Blood microRNA 202-3p associates with the risk of essential hypertension by targeting soluble ST2

Abstract

MicroRNA (miR)-202-3p has attracted a great deal of attention in the fields of oncology, gynecology, and metabolic disorders. However, its role in cardiovascular diseases remains to be clarified. We previously found that disruption of miR-202-3p mediated regulation of expression of soluble (s)ST2, a decoy receptor for interleukin (IL)-33, promotes essential hypertension (EH). In the present study, we first measured miR-202-3p expression levels in the blood of 182 EH cases and 159 healthy controls using TaqMan assays. miR-202-3p levels were shown to be significantly higher in EH cases than controls (fold change = 3.58, P<0.001). Logistic regression analysis revealed that higher miR-202-3p expression was associated with an increased occurrence of EH (adjusted odds ratio (OR): 1.57; 95% confidence interval (CI), 1.36–1.82; P<0.001). Addition of miR-202-3p to traditional risk factors showed an additive prediction value for EH. Further functional experiments indicated that miR-202-3p could be induced by angiotensin II (Ang II) and inhibited by Ang II-triggered soluble ST2 (sST2) expression in a negative feedback manner. Moreover, blood miR-202-3p levels were negatively correlated with sST2 expression in vivo. Our study shows that blood miR-202-3p levels were significantly associated with the occurrence of EH. These findings indicate that miR-202-3p exerts a protective role against EH by antagonizing the induction of sST2 by Ang II.

Introduction

Hypertension is a chronic disease characterized by a continuous increase in arterial blood pressure. It is also a critical risk factor for mortality and morbidity in several cardiovascular diseases including stroke, heart failure, and kidney failure [1]. According to a World Health Organization report of 2017, 23.2% of Chinese adults suffer from hypertension, so ∼245 million individuals are affected in China [2]. Essential hypertension (EH), as the most common disease type, accounts for ∼95% of cases. Hypertension pathogenesis is a multifactorial process involving the interaction of genetic and environmental factors. Besides traditional risk factors such as a high-salt diet, smoking, alcohol, and obesity, 30–50% of blood pressure variations can be attributed to genetic factors.

microRNAs (miRNAs) are a class of endogenous non-coding RNAs of 22 nucleotides in length that are involved in the post-transcriptional regulation of target genes by interacting with the 3′ untranslated region (3′ UTR) of mRNAs. As epigenetic factors, miRNAs have received increasing attention in the occurrence and progression of diseases. Moreover, in recent decades, several population-based research and animal model studies have been conducted to explore the differential expression profiles of hypertension-associated miRNAs. Their findings suggested that miRNAs are not only involved in multiple key steps of the onset and development of EH [3–5], but that they could also be used to predict disease risk and severity as novel biomarkers [6–8].

Peripheral blood contains large numbers of white blood cells, platelets, and red blood cells. Previous studies have suggested that changes in the counts, species, and intracellular gene expression profiles of leukocytes are closely related to hypertension development [9,10]. Therefore, work has focused on the association between blood cell miRNAs and EH occurrence as well as underlying biological mechanisms. Torres-Paz et al. showed that the up-regulation of miR-33a-5p expression in monocytes was significantly positively correlated with carotid intima thickness and increased the risk of hypertension in a Mexican population [11]. Additionally, Yin et al. reported that the expression of miR-128 in peripheral blood was gradually up-regulated during hypertension progression, which aggravated myocardial injury through inhibiting c-Met [12]. Moreover, Parthenakis et al. found that miR-208b and miR-133a were significantly positively correlated with urinary albumin excretion levels in newly diagnosed hypertension patients, suggesting that they could serve as a new generation of biomarkers for improved monitoring of end organ damage in hypertension [13]. Therefore, we proposed that the identification of EH-associated miRNA in peripheral blood cells and the exploration of underlying mechanisms could provide new perspectives in the diagnosis, treatment, and prevention of this disease.

