Assessment of High Risk for Alzheimer’s Disease Using Plasma Biomarkers in Subjects with Normal Cognition in Taiwan: A Preliminary Study

Author:

Hu Chaur-Jong1234,Chiu Ming-Jang5678,Pai Ming-Chyi9,Yan Sui-Hing10,Wang Pei-Ning111213,Chiu Pai-Yi1415,Lin Chin-Hsien5,Chen Ta-Fu5,Yang Fu-Chi16,Huang Kuo-Lun17,Hsu Yi-Ting18,Hou Yi-Chou192021,Lin Wei-Che22,Lu Cheng-Hsien23,Huang Li-Kai12,Yang Shieh-Yueh24

Affiliation:

1. Department of Neurology, School of Medicine, College of Medicine, Taipei Medical University, Taipei, Taiwan

2. Department of Neurology, Dementia Center, Shuang Ho Hospital, Taipei Medical University, New Taipei City, Taiwan

3. Graduate Institute of Neural Regenerative Medicine, College of Medical Science and Technology, Taipei Medical University, Taipei, Taiwan

4. Taipei Neuroscience Institute, Taipei Medical University, Taipei, Taiwan

5. Department of Neurology, National Taiwan University Hospital, College of Medicine, National Taiwan University, Taipei, Taiwan

6. Graduate Institute of Brain and Mind Sciences, College of Medicine, National Taiwan University, Taipei, Taiwan

7. Department of Psychology, National Taiwan University, Taipei, Taiwan

8. Graduate Institute of Biomedical Electronics and Bioinformatics, National Taiwan University, Taipei, Taiwan

9. Division of Behavioral Neurology, Department of Neurology, National Cheng Kung University Hospital, College of Medicine, National Cheng Kung University, Tainan, Taiwan

10. Department of Neurology, Far Eastern Memorial Hospital, New Taipei City, Taiwan

11. Department of Neurology, Neurological Institute, Taipei Veterans General Hospital, Taipei, Taiwan

12. Department of Neurology, School of Medicine, National Yang-Ming University, Taipei, Taiwan

13. Brain Research Center, National Yang-Ming University, Taipei, Taiwan

14. Department of Neurology, Show Chwan Memorial Hospital, Chunghwa, Taiwan

15. MR-guided Focus Ultrasound Center, Chang Bin Show Chwan Memorial Hospital, Chunghwa, Taiwan

16. Department of Neurology, Tri-Service General Hospital, National Defense Medical Center, Taipei, Taiwan

17. Department of Neurology, Linkou Chang Gung Memorial Hospital, and College of Medicine, Chang Gung University, Taoyuan, Taiwan

18. Department of Neurology, China Medical University Hospital, China Medical University, Taichung, Taiwan

19. Graduate Institute of Clinical Medicine, College of Medicine, Taipei Medical University, Taipei, Taiwan

20. Department of Internal Medicine, Cardinal Tien Hospital, New Taipei City, Taiwan

21. School of Medicine, Fu Jen Catholic University, New Taipei City, Taiwan

22. Department of Diagnostic Radiology, Kaohsiung Chang Gung Memorial Hospital, Chang Gung University College of Medicine, Kaohsiung, Taiwan

23. Department of Neurology, Kaohsiung Chang Gung Memorial Hospital, Chang Gung University College of Medicine, Kaohsiung, Taiwan

24. MagQu Co., Ltd., New Taipei City, Taiwan

Abstract

Background: In Alzheimer’s disease (AD), cognitive impairment begins 10–15 years later than neurodegeneration in the brain. Plasma biomarkers are promising candidates for assessing neurodegeneration in people with normal cognition. It has been reported that subjects with the concentration of plasma amyloid-β 1-42×total tau protein higher than 455 pg2/ml2 are assessed as having a high risk of amnesic mild impairment or AD, denoted as high risk of AD (HRAD). Objective: The prevalence of high-risk for dementia in cognitively normal controls is explored by assaying plasma biomarkers. Methods: 422 subjects with normal cognition were enrolled around Taiwan. Plasma Aβ1-40, Aβ1-42, and T-Tau levels were assayed using immunomagnetic reduction to assess the risk of dementia. Results: The results showed that 4.6% of young adults (age: 20–44 years), 8.5% of middle-aged adults (age: 45–64 years), and 7.3% of elderly adults (age: 65–90 years) had HRAD. The percentage of individuals with HRAD dramatically increased in middle-aged and elderly adults compared to young adults. Conclusion: The percentage of HRAD in cognitively normal subjects are approximately 10%, which reveals that the potentially public-health problem of AD in normal population. Although the subject having abnormal levels of Aβ or tau is not definitely going on to develop cognitive declines or AD, the risk of suffering cognitive impairment in future is relatively high. Suitable managements are suggested for these high-risk cognitively normal population. Worth noting, attention should be paid to preventing cognitive impairment due to AD, not only in elderly adults but also middle-aged adults.

Publisher

IOS Press

Subject

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

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