Actively Recruiting
EGR2 and NLRP3 Pathways in Obstructive Sleep Apnea-Related Cognitive and Mood Disorders
Led by Xinhua Hospital, Shanghai Jiao Tong University School of Medicine · Updated on 2025-08-13
1000
Participants Needed
1
Research Sites
65 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Obstructive sleep apnea-hypopnea syndrome (OSAS) is a common disorder in which repeated airway blockages during sleep lead to low oxygen levels, inflammation, and disrupted sleep. Many OSAS patients-both children and adults-experience problems with memory, attention, and mood, such as anxiety or depression. However, the exact molecular drivers of these brain changes are not fully understood. This observational study will enroll: Children (ages 2-18) and adults (\>18 years) with OSAS, as well as age- and sex-matched healthy volunteers. Clinical assessments: Children will undergo routine ENT examinations (including nasal endoscopy and X-rays); adults will have an overnight sleep study (polysomnography). All participants will complete questionnaires on sleepiness (e.g., ESS), mood (PHQ-9, GAD-7), and cognitive screening (MoCA for adults, age-appropriate scales for children). Sample collection: A small blood draw (3 mL) and, when applicable (e.g., adults undergoing surgery), a tiny subcutaneous fat biopsy. Saliva samples will also be collected. Laboratory tests: Measure expression levels of two key inflammatory pathway genes-EGR2 and NLRP3-in blood cells, saliva, and fat tissue using RNA sequencing, RT-qPCR, and Western Blot. Correlate these molecular markers with sleep parameters (AHI, oximetry), cognitive scores, and mood scores. Data analysis: Develop and validate machine-learning models that integrate data from multiple tissues to predict who is at highest risk for cognitive or mood disturbances.
CONDITIONS
Official Title
EGR2 and NLRP3 Pathways in Obstructive Sleep Apnea-Related Cognitive and Mood Disorders
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Children aged 2 to 18 years with obstructive snoring or sleep apnea signs from initial ENT screening
- Adults over 18 years with suspected OSAS having chronic snoring, witnessed apneas, or daytime sleepiness
- No severe chronic heart, liver, kidney failure, psychiatric disorders, or pregnancy in adults
- Signed informed consent by participant or legal guardian
- Not currently enrolled in another registered clinical trial
You will not qualify if you...
- Congenital craniofacial malformations
- Severe heart, lung, liver, or kidney failure
- Major neurological disease
- Recent use of anti-inflammatory or immunomodulatory medications
- Current psychiatric disorder
- Pregnancy
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Shanghai Xinhua hospital
Shanghai, China
Actively Recruiting
Research Team
J
Jiang, PHD,MD
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
4
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