Evidence map›Paper›PMID 28586842›Full record

ArticleJAMA pediatrics2017

Association Between Prenatal Alcohol Exposure and Craniofacial Shape of Children at 12 Months of Age.

Evelyne Muggli, Harold Matthews, Anthony Penington, Peter Claes, Colleen O'Leary, Della Forster, Susan Donath, Peter J Anderson, Sharon Lewis, Cate Nagle and 4 more

Open access · bronzeAbstract read
In one paragraph

Article in JAMA pediatrics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 62 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
62citing papers in PubMed, 2 pooled it
18.3field-weighted citation impact, top 1% 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

62 citing papers in PubMed, 2 syntheses or guidelines pooled it, 129 citations in OpenAlex.

  1. Pooled it
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  6. Review
  7. Prenatal Alcohol Exposure and Mitochondrial Function in the Brain.Advances in experimental medicine and biology · 2026
    Review
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2 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors at 8 institutions in 2 countries.

Evelyne MuggliPublic Health Genetics, Murdoch Childrens Research Institute, Parkville, Victoria, Australia.
Harold MatthewsDepartment of Paediatrics, University of Melbourne, Victoria, Australia.
Anthony PeningtonDepartment of Paediatrics, University of Melbourne, Victoria, Australia.
Peter ClaesPlastic Surgery, Murdoch Childrens Research Institute, Parkville, Victoria, Australia.
Colleen O'LearyTelethon Kids Institute, Perth, Western Australia, Australia.
Della ForsterJudith Lumley Centre, School of Nursing and Midwifery, College of Science, Health and Engineering, La Trobe University, Melbourne, Victoria, Australia.
Susan DonathDepartment of Paediatrics, University of Melbourne, Victoria, Australia.
Peter J AndersonDepartment of Paediatrics, University of Melbourne, Victoria, Australia.
Sharon LewisPublic Health Genetics, Murdoch Childrens Research Institute, Parkville, Victoria, Australia.
Cate NagleCentre for Quality and Patient Safety Research, Deakin University, Geelong, Victoria, Australia.
Jeffrey M CraigDepartment of Paediatrics, University of Melbourne, Victoria, Australia.
Susan M WhiteDepartment of Paediatrics, University of Melbourne, Victoria, Australia.
Elizabeth J ElliottPaediatrics and Child Health, Children's Hospital Westmead, University of Sydney, Sydney, New South Wales, Australia.
Jane HallidayPublic Health Genetics, Murdoch Childrens Research Institute, Parkville, Victoria, Australia.
Murdoch Children's Research Institute · AUVictorian Clinical Genetics Services · AUUniversity of Melbourne · AUDeakin University · AUKU Leuven · BELa Trobe University · AUThe Kids Research Institute Australia · AUUniversity of Sydney · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Importance: Children who receive a diagnosis of fetal alcohol spectrum disorder may have a characteristic facial appearance in addition to neurodevelopmental impairment. It is not well understood whether there is a gradient of facial characteristics of children who did not receive a diagnosis of fetal alcohol spectrum disorder but who were exposed to a range of common drinking patterns during pregnancy. Objective: To examine the association between dose, frequency, and timing of prenatal alcohol exposure and craniofacial phenotype in 12-month-old children. Design, Setting, and Participants: A prospective cohort study was performed from January 1, 2011, to December 30, 2014, among mothers recruited in the first trimester of pregnancy from low-risk, public maternity clinics in metropolitan Melbourne, Australia. A total of 415 white children were included in this analysis of 3-dimensional craniofacial images taken at 12 months of age. Analysis was performed with objective, holistic craniofacial phenotyping using dense surface models of the face and head. Partial least square regression models included covariates known to affect craniofacial shape. Exposures: Low, moderate to high, or binge-level alcohol exposure in the first trimester or throughout pregnancy. Main Outcomes and Measures: Anatomical differences in global and regional craniofacial shape between children of women who abstained from alcohol during pregnancy and children with varying levels of prenatal alcohol exposure. Results: Of the 415 children in the study (195 girls and 220 boys; mean [SD] age, 363.0 [8.3] days), a consistent association between craniofacial shape and prenatal alcohol exposure was observed at almost any level regardless of whether exposure occurred only in the first trimester or throughout pregnancy. Regions of difference were concentrated around the midface, nose, lips, and eyes. Directional visualization showed that these differences corresponded to general recession of the midface and superior displacement of the nose, especially the tip of the nose, indicating shortening of the nose and upturning of the nose tip. Differences were most pronounced between groups with no exposure and groups with low exposure in the first trimester (forehead), moderate to high exposure in the first trimester (eyes, midface, chin, and parietal region), and binge-level exposure in the first trimester (chin). Conclusions and Relevance: Prenatal alcohol exposure, even at low levels, can influence craniofacial development. Although the clinical significance of these findings is yet to be determined, they support the conclusion that for women who are or may become pregnant, avoiding alcohol is the safest option.

Indexed as

AustraliaBinge DrinkingCohort StudiesCraniofacial AbnormalitiesFaciesFemaleFetal Alcohol Spectrum DisordersHumansInfantMalePregnancyPrenatal Exposure Delayed EffectsPrevalenceProspective StudiesSkullTomography, X-Ray Computed

Identifiers

PMID28586842
PMCPMC6583660
OpenAlexW2622695354

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.