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Updated: Jan 27, 2026

Identification of Circular RNAs using RNA Sequencing
Published on: November 14, 2019
Up-regulation of circular RNA hsa_circ_0037909 promotes essential hypertension
Xingjie Bao1, Xin He1, Shuying Zheng1
1Department of Preventative Medicine, Zhejiang Provincial Key Laboratory of Pathological and Physiological Technology, Medicine School of Ningbo University, Ningbo, China.
Insights
Circular RNAs like hsa_circ_0037909 and microRNA hsa-miR-637 show altered expression in essential hypertension (EH). Their combined analysis may serve as a novel biomarker for early EH diagnosis.
Area of Science:
- Genetics
- Molecular Biology
- Cardiovascular Disease Research
Background:
- Essential hypertension (EH) is a prevalent condition with limited understanding of its genetic basis.
- Circular RNAs (circRNAs), known for their stability, are implicated in molecular regulation and may play a role in EH.
Purpose of the Study:
- To investigate the role of specific circRNAs and microRNAs in the pathogenesis of essential hypertension.
- To evaluate the potential of these molecules as diagnostic biomarkers for EH.
Main Methods:
- Quantitative reverse transcription PCR (qRT-PCR) was used to analyze circRNA and microRNA expression in blood and endothelial cells.
- A case-control study involving 48 pairs of matched participants was conducted.
- Statistical analyses included t-tests, chi-squared tests, logistic regression, and ROC curve analysis.
Main Results:
- Hsa_circ_0037909 expression was significantly higher, while hsa-miR-637 expression was significantly lower in EH patients compared to controls.
- Logistic regression identified hsa-miR-637, hsa_circ_0037909, HDL, and serum creatinine as significant factors in EH.
- The combined analysis of hsa_circ_0037909 and hsa-miR-637 demonstrated excellent diagnostic potential via ROC curve analysis.
Conclusions:
- The combination of hsa_circ_0037909 and hsa-miR-637 shows promise as a significant biomarker for the early detection of essential hypertension.
- Hsa_circ_0037909 may influence EH development by affecting serum creatinine or LDL levels.
Aims:
Essential hypertension (EH) is a high prevalence disease facing a public health challenge. People were little known about the genetics of diagnosing the cause of EH. Circular RNAs that have a continuous cycle of covalent closure, without affected by RNA exonuclease, and are more stable and hard to degrade may involve into the molecule regulation mechanism of EH as an important biomedical.
Methods:
qRT-PCR was used to analyze circRNAs in total volume of human blood and the induced human aortic endothelial cells (HAECs) and human umbilical vein endothelial cells (HUVECs). Our case-control study was involved with 48 pairs of case controls with sex and age (±3 years) match. We conducted t test, Pearson's χ2 test, and receiver operating characteristics (ROC) curve analysis for the corresponding analysis.
Results:
The expression level of hsa_circ_0037909 in EH patients was significantly higher than that in the healthy controls (P = 0.007), and the expression level of hsa-miR-637 in EH patients was significantly lower in than that in the healthy controls (P = 0.039); the same result appears in the HAECs and HUVECs. Hsa-miR-637 (adjusted P = 0.018), hsa_circ_0037909 (adjusted P = 0.005), HDL (adjusted P = 0.024), and serum creatinine (adjusted P = 0.014) were brought into the model which performed logistic regression analysis. The combination of two RNAs was excellent (P < 0.001) through ROC curve analysis. Hsa_circ_0037909 was significantly positively correlated with serum creatinine (P < 0.001) and low-density lipoprotein (LDL) (P = 0.017).
Conclusions:
Our findings suggested that the combination of hsa_circ_0037911 and hsa-miR-637 may be a significant important biomarker for early diagnosis of EH. Hsa_circ_0037909 may affect serum creatinine or LDL leading to the formation of EH.
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