Emerging evidence suggests that miR-202-3p could function as a suppressor for a series of tumors, including osteosarcoma, colorectal cancer, gastric cancer, cervical cancer, and thyroid cancer [14,15]. By controlling a variety of target genes such as cyclin D1, γ-catenin, and bcl-2, miR-202-3p plays an essential role in multiple physiological and pathogenic processes of tumor progression including cell proliferation, invasion, and apoptosis. It has also been reported to be involved in various metabolic and cardiovascular diseases. For example, Fornari et al. found that miR-202-3p regulated Ccr7 and cd247, interfered with immune homeostasis, and led to the occurrence of type 1 diabetes [16]. Recently, Wu et al. showed that miR-202-3p overexpression alleviated myocardial ischemia and reperfusion injury by activating the transforming growth factor β-1/Smads pathway and protecting against myocardial infarction and fibrosis [17].

In 2017, we conducted a case–control study to explore the association between genetic variants in the interleukin (IL)-33/ST2 pathway and the risk of hypertension and found that a common polymorphism within the 3′ UTR of the ST2 gene interrupted the regulation of soluble (s)ST2 expression by miR-202-3p and promoted the occurrence of EH [18]. Because the IL-33 decoy receptor soluble ST2 (sST2) is widely recognized as a risk factor for hypertension [19,20], we hypothesized that the inhibition of sST2 by miR-202-3p was critical for the onset and development of EH. However, the etiological and pathological role of miR-202-3p in EH remained unclear. In the present study, we first conducted a case–control study to validate the association between blood cell levels of miR-202-3p and the occurrence of EH. Then, to investigate the pathological role of miR-202-3p in EH, we analyzed the effects of miR-202-3p on sST2 expression both in vitro and in vivo.

Methods

Study design and population

The 182 EH cases for miRNA detection were consecutively recruited from the Second Affiliated Hospital of Nanchang University in Nanchang City, Jiangxi province, China between November 2016 and August 2017. Hypertension was diagnosed as average SBP ≥ 140 mmHg, and/or average diastolic blood pressure (DBP) ≥ 90 mmHg, and/or self-reported current treatment for hypertension with antihypertensive drugs. A total of 159 control subjects were from the same community as the patients. Control subjects showed SBP < 140 mmHg, DBP < 90 mmHg, and had never been treated for hypertension. Blood pressure was measured according to reported guidelines [21]. People participating in the physical examination at the Second Affiliated Hospital of Nanchang University were recruited and frequency matched by age and sex with patients, with determined to be free of EH and peripheral atherosclerotic arterial disease by medical history and clinical examinations. Five milliliters of fresh vein blood samples were collected from each participant with EDTA-anticoagulant tubes. The plasma and blood cells were separated by centrifugation at 2000×g for 10 min at 4°C, and then stored at −80°C until use. The questionnaires were used to collect general characteristics and results of clinical biochemistry tests for all participants by trained interviewers. The study protocol conformed to the ethical guidelines of the 1975 Declaration of Helsinki and was approved by the ethics committee of the Second Affiliated Hospital of Nanchang University, and all participants provided written informed consent.

Total RNA isolation

For miRNA detection in blood samples, approximately 200 μl of blood was used to extract total RNAs using the mirVana PARIS miRNA Isolation Kit (Ambion1556) following the manufacturer’s protocol. For gene expression detection in cultured cells, total RNAs were isolated using TRIzol reagent (Invitrogen) following the manufacturer’s instructions.

qRT-PCR assays

miRNA expression was detected as previously described [22]. In brief, input RNAs were reverse transcribed (RT) using the TaqMan miRNA Reverse Transcription Kit (Applied BioSystems, Foster City, CA) following the manufacturer’s protocol. RT products were diluted 1:5 and subjected to qPCR in triplicate using the TaqMan miRNA Assay Kit (Applied BioSystems, Foster City, CA) according to the manufacturer’s protocol. miRNA expression levels were normalized to U6b and calculated using the equation 2^−ΔC_t, where ΔC_t = cycle threshold (C_t) (miRNA) − C_t (U6b).

For gene expression analysis, first strand cDNA was obtained using SuperS High Capacity cDNA Reverse Transcription Kit (Applied BioSystems). Quantitative PCR was conducted to detect gene expressions using PowerUp™ SYBR™ Green Master Mix (Applied BioSystems). The mRNA levels were normalized to β-actin mRNA levels. The primers for the genes were as follows: β-actin (F: 5′-CCTGGCACCCAGCACAAT-3′, R: 5′-GCCGATC CACACGGAGTACT-3′); and sST2 (F: 5′-GGCACACCGTAAGAC TAAGTAG-3′; R: 5′-CAATTTAAGCAGCAGAGAAGCTCC-3′).

