Evidence map›Paper›PMID 29663709›Full record

ArticleAmerican journal of medical genetics. Part A2018

Soft tissue nasal asymmetry as an indicator of orofacial cleft predisposition.

Charles Zhang, Steven F Miller, Jasmien Roosenboom, George L Wehby, Lina M Moreno Uribe, Jacqueline T Hecht, Frederic W B Deleyiannis, Kaare Christensen, Mary L Marazita, Seth M Weinberg

Abstract readMulticenter Study
In one paragraph

Article in American journal of medical genetics. Part A, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Review
  2. 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

10 authors.

Charles ZhangDepartment of Anthropology, University of Pittsburgh, Pittsburgh, Pennsylvania.
Steven F MillerDepartment of Anatomy, Midwestern University, Downers Grove, Illinois.
Jasmien RoosenboomCenter for Craniofacial and Dental Genetics, Department of Oral Biology, University of Pittsburgh, Pittsburgh, Pennsylvania.
George L WehbyDepartment of Health Management and Policy, University of Iowa, Iowa City, Iowa.
Lina M Moreno UribeDepartment of Orthodontics, University of Iowa, Iowa City, Iowa.
Jacqueline T HechtDepartment of Pediatrics, University of Texas McGovern Medical Center, Houston, Texas.
Frederic W B DeleyiannisDepartment of Pediatric Plastic Surgery, Children's Hospital of Colorado, Aurora, Colorado.
Kaare ChristensenInstitute of Public Health, University of Southern Denmark, Odense, Denmark.
Mary L MarazitaCenter for Craniofacial and Dental Genetics, Department of Oral Biology, University of Pittsburgh, Pittsburgh, Pennsylvania.
Seth M WeinbergCenter for Craniofacial and Dental Genetics, Department of Oral Biology, University of Pittsburgh, Pittsburgh, Pennsylvania.ORCID 0000-0001-9467-4556

Funding

Extending the Phenotype of Nonsyndromic Orofacial CleftsR01DE016148 · NIDCR · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI MARAZITA, MARY L., WEINBERG, SETH M · 2004 to 2018
$19.7M
3D Analysis of Normal Facial Variation: Data Repository and Genetics (Research)U01DE020078 · NIDCR · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI MARAZITA, MARY L., WEINBERG, SETH M · 2009 to 2013
$2.0M
Health outcomes and improved phenotypic characterization of cleft lip and palateR01DD000295 · DD · UNIVERSITY OF IOWA · PI WEHBY, GEORGE L · 2007 to 2009
$1.4M
NCBDD CDC HHS R01 DD000295NIDCR NIH HHS R01 DE016148NIDCR NIH HHS U01 DE020078
6 · The paper itself

Abstract

The biological relatives of offspring with nonsyndromic orofacial clefts have been shown to exhibit distinctive facial features, including excess asymmetry, which are hypothesized to indicate the presence of genetic risk factors. The significance of excess soft tissue nasal asymmetry in at-risk relatives is unclear and was examined in the present study. Our sample included 164 unaffected parents from families with a history of orofacial clefting and 243 adult controls. Geometric morphometric methods were used to analyze the coordinates of 15 nasal landmarks collected from three-dimensional facial surface images. Following generalized Procrustes analysis, Procrustes ANOVA and MANOVA tests were applied to determine the type and magnitude of nasal asymmetry present in each group. Group differences in mean nasal asymmetry were also assessed via permutation testing. We found that nasal asymmetry in both parents and controls was directional in nature, although the magnitude of the asymmetry was greater in parents. This was confirmed with permutation testing, where the mean nasal asymmetry was significantly different (p < .0001) between parents and controls. The asymmetry was greatest for midline structures and the nostrils. When subsets of parents were subsequently analyzed and compared (parents with bilateral vs. unilateral offspring; parents with left vs. right unilateral offspring), each group showed a similar pattern of asymmetry and could not be distinguished statistically. Thus, the side of the unilateral cleft (right vs. left) in offspring was not associated with the direction of the nasal asymmetry in parents.

Indexed as

AdultCase-Control StudiesCleft PalateFacial AsymmetryFemaleGenetic Predisposition to DiseaseHumansMaleMiddle AgedNoseParentscleft lip and palategeometric morphometricsshape variationstereophotogrammetry

Identifiers

PMID29663709
PMCPMC5992056

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Registered trials

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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.