Evidence map›Paper›PMID 35526059›Full record

SynthesisEuropean journal of medical research2022

Association of vitamin D receptor gene rs739837 polymorphism with type 2 diabetes and gestational diabetes mellitus susceptibility: a systematic review and meta-analysis.

Qiaoli Zeng, Dehua Zou, Yue Wei, Yingguang Ouyang, Zhaohang Lao, Runmin Guo

Open access · goldAbstract readMeta-AnalysisSystematic Review
In one paragraph

Synthesis in European journal of medical research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 3 pooled it
4.1field-weighted citation impact, top 5% 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

15 citing papers in PubMed, 3 syntheses or guidelines pooled it, 29 citations in OpenAlex.

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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

6 authors at 3 institutions in 2 countries.

Qiaoli Zeng *Department of Internal Medicine, Shunde Women and Children's Hospital (Maternity and Child Healthcare Hospital of Shunde Foshan), Guangdong Medical University, Foshan, 528300, Guangdong, People's Republic of China.
Dehua Zou *State Key Laboratory for Quality Research of Chinese Medicines, Macau University of Science and Technology, Taipa, Macau (SAR), People's Republic of China.
Yue Wei *Department of Ultrasound, Shunde Women and Children's Hospital (Maternity and Child Healthcare Hospital of Shunde Foshan), Guangdong Medical University, Foshan, 528300, Guangdong, People's Republic of China.
Yingguang OuyangDepartment of General Affairs, Shunde Women and Children's Hospital (Maternity and Child Healthcare Hospital of Shunde Foshan), Guangdong Medical University, Foshan, 528300, Guangdong, People's Republic of China. 178512944@qq.com.
Zhaohang LaoDepartment of Ultrasound, Shunde Women and Children's Hospital (Maternity and Child Healthcare Hospital of Shunde Foshan), Guangdong Medical University, Foshan, 528300, Guangdong, People's Republic of China. xilinold@sohu.com.
Runmin GuoDepartment of Internal Medicine, Shunde Women and Children's Hospital (Maternity and Child Healthcare Hospital of Shunde Foshan), Guangdong Medical University, Foshan, 528300, Guangdong, People's Republic of China. 1314ivu@126.com.
Guangdong Medical College · CNFoshan Maternity and Child Health Care Hospital · CNMacau University of Science and Technology · MO

Funding

Doctoral scientific research Initiate funding project of Shunde Women and Children's Hospital of Guangdong Medical University(Maternity & Child Healthcare Hospital of Shunde Foshan) 2020BSQD007Guangdong Medical University Research Foundation GDMUM2020008Guangdong Medical University Research Foundation GDMUM2020012Medical Research Project of Foshan Health Bureau 20210188Medical Research Project of Foshan Health Bureau 20210289National Natural Science Foundation of China 81873649
6 · The paper itself

Abstract

backgroundIncreasing evidence shows that genetic variants of genes in the diabetes mellitus (DM) metabolic pathway, such as the vitamin D receptor (VDR) gene rs739837 polymorphism, increase the risk of DM susceptibility. However, the findings have been inconsistent. The present study was performed to evaluate the association of VDR gene rs739837 and type 2 diabetes (T2DM) or gestational diabetes mellitus (GDM) risk.

methodsA comprehensive meta-analysis and a subgroup analysis were conducted to assess the association between VDR rs739837 and T2DM or GDM among five genetic models (dominant, recessive, homozygote heterozygote, and allele models) using a fixed or random model.

resultsThe meta-analysis included 9 studies. In the overall analysis, the results showed that VDR rs739837 was associated with an increased risk of T2DM or GDM in the allele model (T vs. G: OR = 1.088; 95% CI: 1.018-1.163; P = 0.012) and dominant model (TT + GT vs. GG: OR = 1.095; 95% CI: 1.001-1.197; P = 0.047). In the subgroup analysis, VDR rs739837 was also associated with an increased risk of T2DM in the allele model (T vs. G: OR = 1.159; 95% CI: 1.055-1.273; P = 0.002) and dominant model (TT + GT vs. GG: OR = 1.198; 95% CI: 1.048-1.370; P = 0.008). However, VDR rs739837 was not associated with GDM.

conclusionsSignificant associations were found between the VDR rs739837 polymorphism and T2DM susceptibility, but not with GDM.

Indexed as

Diabetes, GestationalDiabetes Mellitus, Type 2Receptors, CalcitriolAllelesCase-Control StudiesFemaleGenetic Predisposition to DiseaseHumansPolymorphism, Single NucleotidePregnancyReceptors, CalcitriolVDR protein, humanGestational diabetes mellitusMeta-analysisrs739837SusceptibilityType 2 diabetes mellitusVitamin D receptor

Identifiers

PMID35526059
PMCPMC9080160
OpenAlexW4228998778

What OpenQuestion holds

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LicenceCC BY
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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.