Evidence map›Paper›PMID 22193458›Full record

ArticleMolecular and cellular biochemistry2012

MAOA, MTHFR, and TNF-β genes polymorphisms and personality traits in the pathogenesis of migraine.

Masakazu Ishii, Shunichi Shimizu, Yuki Sakairi, Ayumu Nagamine, Yuika Naito, Yukiko Hosaka, Yuko Naito, Tatsuya Kurihara, Tomomi Onaya, Hideto Oyamada and 8 more

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Article in Molecular and cellular biochemistry, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 4 pooled it
2.9field-weighted citation impact, top 9% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

12 citing papers in PubMed, 4 syntheses or guidelines pooled it, 39 citations in OpenAlex.

  1. Pooled it
  2. Personality profile and depression in migraine: a meta-analysis.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2020
    Pooled it
  3. Pooled it
  4. Pooled it
  5. Review
  6. Review
  7. Clinical Response to Valproate in Patients with Migraine.Journal of clinical neurology (Seoul, Korea) · 2016
    Article
  8. Article
  9. Article
  10. Maternal personality profile of children affected by migraine.Neuropsychiatric disease and treatment · 2013
    Article
  11. Article
  12. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

18 authors at 4 institutions in 1 country.

Masakazu IshiiDepartment of Pathophysiology, School of Pharmacy, Showa University, 1-5-8 Hatanodai, Shinagawa-ku, Tokyo 142-8555, Japan. masakazu@pharm.showa-u.ac.jp
Shunichi Shimizu
Yuki Sakairi
Ayumu Nagamine
Yuika Naito
Yukiko Hosaka
Yuko Naito
Tatsuya Kurihara
Tomomi Onaya
Hideto Oyamada
Atsuko Imagawa
Kenji Shida
Johji Takahashi
Katsuji Oguchi
Yutaka Masuda
Hajime Hara
Shino Usami
Yuji Kiuchi
Showa University · JPShowa University Fujigaoka Hospital · JPShowa Pharmaceutical University · JPShowa University Fujigaoka Rehabilitation Hospital

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Migraine is a multifactorial disease with various factors, such as genetic polymorphisms and personality traits, but the contribution of those factors is not clear. To clarify the pathogenesis of migraine, the contributions of genetic polymorphisms and personality traits were simultaneously investigated using multivariate analysis. Ninety-one migraine patients and 119 non-headache healthy volunteers were enrolled. The 12 gene polymorphisms analysis and NEO-FFI personality test were performed. At first, the univariate analysis was performed to extract the contributing factors to pathogenesis of migraine. We then extracted the factors that independently contributed to the pathogenesis of migraine using multivariate stepwise logistic regression analysis. Using the multivariate analysis, three gene polymorphisms including monoamine oxidase A (MAOA) T941G, methylenetetrahydrofolate reductase (MTHFR) C677T, and tumor necrosis factor beta (TNF-β) G252Α, and the neuroticism and conscientiousness scores in NEO-FFI were selected as significant factors that independently contributed to the pathogenesis of migraine. Their odds ratios were 1.099 (per point of neuroticism score), 1.080 (per point of conscientiousness score), 2.272 (T and T/T or T/G vs G and G/G genotype of MAOA), 1.939 (C/T or T/T vs C/C genotype of MTHFR), and 2.748 (G/A or A/A vs G/G genotype of TNF-β), respectively. We suggested that multiple factors, such as gene polymorphisms and personality traits, contribute to the pathogenesis of migraine. The contribution of polymorphisms, such as MAOA T941G, MTHFR C677T, and TNF-β G252A, were more important than personality traits in the pathogenesis of migraine, a multifactorial disorder.

Indexed as

PersonalityPolymorphism, GeneticAdultCase-Control StudiesChi-Square DistributionFemaleGene FrequencyGenetic Predisposition to DiseaseHumansJapanLogistic ModelsLymphotoxin-alphaMaleMethylenetetrahydrofolate Reductase (NADPH2)Middle AgedMigraine DisordersLymphotoxin-alphaMethylenetetrahydrofolate Reductase (NADPH2)Monoamine Oxidase

Identifiers

PMID22193458
OpenAlexW2084476052

What OpenQuestion holds

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Read underepoch 390

Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.