Department of Geriatrics, Tianjin NanKai Hospital, No. 6 Changjiang Road, Nankai District, Tianjin City, 300100, China.
Department of Neurology, Tianjin NanKai Hospital, Tianjin City, 300100, China.
BMC Cardiovasc Disord. 2021 Mar 24;21(1):150. doi: 10.1186/s12872-021-01960-4.
Atherosclerosis (AS) is a leading cause of vascular disease worldwide. MicroRNAs (miRNAs) play an essential role in the development of AS. However, the miRNAs-based biomarkers for the diagnosis of AS are still limited. Here, we aimed to identify the miRNAs significantly related to AS and construct the predicting model based on these miRNAs for distinguishing the AS patients from healthy cases.
The miRNA and mRNA expression microarray data of blood samples from patients with AS and healthy cases were obtained from the GSE59421 and GSE20129 of Gene Expression Omnibus (GEO) database, respectively. Weighted Gene Co-expression Network Analysis (WGCNA) was performed to evaluate the correlation of the miRNAs and mRNAs with AS and identify the miRNAs and mRNAs significantly associated with AS. The potentially critical miRNAs were further optimized by functional enrichment analysis. The logistic regression models were constructed based on these optimized miRNAs and validated by threefold cross-validation method.
WGCNA revealed 42 miRNAs and 532 genes significantly correlated with AS. Functional enrichment analysis identified 12 crucial miRNAs in patients with AS. Moreover, 6 miRNAs among the identified 12 miRNAs, were selected using a stepwise regression model, in which four miRNAs, including hsa-miR-654-5p, hsa-miR-409-3p, hsa-miR-485-5p and hsa-miR-654-3p, were further identified through multivariate regression analysis. The threefold cross-validation method showed that the AUC of logistic regression model based on the four miRNAs was 0.7308, 0.8258, and 0.7483, respectively, with an average AUC of 0.7683.
We identified a total of four miRNAs, including hsa-miR-654-5p and hsa-miR-409-3p, are identified as the potentially critical biomarkers for AS. The logistic regression model based on the identified 2 miRNAs could reliably distinguish the patients with AS from normal cases.
动脉粥样硬化(AS)是全球血管疾病的主要原因。 microRNAs(miRNAs)在 AS 的发展中起着至关重要的作用。然而,基于 miRNA 的 AS 诊断生物标志物仍然有限。在这里,我们旨在确定与 AS 显著相关的 miRNAs,并基于这些 miRNAs 构建预测模型,以区分 AS 患者和健康病例。
从基因表达综合数据库(GEO)的 GSE59421 和 GSE20129 中分别获得了 AS 患者和健康对照者血液样本的 miRNA 和 mRNA 表达微阵列数据。采用加权基因共表达网络分析(WGCNA)评估 miRNA 和 mRNAs 与 AS 的相关性,并确定与 AS 显著相关的 miRNA 和 mRNAs。进一步通过功能富集分析对潜在关键 miRNA 进行优化。基于这些优化的 miRNAs 构建逻辑回归模型,并通过三折交叉验证方法进行验证。
WGCNA 显示 42 个 miRNA 和 532 个基因与 AS 显著相关。功能富集分析确定了 12 个 AS 患者中关键的 miRNA。此外,通过逐步回归模型选择了 12 个 miRNA 中的 6 个 miRNA,其中包括 hsa-miR-654-5p、hsa-miR-409-3p、hsa-miR-485-5p 和 hsa-miR-654-3p,通过多元回归分析进一步确定。三折交叉验证方法显示基于 4 个 miRNA 的逻辑回归模型的 AUC 分别为 0.7308、0.8258 和 0.7483,平均 AUC 为 0.7683。
我们总共鉴定了 4 个 miRNA,包括 hsa-miR-654-5p 和 hsa-miR-409-3p,它们被认为是 AS 的潜在关键生物标志物。基于所鉴定的 2 个 miRNA 的逻辑回归模型可以可靠地区分 AS 患者和正常病例。