Evidence map›Paper›PMID 30927385›Full record

ArticleBirth defects research2019

Evaluation of prenatal diabetes mellitus and other risk factors for craniofacial microsomia.

Babette Siebold, Carrie L Heike, Brian G Leroux, Matthew L Speltz, Amelia F Drake, Alexis L Johns, Kathleen A Kapp-Simon, Leanne Magee, Daniela V Luquetti

Open access · greenAbstract read
In one paragraph

Article in Birth defects research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.7field-weighted citation impact, top 25% 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

3 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Article
  3. 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

9 authors at 6 institutions in 1 country.

Babette SieboldCenter for Developmental Biology and Regenerative Medicine, Seattle Children's Research Institute, Seattle, Washington.
Carrie L HeikeCenter for Developmental Biology and Regenerative Medicine, Seattle Children's Research Institute, Seattle, Washington.
Brian G LerouxDepartment of Biostatistics, University of Washington School of Dentistry, Seattle, Washington.
Matthew L SpeltzCenter for Developmental Biology and Regenerative Medicine, Seattle Children's Research Institute, Seattle, Washington.
Amelia F DrakeDepartment of Otolaryngology/Head and Neck Surgery, University of North Carolina, Chapel Hill, North Carolina.
Alexis L JohnsDivision of Plastic and Maxillofacial Surgery, Children's Hospital of Los Angeles, Los Angeles, California.
Kathleen A Kapp-SimonCleft-Craniofacial Center, Shriners Hospital for Children, Chicago, Illinois.
Leanne MageeDivision of Plastic and Reconstructive Surgery, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
Daniela V LuquettiCenter for Developmental Biology and Regenerative Medicine, Seattle Children's Research Institute, Seattle, Washington.ORCID 0000-0001-6059-7708
Seattle Children's Hospital · USChildren's Hospital of Los Angeles · USChildren's Hospital of Philadelphia · USUniversity of Illinois Chicago · USUniversity of North Carolina at Chapel Hill · USUniversity of Washington · US

Funding

Transform Dissemination and Implementation Science in CTSA ProgramsUL1TR002319 · NCATS · UNIVERSITY OF WASHINGTON · PI John K. Amory · 2017 to 2026
$100.0M
Institute of Translational Health SciencesUL1TR000423 · NCATS · UNIVERSITY OF WASHINGTON · PI DISIS, MARY L. · 2012 to 2016
$49.4M
CFM: Longitudinal Outcomes in Children pre-Kindergarten (CLOCK)R01DE022438 · NIDCR · SEATTLE CHILDREN'S HOSPITAL · PI HEIKE, CARRIE LYN, SPELTZ, MATTHEW LOUIS · 2012 to 2018
$4.7M
NCATS NIH HHS UL1 TR000423NCATS NIH HHS UL1 TR002319NIDCR NIH HHS R01 DE022438
6 · The paper itself

Abstract

objectivesCraniofacial microsomia (CFM) is a congenital condition that typically involves hypoplasia of the ear and jaw. It is often associated with adverse effects such as hearing loss and sleep-disordered breathing. There is little research on its etiology.

methodsWe conducted a case-control study from maternal interview data collected from mothers of infants with and without CFM. The study included 108 children with and 84 children without CFM. Logistic regression with adjustment for demographic factors was used to evaluate associations between maternal exposures of interest and risk for CFM overall, as well as for different phenotypic sub-groups of children on the CFM spectrum.

resultsWe found a statistically significant association between diabetes mellitus (DM) and CFM (OR 4.01, 95% CI 1.6-10.5). The association was slightly attenuated after adjustment for BMI. Higher parity was also associated with increased risk for CFM (OR 2.0, 95% CI 1.0-4.0). Vitamin A consumption and/or liver consumption was associated with a 70% lower risk compared with non-users (OR 0.3, 95% 0.1-0.8). Maternal age at the time of pregnancy was not associated with CFM.

conclusionsThese analyses contribute evidence linking maternal DM with an elevated risk of having an infant with CFM, which is consistent with previous research and adds to the body of knowledge about the strength of this association. Further study is warranted to understand the potential mechanisms underlying the effect of DM in the developing embryo.

Indexed as

AdultCase-Control StudiesDiabetes ComplicationsDiabetes MellitusFemaleGoldenhar SyndromeHumansInfantMaleMothersPregnancyPrenatal Exposure Delayed EffectsRisk FactorsUnited Statesanotiacraniofacial microsomiadiabeteshemifacial microsomiamicrotiaOAVS

Identifiers

PMID30927385
PMCPMC6602800
OpenAlexW2929224003

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.