Chemicals, cell culture and transfection

Human acute monocytic leukemia cell line THP-1 cells, purchased from the type culture collection of the Chinese Academy of Sciences (Shanghai, China), were maintained in RPMI-1640 medium (Gibco) supplemented with 10% fetal bovine serum (FBS), sodium pyruvate and GlutaMax. Angiotensin II (Ang II) was purchase from Sigma–Aldrich Chemical Reagent Co., Ltd (St. Louis, Missouri, U.S.A.). miRNA mimics and inhibitor were synthesized by Ruibo Bio Co., Ltd. (Guangzhou, China) and transfected into cells alone or with the reporter plasmids using Lipofectamine 3000 (Invitrogen) in accordance with the manufacturer’s protocol. All experiments were conducted with cells at a logarithmic stage of growth curve.

Biological variable determination

The levels of biological variables such as total cholesterol (TC), triglyceride (TG), and fasting blood glucose (FBG) etc. were measured by standard laboratory procedures at the Department of Clinical Laboratory, The Second Affiliated Hospital of Nanchang University.

Statistical analysis

The general characteristics of cases and controls are presented as mean ± standard deviation (SD), median with interquartile range (IQR) or number with percentage. Comparison of the differences was conducted by Student’s t test, Mann–Whitney U test, or the Chi-square test depending on the distribution of data. The difference in circulating miR-202-3p levels between cases and controls was examined by Student’s t test. The odds ratios (ORs) and 95% confidence intervals (CIs) were calculated to indicate the association of miR-202-3p expression with the occurrence of EH by unconditional logistic regression model, with an adjustment of traditional risk factors including age, sex, smoking, drinking, TC, fasting glucose (FG), and family history of hypertension. The ability for miR-202-3p to discriminate EH cases from controls was analyzed by receiver operating characteristic (ROC) curves and reclassification analysis in two models. The baseline model was composed of traditional risk factors, and the extended model incorporated miR-202-3p expression with traditional risk factors. Correlations between miRNA expression and clinical parameters were analyzed by the Pearson or Spearman correlation tests. All statistical analyses were performed using SPSS 12.0 software (Statistical Package for the Social Sciences, Chicago, IL, U.S.A.). A value of P<0.05 was considered significant (two-tailed).

Results

General characteristics of the study population

General characteristics of the population are shown in Table 1. Sex ratios of case and control groups were similar, but the age (59–72 years), creatinine (65.81, 101.23), homocysteine (11.64, 18.35), uric acid (300.51, 481.51), body mass index (BMI, 25.14 ± 3.64), and alcohol consumption (20.2%) of EH patients were significantly higher than the healthy control group (P<0.05). In contrast, the levels of TC (4.42 ± 1.17 mmol/l), high-density lipoprotein cholesterol (HDL-c; 1.05 ± 0.27 mmol/l), low-density lipoprotein cholesterol (LDL-c; 2.81 ± 1.05 mmol/l), and a history of hypertension (18.5%) were significantly lower than those in the control group (P<0.05), possibly because of the application of cholesterol-lowering medications in this population. No significant differences were found for the other variables between the two groups.

Table 1. General characteristics of the study population.

Variables	Control (n=159)	EH (n=182)	P-value
Age, years	60 (50, 67)	64 (59, 72)	0.0011
Male, %	55.3	52.2	0.5612
FG, mmol/l	5.12 (4.80, 5.63)	5.19 (4.77, 5.90)	0.3761
TC, mmol/l	5.24 ± 0.98	4.42 ± 1.17	<0.0013
TG, mmol/l	1.26 (0.91, 1.84)	1.25 (1.00, 1.73)	0.5961
HDL-c, mmol/l	1.25 ± 0.29	1.05 ± 0.27	<0.0013
LDL-c, mmol/l	3.31 ± 0.84	2.81 ± 1.05	<0.0013
Creatinine	69.35 (59.60, 80.11)	79.28 (65.81, 101.23)	<0.0011
Homocysteine	12.17 (10.66, 15)	13.86 (11.64, 18.35)	0.0021
Uric acid	323.20 (282.73, 395.72)	381.94 (300.51, 481.51)	<0.0011
PLT (×109/l)	212.92 ± 55.18	205.74 ± 66.01	0.2843
PDW, %	13.4 (11.8, 15.3)	12.8 (11.5, 14.88)	0.2431
MPV, fl	11.00 (10.3, 11.9)	10.90 (10.23, 11.80)	0.6241
PCT	0.24 ± 0.05	0.23 ± 0.06	0.1243
BMI	23.58 ± 3.06	25.14 ± 3.64	<0.0013
miR-202-3p	−1.71 ± 2.27	0.13 ± 1.94	<0.0013
Smoking, %	22.3	18.5	0.3942
Drinking, %	8.9	20.2	0.0042
Family history of hypertension, %	29.9	18.5	0.0152

