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丝氨酸羟甲基转移酶 1 基因甲基化与缺血性脑卒中的关系。

The association between serine hydroxymethyl transferase 1 gene hypermethylation and ischemic stroke.

机构信息

Department of Cardiology, Yuyao people's Hospital, Ningbo, Zhejiang, China.

Department of Internal medicine, Yuyao people's Hospital, Ningbo, Zhejiang, China.

出版信息

Bosn J Basic Med Sci. 2021 Aug 1;21(4):454-460. doi: 10.17305/bjbms.2020.5188.

Abstract

This study aimed to determine the correlation between serine hydroxymethyl transferase 1 (SHMT1) gene methylation and ischemic stroke. A total of 202 age- and sex-matched individuals were included. Quantitative methylation-specific polymerase chain reaction (qMSP-PCR) was used to analyze the DNA methylation level. The plasma homocysteine (Hcy) concentration was much higher in ischemic cases than in controls (p = 0.009), while the high-density lipoprotein (HDL) levels in stroke cases were considerably lower than in controls (p = 0.005). A significantly higher level of SHMT1 methylation was observed in the ischemic strokes (58.82 ± 17.83%) compared to that in the controls (42.59 ± 20.76%, p < 0.001). The SHMT1 methylation level was strongly correlated with HDL concentration in the healthy controls (r = 0.517, p < 0.001), while the high plasma level of Hcy showed strong association with SHMT1 methylation in ischemic strokes (r = 0.346, p < 0.001). Receiver operating characteristic (ROC) analysis of curve indicated that SHMT1 methylation has been an acceptable indicator for ischemic stroke in female patients [all sexes, area under the curve (AUC) = 0.71, p < 0.001; male patients AUC = 0.62, p = 0.032; and female patients AUC = 0.79, p < 0.001] and in all ages (AUC = 0.71, p < 0.001). In our samples, DNA methylation levels of the STHMI gene were significantly correlated with ischemic stroke in Han Chinese. STHMI hypermethylation was significantly associated with the high Hcy concentration in ischemic stroke and had value as a potential indicator for female ischemic stroke.

摘要

本研究旨在探讨丝氨酸羟甲基转移酶 1(SHMT1)基因甲基化与缺血性脑卒中的相关性。共纳入 202 例年龄和性别匹配的个体。采用定量甲基化特异性聚合酶链反应(qMSP-PCR)分析 DNA 甲基化水平。缺血性脑卒中组的血浆同型半胱氨酸(Hcy)浓度明显高于对照组(p=0.009),而高密度脂蛋白(HDL)水平明显低于对照组(p=0.005)。与对照组(42.59±20.76%)相比,缺血性脑卒中患者的 SHMT1 甲基化水平显著升高(58.82±17.83%,p<0.001)。健康对照组中 SHMT1 甲基化水平与 HDL 浓度呈强相关性(r=0.517,p<0.001),而缺血性脑卒中患者中高血浆 Hcy 水平与 SHMT1 甲基化呈强相关性(r=0.346,p<0.001)。曲线的接收者操作特征(ROC)分析表明,SHMT1 甲基化可作为女性缺血性脑卒中患者的一个较好的诊断指标[所有性别,曲线下面积(AUC)=0.71,p<0.001;男性患者 AUC=0.62,p=0.032;女性患者 AUC=0.79,p<0.001],也可作为所有年龄组的诊断指标(AUC=0.71,p<0.001)。在我们的样本中,SHMT1 基因的 DNA 甲基化水平与汉族人群的缺血性脑卒中显著相关。SHMT1 过度甲基化与缺血性脑卒中高 Hcy 浓度显著相关,可能作为女性缺血性脑卒中的潜在标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/797b/8292870/0630ba24635a/BJBMS-21-454-g002.jpg

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