Literature DB >> 28360555

Endothelial Nitric Oxide Synthase and Angiotensin Converting Enzyme Gene Polymorphisms in Migraine Patients.

Tammam Sipahi1, Babürhan Güldiken2, Levent Kabayel3, Orkide Palabiyik1, Hülya Özkan3, Tülay Okman Kiliç4, Necdet Süt5, Nilda Turgut6.   

Abstract

INTRODUCTION: In this study, we investigated the association of migraine with the Variable Number of Tandem Repeats (VNTR), repeated as 27 base pair, gene polymorphism in intron 4 of the endothelial nitric oxide synthase (eNOS) and the insertion/deletion of angiotensin converting enzyme (ACE) gene polymorphisms.
METHODS: One hundred and five migraine and ninety seven healthy female control subjects were enrolled in the study. The patients were subdivided as migraine with aura and without aura, and the frequency and severity of migraine headaches were recorded. The eNOS VNTR (eNOS 4 a/b) and ACE insertion/deletion gene polymorphisms (ACE I/D) were assessed by polymerase chain reactions. RESULT: The allele and genotype frequencies of eNOS 4 a/b gene polymorphism showed no difference between the migraine and control groups. The genotypic distribution of the ACE I/D gene polymorphism in the migraine group significantly differed from that in the control group. The DD and ID genotype increased the risk of migraine as much as 2.571 (95% CI-1.138-5.811) and 4.453 (95% CI-2.006-9.883) compared to the II genotype. The same increased risk sustained for both genotypes in the migraine with aura subgroup, but only the ID genotype remained as the risk factor in the migraine without aura subgroup (OR-3.750, 95% CI-1.493-9.420). No association of gene polymorphisms with migraine frequency and severity was observed.
CONCLUSION: Our findings support the relationship between migraine and the ACE I/D gene polymorphism. However, no association was found between migraine and the eNOS 4 a/b gene polymorphism.

Entities:  

Keywords:  Migraine; angiotensin converting enzyme; genetic polymorphism; nitric oxide synthase

Year:  2013        PMID: 28360555      PMCID: PMC5363447          DOI: 10.4274/npa.y6665

Source DB:  PubMed          Journal:  Noro Psikiyatr Ars        ISSN: 1300-0667            Impact factor:   1.339


  31 in total

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Authors:  K Gardner
Journal:  Can J Neurol Sci       Date:  1999-11       Impact factor: 2.104

Review 3.  Molecular genetics of migraine headaches: a review.

Authors:  P Montagna
Journal:  Cephalalgia       Date:  2000-02       Impact factor: 6.292

4.  Endothelial nitric oxide synthase haplotypes associated with aura in patients with migraine.

Authors:  Flavia M Gonçalves; Alisson Martins-Oliveira; Jose G Speciali; Marcelo R Luizon; Tatiane C Izidoro-Toledo; Pamela S Silva; Fabiola Dach; Jose E Tanus-Santos
Journal:  DNA Cell Biol       Date:  2011-02-20       Impact factor: 3.311

Review 5.  5-HTTLPR polymorphism in the serotonin transporter gene and migraine: a systematic review and meta-analysis.

Authors:  Markus Schürks; Pamela M Rist; Tobias Kurth
Journal:  Cephalalgia       Date:  2010-03-26       Impact factor: 6.292

Review 6.  Sex hormone receptor gene polymorphisms and migraine: a systematic review and meta-analysis.

Authors:  Markus Schürks; Pamela M Rist; Tobias Kurth
Journal:  Cephalalgia       Date:  2010-05-04       Impact factor: 6.292

7.  Angiotensin-converting enzyme gene deletion polymorphism determines an increase in frequency of migraine attacks in patients suffering from migraine without aura.

Authors:  S Paterna; P Di Pasquale; A D'Angelo; G Seidita; A Tuttolomondo; A Cardinale; T Maniscalchi; G Follone; A Giubilato; M Tarantello; G Licata
Journal:  Eur Neurol       Date:  2000       Impact factor: 1.710

8.  Association of the insertion/deletion polymorphism of the angiotensin I-converting enzyme gene in patients of migraine with aura.

Authors:  Hisanori Kowa; Emi Fusayasu; Tamami Ijiri; Kumiko Ishizaki; Kenichi Yasui; Kazuhiro Nakaso; Masayoshi Kusumi; Takao Takeshima; Kenji Nakashima
Journal:  Neurosci Lett       Date:  2005-02-10       Impact factor: 3.046

9.  A smoking-dependent risk of coronary artery disease associated with a polymorphism of the endothelial nitric oxide synthase gene.

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Journal:  Nat Med       Date:  1996-01       Impact factor: 53.440

10.  PCR detection of the insertion/deletion polymorphism of the human angiotensin converting enzyme gene (DCP1) (dipeptidyl carboxypeptidase 1).

Authors:  B Rigat; C Hubert; P Corvol; F Soubrier
Journal:  Nucleic Acids Res       Date:  1992-03-25       Impact factor: 16.971

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