Evidence map›Paper›PMID 32654027›Full record

ArticleDiabetologia2020

The Pacific-specific CREBRF rs373863828 allele protects against gestational diabetes mellitus in Māori and Pacific women with obesity.

Mohanraj Krishnan, Rinki Murphy, Karaponi A M Okesene-Gafa, Maria Ji, John M D Thompson, Rennae S Taylor, Tony R Merriman, Lesley M E McCowan, Christopher J D McKinlay

Open access · bronzeAbstract read
PubMed Publisher
In one paragraph

Article in Diabetologia, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 1 pooled it
1.5field-weighted citation impact, top 13% 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

17 citing papers in PubMed, 1 synthesis or guideline pooled it, 26 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

9 authors at 1 institution in 1 country.

Mohanraj KrishnanDepartment of Obstetrics and Gynaecology, University of Auckland, Auckland, New Zealand.
Rinki MurphyDepartment of Medicine, University of Auckland, Private Bag 92019, Auckland, 1142, New Zealand. r.murphy@auckland.ac.nz.ORCID 0000-0002-0043-2423
Karaponi A M Okesene-GafaDepartment of Obstetrics and Gynaecology, University of Auckland, Auckland, New Zealand.
Maria JiDepartment of Obstetrics and Gynaecology, University of Auckland, Auckland, New Zealand.
John M D ThompsonDepartment of Obstetrics and Gynaecology, University of Auckland, Auckland, New Zealand.
Rennae S TaylorDepartment of Obstetrics and Gynaecology, University of Auckland, Auckland, New Zealand.
Tony R MerrimanMaurice Wilkins Centre for Molecular Biodiscovery, University of Auckland, Auckland, New Zealand.
Lesley M E McCowanDepartment of Obstetrics and Gynaecology, University of Auckland, Auckland, New Zealand.
Christopher J D McKinlayCounties Manukau Health, Auckland, New Zealand. c.mckinlay@auckland.ac.nz.ORCID 0000-0003-1088-9467
University of Auckland · NZ

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aims/hypothesisThe CREBRF rs373863828 minor (A) allele is associated with increased BMI but reduced prevalence of type 2 diabetes in Māori and Pacific people. Given the shared aetiology of type 2 diabetes and gestational diabetes mellitus (GDM), we tested for an association between the CREBRF rs373863828 variant and GDM.

methodsWe conducted a prospective cohort study of Māori and Pacific women nested within a nutritional intervention study for pregnant women with obesity. Women were enrolled at 12-17 weeks' gestation and underwent anthropometry and collection of buffy coats for later genetic testing. GDM was diagnosed by 75 g OGTT at 24-28 weeks' gestation using the International Association of Diabetes and Pregnancy Study Groups criteria. Genotyping was performed by real-time PCR with a custom CREBRF rs373863828 probe-set. The association between CREBRF rs373863828 and GDM was analysed separately by ethnic group using logistic regression, with effect estimates combined in a meta-analysis.

resultsOf 112 Māori and Pacific pregnant women with obesity, 31 (28%) carried the CREBRF rs373863828 A allele (A/G or A/A) and 35 (31%) developed GDM. Women who carried the CREBRF rs373863828 A allele did not differ in BMI when compared with non-carriers (G/G). There was a fivefold reduction in the likelihood of GDM per CREBRF rs373863828 A allele (OR 0.19 [95% CI 0.05, 0.69], p = 0.01), independent of age, BMI and family history of diabetes (adjusted OR 0.13 [95% CI 0.03, 0.53], p = 0.004). GDM was diagnosed in 10% and 40% of women with and without the CREBRF rs373863828 A allele, respectively (no woman with the A/A genotype developed GDM). CONCLUSIONS/

interpretationThe CREBRF rs373863828 (A) allele is associated with reduced likelihood of GDM in Māori and Pacific women with obesity and may improve GDM risk prediction. Graphical abstract.

Indexed as

AdultDiabetes, GestationalFemaleGenetic Predisposition to DiseaseHumansMutation, MissenseObesityPregnancyPregnancy ComplicationsProtective FactorsTumor Suppressor ProteinsYoung AdultCREB3 regulatory factor, humanTumor Suppressor ProteinsCREBRFGestational diabetes mellitusMaternal obesityType 2 diabetes mellitus

Identifiers

PMID32654027
OpenAlexW3041065482

What OpenQuestion holds

Textmetadata
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.