Evidence map›Paper›PMID 20959425›Full record

SynthesisCephalalgia : an international journal of headache2010

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

Markus Schürks, Pamela M Rist, Tobias Kurth

Open access · greenAbstract readMeta-AnalysisSystematic Review
In one paragraph

Synthesis in Cephalalgia : an international journal of headache, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed, 2 pooled it
3.0field-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

25 citing papers in PubMed, 2 syntheses or guidelines pooled it, 48 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Review
  4. Review
  5. Review
  6. Article
  7. Article
  8. Correlation betweenTranslational pediatrics · 2022
    Article
  9. Review
  10. Review
  11. Article
  12. The New *G29A and G1222A ofFrontiers in molecular neuroscience · 2018
    Article
  13. Review
  14. Review
  15. Review
  16. Childhood Maltreatment in the Migraine Patient.Current treatment options in neurology · 2016
    Review
  17. Childhood Maltreatment and Headache Disorders.Current pain and headache reports · 2016
    Article
  18. Article
  19. Article
  20. Review
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

3 authors at 2 institutions in 3 countries.

Markus SchürksBrigham and Women's Hospital, Harvard Medical School, Boston, MA 02215-1204, USA. mschuerks@rics.bwh.harvard.edu
Pamela M Rist
Tobias Kurth
Harvard University · USBrigham and Women's Hospital · US

Funding

TRAINING PROGRAM IN EPIDEMIOLOGIC RESEARCH ON AGINGT32AG000158 · NIA · BRIGHAM AND WOMEN'S HOSPITAL · PI GAZIANO, J. MICHAEL · 1988 to 2015
$2.1M
NIA NIH HHS T32 AG000158
6 · The paper itself

Abstract

BACKGROUND AND

methodsData on the association between the SLC6A4 5-HTTLPR polymorphism and migraine are conflicting. We performed a systematic review and meta-analysis among studies published up to September 2009. For each study with genotype information, we calculated odds ratios (OR) and 95% confidence intervals (CI) assuming additive, dominant, and recessive genetic models. We then calculated pooled ORs and 95% CIs.

resultsAmong the ten studies identified there was no overall association between the polymorphism and any migraine for Europeans or Asians. However, European women carrying the S allele had an increased risk for any migraine (dominant model: pooled OR=2.02; 95% CI 1.24-3.28). Results among Europeans further suggested an increased risk for migraine with aura among carriers of the S/S genotype (recessive model: pooled OR=1.41; 95% CI 0.83-2.40).

conclusionsWhile our results indicate no overall association between the SLC6A4 5-HTTLPR polymorphism and migraine among Europeans and Asians, gender and migraine aura status may have modifying roles among Europeans.

Indexed as

Genetic Predisposition to DiseasePolymorphism, Single NucleotideAsian PeopleFemaleHumansMaleMigraine DisordersOdds RatioSerotonin Plasma Membrane Transport ProteinsWhite PeopleSerotonin Plasma Membrane Transport ProteinsSLC6A4 protein, human

Identifiers

PMID20959425
PMCPMC3055240
OpenAlexW2168557513

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

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.