Evidence map›Paper›PMID 36380655›Full record

ArticleAmerican journal of medical genetics. Part A2023

Growth charts for Marfan syndrome in the Netherlands and analysis of genotype-phenotype relationships.

Peter Lauffer, Gerard Pals, Aeilko H Zwinderman, Floor A M Postema, Marieke J H Baars, Eelco Dulfer, Yvonne Hilhorst-Hofstee, Arjan C Houweling, Marlies Kempers, Ingrid P C Krapels and 7 more

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In one paragraph

Article in American journal of medical genetics. Part A, 2023. 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
1.1field-weighted citation impact, top 20% 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.

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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

17 authors at 9 institutions in 2 countries.

Peter LaufferDepartment of Pediatric Endocrinology, Emma Children's Hospital, Amsterdam University Medical Center, University of Amsterdam, Amsterdam, The Netherlands.ORCID 0000-0002-1174-7340
Gerard PalsDepartment of Human Genetics, Amsterdam University Medical Center, University of Amsterdam, Amsterdam, The Netherlands.
Aeilko H ZwindermanDepartment of Clinical Epidemiology, Bioinformatics and Biostatistics, Amsterdam University Medical Center, University of Amsterdam, Amsterdam, The Netherlands.
Floor A M PostemaDepartment of Pediatrics, Emma Children's Hospital, Amsterdam University Medical Center, University of Amsterdam, Amsterdam, The Netherlands.
Marieke J H BaarsDepartment of Human Genetics, Amsterdam University Medical Center, University of Amsterdam, Amsterdam, The Netherlands.
Eelco DulferDepartment of Clinical Genetics, University Medical Center Groningen, Groningen, The Netherlands.
Yvonne Hilhorst-HofsteeDepartment of Clinical Genetics, Leiden University Medical Center, Leiden, The Netherlands.
Arjan C HouwelingDepartment of Human Genetics, Amsterdam University Medical Center, Vrije Universiteit Amsterdam, Amsterdam, The Netherlands.
Marlies KempersDepartment of Clinical Genetics, Radboud University Medical Center, Nijmegen, The Netherlands.
Ingrid P C KrapelsDepartment of Clinical Genetics, Maastricht University Medical Center, Maastricht, The Netherlands.
Ingrid M B H van de LaarDepartment of Clinical Genetics, Erasmus Medical Center, Rotterdam, The Netherlands.
Bart LoeysDepartment of Clinical Genetics, Radboud University Medical Center, Nijmegen, The Netherlands.
Alexander M J SpaansGrowth Analyser B.V., Rotterdam, The Netherlands.
Jessica Warnink-KavelaarsDepartment of Rehabilitation Medicine, Emma Children's Hospital, Amsterdam Movement Sciences, Rehabilitation and Development, Amsterdam University Medical Center, University of Amsterdam, Amsterdam, The Netherlands.
Vivian de WaardDepartment of Medical Biochemistry, Amsterdam University Medical Center, University of Amsterdam, Amsterdam Cardiovascular Sciences, Amsterdam, The Netherlands.
Jan M WitDepartment of Pediatrics, Willem-Alexander Children's Hospital, Leiden University Medical Center, Leiden, The Netherlands.
Leonie A MenkeDepartment of Pediatrics, Emma Children's Hospital, Amsterdam University Medical Center, University of Amsterdam, Amsterdam, The Netherlands.
Amsterdam University Medical Centers · NLEmma Kinderziekenhuis · NLLeiden University Medical Center · NLRadboud University Nijmegen · NLErasmus MC · NLMaastricht University · NLRotterdam University of Applied Sciences · NLUniversity Medical Center Groningen · NLVrije Universiteit Amsterdam · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

To optimize care for children with Marfan syndrome (MFS) in the Netherlands, Dutch MFS growth charts were constructed. Additionally, we aimed to investigate the effect of FBN1 variant type (haploinsufficiency [HI]/dominant negative [DN]) on growth, and compare MFS-related height increase across populations. Height and weight data of individuals with MFS aged 0-21 years were retrospectively collected. Generalized Additive Models for Location, Scale and Shape (GAMLSS) was used for growth chart modeling. To investigate genotype-phenotype relationships, FBN1 variant type was included as an independent variable in height-for-age and BMI-for-age models. MFS-related height increase was compared with that of previous MFS growth studies from the United States, Korea, and France. Height and weight data of 389 individuals with MFS were included (210 males). Height-for-age, BMI-for-age, and weight-for-height charts reflected the tall and slender MFS habitus throughout childhood. Mean increase in height of individuals with MFS compared with the general Dutch population was significantly lower than in the other three MFS populations compared to their reference populations. FBN1-HI variants were associated with taller height in both sexes, and decreased BMI in females (p-values <0.05). This Dutch MFS growth study broadens the notion that genetic background and MFS variant type (HI/DN) influence tall and slender stature in MFS.

Indexed as

Marfan SyndromeFemaleFibrillin-1GenotypeGrowth ChartsHumansMaleMutationNetherlandsPhenotypeRetrospective StudiesFibrillin-1dominant-negative variantgrowth chartshaploinsufficiency variantheightMarfan syndromeweight

Identifiers

PMID36380655
PMCPMC10099852
OpenAlexW4309157625

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.