Data are expressed as mean ± SD, median (25th, 75th quartiles) or percentages.

Abbreviations: MPV, mean platelet volume; PCT, plateletcrit; PDW, platelet distribution width; PLT, blood platelet count.

¹Mann–Whitney U test for the differences between EH patients and controls.

²Chi-square test for the difference in the distribution frequencies between EH patients and controls.

³Student’s t test for the difference between EH patients and controls.

Association between miR-202-3p blood levels and EH

As shown in Figure 1, the level of miR-202-3p in peripheral blood cells was significantly higher in EH patients than in controls (log-transformed expression levels relative to U6b, 0.13 ± 1.94 vs. –1.71 ± 2.27; P<0.001). Logistic regression analysis indicated that higher levels of miR-202-3p were associated with an increased risk of EH (adjusted OR: 1.57; 95% CI: 1.36−1.82; P<0.001; Table 2) after adjusting for age, sex, smoking, drinking, BMI, TC, FG, and a history of hypertension.

Figure 1. Expression levels of miR-202-3p in EH patients and control subjects.

The expression of miR-202-3p was detected in 159 patients and 168 control subjects. Relative expression levels were normalized to U6b and then log 2-transformed. The whiskers of the plots represent the 2.5–97.5 percentiles. ***, P<0.001, miR-202-3p expression in EH patients vs. controls.

Table 2. Association of the expression level of miR-202-3p with EH.

Variables	OR (95% CI)1	P-value
Age	1.04 (1.01–1.07)	0.007
Male	0.54 (0.27–1.08)	0.083
Smoking	1.20 (0.53–2.71)	0.669
Drinking	0.40 (0.16–1.01)	0.053
BMI	1.20 (1.10–1.31)	<0.001
TC	0.48 (0.36–0.64)	<0.001
FG	1.14 (0.94–1.40)	0.192
Family history of hypertension, %	1.59 (0.81–3.10)	0.176
miR-202-3p	1.57 (1.36–1.82)	<0.001

¹By logistic regression analysis adjusted with age, sex, smoking, drinking, BMI, TC, FG, and family history of hypertension.

Diagnostic value of miR-202-3p

As shown in Table 3, the area under the ROC curve was similar between the baseline model (0.77; 95% CI, 0.71–0.82; P<0.001) and the combined miR-202-3p prediction model (0.84; 95% CI: 0.79–0.88; P<0.001). The net reclassification improvement (NRI) and integrated discrimination improvement (IDI) were calculated to determine the ability of miRNA to reclassify patients misclassified by the baseline model. The results showed that miR-202-3p was able to reclassify a significant portion of patients with an NRI of 94.3% (95% CI: 75.0–113.5; P<0.001) and an IDI of 0.131 (95% CI: 0.094–0.167; P<0.001).

Table 3. AUC, NRI, and IDI calculations for miR-202-3p.

Variables	miR-202-3p	P-value
Baseline model AUC (95% CI)	0.77 (0.71, 0.82)	<0.0001
Extended model AUC (95% CI)	0.84 (0.79, 0.88)	<0.0001
NRI, % (95% CI)	94.3 (75.0, 113.5)	<0.0001
IDI, (95% CI)	0.131 (0.094, 0.167)	<0.0001

AUC calculations are based on a multivariate logistic regression analysis including age, sex, smoking, drinking, diabetes mellitus, TG and family history of hypertension (baseline model) or the addition of miR-202-3p (extended model). Abbreviation: AUC, area under the ROC curve.

