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This study investigates whether variants in the \u003Cjats:styled-content style=\"fixed-case\">BDNF\u003C\u002Fjats:styled-content> gene are associated with migraine in an \u003Cjats:styled-content style=\"fixed-case\">A\u003C\u002Fjats:styled-content>ustralian case‐control population.\u003C\u002Fjats:p>\u003C\u002Fjats:sec>\u003Cjats:sec>\u003Cjats:title>Background\u003C\u002Fjats:title>\u003Cjats:p>\u003Cjats:styled-content style=\"fixed-case\">BDNF\u003C\u002Fjats:styled-content> 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 \u003Cjats:styled-content style=\"fixed-case\">BDNF\u003C\u002Fjats:styled-content>, in particular the functional \u003Cjats:styled-content style=\"fixed-case\">V\u003C\u002Fjats:styled-content>al66\u003Cjats:styled-content style=\"fixed-case\">M\u003C\u002Fjats:styled-content>et polymorphism (rs6265), have been found to be associated with a number of psychiatric disorders, cognitive function, and obesity. As \u003Cjats:styled-content style=\"fixed-case\">BDNF\u003C\u002Fjats:styled-content> has been found to be differentially expressed in a number of aspects related to migraine, we tested for association between single nucleotide polymorphisms (\u003Cjats:styled-content style=\"fixed-case\">SNPs\u003C\u002Fjats:styled-content>) in \u003Cjats:styled-content style=\"fixed-case\">BDNF\u003C\u002Fjats:styled-content> and migraine.\u003C\u002Fjats:p>\u003C\u002Fjats:sec>\u003Cjats:sec>\u003Cjats:title>Methods\u003C\u002Fjats:title>\u003Cjats:p>Five \u003Cjats:styled-content style=\"fixed-case\">SNPs\u003C\u002Fjats:styled-content> in the \u003Cjats:styled-content style=\"fixed-case\">BDNF\u003C\u002Fjats:styled-content> locus (rs1519480, rs6265, rs712507, rs2049046, and rs12273363) were genotyped initially in a cohort of 277 migraine cases, including 172 diagnosed with migraine with aura (\u003Cjats:styled-content style=\"fixed-case\">MA\u003C\u002Fjats:styled-content>) and 105 with migraine without aura (\u003Cjats:styled-content style=\"fixed-case\">MO\u003C\u002Fjats:styled-content>), and 277 age‐ and sex‐matched controls. Three of these \u003Cjats:styled-content style=\"fixed-case\">SNPs\u003C\u002Fjats:styled-content> (rs6265, rs2049046, and rs12273363) were subsequently genotyped in a second cohort of 580 migraineurs, including 473 diagnosed with \u003Cjats:styled-content style=\"fixed-case\">MA\u003C\u002Fjats:styled-content> and 105 with \u003Cjats:styled-content style=\"fixed-case\">MO\u003C\u002Fjats:styled-content>, and 580 matched controls.\u003C\u002Fjats:p>\u003C\u002Fjats:sec>\u003Cjats:sec>\u003Cjats:title>Results\u003C\u002Fjats:title>\u003Cjats:p>\u003Cjats:styled-content style=\"fixed-case\">BDNF SNPs\u003C\u002Fjats:styled-content> rs1519480, rs6265, rs712507, and rs12273363 were not significantly associated with migraine. However, rs2049046 showed a significant association with migraine, and in particular, \u003Cjats:styled-content style=\"fixed-case\">MA\u003C\u002Fjats:styled-content> in the first cohort. In the second cohort, although an increase in the rs2049046 \u003Cjats:styled-content style=\"fixed-case\">T\u003C\u002Fjats:styled-content>‐allele frequency was observed in migraine cases, and in both \u003Cjats:styled-content style=\"fixed-case\">MA\u003C\u002Fjats:styled-content> and \u003Cjats:styled-content style=\"fixed-case\">MO\u003C\u002Fjats:styled-content> 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 \u003Cjats:styled-content style=\"fixed-case\">MA\u003C\u002Fjats:styled-content> subgroup.\u003C\u002Fjats:p>\u003C\u002Fjats:sec>\u003Cjats:sec>\u003Cjats:title>Conclusion\u003C\u002Fjats:title>\u003Cjats:p>This study confirmed previous studies that the functional \u003Cjats:styled-content style=\"fixed-case\">BDNF SNP\u003C\u002Fjats:styled-content> rs6265 (\u003Cjats:styled-content style=\"fixed-case\">V\u003C\u002Fjats:styled-content>al66\u003Cjats:styled-content style=\"fixed-case\">M\u003C\u002Fjats:styled-content>et) is not associated with migraine. However, we found that rs2049046, which resides at the 5' end of one the \u003Cjats:styled-content style=\"fixed-case\">BDNF\u003C\u002Fjats:styled-content> transcripts, may be associated with migraine, suggesting that further investigations of this \u003Cjats:styled-content style=\"fixed-case\">SNP\u003C\u002Fjats:styled-content> may be warranted.\u003C\u002Fjats:p>\u003C\u002Fjats:sec>",{"EN":160},"Investigation of Brain‐Derived Neurotrophic Factor (\u003Cscp>BDNF\u003C\u002Fscp>) Gene Variants in Migraine",{"VOID":162},"24708359",{"VOID":164},"10.1111\u002Fhead.12351","PUBLICATION","VERIFIED","Auto Verify",[169],"EN","https:\u002F\u002Fheadachejournal.onlinelibrary.wiley.com\u002Fdoi\u002F10.1111\u002Fhead.12351",[172,191,208,225,242],{"id":173,"sortIndex":24,"researcher":23,"roles":174,"affiliations":175,"properties":184,"displayName":188,"givenName":23,"familyName":23},"5c4fdead-0fa3-4c3f-b143-f40b4ef82aad",[],[176],{"id":177,"sortIndex":24,"affiliation":178,"properties":23},"65660d9c-ab25-4212-87f5-35935e8ad9c5",{"id":177,"createTime":23,"updateTime":23,"relativeEntities":179,"slug":23,"properties":180,"entityType":23,"verifyStatus":23,"verifyTime":23,"verifyNote":23,"languages":23,"translateLanguages":23,"viewCount":23,"url":23,"parentIds":183,"statistic":23},[],{"title":181},{"VI":182},"Genomics Research Centre, Institute of Health and Biomedical Innovation, Queensland University of Technology, Brisbane QLD, Australia",[],{"orcid":185,"title":187,"openalex":189},{"VOID":186},"https:\u002F\u002Forcid.org\u002F0000-0002-8512-1498",{"EN":188},"Heidi G. 