Evidence map›Paper›PMID 31592117›Full record

ArticleEndocrinology, diabetes & metabolism2019

Normal foetal kidney volume in offspring of women treated for gestational diabetes.

Stacey Hokke, Natasha de Zoysa, Bethany L Carr, Veronica Abruzzo, Peter R Coombs, Carolyn A Allan, Christine East, Julie R Ingelfinger, Victor G Puelles, Mary J Black and 5 more

Open access · goldAbstract read
In one paragraph

Article in Endocrinology, diabetes & metabolism, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.1field-weighted citation impact, top 19% 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

5 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Review
  3. Observational
  4. Review
  5. 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

15 authors at 7 institutions in 3 countries.

Stacey HokkeDevelopment and Stem Cells Program Department of Anatomy and Developmental Biology Biomedicine Discovery Institute Monash University Clayton Vic. Australia.
Natasha de ZoysaDevelopment and Stem Cells Program Department of Anatomy and Developmental Biology Biomedicine Discovery Institute Monash University Clayton Vic. Australia.
Bethany L CarrMonash Women's Maternity Services Monash Health Clayton Vic. Australia.
Veronica AbruzzoMonash Women's Maternity Services Monash Health Clayton Vic. Australia.
Peter R CoombsDiagnostic Imaging Monash Health Clayton Vic. Australia.
Carolyn A AllanEndocrine Services in Pregnancy Monash Health Clayton Vic. Australia.
Christine EastMonash Women's Maternity Services Monash Health Clayton Vic. Australia.
Julie R IngelfingerPediatric Nephrology Mass General Hospital for Children at MGH Boston MA USA.
Victor G PuellesDevelopment and Stem Cells Program Department of Anatomy and Developmental Biology Biomedicine Discovery Institute Monash University Clayton Vic. Australia.
Mary J BlackDevelopment and Stem Cells Program Department of Anatomy and Developmental Biology Biomedicine Discovery Institute Monash University Clayton Vic. Australia.
Danica RyanDevelopment and Stem Cells Program Department of Anatomy and Developmental Biology Biomedicine Discovery Institute Monash University Clayton Vic. Australia.
James A ArmitageDevelopment and Stem Cells Program Department of Anatomy and Developmental Biology Biomedicine Discovery Institute Monash University Clayton Vic. Australia.
Euan M WallaceDepartment of Obstetrics and Gynaecology Monash University Clayton Vic. Australia.
John F BertramDevelopment and Stem Cells Program Department of Anatomy and Developmental Biology Biomedicine Discovery Institute Monash University Clayton Vic. Australia.
Luise A Cullen-McEwenDevelopment and Stem Cells Program Department of Anatomy and Developmental Biology Biomedicine Discovery Institute Monash University Clayton Vic. Australia.ORCID https://orcid.org/0000-0003-2229-5762
Discovery Institute · USMonash Health · AUDeakin University · AUHudson Institute of Medical Research · AUMassachusetts General Hospital · USMonash University · AUUniversität Hamburg · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimsThe worldwide prevalence of gestational diabetes mellitus (GDM) is increasing. Studies in rodent models indicate that hyperglycaemia during pregnancy alters kidney development, yet few studies have examined if this is so in humans. The objective of this study was to evaluate the association of treated GDM with foetal kidney size. MATERIALS AND

methodsParticipants were recruited from an Australian tertiary hospital, and clinical data were collected from women without GDM and women diagnosed and treated for GDM and their offspring. Participants underwent an obstetric ultrasound at 32-34 weeks gestation for foetal biometry and foetal kidney volume measurement.

resultsSixty-four non-GDM and 64 GDM women participated in the study. Thirty percent of GDM women were diagnosed with fasting hyperglycaemia, while 89% had an elevated 2-hour glucose level. Maternal age, weight and body mass index were similar in women with and without GDM. Estimated foetal weight, foetal kidney dimensions, total foetal kidney volume and birth weight were similar in offspring of women with and without GDM.

conclusionsWe conclude that a period of mild hyperglycaemia prior to diagnosis of GDM and treatment initiation, which coincides with a period of rapid nephron formation and kidney growth, does not alter kidney size at 32-34 weeks gestation.

Indexed as

foetal kidney volumegestational diabeteskidney development

Identifiers

PMID31592117
PMCPMC6775447
OpenAlexW2971309299

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.