently and positively associated with left atrium dimension and atrial fibrillation duration [26]. Another report suggested that miR-10b and miR-138–2, which are significantly increased in the left atrium of individuals with AF-associated rheumatic mitral valve disease (RMVD), are responsible for morphological and physiological phenotype differences between the left and right atria [27].

MiRNAs may participate in the AF regulation process through various mechanisms. For instance, miR-155-5p and miR-24-3p levels are greatly reduced in post-ablation AF patients compared with AF patients not administered ablation [28]. In addition, NO levels were much lower in the AF + group compared with the AF- group. In a swine model of AF, as targets of miR-155-5p and miR-24-3p, eNOS and NO had increased amounts with decreasing miR-155-5p and miR-24-3p amounts, indicating that the above miRNAs are involved in the pathogenesis of AF via eNOS and NO regulation [28]. Meanwhile, miR-21 was detected in atrial myocytes from patients in the sinus rhythm, with significantly greater expression in chronic atrial fibrillation myocytes [29]. In addition, miR-21 showed inverse correlations with α1c subunit of the calcium channel (CACNA1C) gene expression and I(Ca,L) density [29].

The present study also found that IL-6, hs-CRP, and NT-proBNP levels were positively correlated with miR-222 levels in all participants. These findings suggest that miRNA-222, IL-6, hs-CRP, and NT-proBNP might be involved in the exacerbation of DVHD accompanied by AF through the following potential mechanisms. Studies showed that valve degeneration is related to lipid deposition and inflammation [30]. In addition, miR-148a-3p was shown to be involved in the inflammatory response of the valve [31]. The present study found that miR-222, IL-6, and hs-CRP levels were significantly elevated in patients with DVHD, suggesting that inflammatory responses are involved in the development of degenerative valvular disease. Indeed, hs-CRP is a marker of low-grade systemic inflammation, and IL-6 is a proinflammatory cytokine [32, 33]. Investigation of the involvement of miRNAs in the regulation of heart aging through inflammatory responses showed that the miRNA let-7 inhibits angiotensin II-induced cardiomyopathy and fibrosis by inhibiting the expression of IL-6 and multiple collagens in the heart [34]. Patel et al. [35] found that changes in shear-sensitive miRNAs in aortic valve endothelial cells are involved in the development and progression of aortic valve diseases. Rathan et al. [36] showed that miRNA-214 is a shear-dependent miRNA that regulates key mechanosensitive genes related to aortic valve calcification, such as transforming growth factor (TGF)-β1. Animal experiments also showed that the IL-6 signal transduction pathway is involved in the mechanobiological response of aortic valve interstitial cells to promote aortic valve calcification [37]. Studies showed that RNAs affect valve calcification by regulating the levels of osteocalcin [38]. MiR-138 inhibits aortic valve calcification by inhibiting osteogenic differentiation of interstitial valve cells [39]. IL-6 expression is elevated in human calcific aortic valve disease, and phosphate-induced valve mineralization chiefly relies on IL-6 expression [40]. Studies showed that the expression of hypoxia-induced miR-210 is increased in peripheral plasma, monocytes, and skeletal muscle of rats with heart failure [41]. The levels of miRNA-222 in peripheral blood from patients with coronary artery stenosis are increased during dobutamine stress echocardiograms [42]. Therefore, miRNAs participate in DVHD through inflammatory responses, mechanical stress, calcification and osteogenesis, and oxidative stress. Of note, many of those miRNAs are also involved in AF [27‐29], and there is a possibility of synergistic effects among those involved in DVHD and AF. Additional transcriptome-wide studies are necessary to identify those relationships.

This study had limitations. First, the sample size was small, and only one miRNA was assessed. Further studies are necessary to examine the roles of miRNAs in DVHD. In addition, the panel of inflammatory markers was limited, and oxidative stress assessment and quantification of valve calcification were not performed. Finally, the clinical history of patients and DVHD severity were not taken into consideration, which might highly bias our findings. Therefore, previous myocardial infarction, stroke, chronic kidney disease and liver disease should be evaluated for their effects on miRNA-222, IL-6 and NT-proBNP.

Overall, miR222 and inflammatory responses may be involved in the exacerbation of DVHD by AF. Combined detection of miRNA-222, IL-6, and NT-proBNP could assist in the evaluation and clinical management of DVHD.