Biomarker Changes during 20 Years Preceding Alzheimer's Disease

被引:61
|
作者
Jia, Jianping [1 ,2 ,3 ,5 ]
Ning, Yuye [1 ]
Chen, Meilin [1 ]
Wang, Shuheng [1 ]
Yang, Hao [1 ]
Li, Fangyu [1 ]
Ding, Jiayi [1 ]
Li, Yan [1 ]
Lyu, Jihui [6 ]
Zhao, Bote [1 ]
Yang, Shanshan [8 ]
Yan, Xin [7 ]
Wang, Yue [4 ]
Qin, Wei [1 ]
Wang, Qi [1 ]
Li, Ying [1 ]
Zhang, Jintao [9 ]
Liang, Furu [10 ]
Liao, Zhengluan [11 ]
Wang, Shan [12 ]
机构
[1] Capital Med Univ, Xuanwu Hosp, Innovat Ctr Neurol Disorders, Dept Neurol, 45 Changchun St, Beijing 100053, Peoples R China
[2] Capital Med Univ, Clin Ctr Neurodegenerat Dis & Memory Impairment, Beijing Key Lab Geriatr Cognit Disorders, Beijing, Peoples R China
[3] Capital Med Univ, Beijing Inst Brain Disorders, Ctr Alzheimers Dis, Collaborat Innovat Ctr Brain Disorders, Beijing, Peoples R China
[4] Capital Med Univ, Beijing Anding Hosp, Dept Neurol, Beijing, Peoples R China
[5] Minist Educ, Key Lab Neurodegenerat Dis, Beijing, Peoples R China
[6] Beijing Geriatr Hosp, Ctr Cognit Disorders, Beijing, Peoples R China
[7] Beijing Jishuitan Hosp, Dept Neurol, Beijing, Peoples R China
[8] Daqing Oilfield Gen Hosp, Dept Neurol, Daqing, Peoples R China
[9] Peoples Liberat Army, Dept Neurol, Hosp 960, Jinan, Peoples R China
[10] Baotou Cent Hosp, Dept Neurol, Baotou, Peoples R China
[11] Zhejiang Prov Peoples Hosp, Dept Psychiat, Hangzhou, Peoples R China
[12] Hebei Med Univ, Hosp 2, Dept Neurol, Shijiazhuang, Peoples R China
来源
NEW ENGLAND JOURNAL OF MEDICINE | 2024年 / 390卷 / 08期
基金
中国国家自然科学基金; 北京市自然科学基金;
关键词
HYPOTHETICAL MODEL; DEMENTIA; PREVALENCE; MARKERS; SCALE;
D O I
10.1056/NEJMoa2310168
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Biomarker changes that occur in the period between normal cognition and the diagnosis of sporadic Alzheimer's disease have not been extensively investigated in longitudinal studies.Methods We conducted a multicenter, nested case-control study of Alzheimer's disease biomarkers in cognitively normal participants who were enrolled in the China Cognition and Aging Study from January 2000 through December 2020. A subgroup of these participants underwent testing of cerebrospinal fluid (CSF), cognitive assessments, and brain imaging at 2-year-to-3-year intervals. A total of 648 participants in whom Alzheimer's disease developed were matched with 648 participants who had normal cognition, and the temporal trajectories of CSF biochemical marker concentrations, cognitive testing, and imaging were analyzed in the two groups.Results The median follow-up was 19.9 years (interquartile range, 19.5 to 20.2). CSF and imaging biomarkers in the Alzheimer's disease group diverged from those in the cognitively normal group at the following estimated number of years before diagnosis: amyloid-beta (A beta)42, 18 years; the ratio of A beta 42 to A beta 40, 14 years; phosphorylated tau 181, 11 years; total tau, 10 years; neurofilament light chain, 9 years; hippocampal volume, 8 years; and cognitive decline, 6 years. As cognitive impairment progressed, the changes in CSF biomarker levels in the Alzheimer's disease group initially accelerated and then slowed.Conclusions In this study involving Chinese participants during the 20 years preceding clinical diagnosis of sporadic Alzheimer's disease, we observed the time courses of CSF biomarkers, the times before diagnosis at which they diverged from the biomarkers from a matched group of participants who remained cognitively normal, and the temporal order in which the biomarkers became abnormal. (Funded by the Key Project of the National Natural Science Foundation of China and others; ClinicalTrials.gov number, NCT03653156.) In the 20 years before diagnosis, the time points at which biomarkers for sporadic Alzheimer's disease diverged from those associated with normal cognition ranged from 6 years to 18 years.
引用
收藏
页码:712 / 722
页数:11
相关论文
共 50 条
  • [41] Retinal oximetry as a biomarker for Alzheimer's disease
    Traustadottir, Valgerdur Dora Dora
    Olafsdottir, Olof Birna
    Saevarsdottir, Hrafnhildur Sif
    Hardarson, Sveinn Hakon
    Snaedal, Jon
    Stefansson, Einar
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2017, 58 (08)
  • [42] Flotillin: A Promising Biomarker for Alzheimer's Disease
    Angelopoulou, Efthalia
    Paudel, Yam Nath
    Shaikh, Mohd. Farooq
    Piperi, Christina
    JOURNAL OF PERSONALIZED MEDICINE, 2020, 10 (02):
  • [43] Circulating Biomarker Panels in Alzheimer's Disease
    Zafari, Sachli
    Backes, Christina
    Meese, Eckart
    Keller, Andreas
    GERONTOLOGY, 2015, 61 (06) : 497 - 503
  • [44] A molecular biomarker for the diagnosis of Alzheimer's disease
    Nature Clinical Practice Neurology, 2006, 2 (12): : 642 - 642
  • [45] The biomarker signature of preclinical Alzheimer's disease
    Molinuevo, J. L.
    JOURNAL OF NEUROLOGY, 2013, 260 : S9 - S10
  • [46] Selenium as a potential biomarker for Alzheimer's disease
    Cardoso, B.
    Roberts, B.
    Bush, A.
    Hare, D.
    JOURNAL OF NEUROCHEMISTRY, 2015, 134 : 348 - 349
  • [47] Complement activation as a biomarker for Alzheimer's disease
    Aiyaz, Mohammed
    Lupton, Michelle K.
    Proitsi, Petroula
    Powell, John F.
    Lovestone, Simon
    IMMUNOBIOLOGY, 2012, 217 (02) : 204 - 215
  • [48] Neurogranin as a Novel Biomarker in Alzheimer's Disease
    Agnello, Luisa
    Gambino, Caterina Maria
    Lo Sasso, Bruna
    Bivona, Giulia
    Milano, Salvatore
    Ciaccio, Anna Maria
    Piccoli, Tommaso
    La Bella, Vincenzo
    Ciaccio, Marcello
    LABORATORY MEDICINE, 2021, 52 (02) : 188 - 196
  • [49] β-Amyloid Biomarker Detection for Alzheimer’s Disease
    Li C.-Z.
    Grajales S.
    Shuang S.
    Dong C.
    Nair M.
    Journal of Analysis and Testing, 2017, 1 (2)
  • [50] Clinical evaluation as a biomarker for Alzheimer's disease
    Cummings, Jeffrey L.
    JOURNAL OF ALZHEIMERS DISEASE, 2005, 8 (04) : 327 - 337