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main objective of this study is to determine whether change in migraine frequency is correlated with a denervation pattern of the corrugator muscle after local botulinum toxin type A injections.\u003C\u002Fjats:p>\u003Cjats:p>Background.—Recent studies suggest botulinum toxin type A is effective in preventing migraine. Relaxation of the corrugator muscle may be one of multiple targets of botulinum toxin type A in relieving migraine pain.\u003C\u002Fjats:p>\u003Cjats:p>Methods.—The pretreatment amplitude of the compound muscle action potential (CMAP) was obtained in 10 patients with a migraine frequency of two to six attacks per month following stimulation of the temporal branch of the facial nerve. Patients were subsequently injected with 20 units of botulinum toxin type A at predefined sites in the procerus and corrugator muscles. CMAP was obtained on days 7, 30, 60, and 90 after injection. Migraine frequency, as reported in headache diaries, was compared with the amplitudes obtained.\u003C\u002Fjats:p>\u003Cjats:p>Results.—A 50% decrease in CMAP was demonstrated in the total group by day 7. Maximal decline of CMAP was observed by day 30, and was sustained at day 60. Migraine frequency declined by 50% or more in 7 of 10 patients by day 60. Migraine response to botulinum toxin type A treatment did not correlate with the denervation pattern.\u003C\u002Fjats:p>\u003Cjats:p>Conclusion.—Relaxation of the corrugator muscles is not solely responsible for the pain relief in migraine patients treated with botulinum toxin type A.\u003C\u002Fjats:p>",{"EN":737},"Mechanism of Action of Botulinum Toxin Type A in Migraine Prevention: A Pilot Study",{"VOID":739},"15330827",{"VOID":741},"10.1111\u002Fj.1526-4610.2004.04148.x","2024-12-04T12:31:55.142+00:00","Author affiliation is blank",[169],"https:\u002F\u002Fheadachejournal.onlinelibrary.wiley.com\u002Fdoi\u002F10.1111\u002Fj.1526-4610.2004.04148.x",[747,764,773],{"id":748,"sortIndex":24,"researcher":23,"roles":749,"affiliations":750,"properties":759,"displayName":761,"givenName":23,"familyName":23},"d4d0f0c9-f304-4d86-86fa-5ac1f4521bc7",[],[751],{"id":752,"sortIndex":24,"affiliation":753,"properties":23},"24172dd4-3270-42c0-b09c-247ce8109a5b",{"id":752,"createTime":23,"updateTime":23,"relativeEntities":754,"slug":23,"properties":755,"entityType":23,"verifyStatus":23,"verifyTime":23,"verifyNote":23,"languages":23,"translateLanguages":23,"viewCount":23,"url":23,"parentIds":758,"statistic":23},[],{"title":756},{"EN":757},"Department of Neurology and Neurophysiology, University of Pretoria, South Africa.",[],{"title":760,"openalex":762},{"EN":761},"Johan A. 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It can be seen as a reaction of the organism, probably determined by the hypothalamus and released by a variety of extrinsic and intrinsic factors. Several factors may determine attacks at different times within a patient's lifetime. Vascular reactions are secondary to the primary cerebral mechanism, and account for many of the symptoms, notably the headache. The prodrome, aura, and the incubation during sleep are part of the attack.\u003C\u002Fjats:p>\u003Cjats:p>Emotional disturbance is the commonest single trigger mechanism, and is the most important cause of frequent and severe attacks. There is, however, nothing specific about the emotional stimulus, nor is there a consistent personality type in migraine subjects. Certain personality reactions and patterns of behavior recur in migraine subjects; a tendency to anxiety reactions, sensitivity to stress and difficulty in handling aggressive and hostile drives. In this respect, migraine is similar to many other “psychosomatic diseases” without demonstrable pathology but characterized by disorders of homeostasis. In some patients extrinsic physical and biochemical precipitants are prominent and the “psychosomatic element” is slight. 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contraction headache and migraine patients were compared for symptoms of muscular and vascular activity, and responsiveness to frontalis electromyogram (EMG) biofeedback therapy. Locations of head pain were non‐specific to the diagnostic groups. Migraine patients had higher frontalis EMG activity than muscle contraction headache patients and headache‐free controls. Both headache groups had higher neck EMG activity than controls. Pulse velocities in the superficial temporal arteries were similar in the two headache patient groups but different from controls. It is suggested that muscle contraction headache and migraine patients have similar physiologic predisposition for headaches. 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