Department of Neurology, The Affiliated Hospital of Kangda College of Nanjing Medical University/The First People's Hospital of Lianyungang, Lianyungang, Jiangsu Province, China.
Department of Clinical Medicine, Xuzhou Medical University, Xuzhou, Jiangsu Province, China.
PLoS One. 2020 Sep 30;15(9):e0239856. doi: 10.1371/journal.pone.0239856. eCollection 2020.
Cyclooxygenase-2 (COX-2) is known to be involved in the pathogenesis of migraine, and some polymorphisms are known to affect the expression of COX-2. This retrospective case-control study aimed to explore the associations between the -765 G>C (rs20417), -1759 G>A (rs3218625), and -8473 C>T (rs5275) COX-2 polymorphisms and migraine in Chinese Han individuals. One hundred and ten unrelated Han Chinese patients with migraine and 108 healthy controls were recruited between 03/2014 and 08/2016 at the First Affiliated Hospital of Nanjing Medical University and the First People's Hospital of Lianyungang City. The genotypes of all polymorphisms in controls followed the Hardy-Weinberg equilibrium (P = 0.215, P = 0.884, and P = 0.689). There were differences in the genotype and allele distributions of the COX-2-1759G>A (Gly587Arg) polymorphism between the migraine and control groups (P = 0.038 and P = 0.040, respectively). Compared with the COX-2-1759AG genotype, GG genotype carriers had an increased risk of migraine (odds ratio (OR) = 8.720, 95% confidence interval (CI): 1.072-70.960, P = 0.038). The frequency of the COX-2-1759A allele in patients with migraine was significantly lower than the controls (OR = 0.119, 95%CI: 0.015-0.957, P = 0.040). Adjusted age and sex, a statistical difference was found in the dominant model of COX-2-1759 G>A (OR = 0.118, 95% CI 0.014 to 0.962, P = 0.046). No significant difference was detected regarding the -765G>C and -8473T>C polymorphisms between the two groups. The COX-2 1759A allele might be involved in the development of migraine in Chinese Han individuals, but this will have to be confirmed in large-scale studies.
环氧化酶-2(COX-2)已知与偏头痛的发病机制有关,一些多态性已知会影响 COX-2 的表达。本回顾性病例对照研究旨在探讨中国汉族人群 COX-2-765G>C(rs20417)、-1759G>A(rs3218625)和-8473C>T(rs5275)多态性与偏头痛之间的关联。2014 年 3 月至 2016 年 8 月,在南京医科大学第一附属医院和连云港市第一人民医院,招募了 110 名无亲缘关系的汉族偏头痛患者和 108 名健康对照者。对照组所有多态性的基因型均符合 Hardy-Weinberg 平衡(P=0.215、P=0.884 和 P=0.689)。偏头痛组和对照组 COX-2-1759G>A(Gly587Arg)多态性的基因型和等位基因分布存在差异(P=0.038 和 P=0.040)。与 COX-2-1759AG 基因型相比,GG 基因型携带者偏头痛的风险增加(比值比(OR)=8.720,95%置信区间(CI):1.072-70.960,P=0.038)。偏头痛患者 COX-2-1759A 等位基因的频率明显低于对照组(OR=0.119,95%CI:0.015-0.957,P=0.040)。调整年龄和性别后,在 COX-2-1759G>A 的显性模型中发现有统计学差异(OR=0.118,95%CI 0.014-0.962,P=0.046)。两组间 COX-2-765G>C 和-8473T>C 多态性无显著性差异。COX-2 1759A 等位基因可能参与中国汉族人群偏头痛的发生,但这需要在大规模研究中进一步证实。