Evidence map›Paper›PMID 37509275›Full record

ArticleCancers2023

Sensory Processing in Children and Adolescents with Neurofibromatosis Type 1.

Natalie A Pride, Kristina M Haebich, Karin S Walsh, Francesca Lami, Melissa Rouel, Alice Maier, Anita K Chisholm, Jennifer Lorenzo, Stephen J C Hearps, Kathryn N North and 1 more

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 3 pooled it
1.4field-weighted citation impact, top 17% 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

6 citing papers in PubMed, 3 syntheses or guidelines pooled it, 7 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Article
  5. Article
  6. 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

11 authors at 5 institutions in 2 countries.

Natalie A PrideKids Neuroscience Centre, The Children's Hospital at Westmead, Sydney, NSW 2145, Australia.
Kristina M HaebichMurdoch Children's Research Institute, Parkville, VIC 3052, Australia.
Karin S WalshCenter for Neuroscience and Behavioral Medicine, Children's National Hospital, George Washington University School of Medicine, Washington, DC 20052, USA.ORCID 0000-0001-9637-2164
Francesca LamiMurdoch Children's Research Institute, Parkville, VIC 3052, Australia.ORCID 0000-0002-9706-315X
Melissa RouelKids Neuroscience Centre, The Children's Hospital at Westmead, Sydney, NSW 2145, Australia.
Alice MaierMurdoch Children's Research Institute, Parkville, VIC 3052, Australia.
Anita K ChisholmMurdoch Children's Research Institute, Parkville, VIC 3052, Australia.
Jennifer LorenzoKids Neuroscience Centre, The Children's Hospital at Westmead, Sydney, NSW 2145, Australia.
Stephen J C HearpsMurdoch Children's Research Institute, Parkville, VIC 3052, Australia.ORCID 0000-0003-2984-1172
Kathryn N NorthMurdoch Children's Research Institute, Parkville, VIC 3052, Australia.
Jonathan M PayneMurdoch Children's Research Institute, Parkville, VIC 3052, Australia.ORCID 0000-0001-9565-3845
The University of Melbourne · AUChildren's Hospital at Westmead · AURoyal Children's Hospital · AUGeorge Washington University · USMurdoch Children's Research Institute · AU

Funding

Murdoch Children's Research Institute Awarded to JMPUnited States Department of Defense W81XWH-15-1-0619
6 · The paper itself

Abstract

Despite the evidence of elevated autistic behaviors and co-occurring neurodevelopmental difficulties in many children with neurofibromatosis type 1 (NF1), we have a limited understanding of the sensory processing challenges that may occur with the condition. This study examined the sensory profile of children and adolescents with NF1 and investigated the relationships between the sensory profiles and patient characteristics and neuropsychological functioning. The parent/caregivers of 152 children with NF1 and 96 typically developing children completed the Sensory Profile 2 (SP2), along with standardized questionnaires assessing autistic behaviors, ADHD symptoms, internalizing symptoms, adaptive functioning, and social skills. Intellectual functioning was also assessed. The SP2 data indicated elevated sensory processing problems in children with NF1 compared to typically developing children. Over 40% of children with NF1 displayed differences in sensory registration (missing sensory input) and were unusually sensitive to and unusually avoidant of sensory stimuli. Sixty percent of children with NF1 displayed difficulties in one or more sensory modalities. Elevated autistic behaviors and ADHD symptoms were associated with more severe sensory processing difficulties. This first detailed assessment of sensory processing, alongside other clinical features, in a relatively large cohort of children and adolescents with NF1 demonstrates the relationships between sensory processing differences and adaptive skills and behavior, as well as psychological well-being. Our characterization of the sensory profile within a genetic syndrome may help facilitate more targeted interventions to support overall functioning.

Indexed as

adaptive skillsADHDanxietyautisticneurofibromatosis type 1sensory modulationsensory processing

Identifiers

PMID37509275
PMCPMC10377664
OpenAlexW4384341508

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.