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Sleep profile in patients with septo-optic-pituitary dysplasia: protocol for a prospective cohort study
Ludovica Pasca1,2, Federica Morelli1,3, Guido Catalano1,2
1IRCCS Mondino Foundation, Pavia, Italy.
Insights
This study investigates sleep disturbances and melatonin profiles in children with septo-optic-pituitary dysplasia (SOD), comparing them to children with visual impairments or agenesis of the corpus callosum.
Area of Science:
- Pediatric Endocrinology
- Sleep Medicine
- Neurodevelopmental Disorders
Background:
- Children with septo-optic-pituitary dysplasia (SOD) exhibit sleep issues like fragmentation and circadian rhythm disruption.
- These sleep disturbances are potentially linked to structural/functional SOD abnormalities affecting brain midline and visual input.
- The specific impact of these factors on melatonin secretion and sleep in SOD patients is not well understood.
Purpose of the Study:
- To assess sleep quality, characteristics, and melatonin profiles in pediatric SOD patients.
- To compare sleep and melatonin findings in SOD patients with those in children with isolated bilateral visual impairment and agenesis of the corpus callosum.
Main Methods:
- Prospective recruitment of SOD patients aged 3-18 years.
- Assessment of sleep using actigraphy, standardized questionnaires, and sleep EEG.
- Evaluation of plasma and salivary melatonin profiles at baseline and follow-up.
Main Results:
- Data collection ongoing; results to be disseminated upon study completion.
Conclusions:
- Further research is needed to elucidate the relationship between SOD, melatonin, and sleep disturbances.
- Understanding these connections may lead to targeted interventions for improved sleep in affected children.
Introduction:
Children 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.
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