Sutherland Heidi G, Maher Bridget H, Rodriguez-Acevedo Astrid J, Haupt Larisa M, Griffiths Lyn R
Genomics Research Centre, Institute of Health and Biomedical Innovation, Queensland University of Technology, Brisbane, Qld, Australia.
Headache. 2014 Jul-Aug;54(7):1184-93. doi: 10.1111/head.12351. Epub 2014 Apr 7.
A number of observations have suggested that brain-derived neurotrophic factor (BDNF) plays a role in migraine pathophysiology. This study investigates whether variants in the BDNF gene are associated with migraine in an Australian case-control population.
BDNF has an important role in neural growth, development, and survival in the central nervous system and is an important modulator of central and peripheral pain responses. Variants in BDNF, in particular the functional Val66Met polymorphism (rs6265), have been found to be associated with a number of psychiatric disorders, cognitive function, and obesity. As BDNF has been found to be differentially expressed in a number of aspects related to migraine, we tested for association between single nucleotide polymorphisms (SNPs) in BDNF and migraine.
Five SNPs in the BDNF locus (rs1519480, rs6265, rs712507, rs2049046, and rs12273363) were genotyped initially in a cohort of 277 migraine cases, including 172 diagnosed with migraine with aura (MA) and 105 with migraine without aura (MO), and 277 age- and sex-matched controls. Three of these SNPs (rs6265, rs2049046, and rs12273363) were subsequently genotyped in a second cohort of 580 migraineurs, including 473 diagnosed with MA and 105 with MO, and 580 matched controls.
BDNF SNPs rs1519480, rs6265, rs712507, and rs12273363 were not significantly associated with migraine. However, rs2049046 showed a significant association with migraine, and in particular, MA in the first cohort. In the second cohort, although an increase in the rs2049046 T-allele frequency was observed in migraine cases, and in both MA and MO subgroups, it was not significantly different from controls. Analysis of data combined from both cohorts for rs2049046 showed significant differences in the genotypic and allelic distributions for this marker in both migraine and the MA subgroup.
This study confirmed previous studies that the functional BDNF SNP rs6265 (Val66Met) is not associated with migraine. However, we found that rs2049046, which resides at the 5' end of one the BDNF transcripts, may be associated with migraine, suggesting that further investigations of this SNP may be warranted.
多项观察结果表明,脑源性神经营养因子(BDNF)在偏头痛病理生理学中发挥作用。本研究调查BDNF基因变异是否与澳大利亚病例对照人群中的偏头痛相关。
BDNF在中枢神经系统的神经生长、发育和存活中起重要作用,是中枢和外周疼痛反应的重要调节因子。已发现BDNF变异,特别是功能性Val66Met多态性(rs6265),与多种精神疾病、认知功能和肥胖有关。由于已发现BDNF在与偏头痛相关的多个方面存在差异表达,我们测试了BDNF单核苷酸多态性(SNP)与偏头痛之间的关联。
最初在277例偏头痛患者队列中对BDNF基因座中的5个SNP(rs1519480、rs6265、rs712507、rs2049046和rs12273363)进行基因分型,其中包括172例诊断为有先兆偏头痛(MA)和105例无先兆偏头痛(MO)患者,以及277例年龄和性别匹配的对照。随后在第二个队列中对其中3个SNP(rs