Exploring the Association Between Cognitive Function, Obstructive Sleep Apnea and Brain Imaging and the Determinants of Neurocognitive Decline in Subjects With Subjective or Mild Cognitive Impairment
Led by The University of Hong Kong · Updated on 2025-04-02
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13 weeks
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What this Trial Is About
Obstructive sleep apnea (OSA) causes repeated airway blockage during sleep, leading to low oxygen levels and disrupted sleep. This condition is linked to higher risks of mild cognitive impairment (MCI) and Alzheimer's disease. The study investigates how OSA, sleep patterns, and brain changes relate to cognitive decline in people with subjective or mild cognitive impairment. Researchers aim to understand if treating OSA can slow down cognitive decline and brain amyloid buildup, a feature of Alzheimer's disease.
Participants with subjective or mild cognitive impairment will be observed with or without treatment using continuous positive airway pressure (CPAP) or other clinical management for OSA. Sleep questionnaires, cognitive tests, and home sleep apnea tests will be used at the start and during follow-ups at 6 months, 1 year, 2 years, and 3 years. A subgroup of 90 participants will receive PET-MRI brain scans at baseline to assess amyloid levels and brain changes related to OSA severity.
Throughout the study, participants will complete repeated assessments of cognitive abilities, sleep quality, daytime sleepiness, insomnia, and mood. Researchers will monitor neurocognitive function changes using tests such as ADAS-Cog and MoCA. The study will analyze the impact of OSA and its treatment on brain imaging and cognitive outcomes over three years. The University of Hong Kong sponsors this observational study, which runs until March 2027.
CONDITIONS
Brief Title
Sleep Apnea, Neurocognitive Decline and Brain Imaging in Patients With Subjective or Mild Cognitive Impairment
Who Can Participate
Age: 50Years - 80Years
All Genders
Eligibility Criteria
You may qualify if you...
Aged 50 to 80 years
Diagnosis of mild cognitive impairment based on Peterson's criteria
Diagnosis of subjective cognitive impairment with subjective complaints but normal cognitive test scores
Able to speak and read Chinese
Adequate vision and hearing to perform cognitive tests
Subjects with moderate-severe OSA or no OSA based on sleep study invited for PET-MRI brain scan
You will not qualify if you...
Diagnosed psychiatric illness with or without medication, such as major depressive disorder
Other clear organic causes of cognitive impairment like vascular cognitive impairment, brain tumour, dementia with Lewy body, Parkinson's disease, neurosyphilis, autoimmune encephalitis, substance or alcohol abuse
Active cancer diagnosis under treatment
Contraindications to PET-CT or MRI brain scan (excluded from neuroimaging studies)
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Your Study Journey
Screening
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Diagnostic Evaluation
Duration - At baseline
Participants undergo baseline assessments including sleep questionnaires, neurocognitive tests, home sleep apnea test, and PET-MRI brain imaging for a subset of subjects.
1 visit (in-person)
Monitoring
Duration - 3 years
Participants are observed over time to assess changes in neurocognitive function, sleep profiles, and symptoms of sleep apnea and related conditions.
Visits at 6 months, 1 year, 2 years, and 3 years (in-person)
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