Correlation between miR-202-3p expression and clinical variables

Conventional risk factors including smoking, drinking, and a history of hypertension contribute to the occurrence of EH. Therefore, we next analyzed the correlation between miR-202-3p and various clinical variables. As shown in Table 4, blood levels of miR-202-3p were significantly positively correlated with male sex (r = 0.114, P=0.036), drinking (r = 0.115, P=0.036), and BMI (r = 0.14, P=0.011). It is also widely accepted that lipid and glucose metabolism play critical roles in the development of EH. Our findings suggested that blood miR-202-3p levels were significantly negatively correlated with those of TC (r = −0.127, P=0.021) and HDL-c (r = −0.15, P=0.006). Moreover, miR-202-3p was significantly positively correlated with creatinine (r = 0.115, P=0.034), uric acid (r = 0.115, P=0.034), and homocysteine (r = 0.186, P=0.006) and negatively correlated with platelet count in EH patients (r = −0.108, P=0.048). No significant correlations were found with other variables.

Table 4. Correlation analysis between miR-202-3p expression and clinical variables in combined population.

Variables	r	P-value
Age	0.002	0.9711
Sex	0.114	0.0361
Smoking	−0.06	0.271
Drinking	0.115	0.0361
Family history of hypertension %	−0.011	0.8461
TG	0.055	0.3221
TC	−0.127	0.0212
HDL-c	−0.15	0.0062
LDL-c	−0.09	0.1042
FG	0.038	0.4951
BMI	0.14	0.0112
Creatinine	0.115	0.0341
Uric acid	0.115	0.0341
Homocysteine	0.186	0.0061
MPV	0.09	0.1011
PCT	−0.095	0.0842
PDW	0.078	0.1591
PLT	−0.108	0.0482

Abbreviations: MPV, mean platelet volume; PCT, plateletcrit; PDW, platelet distribution width; PLT, blood platelet.

¹Spearman correlation test.

²Pearson correlation test.

miR-202-3p inhibits sST2 expression induced by Ang II

It is widely accepted that vascular inflammation contributes greatly to the pathogenesis of EH [23]. To reveal the underlying mechanism by which miR-202-3p is involved in EH pathogenesis, we applied the prohypertensive reagent Ang II to human THP-1 macrophage cells to induce an inflammatory response. As shown in Figure 2B, the endogenous expression of miR-202-3p in THP-1 cells was gradually up-regulated by Ang II in a dose-dependent manner. Because we previously found that sST2 was controlled by miR-202-3p [18]. We next examined the effects of miR-202-3p on sST2 expression in the Ang II-induced monocytic inflammatory response. Figure 2A shows that the expression of sST2 increased sharply after Ang II stimulation, and that this could be abrogated by miR-202-3p transfection (Figure 2C).

Figure 2. miR-202-3p inhibits sST2 expression induced by Ang II.

Human macrophage THP-1 cells were seeded into six-well plate and starved overnight. After that, cells were treated with different concentrations of Ang II (0, 0.1, 1 and 10 μM) for 24 h, respectively. After that, cells were harvested to analyze the expression of sST2 (A) and miR-202-3p (B). The mRNA levels were normalized to β-ACTIN mRNA and the levels of miRNA were normalized to U6b. All data were expressed as mean ± SD and the differences of gene expression between groups treated with different doses of ang II were examined by Student’s t test. *P<0.05, **P<0.01, ***P<0.005 vs untreated control. (C) THP-1 cells were seeded into six-well plate and transfected with miR-202-3p mimic or negative control mimic (NC). At 24 h post transfected, cells were further stimulated with 10 μM Ang II for another 24 h. After that, cells were collected to analyze the expression of sST2. The difference of gene expression between groups transfected with miR-202-3p and negative control was examined by Student’s t test. **P<0.01 vs untreated control, *P<0.05 vs negative control mimic. All data represent three independent experiments.

Blood cell levels of miR-202-3p were negatively correlated with sST2 expression in PBMCs

To validate the regulation of sST2 by miR-202-3p in vivo, we examined the correlation between blood levels of miR-202-3p and sST2 expression in PBMCs from 30 healthy controls. As shown in Figure 3, miR-202-3p levels were significantly negatively correlated with the expression of sST2 (r = –0.768, P<0.001).

