Evidence map›Paper›PMID 35063470›Full record

ArticleThe Journal of pediatrics2022

Anthropometric Measures Correspond with Functional Motor Outcomes in Females with Rett Syndrome.

Kathleen J Motil, Suzanne Geerts, Fran Annese, Jeffrey L Neul, Tim Benke, Eric Marsh, David Lieberman, Steven A Skinner, Daniel G Glaze, Peter Heydemann and 6 more

Abstract read
In one paragraph

Article in The Journal of pediatrics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Review
  6. Review
  7. Rett syndrome: The Natural History Study journey.Annals of the Child Neurology Society · 2024
    Review
  8. Article
  9. Review
  10. Review
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

16 authors.

Kathleen J MotilChildren's Nutrition Research Center, Baylor College of Medicine, Houston, TX.
Suzanne GeertsSparks Clinics/Nutrition, University of Alabama at Birmingham, Birmingham, AL.
Fran AnneseGenetics Center, Greenwood Genetic Center, Greenwood, SC.
Jeffrey L NeulDepartment of Pediatrics/Child Neurology, Vanderbilt Kennedy Center, Vanderbilt University Medical Center, Nashville, TN.
Tim BenkeDepartment of Pediatrics/Child Neurology, University of Colorado-Denver, Denver, CO.
Eric MarshDepartment of Pediatrics/Child Neurology, Children's Hospital of Philadelphia, University of Pennsylvania, Philadelphia, PA.
David LiebermanDepartment of Child Neurology, Children's Hospital Boston, Harvard University, Boston, MA.
Steven A SkinnerGenetics Center, Greenwood Genetic Center, Greenwood, SC.
Daniel G GlazeDepartment of Pediatrics/Child Neurology, Baylor College of Medicine, Houston, TX.
Peter HeydemannDepartment of Pediatrics/Child Neurology, Rush Medical Center, Chicago, IL.
Arthur BeisangDepartment of Pediatrics, Gillette Children's Hospital, St. Paul, MN.
Shannon StandridgeDepartment of Pediatrics/Child Neurology, Cincinnati Children's Hospital, Cincinnati, OH.
Robin RytherDepartment of Pediatrics/Child Neurology, Washington University, St. Louis, MO.
Jane B LaneDepartment of Pediatrics/Child Neurology, University of Alabama at Birmingham, Birmingham, AL.
Lloyd EdwardsSchool of Public Health/Biostatistics, University of Alabama at Birmingham, Birmingham, AL.
Alan K PercyDepartment of Pediatrics/Child Neurology, University of Alabama at Birmingham, Birmingham, AL. Electronic address: apercy@uab.edu.

Funding

Training and Career Development ComponentU54HD061222 · NICHD · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI PERCY, ALAN KENNETH · 2009 to 2019
$12.4M
Overall: Eunice Kennedy Shriver Intellectual and Developmental Disabilities Research Center at VanderbiltP50HD103537 · NICHD · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Lea K Davis · 2020 to 2026
$10.3M
NICHD NIH HHS P50 HD103537NICHD NIH HHS U54 HD061222
6 · The paper itself

Abstract

objectiveTo characterize growth and anthropometric measurements in females with Rett syndrome and compare these measurements with functional outcomes. STUDY

designWe obtained longitudinal growth and anthropometric measurements from 1154 females with classic and atypical Rett syndrome seen between 2006 and 2019 in the US Natural History Study. We calculated the Clinical Severity Score, Motor Behavior Assessment score, and arm and leg muscle areas and recorded the functional assessments of arm and hand use and ambulation. We compared growth and anthropometric variables from females with Rett syndrome in regard to normative data. We analyzed Clinical Severity Score, Motor Behavior Assessment, and anthropometric measurements in regard to functional assessments.

resultsGrowth and anthropometric measurements were significantly lower in females with classic and severe atypical Rett syndrome compared with those classified as mild atypical Rett syndrome and deviated from normative patterns among all 3 groups. Suprailiac skinfold measurements correlated with body mass index measurements in each group. Lower leg muscle area measurements were significantly greater among females in all 3 Rett syndrome groups who ambulated independently compared with those who did not. In females with classic Rett syndrome, arm, thigh, and lower leg muscle area measurements increased significantly over time and were significantly greater among those who had purposeful arm and hand use and independent ambulation compared with those who did not.

conclusionsThe pattern of growth and anthropometric measures in females with Rett syndrome differs from normative data and demonstrates clear differences between classic and mild or severe atypical Rett syndrome. Anthropometric measures correspond with functional outcomes and could provide markers supporting efficacy outcomes in clinical trials.

Indexed as

Rett SyndromeAnthropometryFemaleHumansMethyl-CpG-Binding Protein 2WalkingMethyl-CpG-Binding Protein 2

Identifiers

PMID35063470
PMCPMC9086122

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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.