Evidence map›Paper›PMID 28625035›Full record

ArticleAsia Pacific journal of clinical nutrition2017

Programming of infant neurodevelopment by maternal obesity: potential role of maternal inflammation and insulin resistance.

Mira Dewi, Susan E Carlson, Kathleen M Gustafson, Debra K Sullivan, Jo A Wick, Holly R Hull

Abstract read
In one paragraph

Article in Asia Pacific journal of clinical nutrition, 2017. 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
0.8field-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, 6 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  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

6 authors at 2 institutions in 2 countries.

Mira DewiDepartment of Dietetics and Nutrition, School of Health Professions, University of Kansas Medical Center, Kansas City, KS, USA.
Susan E CarlsonDepartment of Community Nutrition, Faculty of Human Ecology, Bogor Agricultural University, Bogor, Indonesia.
Kathleen M GustafsonDepartment of Neurology, School of Medicine, Hoglund Brain Imaging Center, University of Kansas Medical Center, Kansas City, KS, USAa.
Debra K SullivanDepartment of Community Nutrition, Faculty of Human Ecology, Bogor Agricultural University, Bogor, Indonesia.
Jo A WickDepartment of Biostatistics, School of Medicine, University of Kansas Medical Center, Kansas City, KS, USA.
Holly R HullDepartment of Dietetics and Nutrition, School of Health Professions, University of Kansas Medical Center, Kansas City, KS, USA. Email: hhull@kumc.edu.
IPB University · IDUniversity of Kansas Medical Center · US

Funding

Heartland Institute for Clinical and Translational ResearchUL1TR000001 · NCATS · UNIVERSITY OF KANSAS MEDICAL CENTER · PI BAROHN, RICHARD J. · 2012 to 2015
$13.0M
Kansas BIRCWH Career Development Program Women's HealthK12HD052027 · NICHD · UNIVERSITY OF KANSAS MEDICAL CENTER · PI CARLSON, SUSAN E · 2005 to 2014
$5.0M
NCATS NIH HHS UL1 TR000001NICHD NIH HHS K12 HD052027
6 · The paper itself

Abstract

BACKGROUND AND

objectivesRecent studies show that maternal obesity is associated with impaired offspring neurodevelopmental outcomes. The mechanism underlying the association is unclear. However, there is evidence to suggest a role for intra-uterine exposure to inflammation and insulin resistance (IR). We aimed to determine if maternal IR and inflammation were associated to fetal neurodevelopment as indicated by fetal heart rate variability (HRV), an index of fetal cardiac autonomic nervous system development. METHODS AND STUDY

designA total of 44 healthy maternal-fetal pairs (maternal pre-pregnancy BMI distribution: n=20 normal weight, 8 overweight, 16 obese) were analyzed. We assessed maternal inflammation (plasma IL-6 and TNF-α) and IR (HOMA index). Fetal HRV, a proxy for fetal neurodevelopment, was assessed using fetal magnetocardiogram at the 36th week of pregnancy. The relationships between maternal inflammation and IR with fetal HRV (SD1 and SD2) were estimated individually by Pearson bivariate correlations.

resultsNo correlations were observed between the fetal HRV components with maternal HOMA-IR and maternal plasma levels of IL-6 and TNF-α (all p<0.05). However, the negative association between maternal TNF-α level and fetal SD2 approached significance (correlation coefficient=-0.29, 95% confidence interval=-0.62,-0.03, p=0.07).

conclusionMaternal IR and inflammation during pregnancy were not associated with fetal cardiac autonomic nervous system development. Further studies with a larger sample size and more maternal inflammatory indicators are needed to explore these relationships.

Indexed as

Pregnancy ComplicationsAdultBody Mass IndexCentral Nervous SystemCytokinesFemaleGene Expression RegulationHeart RateHomeostasisHumansInfant, NewbornInflammationInsulin ResistanceObesityPregnancyPrenatal Exposure Delayed EffectsCytokines

Identifiers

PMID28625035
PMCPMC6939379
OpenAlexW2968525714

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.