Osteopontin: A novel marker of pre-symptomatic sporadic Alzheimer's disease

被引:2
|
作者
Quesnel, Marc James [1 ,2 ]
Labonte, Anne [2 ,3 ]
Picard, Cynthia [2 ,3 ]
Bowie, Daniel C. [1 ,2 ]
Zetterberg, Henrik [4 ,5 ,6 ,7 ,8 ,9 ]
Blennow, Kaj [4 ,5 ,10 ,11 ,12 ,13 ]
Brinkmalm, Ann [4 ,5 ]
Villeneuve, Sylvia [1 ,2 ,3 ]
Poirier, Judes [1 ,2 ,3 ]
机构
[1] McGill Univ, Montreal, PQ, Canada
[2] Douglas Mental Hlth Univ Inst, Verdun, PQ, Canada
[3] Douglas Mental Hlth Univ Inst, Ctr Studies Prevent Alzheimers Dis, 6875,LaSalle, Verdun, PQ H4H1R3, Canada
[4] Univ Gothenburg, Sahlgrenska Acad, Inst Neurosci & Physiol, Dept Psychiat & Neurochem,SU Sahlgrenska, Gothenburg, Sweden
[5] Sahlgrens Univ Hosp, Clin Neurochem Lab, SU Molndals Sjukhus, Molndal, Sweden
[6] UCL Inst Neurol, Dept Neurodegenerat Dis, Queen Sq, London, England
[7] UCL, UK Dementia Res Inst, London, England
[8] Hong Kong Sci Pk, Hong Kong Ctr Neurodegenerat Dis, Shatin, Hong Kong, Peoples R China
[9] Univ Wisconsin, Wisconsin Alzheimers Dis Res Ctr, Sch Med & Publ Hlth, Madison, WI USA
[10] Sorbonne Univ, Pitie Salpetriere Hosp, Paris Brain Inst, ICM, Paris, France
[11] Univ Sci & Technol China, Neurodegenerat Disorder Res Ctr, Div Life Sci & Med, Hefei, Peoples R China
[12] Univ Sci & Technol China, Inst Aging & Brain Disorders, Dept Neurol, Hefei, Peoples R China
[13] First Affiliated Hosp USTC, Hefei, Peoples R China
基金
加拿大健康研究院; 瑞典研究理事会; 美国国家卫生研究院; 欧盟地平线“2020”;
关键词
Alzheimer's disease; autopsied brains; biomarkers; cerebral ventricles; cerebrospinal fluid; mRNA; neuroinflammation; osteopontin; positron emission tomography; post mortem; Pre-symptomatic; secreted phosphoprotein 1; synaptic markers; CEREBROSPINAL-FLUID; BIOMARKERS; PROGRESSION; ACTIVATION; CORRELATE; VARIANTS; TAU;
D O I
10.1002/alz.14065
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
INTRODUCTION: We investigate the role of osteopontin (OPN) in participants with Pre-symptomatic Alzheimer's disease (AD), mild cognitive impairment (MCI), and in AD brains. METHODS: Cerebrospinal fluid (CSF) OPN, AD, and synaptic biomarker levels were measured in 109 cognitively unimpaired (CU), parental-history positive Pre-symptomatic Evaluation of Experimental or Novel Treatments for Alzheimer's Disease (PREVENT-AD) participants, and in 167 CU and 399 participants with MCI from the Alzheimer's Disease Neuroimaging Initiative (ADNI) cohort. OPN levels were examined as a function of amyloid beta (A beta) and tau positivity. Survival analyses investigated the link between OPN and rate of conversion to AD. RESULTS: In PREVENT-AD, CSF OPN was positively correlated with synaptic biomarkers. In PREVENT-AD and ADNI, OPN was elevated in CSF A beta(42/40)(+)/total tau(+) and CSF A beta(42/40)(+)/phosphorylated tau181(+) individuals. In ADNI, OPN was increased in A beta(+) positron emission tomography (PET) and tau(+) PET individuals, and associated with an accelerated rate of conversion to AD. OPN was elevated in autopsy-confirmed AD brains. DISCUSSION: Strong associations between CSF OPN and key markers of AD pathophysiology suggest a significant role for OPN in tau neurobiology, particularly in the early stages of the disease.
引用
收藏
页码:6008 / 6031
页数:24
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