Association of CALCA and RAMP1 gene polymorphisms with migraine in a Chinese population

被引:0
|
作者
An, Xingkai [1 ]
Yu, Zhenzhen [1 ]
Fang, Jie [1 ]
Lin, Qing [1 ]
Lu, Congxia [1 ]
Ma, Qilin [1 ]
Qu, Hongli [1 ]
机构
[1] Xiamen Univ, Affiliated Hosp 1, Dept Neurol, Xiamen, Peoples R China
基金
中国国家自然科学基金;
关键词
Migraine; CALCA; RAMP1; CGRP; polymorphism; China; CGRP; ANTAGONISTS;
D O I
暂无
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background & Objective: The calcitonin gene-related peptide (CGRP) has a central role in the pathogenesis of migraine, but variations in CGRP-related genes, including the calcitonin gene-related polypeptide-alpha (CALCA) gene and the receptor activity modifying 1 (RAMP1) gene, have not been found to link with migraine in Australian population. The goals of this study were to determine whether variants in the two genes are related to migraine in Chinese population. Methods: Using a case-control approach, rs3781719 and rs145837941 in the CALCA gene and rs3754701 and rs7590387 at the RAMP1 locus was analyzed in a cohort of 504 migraine cases and 529 ethnically matched controls. Genotyping was performed using Sequenom MALDI-TOF mass spectrometry iPLEX platform. Results: The CALCA gene rs145837941 variant was not found in migraine or control group. No significant difference in genotypic and allelic distribution was observed in the other three polymorphisms between migraine cases and controls. All the three SNPs were also not selected as significant factors that independently contributed to susceptibility to migraine in multivariate analysis. In the subgroup analysis, the CALCA rs3781719 seemed to be a significant risk for migraine with aura, but was not statistically significant after FDR correction. Moreover, there was no synergistic relationship between the three SNPs in the multifactor dimensionality reduction analysis for explore locus-locus interactions. Conclusion: Our data suggested that variants in CALCA gene and RAMP1 gene were not associated with migraine in the Han-Chinese population.
引用
收藏
页码:221 / 225
页数:5
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