Dipartimento di Medicina Molecolare e Biotecnologie Mediche, Università di Napoli Federico II, 80131 Naples, Italy.
CEINGE-Biotecnologie Avanzate, 80145 Naples, Italy.
Medicina (Kaunas). 2021 Jul 17;57(7):723. doi: 10.3390/medicina57070723.
: ischemic stroke (IS) is among the most frequent causes of death worldwide; thus, it is of paramount relevance to know predisposing factors that may help to identify and treat the high-risk subjects. :we tested nine variants in genes involved in thrombotic pathway in 282 patients that experienced IS and 87 that had transient ischemic attacks (TIA) in comparison to 430 subjects from the general population (GP) of the same geographic area (southern Italy). We included cases of young and child IS to evaluate the eventual differences in the role of the analyzed variants. : we did not observe significant differences between TIA and the GP for any of the variants, while the allele frequencies of methylene-tetrahydrofolate reductase (MTHFR) C677T, beta-fibrinogen -455G>A and factor (FXIII) V34L were significantly higher in patients with IS than in the subjects from the GP. No significant interaction was observed with sex. : the present data argue that some gene variants have a role in IS and this appears to be an interesting possibility to be pursued in large population studies to help design specific strategies for IS prevention.
: 缺血性脑卒中 (IS) 是全球最常见的死亡原因之一;因此,了解可能有助于识别和治疗高危人群的易患因素至关重要。: 我们在 282 名经历过 IS 的患者和 87 名经历过短暂性脑缺血发作 (TIA) 的患者中检测了涉及血栓形成途径的 9 个基因变体,并与来自同一地理区域(意大利南部)的 430 名普通人群 (GP) 进行了比较。我们纳入了年轻和儿童 IS 病例,以评估分析变体的潜在差异。: 我们没有观察到任何变体在 TIA 和 GP 之间存在显著差异,而亚甲基四氢叶酸还原酶 (MTHFR) C677T、β-纤维蛋白原 -455G>A 和因子 (FXIII) V34L 的等位基因频率在 IS 患者中明显高于 GP 中的受试者。没有观察到性别之间的显著相互作用。: 目前的数据表明,一些基因变体在 IS 中起作用,这似乎是一个有趣的可能性,可以在大规模人群研究中进一步探讨,以帮助制定 IS 预防的具体策略。