Evidence map›Paper›PMID 30390345›Full record

ArticleJournal of clinical laboratory analysis2019

Analysis of estrogen and progesterone receptor gene polymorphisms in leiomyoma.

Muhammed Toprak, Omer Ates, Asker Zeki Ozsoy, Nihan Bozkurt, Saime Sezer Sondas, Bülent Cakmak, Hatice Yılmaz Dogru, İlhan Bahri Delibas, Fazlı Demirturk

Open access · bronzeAbstract read
In one paragraph

Article in Journal of clinical laboratory analysis, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 1 pooled it
0.8field-weighted citation impact, top 23% 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

4 citing papers in PubMed, 1 synthesis or guideline pooled it, 9 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. 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

9 authors at 1 institution in 1 country.

Muhammed ToprakFaculty of Medicine, Department of Obstetrics and Gynecology, Gaziosmanpasa University, Tokat, Turkey.
Omer AtesFaculty of Medicine, Department of Medical Biology, Gaziosmanpasa University, Tokat, Turkey.
Asker Zeki OzsoyFaculty of Medicine, Department of Obstetrics and Gynecology, Gaziosmanpasa University, Tokat, Turkey.
Nihan BozkurtFaculty of Medicine, Department of Medical Biology, Gaziosmanpasa University, Tokat, Turkey.ORCID http://orcid.org/0000-0002-2283-0828
Saime Sezer SondasFaculty of Medicine, Department of Medical Biology, Gaziosmanpasa University, Tokat, Turkey.
Bülent CakmakFaculty of Medicine, Department of Obstetrics and Gynecology, Gaziosmanpasa University, Tokat, Turkey.
Hatice Yılmaz DogruFaculty of Medicine, Department of Obstetrics and Gynecology, Gaziosmanpasa University, Tokat, Turkey.
İlhan Bahri DelibasFaculty of Medicine, Department of Obstetrics and Gynecology, Gaziosmanpasa University, Tokat, Turkey.
Fazlı DemirturkFaculty of Medicine, Department of Obstetrics and Gynecology, Gaziosmanpasa University, Tokat, Turkey.
Tokat Gaziosmanpaşa Üniversitesi · TR

Funding

Gaziosmanpasa University Scientific Research Projects Fund
6 · The paper itself

Abstract

backgroundLeiomyoma, one of the most common benign tumors, causes morbidity during the reproductive years in women. The molecular pathogenesis of the disease is not clear. Leiomyomas are hormone-sensitive tumors affecting around 20%-25% of women. Gene polymorphism studies could be important and explaining in the evaluation of multifactorial diseases such as leiomyoma. Polymorphisms involving genes responsible for the synthesis and signalization of steroid hormones could be used as genetic markers for hormone-related conditions. The purpose of this study was to analyze the effect of ERα-351 XbaI A/G, ERα-397 PvuII T/C, and progesterone receptor (PGR) PROGINS polymorphisms on the development of leiomyomas. MATERIAL AND

methodsIn this study, 213 samples (103 leiomyoma patients and 110 healthy controls) participated. The ERα-351 XbaI A/G and ERα-397 PvuII T/C gene polymorphisms were analyzed using PCR-RFLP method. PGR PROGINS polymorphism was analyzed by PCR method with specific primers.

resultsThe genotype distribution and allele frequency of the ERα-351 XbaI A/G, ERα-397 PvuII T/C, and PGR PROGINS polymorphisms were not statistically different between leiomyoma patient and control groups (p > 0.05).

conclusionThis study reflects that ERα and PGR PROGINS polymorphisms may not be one of the many genetic factors for leiomyoma susceptibility.

Indexed as

AdultCase-Control StudiesFemaleHumansLeiomyomaMiddle AgedPolymerase Chain ReactionPolymorphism, GeneticReceptors, EstrogenReceptors, ProgesteroneReceptors, EstrogenReceptors, Progesteroneestrogengene polymorphismleiomyomaPCRprogesterone receptor

Identifiers

PMID30390345
PMCPMC6818596
OpenAlexW2898942298

What OpenQuestion holds

Textmetadata
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.