Figure 3. Blood levels of miR-202-3p were negatively correlated with sST2 expression in PBMCs.

Human fresh vein blood samples from 30 healthy controls were collected and centrifuged to remove plasma. Then, the remnants were mixed with TRIzol LS reagent immediately. Total RNA was extracted to monitor the levels of miR-202-3p and sST2 expression by Quantitative PCR. The correlation of miR-202-3p levels with sST2 expression were examined by Pearson correlation test.

Discussion

In the present study, we proposed a negative feedback mechanism mediated by miR-202-3p against EH and obtained the following supporting evidence. First, our large sample case–control study found that higher miR-202-3p levels of blood cells were associated with an increased occurrence of EH. ROC curve and reclassification analysis indicated that the combination of miR-202-3p with traditional risk factors improved the predictive value of EH risk. Then, we showed that the expression of both sST2 and miR-202-3p could be induced by Ang II in a dose-dependent manner and that miR-202-3p overexpression inhibited the up-regulation of sST2 triggered by Ang II. Further, an in vivo assay suggested that miR-202-3p levels were negatively correlated with sST2 expression in the peripheral blood cells of 30 healthy controls. Collectively, our results suggest that miR-202-3p is involved in the development of EH partially by down-regulating sST2 expression via a feedback manner.

Systemic and local inflammation are both known to play an important role in the pathogenesis of EH. IL-33 is a newly discovered member of the IL-1 family that induces a Th2-type immune response by interacting with the ST2 receptor on cell membranes [24]. The ST2 gene encodes four isomers: sST2, ST2L, ST2V, and ST2LV, of which sST2 acts as a decoy receptor for IL-33, blocking the IL-33/ST2 signaling pathway by binding to IL-33, and inhibiting Th2-type inflammatory immune responses [25,26]. IL-1RAcP, another gene in this pathway, determines the affinity between IL-33 and ST2 [27]. In recent years, multiple pieces of evidence have shown that the IL-33/ST2 pathway has a crucial function in the pathogenesis of EH. The relationship between sST2 and hypertension has attracted particular attention. Ho et al. found that increased plasma concentrations of sST2 were significantly associated with EH risk [28], while Yin et al. suggested that sST2 plasma levels could be used as a biomarker for EH risk prediction [29].

In the present study, we revealed that blood cell levels of miR-202-3p were significantly increased in EH patients compared with controls and that higher levels were associated with an increased risk of EH, and addition of miR-202-3P to the traditional risk factor model increased the prediction probability. Further functional analysis suggested an underlying mechanism involving the exertion of anti-hypertensive effects by miR-202-3p partially through the suppression of sST2 in vascular inflammation. This is in-line with our previous study that indicated that the disruption of sST2 expression regulation by miR-202-3p contributed significantly to EH development [18]. To the best of our knowledge, this study documented a significant risk predicting value of miR-202-3p for the occurrence of EH for the first time. Although past studies have focused on the anti-tumor role of miR-202-3p, our study and others’ suggested that miR-202-3p played a critical role in the development of diverse cardiovascular diseases [17,18].

Gene annotation enrichment analysis for potential targets of miR-202-3p suggested that it might be implicated in cardiovascular and metabolic diseases (data not shown). We also conducted a population-based study and cell experiments to determine the etiological role of miR-202-3p in EH development. Our findings suggested that higher blood levels of miR-202-3p associated with an increased risk of EH and that sST2 is a critical target for miR-202-3p to exert anti-hypertensive effects. However, sST2 might not be the only target of miR-202-3p in EH pathogenesis. For example, the target genes CCR7 and CD247 were shown to be involved in the regulation of immune inflammatory cell function, contributing to end organ damage in hypertension [30,31]. Moreover, TRPM6, an identified target of miR-202-3p, encodes a transient receptor potential ion channel that plays an important role in the regulation of vascular tone and blood pressure [32,17], while MALAT-1, a long noncoding RNA targeted by miR-202-3p, was involved in vascular remodeling and promoted hypertension [33,34]. To the best of our knowledge, this study is the first to illustrate a mechanistic link between miR-202-3p and EH. However, additional efforts should be made to comprehensively reveal the mechanism by which miR-202-3p influences EH development.

