Evidence map›Paper›PMID 39819934›Full record

ArticleBMJ open2025

Sleep profile in patients with septo-optic-pituitary dysplasia: protocol for a prospective cohort study.

Ludovica Pasca, Federica Morelli, Guido Catalano, Carlo Alberto Quaranta, Helene Vitali, Elena Ballante, Francesca Dattrino, Francesca Crema, Paola Rota, Costanza Varesio and 4 more

Registry-linked trialAbstract readClinical Trial Protocol
In one paragraph

Article in BMJ open, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06262152 (Characterization of Sleep Features in Pediatric Patients With Septa-optic Dysplasia), which is not on this map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–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.

NCT06262152 unknown statusnot on this map

Characterization of Sleep Features in Pediatric Patients With Septa-optic Dysplasia

TypeobservationalSponsorIRCCS National Neurological Institute "C. Mondino" FoundationRan2023 to 2025Enrolled45ConditionsSepto-Optic Dysplasia, Agenesis of Corpus Callosum, BlindnessArmsActigraphy, blood and salivary sample, and sleep evaluation
3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Ludovica PascaIRCCS Mondino Foundation, Pavia, Italy.ORCID http://orcid.org/0000-0003-4382-0095
Federica MorelliIRCCS Mondino Foundation, Pavia, Italy.
Guido CatalanoIRCCS Mondino Foundation, Pavia, Italy.
Carlo Alberto QuarantaIRCCS Mondino Foundation, Pavia, Italy.
Helene VitaliUnit for Visually Impaired People, Istituto Italiano di Tecnologia, Genoa, Italy.
Elena BallanteIRCCS Mondino Foundation, Pavia, Italy.
Francesca DattrinoIRCCS Mondino Foundation, Pavia, Italy.
Francesca CremaClinical and Experimental Pharmacology Unit, Department of Internal Medicine and Therapeutics, University of Pavia, Pavia, Italy.
Paola RotaDepartment of Biomedical, Surgical and Dental Sciences, University of Milan, Milano, Italy.
Costanza VaresioIRCCS Mondino Foundation, Pavia, Italy.
Valentina De GiorgisIRCCS Mondino Foundation, Pavia, Italy.
Romina RomanielloIRCCS Mondino Foundation, Pavia, Italy.
Sabrina SignoriniIRCCS Mondino Foundation, Pavia, Italy.
Valentina FrancoIRCCS Mondino Foundation, Pavia, Italy valentina.franco@unipv.it.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionChildren with septo-optic-pituitary dysplasia (SOD) may experience a range of visual impairments and hormonal dysfunctions beyond developmental delay/intellectual disability. The literature describes sleep fragmentation, circadian rhythm disruptions and reduced sleep efficiency. These manifestations are believed to be closely linked to both structural and functional abnormalities associated with SOD, potentially disrupting the natural circadian rhythm. Both anomalies in midline brain structures and decreased visual input could potentially impact melatonin secretion, although a distinct melatonin profile for SOD patients has yet to be identified. Furthermore, the specific contribution of these factors to sleep disturbances in SOD remains unexplored. The aim of this study is to evaluate the quality of sleep and its characteristics, along with the melatonin profile, among paediatric patients diagnosed with SOD. A comparison will be made between these findings and those of children with isolated bilateral visual impairment, as well as patients with agenesis of the corpus callosum. METHODS AND ANALYSIS: Participants aged between 3 and 18 years previously diagnosed with SOD will be recruited prospectively. Each participant will be assessed at baseline and at each follow-up visit scheduled to evaluate the clinical course. Sleep quality and daytime sleepiness changes will be tracked using actigraphic assessment, standardised sleep questionnaires and a sleep EEG. Additionally, plasma and salivary melatonin profiles will be assessed for each participant. ETHICS AND DISSEMINATION: This study has been approved by local Ethics Committee (N°0049187/23). The study findings will be shared through publication in an international peer-reviewed journal and presented at both national and international conferences. TRIAL REGISTRATION NUMBER: NCT06262152.

Indexed as

MelatoninSepto-Optic DysplasiaSleepSleep QualitySleep Wake DisordersAdolescentChildChild, PreschoolCircadian RhythmElectroencephalographyFemaleHumansMaleProspective StudiesResearch DesignSalivaMelatoninDevelopmental neurology & neurodisabilityNeurobiologyNeuro-ophthalmologyNeurophysiologySLEEP MEDICINE

Identifiers

PMID39819934
PMCPMC11751809

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

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.