Evidence map›Paper›PMID 31808503›Full record

SynthesisBioscience reports2019

A functional polymorphism rs10830963 in melatonin receptor 1B associated with the risk of gestational diabetes mellitus.

Bo Huang, Yu-Kun Wang, Lin-Yuan Qin, Qin Wei, Nian Liu, Min Jiang, Hong-Ping Yu, Xiang-Yuan Yu

Erratum issuedOpen access · goldAbstract readMeta-Analysis
In one paragraph

Synthesis in Bioscience reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

13 citing papers in PubMed, 24 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Article
  6. Review
  7. Genetic variants ofFrontiers in endocrinology · 2023
    Article
  8. Review
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 3 institutions in 1 country.

Bo HuangDepartment of Epidemiology and Health Statistics of Guilin Medical University, Guilin 541100, Guangxi, China.
Yu-Kun WangDepartment of Microbiology of Guangxi University, Nanning 530004, Guangxi, China.
Lin-Yuan QinDepartment of Epidemiology and Health Statistics of Guilin Medical University, Guilin 541100, Guangxi, China.
Qin WeiDepartment of Epidemiology and Health Statistics of Guilin Medical University, Guilin 541100, Guangxi, China.
Nian LiuDepartment of Epidemiology and Health Statistics of Guilin Medical University, Guilin 541100, Guangxi, China.
Min JiangDepartment of Epidemiology and Health Statistics of Guilin Medical University, Guilin 541100, Guangxi, China.
Hong-Ping YuAffiliated Tumor Hospital of Guangxi Medical University, Nanning 530021, Guangxi, China.
Xiang-Yuan YuDepartment of Epidemiology and Health Statistics of Guilin Medical University, Guilin 541100, Guangxi, China.
Guilin Medical University · CNGuangxi University · CNTumor Hospital of Guangxi Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The melatonin receptor 1B (MTNR1B) polymorphism rs10830963 C>G has been reported to be associated with the risk of gestational diabetes mellitus (GDM) with inconsistent results. To clarify the effect of the polymorphism on the risk of GDM, a meta-analysis therefore was performed. Pooled OR with its corresponding 95%CI was used to estimate the strength of the association. Totally 14 eligible studies with a number of 5033 GDM patients and 5614 controls were included in this meta-analysis. Results indicated that the variant G allele was significantly associated with an increased GDM risk (CG vs. CC: OR = 1.25, 95% CI = 1.11-1.40, P < 0.001; GG vs. CC: OR = 1.78, 95% CI = 1.45-2.19, P < 0.001; G vs. C: OR = 1.33, 95% CI = 1.21-1.47, P < 0.001). In the stratified analysis by ethnicity, similar results were found in Asians (CG vs. CC: OR = 1.15, 95%CI = 1.02-1.28, P = 0.020; GG vs. CC: OR = 1.52, 95% CI = 1.23-1.89, P < 0.001; G vs. C: OR = 1.23, 95% CI = 1.10-1.37, P < 0.001) and in Caucasians (CG vs. CC: OR = 1.40, 95% CI = 1.16-1.70, P < 0.001; GG vs. CC: OR = 2.21, 95% CI = 1.54-3.17, P < 0.001; G vs. C: OR = 1.47, 95% CI = 1.24-1.73, P < 0.001). FPRP and TSA analyses confirmed findings support that the rs10830963 G allele increases the risk of GDM, and further functional experimental studies are warranted to explore and clarify the potential mechanism.

Indexed as

Genetic Association StudiesGenetic Predisposition to DiseaseAllelesAsian PeopleDiabetes, GestationalFemaleHumansPolymorphism, Single NucleotidePregnancyReceptor, Melatonin, MT2MTNR1B protein, humanReceptor, Melatonin, MT2Gestational diabetes mellitusmeta analysisMTNR1BPolymorphismTrial sequential analysis

Identifiers

PMID31808503
PMCPMC6923336
OpenAlexW2994531119

What OpenQuestion holds

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Registered trials

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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.