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Article type: Research Article
Authors: Sun, Lina; 1; * | Guo, Chunnib; 1 | Song, Yanc; 1 | Sheng, Jianhuaa; * | Xiao, Shifua; * | for the Alzheimer’s Disease Neuroimaging Initiative2
Affiliations: [a] Alzheimer’s Disease and Related Disorders Center, Department of Geriatric Psychiatry, Shanghai Mental Health Center, Shanghai Jiao Tong University School of Medicine, Shanghai, P.R. China | [b] Department of Neurology, Shanghai General Hospital, Shanghai, P.R. China | [c] Department of Geriatric Psychiatry; Shanghai Yangpu Mental Health Center, Shanghai, P.R. China
Correspondence: [*] Correspondence to: Shifu Xiao, Jianhua Sheng and Lin Sun, PhD, No. 600 South Wanping Road, Xuhui Distinct, Shanghai, China. Tel.: +86 021 64387250; E-mails: [email protected] (S. Xiao); [email protected] (J. Sheng); [email protected] (L. Sun).
Note: [1] These authors contributed equally to this work.
Note: [2] Data used in preparation of this article were obtained from the Alzheimer’s Disease Neuroimaging Initiative (ADNI) database (https://adni.loni.usc.edu). As such, the investigators within the ADNI contributed to the design and implementation of ADNI and/ or provided data but did not participate in analysis or writing of this report. A complete listing of ADNI investigators can be found at: https://adni.loni.usc.edu/wpcontent/uploads/how_to_apply/ADNI_Acknowledgement_List.pdf
Abstract: Background:Bone morphogenetic protein (BMP) plays important roles in the pathology of Alzheimer’s disease (AD). Objective:We sought blood BMP6 involved in the processes underlying cognitive decline and detected them in association with AD. Methods:A total of 309 participants in Shanghai Mental Health Center (SMHC) and 547 participants in Alzheimer’s disease Neuroimaging Initiative (ADNI) cohort were included. Blood BMP6 and cognitive functions were measured in all subjects of both cohorts at baseline, and in 482 subjects of ADNI cohort after one year. A total of 300 subjects in ADNI cohort were detected cerebrospinal fluid (CSF) tau biomarker, and 244 received 1-year follow-up. Results:AD patients had lower levels of blood BMP6 compared to normal controls, and BMP6 was positively associated with cognitive functions. Longitudinal BMP6 combing with APOE genotype could distinguish probable AD from normal controls. The influence of blood BMP6 on cognition was modulated by tau pathology. Conclusion:Blood BMP6 was associated with cognitive performance and identified as a potential predictor for probable AD.
Keywords: Alzheimer’s disease, APOE, BMP6, mild cognitive impairment, prediction, tau pathology
DOI: 10.3233/JAD-220279
Journal: Journal of Alzheimer's Disease, vol. 88, no. 2, pp. 641-651, 2022
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