Evidence map›Paper›PMID 18805939›Full record

ReviewHuman reproduction update

Functional genetic polymorphisms and female reproductive disorders: part II--endometriosis.

C B Tempfer, M Simoni, B Destenaves, B C J M Fauser

Open access · hybridAbstract readReview
In one paragraph

Review in Human reproduction update. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
10.1field-weighted citation impact, top 2% 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

30 citing papers in PubMed, 105 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
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  7. Article
  8. Defining the genetic profile of endometriosis.Experimental and therapeutic medicine · 2019
    Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Endometriosis and ovarian cancer.World journal of clinical oncology · 2014
    Article
  18. Endometriosis still a challenge.Journal of medicine and life · 2014
    Review
  19. Article
  20. 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

4 authors at 4 institutions in 5 countries.

C B TempferDepartment of Obstetrics and Gynecology, Medical University, Vienna, Austria. clemens.tempfer@meduniwien.ac.at
M Simoni
B Destenaves
B C J M Fauser
Medical University of Vienna · ATMerck & Co., Inc., Rahway, NJ, USA (United States) · USUniversity of Groningen · NLUniversity of Modena and Reggio Emilia · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundEndometriosis has a strong genetic component, and numerous genetic studies have been reported.

methodsWe have systematically reviewed these studies and included 114 in our final selection.

resultsWe found no consistent evidence linking endometriosis with specific polymorphisms in genes encoding inflammatory mediators, proteins involved in sex steroid metabolism, vascular function and tissue remodelling. Although a number of polymorphisms have been associated with endometriosis in selected populations, the associations have not been independently confirmed, either because only single studies were carried out on these markers/genes or because other studies reported no association. The most solid evidence linking specific polymorphisms to endometriosis came from studies investigating glutathione-S-transferase, a phase II detoxification enzyme. Carriage of the GSTT1 null deletion variant showed consistent association with endometriosis with a 29% increased risk; however, it cannot be excluded that this result was due to publication bias, and this association should be independently confirmed in large-scale, well-designed case-control studies.

conclusionsThe evidence of an association between genetic polymorphisms and endometriosis is weak. Carriage of the GSTT1 null deletion may moderately increase the risk of this disease. We suggest that the methodology of association studies should be improved in order to identify and validate associations in endometriosis.

Indexed as

Polymorphism, GeneticCytokinesEndometriosisFemaleGenetic Predisposition to DiseaseGonadal Steroid HormonesHumansCytokinesGonadal Steroid Hormones

Identifiers

PMID18805939
PMCPMC2639061
OpenAlexW2147089104

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.