Multicenter Alzheimer's and Parkinson's disease immune biomarker verification study

被引:32
|
作者
Brosseron, Frederic [1 ,2 ]
Kolbe, Carl-Christian [3 ]
Santarelli, Francesco [1 ,2 ]
Carvalho, Stephanie [4 ]
Antonell, Anna [5 ]
Castro-Gomez, Sergio [1 ]
Tacik, Pawel [1 ]
Namasivayam, Aishwarya Alex [6 ]
Mangone, Graziella [4 ]
Schneider, Reinhard [6 ]
Latz, Eicke [2 ,3 ]
Wuellner, Ullrich [2 ,7 ]
Svenningsson, Per [8 ]
Sanchez-Valle, Raquel [5 ]
Luis Molinuevo, Jose [9 ]
Corvol, Jean-Christophe [4 ]
Heneka, Michael T. [1 ,2 ]
机构
[1] Univ Bonn, Dept Neurodegenerat Dis & Geropsychiat Neurol, Med Ctr, Bonn, Germany
[2] German Ctr Neurodegenerat Dis DZNE, Bonn, Germany
[3] Univ Bonn, Inst Innate Immune, Med Ctr, Bonn, Germany
[4] Sorbonne Univ, Hop Pitie Salpetriere, AP HP,Inst Cerveau & Moelle Epiniere, INSERM,UMRS 1127,CNRS,UMR 7225,ICM,Dept Neurol,Ct, Paris, France
[5] Inst Invest Biomed August Pi & Sunyer IDIBAPS, Hosp Clin, Alzheimers Dis & Other Cognit Disorders Unit, Fundacio Clin Recerca Biomed, Barcelona, Spain
[6] Univ Luxembourg, LCSB, Campus Belval, Belvaux, Luxembourg
[7] Univ Bonn, Dept Neurol, Med Ctr, Bonn, Germany
[8] Karolinska Inst, Dept Clin Neurosci, Stockholm, Sweden
[9] Pasqual Maragall Fdn, Barcelonabeta Brain Res Ctr, Barcelona, Spain
关键词
Aging; Alzheimer's disease; Amyloid; Biomarker; Cerebrospinal fluid; Inflammation; Mild cognitive impairment; Multicenter; Parkinson's disease; Tau; CSF; BLOOD; MICROGLIA; SEX; MIF;
D O I
10.1016/j.jalz.2019.07.018
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Introduction: Multiple immunity biomarkers have been suggested as tracers of neuroinflammation in neurodegeneration. This study aimed to verify findings in cerebrospinal fluid (CSF) samples of Alzheimer's disease (AD) and Parkinson's disease (PD) subjects from the network of the European, Innovative Medicines Initiative-funded project AETIONOMY. Methods: A total of 227 samples from the studies/centres AETIONOMY, ICEBERG, and IDIBAPS were used to analyse 21 selected immunity biomarkers in CSF. Results were compared to data of an independent cohort of 399 subjects previously published. Results: Immunity markers were predominantly and reproducibly associated with pathological levels of tau isoforms, but also with amyloid levels, aging, sex, APOE genotype, and center-specific factors. Discussion: Immunity biomarker levels in CSF reflect molecular and cellular pathology rather than diagnosis in neurodegenerative disorders. Assay standardization and stratification for age and other covariates could improve the power of such markers in clinical applications or intervention studies targeting immune responses in neurodegeneration.
引用
收藏
页码:292 / 304
页数:13
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