Evidence map›Paper›PMID 35119474›Full record

Observational studyTranslational vision science & technology2022

Prevalence of Choroidal Abnormalities and Lisch Nodules in Children Meeting Clinical and Molecular Diagnosis of Neurofibromatosis Type 1.

Mariana Flores Pimentel, Anna Heath, Michael J Wan, Rowaida Hussein, Kate E Leahy, Heather MacDonald, Erika Tavares, Cynthia VandenHoven, Katelyn MacNeill, Peter Kannu and 4 more

Open access · goldAbstract readObservational Study
In one paragraph

Observational study in Translational vision science & technology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.2field-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

8 citing papers in PubMed, 11 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

14 authors at 5 institutions in 1 country.

Mariana Flores PimentelDepartment of Ophthalmology and Visual Sciences, The Hospital for Sick Children, Toronto, Ontario, Canada.
Anna HeathDivision of Biostatistics, Dalla Lana School of Public Health, University of Toronto, Ontario, Canada.
Michael J WanDepartment of Ophthalmology and Visual Sciences, The Hospital for Sick Children, Toronto, Ontario, Canada.
Rowaida HusseinGenetics & Genome Biology, The Hospital for Sick Children, Toronto, Ontario, Canada.
Kate E LeahyDepartment of Ophthalmology and Visual Sciences, The Hospital for Sick Children, Toronto, Ontario, Canada.
Heather MacDonaldDepartment of Ophthalmology and Visual Sciences, The Hospital for Sick Children, Toronto, Ontario, Canada.
Erika TavaresGenetics & Genome Biology, The Hospital for Sick Children, Toronto, Ontario, Canada.
Cynthia VandenHovenDepartment of Ophthalmology and Visual Sciences, The Hospital for Sick Children, Toronto, Ontario, Canada.
Katelyn MacNeillDepartment of Ophthalmology and Visual Sciences, The Hospital for Sick Children, Toronto, Ontario, Canada.
Peter KannuDepartment of Medical Genetics, University of Alberta, Edmonton, Alberta, Canada.
Patricia C ParkinDepartment of Pediatrics, The Hospital for Sick Children, Toronto, Ontario, Canada.
Elise HeonDepartment of Ophthalmology and Visual Sciences, The Hospital for Sick Children, Toronto, Ontario, Canada.
Arun ReginaldDepartment of Ophthalmology and Visual Sciences, The Hospital for Sick Children, Toronto, Ontario, Canada.
Ajoy VincentDepartment of Ophthalmology and Visual Sciences, The Hospital for Sick Children, Toronto, Ontario, Canada.
Hospital for Sick Children · CASickKids Foundation · CAUniversity of Toronto · CAPublic Health Ontario · CAUniversity of Alberta · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeTo determine the prevalence of choroidal abnormalities (CAs) and Lisch nodules (LNs) in children who met the clinical diagnostic criteria (CDC) alone and those with a molecularly confirmed diagnosis (MCD) of neurofibromatosis type 1 (NF1), and to ascertain any differences between the groups.

methodsThis was a cross-sectional observational study. All children who met the CDC and/or had MCD of NF1 and underwent eye examination were included. At least two CAs or LNs between the two eyes were set as a threshold to define the presence of either abnormality. Frequencies alongside 95% confidence intervals (CIs) were calculated. The relationship between patient age and the presence of LNs and/or CAs was estimated using logistic regression.

resultsThe study cohort included 94 patients; CAs (64%) were more prevalent than LNs (41%) (0.22; 95% CI, 0.08-0.36; P = 0.0023). The probability of the presence of LNs was lower than that of CAs across all ages (odds ratio = 0.37; 95% CI, 0.20-0.69; P = 0.00173). CAs were exclusively found in 37% of patients and LNs in 16%; 80% had either CAs or LNs, or both. In the CDC group (n = 41), the difference in prevalence (CAs = 68%, LNs = 51%) did not attain statistical significance (0.17; 95% CI, -0.06 to 0.40; P = 0.18). In the MCD group (n = 53), the difference in prevalence (CAs = 60%, LNs = 34%) was significant (0.26; 95% CI, 0.006-0.47; P = 0.023).

conclusionsCAs were more frequent than LNs in pediatric NF1 patients regardless of age and MCD status. Combining ophthalmological exams with near-infrared imaging will increase the diagnostic reach in pediatric NF1. TRANSLATIONAL RELEVANCE: CAs detected on near-infrared imaging are objective biomarkers in NF1. They are more prevalent and detected earlier in the pediatric population compared with LNs. Hence, the presence of CAs should be routinely ascertained in children suspected with NF1.

Indexed as

HamartomaNeurofibromatosis 1ChildChoroidCross-Sectional StudiesHumansPrevalence

Identifiers

PMID35119474
PMCPMC8819284
OpenAlexW4210624771

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.