Evidence map›Paper›PMID 25132852›Full record

ArticleInternational journal of endocrinology2014

MTNR1B Genetic Variability Is Associated with Gestational Diabetes in Czech Women.

Daniela Vejrazkova, Petra Lukasova, Marketa Vankova, Josef Vcelak, Olga Bradnova, Veronika Cirmanova, Katerina Andelova, Hana Krejci, Bela Bendlova

Open access · goldAbstract read
In one paragraph

Article in International journal of endocrinology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
1.5field-weighted citation impact, top 17% 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, 1 synthesis or guideline pooled it, 26 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. Review
  5. Multigenerational diabetes mellitus.Frontiers in endocrinology · 2023
    Review
  6. Article
  7. Gestational Diabetes Mellitus: A Harbinger of the Vicious Cycle of Diabetes.International journal of molecular sciences · 2020
    Review
  8. Novel Genetic Variants ofFrontiers in endocrinology · 2020
    Article
  9. Article
  10. TheInternational journal of molecular sciences · 2018
    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

9 authors at 3 institutions in 1 country.

Daniela VejrazkovaDepartment of Molecular Endocrinology, Institute of Endocrinology, 11694 Prague 1, Czech Republic.ORCID 0000-0003-2799-2874
Petra LukasovaDepartment of Molecular Endocrinology, Institute of Endocrinology, 11694 Prague 1, Czech Republic.ORCID 0000-0003-2474-2052
Marketa VankovaDepartment of Molecular Endocrinology, Institute of Endocrinology, 11694 Prague 1, Czech Republic.ORCID 0000-0003-1883-7274
Josef VcelakDepartment of Molecular Endocrinology, Institute of Endocrinology, 11694 Prague 1, Czech Republic.ORCID 0000-0002-6546-0580
Olga BradnovaDepartment of Molecular Endocrinology, Institute of Endocrinology, 11694 Prague 1, Czech Republic.ORCID 0000-0002-1015-4391
Veronika CirmanovaDepartment of Molecular Endocrinology, Institute of Endocrinology, 11694 Prague 1, Czech Republic.
Katerina AndelovaInstitute for Mother and Child Care, Prague, 14710 Prague 4, Czech Republic.
Hana KrejciDepartment of Obstetrics and Gynecology, First Faculty of Medicine, Charles University and General University Hospital in Prague, 12000 Prague 2, Czech Republic.
Bela BendlovaDepartment of Molecular Endocrinology, Institute of Endocrinology, 11694 Prague 1, Czech Republic.ORCID 0000-0001-7008-8675
Institute of Endocrinology · CZCharles University · CZÚstav pro Péči o Matku a Dítě · CZ

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The gene MTNR1B encodes a receptor for melatonin. Melatonin receptors are expressed in human β-cells, which implies that genetic variants might affect glucose tolerance. Meta-analysis confirmed that the rs10830963 shows the most robust association. The aim of the study was to assess the rs10830963 in Czech GDM patients and controls and to study relations between the SNP and biochemical as well as anthropometric characteristics. Our cohort consisted of 880 women; 458 were diagnosed with GDM, and 422 were normoglycemic controls without history of GDM. Despite similar BMI, the GDM group showed higher WHR, waist circumference, abdominal circumference, and total body fat content. The risk allele G was more frequent in the GDM group (38.3 versus 29.4% in controls, OR 1.49 CI95% [1.22; 1.82]; P OR = 0.0001). In spite of higher frequency, the G allele in the GDM group was not associated with any markers of glucose metabolism. In contrast, controls showed significant association of the allele G with FPG and with postchallenge glycemia during the oGTT. Frequency analysis indicates that rs10830963 is involved in gestational diabetes in Czech women. However, the association of the SNP with glucose metabolism, which is obvious in controls, is covert in women who have experienced GDM.

Identifiers

PMID25132852
PMCPMC4123535
OpenAlexW2079301735

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.