Cross-Cultural Longitudinal Study on Cognitive Decline (CLoCODE) for Subjective Cognitive Decline in China and Germany: A Protocol for Study Design

Author:

Sheng Can1,Yang Kun23,He Beiqi4,Li Taoran1,Wang Xiaoqi1,Du Wenying1,Hu Xiaochen5,Jiang Jiehui6,Jiang Xueyan147,Jessen Frank578,Han Ying14910

Affiliation:

1. Department of Neurology, Xuanwu Hospital of Capital Medical University, Beijing, China

2. Evidence-Based Medicine Center, Xuanwu Hospital of Capital Medical University, Beijing, China

3. Department of Epidemiology and Biostatistics, School of Public Health, Capital Medical University, Beijing, China

4. Key Laboratory of Biomedical Engineering of Hainan Province, School of Biomedical Engineering, Hainan University, Haikou, China

5. Department of Psychiatry and Psychotherapy, Medical Faculty, University of Cologne, Cologne, Germany

6. Institute of Biomedical Engineering, School of Information and Communication Engineering, Shanghai University, Shanghai, China

7. German Center for Neurodegenerative Diseases (DZNE), Bonn, Germany

8. Excellence Cluster on Cellular Stress Responses in Aging-Associated Diseases (CECAD), University of Cologne, Cologne, Germany

9. Center of Alzheimer’s Disease, Beijing Institute for Brain Disorders, Beijing, China

10. National Clinical Research Center for Geriatric Disorders, Beijing, China

Abstract

Background: Subjective cognitive decline (SCD) is considered as the first symptomatic manifestation of Alzheimer’s disease (AD), which is also affected by different cultural backgrounds. Establishing cross-cultural prediction models of SCD is challenging. Objective: To establish prediction models of SCD available for both the Chinese and European populations. Methods: In this project, 330 SCD from China and 380 SCD from Germany are intended to be recruited. For all participants, standardized assessments, including clinical, neuropsychological, apolipoprotein E (APOE) genotype, blood, and multi-parameter magnetic resonance imaging (MRI) at baseline will be conducted. Participants will voluntarily undergo amyloid positron emission tomography (PET) and are classified into amyloid-β (Aβ) positive SCD (SCD+) and Aβ negative SCD (SCD-). First, baseline data of all SCD individuals between the two cohorts will be compared. Then, key features associated with brain amyloidosis will be extracted in SCD+ individuals, and the diagnosis model will be established using the radiomics method. Finally, the follow-up visits will be conducted every 12 months and the primary outcome is the conversion to mild cognitive impairment or dementia. After a 4-year follow-up, we will extract factors associated with the conversion risk of SCD using Cox regression analysis. Results: At present, 141 SCD from China and 338 SCD from Germany have been recruited. Initial analysis showed significant differences in demographic information, neuropsychological tests, and regional brain atrophy in SCD compared with controls in both cohorts. Conclusion: This project may be of great value for future implications of SCD studies in different cultural backgrounds. Trial registration: ClinicalTrials.gov, NCT04696315. Registered 3 January 2021.

Publisher

IOS Press

Subject

Psychiatry and Mental health,Geriatrics and Gerontology,Clinical Psychology,General Medicine,General Neuroscience

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