Evidence map›Paper›PMID 30515004›Full record

ArticleActa informatica medica : AIM : journal of the Society for Medical Informatics of Bosnia & Herzegovina : casopis Drustva za medicinsku informatiku BiH2018

Association Between - 675 ID, 4G/5G PAI-1 Gene Polymorphism and Pregnancy Loss: A Systematic Review.

Grazyna Adler, Emir Mahmutbegovic, Amina Valjevac, Mateusz A Adler, Nevena Mahmutbegovic, Krzysztof Safranow, Ewa Czerska, Anna Pawinska-Matecka, Iwona Ciechanowicz, Damir Marjanovic

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In one paragraph

Article in Acta informatica medica : AIM : journal of the Society for Medical Informatics of Bosnia & Herzegovina : casopis Drustva za medicinsku informatiku BiH, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

5 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. 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

10 authors at 5 institutions in 3 countries.

Grazyna AdlerDepartment of Studies in Antropogenetics and Biogerontology, Pomeranian Medical University, Szczecin, Poland.
Emir MahmutbegovicInstitution of Health Protection of Women and Motherhood Canton Sarajevo, Sarajevo, Bosnia and Herzegovina.
Amina ValjevacLaboratory for Molecular Medicine, Center for Genetics, Medical Faculty, University of Sarajevo, Sarajevo, Sarajevo, Bosnia and Herzegovina.
Mateusz A AdlerWarsaw School of Economics, Warsaw, Poland.
Nevena MahmutbegovicNeurology Clinic, Clinical Center of University of Sarajevo, Sarajevo, Bosnia and Herzegovina.
Krzysztof SafranowDepartment of Biochemistry and Medical Chemistry, Pomeranian Medical University, Szczecin, Polandl.
Ewa CzerskaCentral Laboratory, Regional Hospital, Szczecin, Poland.
Anna Pawinska-MateckaCentral Laboratory, Regional Hospital, Szczecin, Poland.
Iwona CiechanowiczPomeranian Medical University, Szczecin, Poland.
Damir MarjanovicInternational Burch University, Bosnia and Herzegovina.
Pomeranian Medical University · PLUniversity of Szczecin · PLInternational Burch University · BASGH Warsaw School of Economics · PLUniversity of Sarajevo · BA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionSeveral analysis for different population conclude that endothelial plasminogen activator inhibitor 1 gene polymorphism, -675 ID, 4G/5G

aimTherefore, we decided to investigate the -675 ID, 4G/5G

resultsAmong European populations, the statistically significant association between 4G allele and recurrent PL only in Czechs and Bulgarian women was found (p<0.002 and p=0.018, respectively); while, among populations outside Europe in Iranian, Tunisian and Turkish women (each p<0.001).

conclusionsWe concluded, that both in Europe and elsewhere in the world, the high frequency of 4G allele in population, is not unambiguously linked with the risk of pregnancy loss.

Indexed as

genetic riskPAI-1 genepolymorphismpregnancy loss

Identifiers

PMID30515004
PMCPMC6195400
OpenAlexW2890116725

What OpenQuestion holds

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LicenceCC BY-NC
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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.