基础医学与临床 ›› 2020, Vol. 40 ›› Issue (4): 451-455.

• 研究论文 • 上一篇    下一篇

SHMT1基因启动子甲基化与缺血性卒中相关

胡景岑1, 李链1, 王淑瑜1, 许磊1, 杨德伦1, 韩丽媛1*, 许国栋1,2*   

  1. 1.宁波大学 浙江省病理生理学技术研究重点实验室, 浙江 宁波 315211;
    2.宁波市医疗中心李惠利医院病案室, 浙江 宁波 315211
  • 收稿日期:2019-10-15 修回日期:2020-01-02 出版日期:2020-04-05 发布日期:2020-04-06
  • 通讯作者: *hanliyuan@nbu.edu.cn; 18815281025@163.com
  • 基金资助:
    国家自然科学基金(81402745);浙江省自然科学基金(LY17H260002);浙江省大学生科技创新活动计划(2018R405092)

Association between SHMT1 gene promoter methylation and ischemic stroke

HU Jing-cen1, LI Lian1, WANG Shu-yu1, XU Lei1, YANG De-lun1, HAN Li-yuan1*, XU Guo-dong1,2*   

  1. 1. Zhejiang Key Laboratory of Pathophysiology Technological Research, Ningbo University, Ningbo 315211;
    2. Medical Record Statistics Room, Ningbo Medical Center Lihuili Hospital, Ningbo 315211, China
  • Received:2019-10-15 Revised:2020-01-02 Online:2020-04-05 Published:2020-04-06
  • Contact: *hanliyuan@nbu.edu.cn; 18815281025@163.com

摘要: 目的 探究丝氨酸羟甲基转移酶(SHMT1)基因甲基化与缺血性卒中的关系。方法 采用甲基化特异性实时定量PCR测定290名健康对照组和141例缺血性卒中病例组(卒中组)的SHMT1甲基化水平。结果 卒中组SHMT1甲基化水平为24.87% (16.97~35.46)高于对照组的6.58 % (2.43~15.14) (P<0.05)。在调整相关危险因素后, SHMT1甲基化是卒中的危险因素(OR=1.051, 95% CI=1.034~1.068)。受试者工作特征曲线下面积为0.804,95% CI=0.760~0.849 (P<0.01)。在对照组发现尿酸与SHMT1甲基化相关(rs=0.17,P<0.01),在卒中组发现三酰甘油与SHMT1甲基化相关 (rs=0.18,P<0.05)。SHMT1甲基化表达与mRNA的表达呈负相关(r=-0.472,P<0.01)。结果 缺血性卒中患者中SHMT1基因启动子呈高甲基化状态, SHMT1低表达,且SHMT1高甲基化是卒中的危险因素。

关键词: 缺血性卒中, 丝氨酸羟甲基转移酶1, DNA启动子, 甲基化

Abstract: Objective To explore the relationship between serine hydroxymethyltransferase (SHMT1) gene methylation and ischemic stroke patients. Methods The quantitative methylation-specific PCR was used to measure the level of SHMT1 promoter methylation in 290 healthy control individuals and 141 ischemic stroke patients. Results The results showed that the SHMT1 methylation level in the stroke group was 24.87(16.97~35.46), higher than that in the control group 6.58(2.43~15.14) (P<0.05). After adjusting for relevant risk factors, SHMT1 methylation was a risk factor for stroke(OR=1.051, 95% CI= 1.034~1.068). Area under the curve was 0.804, 95% CI=0.760~0.849(P<0.01). The level of uric acid was associated with SHMT1 methylation in the control group(rs=0.17, P<0.01), and the level of TG was associated with SHMT1 methylation in the stroke group(rs=0.18, P<0.05). SHMT1 methylation expression was negatively correlated with mRNA expression(r=-0.472, P<0.01). Conclusions The SHMT1 gene is more methylated and results in low expression in ischemic stroke patients, so SHMT1 hypermethylation is a risk factor for stroke.

Key words: ischemic stroke, serine hydroxymethyltransferase 1, DNA promoter, methylation

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