Screening of genetic variants in ADCYAP1R1, MME and 14q21 in a Swedish cluster headache cohort

Screening of genetic variants in ADCYAP1R1, MME and 14q21 in a Swedish cluster headache cohort Background: We have genotyped a Swedish cluster headache case-control population for three genetic variants representing the most significant markers identified in a recently published genome wide association study on cluster headache. The genetic variants were two common polymorphisms; rs12668955 in ADCYAP1R1 (adenylate cyclase activating polypeptide 1 receptor type 1), rs1006417, an intergenic variant on chromosome 14q21 and one rare mutation, rs147564881,in MME (membrane metalloendopeptidase). Results: We screened 542 cluster headache patients and 581 controls using TaqMan real-time PCR on a 7500 fast cycler, and pyrosequencing on a PSQ 96 System. Statistical analysis for genotype and allele association showed that neither of the two common variants, rs12668955 and rs1006417 were associated with cluster headache. The MME mutation was investigated with pyrosequencing in patients, of whom all were wild type. Conclusion: In conclusion rs12668955 and rs1006417 do not impact the risk of developing cluster headache in the Swedish population. Also, rs147564881 does not seem to be enriched within the Swedish cluster headache patient group. Keywords: Ch, Trigeminal autonomic cephalalgia, Neprilysin, PACAP receptor, Association, SNP Background in several candidate genes to CH. Hypocretin receptor 2 Cluster headache (CH) is a severe primary headache af- (HCRTR2) and nitric oxide synthase (NOS) are examples http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png The Journal of Headache and Pain Springer Journals

Screening of genetic variants in ADCYAP1R1, MME and 14q21 in a Swedish cluster headache cohort

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Publisher
Springer Milan
Copyright
Copyright © 2017 by The Author(s).
Subject
Medicine & Public Health; Pain Medicine; Internal Medicine; Neurology
ISSN
1129-2369
eISSN
1129-2377
D.O.I.
10.1186/s10194-017-0798-y
Publisher site
See Article on Publisher Site

Abstract

Background: We have genotyped a Swedish cluster headache case-control population for three genetic variants representing the most significant markers identified in a recently published genome wide association study on cluster headache. The genetic variants were two common polymorphisms; rs12668955 in ADCYAP1R1 (adenylate cyclase activating polypeptide 1 receptor type 1), rs1006417, an intergenic variant on chromosome 14q21 and one rare mutation, rs147564881,in MME (membrane metalloendopeptidase). Results: We screened 542 cluster headache patients and 581 controls using TaqMan real-time PCR on a 7500 fast cycler, and pyrosequencing on a PSQ 96 System. Statistical analysis for genotype and allele association showed that neither of the two common variants, rs12668955 and rs1006417 were associated with cluster headache. The MME mutation was investigated with pyrosequencing in patients, of whom all were wild type. Conclusion: In conclusion rs12668955 and rs1006417 do not impact the risk of developing cluster headache in the Swedish population. Also, rs147564881 does not seem to be enriched within the Swedish cluster headache patient group. Keywords: Ch, Trigeminal autonomic cephalalgia, Neprilysin, PACAP receptor, Association, SNP Background in several candidate genes to CH. Hypocretin receptor 2 Cluster headache (CH) is a severe primary headache af- (HCRTR2) and nitric oxide synthase (NOS) are examples

Journal

The Journal of Headache and PainSpringer Journals

Published: Aug 22, 2017

References

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