Evidence map›Paper›PMID 22768333›Full record

Trial reportPloS one2012

Association of genetic variants of melatonin receptor 1B with gestational plasma glucose level and risk of glucose intolerance in pregnant Chinese women.

Shunyao Liao, Yunqiang Liu, Yuande Tan, Lu Gan, Jie Mei, Wenzhong Song, Shu Chi, Xianjue Dong, Xiaojuan Chen, Shaoping Deng

Open access · goldAbstract readClinical TrialMulticenter Study
In one paragraph

Trial report in PloS one, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed, 1 pooled it
6.8field-weighted citation impact, top 3% 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

25 citing papers in PubMed, 1 synthesis or guideline pooled it, 47 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Review
  8. World journal of gastroenterology · 2021
    Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. TheInternational journal of molecular sciences · 2018
    Article
  14. Article
  15. Review
  16. Melatonin, mitochondria, and the metabolic syndrome.Cellular and molecular life sciences : CMLS · 2017
    Review
  17. Article
  18. Article
  19. Article
  20. Genetics, genomics and metabolomics: new insights into maternal metabolism during pregnancy.Diabetic medicine : a journal of the British Diabetic Association · 2014
    Review
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 6 institutions in 2 countries.

Shunyao LiaoDiabetes Center, Sichuan Academy of Medical Science and Sichuan Provincial People's Hospital, Chengdu, China. shunyaol@yahoo.com
Yunqiang Liu
Yuande Tan
Lu Gan
Jie Mei
Wenzhong Song
Shu Chi
Xianjue Dong
Xiaojuan Chen
Shaoping Deng
Sichuan Academy of Medical Sciences & Sichuan Provincial People's Hospital · CNChongqing Medical University · CNHunan Normal University · CNMassachusetts General Hospital · USNorthwest University · USState Key Laboratory of Biotherapy

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThis study aimed to explore the association of MTNR1B genetic variants with gestational plasma glucose homeostasis in pregnant Chinese women.

methodsA total of 1,985 pregnant Han Chinese women were recruited and evaluated for gestational glucose tolerance status with a two-step approach. The four MTNR1B variants rs10830963, rs1387153, rs1447352, and rs2166706 which had been reported to associate with glucose levels in general non-pregnant populations, were genotyped in these women. Using an additive model adjusted for age and body mass index (BMI), association of these variants with gestational fasting and postprandial plasma glucose (FPG and PPG) levels were analyzed by multiple linear regression; relative risk of developing gestational glucose intolerance was calculated by logistic regression. Hardy-Weinberg Equilibrium was tested by Chi-square and linkage disequilibrium (LD) between these variants was estimated by measures of D' and r(2).

resultsIn the pregnant Chinese women, the MTNR1B variant rs10830963, rs1387153, rs2166706 and rs1447352 were shown to be associated with the increased 1 hour PPG level (p=8.04 × 10(-10), 5.49 × 10(-6), 1.89 × 10(-5) and 0.02, respectively). The alleles were also shown to be associated with gestational glucose intolerance with odds ratios (OR) of 1.64 (p=8.03 × 10(-11)), 1.43 (p=1.94 × 10(-6)), 1.38 (p=1.63 × 10(-5)) and 1.24 (p=0.007), respectively. MTNR1B rs1387153, rs2166706 were shown to be associated with gestational FPG levels (p=0.04). Our data also suggested that, the LD pattern of these variants in the studied women conformed to that in the general populations: rs1387153 and rs2166706 were in high LD, they linked moderately with rs10830963, but might not linked with rs1447352;rs10830963 might not link with rs1447352, either. In addition, the MTNR1B variants were not found to be associated with any other traits tested.

conclusionsThe MTNR1B is likely to be involved in the regulation of glucose homeostasis during pregnancy.

Indexed as

Polymorphism, GeneticAdultAsian PeopleBlood GlucoseChinaFemaleGlucose IntoleranceHumansPregnancyPregnancy ComplicationsPregnancy Trimester, SecondReceptor, Melatonin, MT1Receptor, Melatonin, MT2Blood GlucoseMTNR1B protein, humanReceptor, Melatonin, MT1Receptor, Melatonin, MT2

Identifiers

PMID22768333
PMCPMC3388040
OpenAlexW2152583765

What OpenQuestion holds

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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.