Department of Zoology, University of Jammu, Jammu, India.
Department of Human Genetics, Govt. Gandhi Memorial Science College, Cluster University of Jammu, Jammu, India.
Eur Neurol. 2023;86(1):55-62. doi: 10.1159/000527271. Epub 2022 Nov 25.
Migraine is a neurovascular disorder and is clinically characterized by episodic attacks of mild to severe headaches. Due to the involvement of multiple environmental and genetic factors, it has become a much more complex neurological condition to understand. Apart from the environmental variables, a plethora of genes have been implicated, and one such example is ESR1. The present study was focused to find out the association of two important polymorphisms, namely, PvuII and XbaI of the ESR1 with migraine in the population of Jammu and Kashmir (UT).
The PCR-RFLP genotyping method was utilized to detect PvuII and XbaI polymorphism, and the result was confirmed by statistical analysis.
Although we did not find a signification association of ESR-PvuII polymorphism with migraine susceptibility {OR: 1.14 at 95% CI [0.76-1.71] (p value 0.5)}, a strong association was found with the clinical subtype of migraine; migraine with aura (MA) {OR: 2.014 at 95% CI [1.069-3.792] (p value 0.028)}. Furthermore, a significant association of ESR-XbaI polymorphism was observed with migraine {OR: 1.908 at 95% CI [1.252-2.907] (p value 0.002) and its both clinical subtypes; migraine without aura (MO) {OR: 1.870 at 95% CI [1.186-2.950] (p value 0.006)} and MA {OR: 2.014 at 95% CI [1.069-3.792] (p value 0.028)}.
In conclusion, ESR1-XbaI polymorphism is significantly associated with migraine risk including both subtypes (MA and MO) in the North Indian population of Jammu.
偏头痛是一种神经血管性疾病,临床上以间歇性轻度至重度头痛发作为特征。由于涉及多种环境和遗传因素,它已成为一种更加复杂的神经疾病。除了环境变量外,还有大量的基因被牵连在内,其中一个例子是 ESR1。本研究旨在探讨 ESR1 基因的两个重要多态性,即 PvuII 和 XbaI 与查谟和克什米尔(UT)人群中偏头痛的关联。
利用 PCR-RFLP 基因分型方法检测 ESR1 的 PvuII 和 XbaI 多态性,并通过统计分析进行验证。
虽然我们没有发现 ESR-PvuII 多态性与偏头痛易感性之间有显著关联(OR:95%CI[0.76-1.71]的 1.14倍(p 值 0.5)),但与偏头痛的临床亚型偏头痛伴先兆(MA)之间存在很强的关联(OR:95%CI[1.069-3.792]的 2.014 倍(p 值 0.028))。此外,还观察到 ESR-XbaI 多态性与偏头痛之间存在显著关联(OR:95%CI[1.252-2.907]的 1.908 倍(p 值 0.002)及其两个临床亚型;偏头痛无先兆(MO)(OR:95%CI[1.186-2.950]的 1.870 倍(p 值 0.006))和 MA(OR:95%CI[1.069-3.792]的 2.014 倍(p 值 0.028))。
总之,ESR1-XbaI 多态性与偏头痛风险显著相关,包括查谟和克什米尔北部人群的偏头痛和 MA 两种亚型。