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沙特心血管疾病患者 Toll 样受体 4 多态性。

Toll-like receptor 4 polymorphisms in Saudi population with cardiovascular diseases.

机构信息

Groupe de Recherche en Écologie Buccale, Faculté de Médecine Dentaire, Université Laval, Québec, QC, Canada.

Genome Research Chair, Department of Biochemistry, College of Science King Saud University, Riyadh, Kingdom of Saudi Arabia.

出版信息

Mol Genet Genomic Med. 2019 Sep;7(9):e852. doi: 10.1002/mgg3.852. Epub 2019 Jul 21.

Abstract

BACKGROUND

Toll-like receptors play a substantial role in innate immunity and the effects of TLR4 genetic variants on cardiovascular diseases are still largely unknown. Therefore, we aimed to investigate the effects of TLR4 polymorphisms on cardiovascular diseases risk in the Saudi population.

METHODS

Three tag single-nucleotide polymorphisms (rs2770150, rs10759931, and rs4986790) in TLR4 were studied on 222 unrelated patients with cardiovascular diseases and 190 healthy volunteers.

RESULTS

We found that, in patients over 60 years old, the frequency of the TT genotype in rs2770150 and the variant allele G in rs10759931 were higher compared to the control group. Based on gender, the genotype frequency of rs2770150 increases the risk for cardiovascular diseases in female patients by 3.6-fold. The allele frequency for the G allele of rs10759931 increased the risk for CVDs in male patients by more than 1.5-fold. Furthermore, the genotype frequency of rs2770150 had a significant association with cardiovascular diseases in patients without hypertension and G allele of rs10759931 significantly increased the risk of cardiovascular diseases in patients that smoked. After Bonferroni correction only patients without hypertension showed significant risk of CVD with rs2770150.

CONCLUSION

A deeper understanding of the genetic variability of TLR4 will enable us to better identification of biomarkers for early detection and prognosis, and also enhance the decision-making process of treatments for cardiovascular diseases.

摘要

背景

Toll 样受体在先天免疫中发挥重要作用,TLR4 基因变异对心血管疾病的影响尚不清楚。因此,我们旨在研究 TLR4 多态性对沙特人群心血管疾病风险的影响。

方法

研究了 TLR4 中的三个标签单核苷酸多态性(rs2770150、rs10759931 和 rs4986790),共纳入 222 例心血管疾病患者和 190 例健康志愿者。

结果

我们发现,在 60 岁以上的患者中,rs2770150 的 TT 基因型和 rs10759931 的变异等位基因 G 的频率高于对照组。根据性别,rs2770150 的基因型频率使女性患者患心血管疾病的风险增加 3.6 倍。rs10759931 的 G 等位基因的等位基因频率使男性患者患 CVD 的风险增加了 1.5 倍以上。此外,rs2770150 的基因型频率与无高血压的患者的心血管疾病显著相关,而 rs10759931 的 G 等位基因则显著增加了有吸烟史的患者心血管疾病的风险。经 Bonferroni 校正后,只有无高血压的患者 rs2770150 与 CVD 有显著相关性。

结论

深入了解 TLR4 的遗传变异性将使我们能够更好地识别生物标志物,用于早期检测和预后,也能增强心血管疾病治疗的决策过程。

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