Evidence map›Paper›PMID 31444527›Full record

ArticleDiabetologia2019

Persistent effects of in utero overnutrition on offspring adiposity: the Exploring Perinatal Outcomes among Children (EPOCH) study.

Christine W Hockett, Kylie K Harrall, Brianna F Moore, Anne P Starling, Anna Bellatorre, Katherine A Sauder, Wei Perng, Ann Scherzinger, Kavita Garg, Brandy M Ringham and 2 more

Open access · bronzeAbstract readMulticenter Study
In one paragraph

Article in Diabetologia, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed, 1 pooled it
3.2field-weighted citation impact, top 8% 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

23 citing papers in PubMed, 1 synthesis or guideline pooled it, 35 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

12 authors at 2 institutions in 1 country.

Christine W HockettLifecourse Epidemiology of Adiposity and Diabetes (LEAD) Center, Colorado School of Public Health, 12474 E. 19th Avenue - Mail Stop F426, Aurora, CO, 80045, USA. christine.hockett@ucdenver.edu.
Kylie K HarrallLifecourse Epidemiology of Adiposity and Diabetes (LEAD) Center, Colorado School of Public Health, 12474 E. 19th Avenue - Mail Stop F426, Aurora, CO, 80045, USA.
Brianna F MooreLifecourse Epidemiology of Adiposity and Diabetes (LEAD) Center, Colorado School of Public Health, 12474 E. 19th Avenue - Mail Stop F426, Aurora, CO, 80045, USA.
Anne P StarlingLifecourse Epidemiology of Adiposity and Diabetes (LEAD) Center, Colorado School of Public Health, 12474 E. 19th Avenue - Mail Stop F426, Aurora, CO, 80045, USA.
Anna BellatorreLifecourse Epidemiology of Adiposity and Diabetes (LEAD) Center, Colorado School of Public Health, 12474 E. 19th Avenue - Mail Stop F426, Aurora, CO, 80045, USA.
Katherine A SauderLifecourse Epidemiology of Adiposity and Diabetes (LEAD) Center, Colorado School of Public Health, 12474 E. 19th Avenue - Mail Stop F426, Aurora, CO, 80045, USA.
Wei PerngLifecourse Epidemiology of Adiposity and Diabetes (LEAD) Center, Colorado School of Public Health, 12474 E. 19th Avenue - Mail Stop F426, Aurora, CO, 80045, USA.
Ann ScherzingerDepartment of Radiology, University of Colorado School of Medicine, Aurora, CO, USA.
Kavita GargDepartment of Radiology, University of Colorado School of Medicine, Aurora, CO, USA.
Brandy M RinghamLifecourse Epidemiology of Adiposity and Diabetes (LEAD) Center, Colorado School of Public Health, 12474 E. 19th Avenue - Mail Stop F426, Aurora, CO, 80045, USA.
Deborah H GlueckLifecourse Epidemiology of Adiposity and Diabetes (LEAD) Center, Colorado School of Public Health, 12474 E. 19th Avenue - Mail Stop F426, Aurora, CO, 80045, USA.
Dana DabeleaLifecourse Epidemiology of Adiposity and Diabetes (LEAD) Center, Colorado School of Public Health, 12474 E. 19th Avenue - Mail Stop F426, Aurora, CO, 80045, USA.
Colorado School of Public Health · USUniversity of Colorado Denver · US

Funding

PILOT STUDY--SUBSTRATE METABOLISM IN EXTREMELY LOW BIRTH WEIGHT INFANTSP30DK048520 · NIDDK · UNIVERSITY OF COLORADO DENVER · PI Wendy M Kohrt · 1995 to 2026
$32.6M
Exploring the Fetal Origins Hypothesis in Diverse YouthR01DK068001 · NIDDK · UNIVERSITY OF COLORADO DENVER · PI DABELEA, DANA · 2005 to 2015
$4.5M
Methods and Software for Lifecourse Epidemiology Data and Sample Size AnalysisR01GM121081 · NIGMS · UNIVERSITY OF COLORADO DENVER · PI DABELEA, DANA, GLUECK, DEBORAH HELEN · 2016 to 2019
$2.6M
A Master Course on Power for Multilevel and Longitudinal Health Behavior StudiesR25GM111901 · NIGMS · UNIVERSITY OF FLORIDA · PI GLUECK, DEBORAH HELEN, MULLER, KEITH E · 2014 to 2018
$1.0M
NIDDK NIH HHS P30 DK048520NIDDK NIH HHS R01 DK068001NIGMS NIH HHS R01 GM121081NIGMS NIH HHS R25 GM111901
6 · The paper itself

Abstract

aims/hypothesisWe previously showed that intrauterine exposure to gestational diabetes mellitus (GDM) increases selected markers of adiposity in pre-pubertal adolescents. In the present study, we examined these associations in adolescence, and explored whether they are strengthened as the participants transition through puberty.

methodsData from 597 individuals (505 unexposed, 92 exposed) participating in the longitudinal Exploring Perinatal Outcomes among Children (EPOCH) study in Colorado were collected at two research visits when the participants were, on average, 10.4 and 16.7 years old. Adiposity measures included BMI, waist/height ratio, and visceral and subcutaneous adipose tissue (as determined by MRI). Separate general linear mixed models were used to assess the longitudinal relationships between exposure to maternal GDM and each adiposity outcome. We tested whether the effect changed over time by including an interaction term between exposure and age in our models, and whether the associations were explained by postnatal behaviours.

resultsCompared with unexposed participants, those exposed to maternal GDM had higher BMI (β = 1.28; 95% CI 0.35, 2.21; p < 0.007), waist/height ratio (β = 0.03; 95% CI 0.01, 0.04; p = 0.0004), visceral adipose tissue (β = 4.81; 95% CI 1.08, 8.54; p = 0.01) and subcutaneous adipose tissue (β = 35.15; 95% CI 12.43, 57.87; p < 0.003). The magnitude of these differences did not change over time and the associations did not appear to be explained by postnatal behaviours. CONCLUSIONS/

interpretationOur data provide further evidence that intrauterine exposure to maternal GDM is associated with increased offspring adiposity, an effect that appears early in life and tracks throughout adolescence. Efforts to prevent childhood obesity following intrauterine exposure to maternal GDM should target the prenatal or early life periods.

Indexed as

AdiposityPrenatal Exposure Delayed EffectsAdipose TissueAdolescentBody Mass IndexChildColoradoDiabetes, GestationalFemaleHumansLinear ModelsLongitudinal StudiesMagnetic Resonance ImagingMaleMothersObesityFetal programmingGDMMaternal diabetesObesityPubertySATVAT

Identifiers

PMID31444527
PMCPMC7593989
OpenAlexW2969605419

What OpenQuestion holds

Textmetadata
LicenceTDM
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.