As we all know, high plasma level of uric acid and homocysteine both contribute greatly to EH pathogenesis [35,36]. Notably, we found miR-202-3p expression was positively correlated with uric acid and homocysteine (Table 4), inconsistent with that higher expression of miR-202-3p could be detected in EH patients (Figure 1). Wainwright et al. have indicated that miR-202-3p transcription was directly controlled by a transcription factor SOX9 [37]. Hyperhomocysteinemia and hyperuricemia both could cause an induction of SOX9 expression [38,39]. Thus, we suggest the SOX9-miR-202-3p-sST2 signaling axis might be critical for the development of hypertension complicated by hyperuricemia and hyperhomocysteinemia and our study will focus on it in next step.

miR-202-3p regulates the proliferation, apoptosis, and function of Sertoli cells and plays a critical role in spermatogenesis [40]. Higher expression of miR-202-3p could be detected in males. We speculated the levels of miR-202-3p might affect the incidence of hypertension. Thus, the expressions of miR-202-3p in PBMCs in our population were examined. We failed to detect higher expression of miR-202-3p in both male patients and total males, probably because of small sample size. Even in the controls group, the levels of miR-202-3p in peripheral blood cells were significantly higher in females than in males (log-transformed expression levels relative to U6B, −1.10 ± 2.33 vs. –2.20 ± 2.10, P=0.002).

The present study has a number of limitations. First, miRNAs often exert their effects synergistically. Thus, systematically screening all IL-33/ST2 pathway-targeting miRNAs could help determine the pathomechanism of EH and improve the prediction efficiency. Second, the effect of miR-202-3p in the progression of EH should be evaluated in future clinical studies. Finally, the biological consequence of miR-202-3p depletion on blood pressure variation and end organ damage should be monitored using spontaneous hypertensive rat models.

In summary, our study showed that blood levels of miR-202-3p increased in EH patients and were associated with EH. Further functional analyses suggested that miR-202-3p suppressed sST2 expression in a feedback manner both in vitro and in vivo. Thus, miR-202-3p appears to exert an anti-hypertensive role but more efforts are required to reveal the underlying mechanisms.

Abbreviations

Ang II

angiotensin II

bcl-2

B-cell lymphoma-2

BMI

body mass index

CI

confidence interval

C_t

cycle threshold

DBP

diastolic blood pressure

EH

essential hypertension

FG

fasting glucose

HDL-c

high-density lipoprotein cholesterol

IDI

integrated discrimination improvement

IL

interleukin

IL-1RAcP

interleukin-1 receptor accessory protein

IQR

interquartile range

MALAT-1

metastasis-associated lung adenocarcinoma transcript 1

miR

microRNA

NRI

net reclassification improvement

OR

odds ratio

PBMC

peripheral blood mononuclear cell

qRT-PCR

real-time quantitative reverse transcription polymerase chain reaction

ROC

receiver operating characteristic

SBP

systolic blood pressure

SOX9

SRY-box transcription factor 9

Sst2

soluble ST2

ST2

suppression of tumorigenicity 2

TC

total cholesterol

TRPM6

potential cation channel subfamily M member 6

3′ UTR

3′ untranslated region

Competing Interests

The authors declare that there are no competing interests associated with the manuscript.

Funding

This work was supported by the Natural National Scientific Foundation of China [grant numbers 81602407, 81700372]; the Science and Technology Plan of Health Commission of Jiangxi Province [grant number 20185210]; the Medical Scientific Research Foundation of Guangdong Province of China [grant number B2019020]; the Health, Science and Technology Planning Project of Shantou city (2017); and the Science and Technology Planning Project of Shantou Municipal (medical).

Author Contribution

The study design was performed by Lu Li. Human sample collection was performed by Xinlei Yang and Zuozhong Yu. The experiments were conducted by Danrong Zhong and Yudan Xie. The data collection and analysis were carried out by Dangui Zhang and Lu Li. The draft of the manuscript was written by Lu Li and Fangqin Wu. The manuscript content revision was performed by Xinghua Jiang and Yanqing Wu. The final version approval of the manuscript was done by Fangqin Wu. Fangqin Wu takes responsibility for the integrity of the data analysis.