Actively Recruiting

Age: 50Years - 80Years
All Genders
ID06150352

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

180

Participants Needed

1

Research Sites

13 weeks

Total Duration

On this page

AI-Summary

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

Eligible

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
Not Eligible

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)

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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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)

Trial Site Locations

Total: 1 location

1

Queen Mary Hospital

Hong Kong, Hong Kong

Actively Recruiting

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Research Team

S

Sau Man Mary Ip, MD

Y

Yuen Kwan Agnes Lai, PhD

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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Published Research Related To This Trial

Heterogeneity of Amyloid Binding in Cognitively Impaired Patients Consecutively Recruited from a Memory Clinic: Evaluating the Utility of Quantitative 18F-Flutemetamol PET-CT in Discrimination of Mild Cognitive Impairment from Alzheimer's Disease and Other Dementias.

Yi-Wen Bao, Anson C M Chau, Patrick Ka-Chun Chiu...

https://pubmed.ncbi.nlm.nih.gov/33361593

Assessment of Alzheimer's disease-related biomarkers in patients with obstructive sleep apnea: A systematic review and meta-analysis.

Wenqi Cui, Zhenghao Duan, Zijian Li...

https://pubmed.ncbi.nlm.nih.gov/36313031

Severe Obstructive Sleep Apnea Is Associated with Higher Brain Amyloid Burden: A Preliminary PET Imaging Study.

Melinda L Jackson, Marina Cavuoto, Rachel Schembri...

https://pubmed.ncbi.nlm.nih.gov/33016907

Association of Sleep-Disordered Breathing With Cognitive Function and Risk of Cognitive Impairment: A Systematic Review and Meta-analysis.

Yue Leng, Claire T McEvoy, Isabel E Allen...

https://pubmed.ncbi.nlm.nih.gov/28846764

Sleep Apnea, Sleep Duration and Brain MRI Markers of Cerebral Vascular Disease and Alzheimer's Disease: The Atherosclerosis Risk in Communities Study (ARIC).

Pamela L Lutsey, Faye L Norby, Rebecca F Gottesman...

https://pubmed.ncbi.nlm.nih.gov/27415826

Validation of an electronic image reader training programme for interpretation of [18F]flutemetamol β-amyloid PET brain images.

Christopher J Buckley, Paul F Sherwin, Adrian P L Smith...

https://pubmed.ncbi.nlm.nih.gov/27984539