The HKU Neurocognitive Disorder (NCD) Cohort is a hospital-based, prospective, observational study of older HK Chinese adults with cognitive impairment, with a special focus on studying patients with subjective cognitive decline and mild cognitive impairment.
The HKU Neurocognitive Disorder (NCD) Cohort is a hospital-based, prospective, observational study of older HK Chinese adults with cognitive impairment, with a special focus on studying patients with subjective cognitive decline and mild cognitive impairment, and in particular the biomarkers that predict cognitive and functional decline. Comprehensive profiling of each subject is performed through a multi-domain assessment protocol including detailed demographics, lifestyle factors, neuropsychological battery, mood, MRI, genetics, blood biomarkers, and other patient-centred parameters including level of disability, quality of life and societal engagement. Ongoing annual follow up captures the essential clinical events and changes in neurocognitive function (conversion to MCI or dementia), mood, level of disability and quality of life; as well as repeat blood tests. The HKU NCD Cohort is the first-ever Asian dementia cohort to be formally included into the Dementia Platforms UK, achieving an international collaborative status with other UK-based cohorts. The study neuropsychological battery is aligned with the NACC UDS3 battery.
Study Type
OBSERVATIONAL
Enrollment
500
Cognitive impairment status (SCD, MCI, dementia), HK-MoCA, Clinical Dementia Rating (CDR sum of squares), Geriatric Depression Scale (GDS-15), Neuropsychiatric Index (NPI), Barthel Index, Lawton's IADL, Life-Space Assessment, Mini-Nutrition Assessment (MNA), Quality of Life for Alzheimer's Disease (QoL-AD, patient and carer parts), frailty status (FRAIL scale), handgrip strength, walking speed, exercise status, sleep quality, Charlson comorbidity index (CCI, age-adjusted). NACC: Story recall, Benson's complex figure copy, colour trail test (black \& white), verbal fluency, digit forward and backward span.
MRI: T1, T2, FLAIR, SWI, DTI, fMRI, ASL, MRS, for selected patients
Stored samples (unanalysed): serum, plasma, buffy coat (PBMC); also processed for microvesicles and exosome analysis
Department of Medicine, Queen Mary Hospital, The University of Hong Kong
Hong Kong, Hong Kong
RECRUITINGCognitive decline
Change in total HK-MoCA score between baseline and follow-up
Time frame: 1 year
Functional decline
Change in Lawton's IADL score between baseline and follow-up
Time frame: 1 year
Neuropsychiatric decline
Change in Neuropsychiatric Index (NPI) between baseline and follow-up
Time frame: 1 year
Quality of life decline
Change in QoL-AD score between baseline and follow-up
Time frame: 1 year
Change in cognitive impairment status
Progression to mild cognitive impairment (MCI) or dementia status
Time frame: 1 year
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128-channel EEG with ERP for Go/NoGo and Prospective Memory (PM) tasks for selected patients
F18 Flutametamol PET CT for selected patients