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TBXAS1 基因多态性与中国汉族人群代谢综合征缺血性脑卒中风险相关。

TBXAS1 Gene Polymorphism Is Associated with the Risk of Ischemic Stroke of Metabolic Syndrome in a Chinese Han Population.

机构信息

The Key Laboratory of Cardiovascular Remodeling and Function Research, Chinese Ministry of Education, Chinese National Health Commission and Chinese Academy of Medical Sciences, the State and Shandong Province Joint Key Laboratory of Translational Cardiovascular Medicine, Qilu Hospital of Shandong University, Jinan, Shandong, China.

Department of Geriatric Medicine, Qilu Hospital of Shandong University, Key Laboratory of Cardiovascular Proteomics of Shandong Province, Jinan, China.

出版信息

Dis Markers. 2022 Jul 25;2022:9717510. doi: 10.1155/2022/9717510. eCollection 2022.

Abstract

OBJECTIVE

To investigate the association between thromboxane A synthase 1 () gene polymorphism and metabolic syndrome (MS) and explore whether gene polymorphism could act as biomarkers in MS and its components or whether it could play a role in MS-related damage.

METHODS

A total of 3072 eligible subjects were obtained, of which 1079 cases were controls and 1993 cases were MS patients. Subjects were followed up for 5 years, and the endpoint were recorded. The gene polymorphism of was detected by using the Sequenom MassArray method.

RESULTS

Significant differences were observed in ischemic stroke and NC_000007.14: g.139985896C>T ( < 0.05). The incidence of ischemic stroke was significantly higher in T allele carriers than in C ( < 0.05). C allele was the protective factor of the onset of ischemic stroke. There were negative interactions between C allele and waist circumference (WC), systolic blood pressure (SBP), diastolic blood pressure (DBP), triglycerides (TG), high-density lipoprotein cholesterol (HDL-C), and fasting plasma glucose (FPG).

CONCLUSION

These findings suggest that NC_000007.14: g.139985896C>T was related to the incidence of ischemic stroke in the whole and MS population, and individuals who carry the C allele have a reduced risk of ischemic stroke, which may be used as a promising biomarker of disease risk in patients with MS.

摘要

目的

探讨血栓素 A 合酶 1()基因多态性与代谢综合征(MS)的关系,探讨基因多态性是否可作为 MS 及其各组分的生物标志物,或是否可在 MS 相关损伤中发挥作用。

方法

共纳入 3072 例符合条件的研究对象,其中 1079 例为对照组,1993 例为 MS 患者。对患者进行 5 年随访,记录终点事件。采用 Sequenom MassArray 法检测的基因多态性。

结果

在缺血性脑卒中与 NC_000007.14:g.139985896C>T 处(<0.05)存在显著差异。T 等位基因携带者的缺血性脑卒中发生率明显高于 C(<0.05)。C 等位基因是缺血性脑卒中发病的保护因素。C 等位基因与腰围(WC)、收缩压(SBP)、舒张压(DBP)、甘油三酯(TG)、高密度脂蛋白胆固醇(HDL-C)、空腹血糖(FPG)之间存在负交互作用。

结论

这些发现提示 NC_000007.14:g.139985896C>T 与全人群和 MS 人群的缺血性脑卒中发生率相关,携带 C 等位基因的个体发生缺血性脑卒中的风险降低,其或可作为 MS 患者疾病风险的有前途的生物标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9ec8/9343182/94dec6123259/DM2022-9717510.001.jpg

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