Evidence map›Paper›PMID 34949201›Full record

ArticleOrphanet journal of rare diseases2021

Growth in achondroplasia including stature, weight, weight-for-height and head circumference from CLARITY: achondroplasia natural history study-a multi-center retrospective cohort study of achondroplasia in the US.

Julie E Hoover-Fong, Kerry J Schulze, Adekemi Y Alade, Michael B Bober, Ethan Gough, S Shahrukh Hashmi, Jacqueline T Hecht, Janet M Legare, Mary Ellen Little, Peggy Modaff and 6 more

Abstract readMulticenter Study
In one paragraph

Article in Orphanet journal of rare diseases, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed, 1 pooled it
–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

35 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Guideline
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  5. Article
  6. C-Type Natriuretic Peptide Derivatives: Orthopaedic Implications in Achondroplasia.Journal of the Pediatric Orthopaedic Society of North America · 2026
    Review
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  13. Observational
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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.

Julie E Hoover-FongGreenberg Center for Skeletal Dysplasias, McKusick-Nathans Department of Genetic Medicine, Johns Hopkins University, 733 N. Broadway Suite 579, Baltimore, MD, 21205, USA. jhoover2@jhmi.edu.ORCID 0000-0002-1242-5626
Kerry J SchulzeGreenberg Center for Skeletal Dysplasias, McKusick-Nathans Department of Genetic Medicine, Johns Hopkins University, 733 N. Broadway Suite 579, Baltimore, MD, 21205, USA.
Adekemi Y AladeGreenberg Center for Skeletal Dysplasias, McKusick-Nathans Department of Genetic Medicine, Johns Hopkins University, 733 N. Broadway Suite 579, Baltimore, MD, 21205, USA.
Michael B BoberNemours/AI duPont Hospital for Children, Wilmington, DE, USA.
Ethan GoughGreenberg Center for Skeletal Dysplasias, McKusick-Nathans Department of Genetic Medicine, Johns Hopkins University, 733 N. Broadway Suite 579, Baltimore, MD, 21205, USA.
S Shahrukh HashmiMcGovern Medical School, University of Texas Health, Houston, TX, USA.
Jacqueline T HechtMcGovern Medical School, University of Texas Health, Houston, TX, USA.
Janet M LegareUniversity of Wisconsin School of Medicine and Public Health, Madison, WI, USA.
Mary Ellen LittleNemours/AI duPont Hospital for Children, Wilmington, DE, USA.
Peggy ModaffUniversity of Wisconsin School of Medicine and Public Health, Madison, WI, USA.
Richard M PauliUniversity of Wisconsin School of Medicine and Public Health, Madison, WI, USA.
David F Rodriguez-BuriticaMcGovern Medical School, University of Texas Health, Houston, TX, USA.
Maria E SernaMcGovern Medical School, University of Texas Health, Houston, TX, USA.
Cory SmidUniversity of Wisconsin School of Medicine and Public Health, Madison, WI, USA.
Chengxin LiuGreenberg Center for Skeletal Dysplasias, McKusick-Nathans Department of Genetic Medicine, Johns Hopkins University, 733 N. Broadway Suite 579, Baltimore, MD, 21205, USA.
John McGreadyGreenberg Center for Skeletal Dysplasias, McKusick-Nathans Department of Genetic Medicine, Johns Hopkins University, 733 N. Broadway Suite 579, Baltimore, MD, 21205, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAchondroplasia is the most common genetic skeletal disorder causing disproportionate short stature/dwarfism. Common additional features include spinal stenosis, midface retrusion, macrocephaly and a generalized spondylometaphyseal dysplasia which manifest as spinal cord compression, sleep disordered breathing, delayed motor skill acquisition and genu varus with musculoskeletal pain. To better understand the interactions and health outcomes of these potential complications, we embarked on a multi-center, natural history study entitled CLARITY (achondroplasia natural history study). One of the CLARITY objectives was to develop growth curves (length/height, weight, head circumference, weight-for-height) and corresponding reference tables of mean and standard deviations at 1 month increments from birth through 18 years for clinical use and research for achondroplasia patients.

methodsAll available retrospective anthropometry data including length/height, weight and head circumference from achondroplasia patients were collected at 4 US skeletal dysplasia centers (Johns Hopkins University, AI DuPont Hospital for Children, McGovern Medical School University of Texas Health, University of Wisconsin School of Medicine and Public Health). Weight-for-age values beyond 3 SD above the mean were excluded from the weight-for-height and weight-for-age curves to create a stricter tool for weight assessment in this population.

resultsOver 37,000 length/height, weight and head circumference measures from 1374 patients with achondroplasia from birth through 75 years of age were compiled in a REDCap database. Stature and weight data from birth through 18 years of age and head circumference from birth through 5 years of age were utilized to construct new length/height-for-age, weight-for-age, head circumference-for-age and weight-for-height curves.

conclusionAchondroplasia-specific growth curves are essential for clinical care of growing infants and children with this condition. In an effort to provide prescriptive, rather than purely descriptive, references for weight in this population, extreme weight values were omitted from the weight-for-age and weight-for-height curves. This well-phenotyped cohort may be studied with other global achondroplasia populations (e.g. Europe, Argentina, Australia, Japan) to gain further insight into environmental or ethnic influences on growth.

Indexed as

AchondroplasiaBody HeightChildCohort StudiesGrowth ChartsHumansInfantRetrospective StudiesAchondroplasiaAnthropometryHead circumferenceHeight/lengthWeight

Identifiers

PMID34949201
PMCPMC8697459

What OpenQuestion holds

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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.