Evidence map›Paper›PMID 36497438›Full record

ArticleCancers2022

Demographic and Disease-Related Predictors of Socioemotional Development in Children with Neurofibromatosis Type 1 and Plexiform Neurofibromas: An Exploratory Study.

Yang Hou, Xian Wu, Dan Liu, Staci Martin, Mary Anne Toledo-Tamula, Taryn Allen, Andrea Baldwin, Andy Gillespie, Anne Goodwin, Brigitte C Widemann and 1 more

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 1 pooled it
1.0field-weighted citation impact, top 22% 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, 1 synthesis or guideline pooled it, 8 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Article
  5. Parent-child discrepancies in reports of child psychosocial functioning in neurofibromatosis type 1.Journal of family psychology : JFP : journal of the Division of Family Psychology of the American Psychological Association (Division 43) · 2025
    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 3 institutions in 1 country.

Yang HouDepartment of Behavioral Sciences and Social Medicine, Florida State University, Tallahassee, FL 32306, USA.ORCID 0000-0002-7360-5751
Xian WuDepartment of Behavioral Sciences and Social Medicine, Florida State University, Tallahassee, FL 32306, USA.
Dan LiuDepartment of Behavioral Sciences and Social Medicine, Florida State University, Tallahassee, FL 32306, USA.
Staci MartinPediatric Oncology Branch, National Cancer Institute, Bethesda, MD 20814, USA.
Mary Anne Toledo-TamulaClinical Research Directorate, Frederick National Laboratory for Cancer Research, Frederick, MD 20702, USA.
Taryn AllenPediatric Oncology Branch, National Cancer Institute, Bethesda, MD 20814, USA.
Andrea BaldwinClinical Research Directorate, Frederick National Laboratory for Cancer Research, Frederick, MD 20702, USA.
Andy GillespiePediatric Oncology Branch, National Cancer Institute, Bethesda, MD 20814, USA.
Anne GoodwinPediatric Oncology Branch, National Cancer Institute, Bethesda, MD 20814, USA.
Brigitte C WidemannPediatric Oncology Branch, National Cancer Institute, Bethesda, MD 20814, USA.
Pamela L WoltersPediatric Oncology Branch, National Cancer Institute, Bethesda, MD 20814, USA.ORCID 0000-0001-9319-6281
National Cancer Institute · USFlorida State University · USFrederick National Laboratory for Cancer Research · US

Funding

WORK ORDER 126643 B539 EXPAND IC SUITE75N91019D00024 · NIAID · LEIDOS BIOMEDICAL RESEARCH, INC. · PI PENDLETON, RICHARD · 2019 to 2025
$3932.6M
Congressionally Directed Medical Research Programs W81XWH2110504NCI NIH HHS 75N91019D00024NIH HHS Intramural Research ProgramUniversity of Kentucky Faculty Startup Funding
6 · The paper itself

Abstract

Individuals with neurofibromatosis type 1 (NF1) and plexiform neurofibromas (PNs) have a higher risk for socioemotional problems. The current study aims to identify the socioemotional developmental pattern and its predictors across childhood and adolescence in individuals with NF1 and PNs. Participants included 88 children with NF1 and PNs (aged 6-18 years old, M = 12.05, SD = 3.62, 57% male) in a natural history study. Neuropsychological assessments were administered three times over six years. There are large variabilities in socioemotional development in the study participants. Developmental patterns varied across socioemotional domains, respondent type (parent-report [PR] vs. child-report [CR]), demographic factors, and NF1 disease-related factors. For instance, lower parental education was associated with a greater decline in internalizing problems (PR) but a greater increase in school disconnectedness (CR) over time. Non-White (vs. White) children were more likely to experience increased adaptive skills (PR) but decreased personal adjustment (CR). Children with more visible tumors experienced a greater decrease in school disconnectedness (CR). Children with more NF1 complications experienced a greater decrease in externalizing problems (PR). These findings indicate the necessity of using multi-informants and investigating subdomains of socioemotional functions. They also highlight the importance of developing individualized approaches to patient care and interventions.

Indexed as

adaptive skillsbehavioral problemsexternalizing problemsinternalizing problemsneurofibromatosis type 1personal adjustmentplexiform neurofibromasschool problemssocioemotional function

Identifiers

PMID36497438
PMCPMC9737030
OpenAlexW4311108326

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.