The Alzheimer's Association appropriate use recommendations for blood biomarkers in Alzheimer's disease

被引:292
|
作者
Hansson, Oskar [1 ,2 ]
Edelmayer, Rebecca M. [3 ]
Boxer, Adam L. [4 ]
Carrillo, Maria C. [3 ]
Mielke, Michelle M. [5 ]
Rabinovici, Gil D. [4 ]
Salloway, Stephen [6 ,7 ]
Sperling, Reisa [8 ]
Zetterberg, Henrik [9 ,10 ,11 ,12 ,13 ]
Teunissen, Charlotte E. [14 ]
机构
[1] Lund Univ, Dept Clin Sci Malmo, Memory Res Unit, Clin, Malmo, Sweden
[2] Skane Univ Hosp, Memory Clin, SE-20502 Malmo, Sweden
[3] Alzheimers Assoc, Chicago, IL USA
[4] Univ Calif San Francisco, Dept Neurol, Memory & Aging Ctr, San Francisco, CA USA
[5] Wake Forest Univ, Bowman Gray Sch Med, Dept Epidemiol & Prevent, Winston Salem, NC USA
[6] Brown Univ, Dept Neurol, Alpert Med Sch, Providence, RI USA
[7] Brown Univ, Dept Psychiat, Alpert Med Sch, Providence, RI USA
[8] Harvard Med Sch, Massachusetts Gen Hosp, Ctr Alzheimer Res & Treatment, Brigham & Womens Hosp, Boston, MA 02115 USA
[9] Univ Gothenburg, Inst Neurosci & Physiol, Dept Psychiat & Neurochem, Sahlgrenska Acad, Molndal, Sweden
[10] Sahlgrens Univ Hosp, Clin Neurochem Lab, Molndal, Sweden
[11] UCL Inst Neurol, Dept Neurodegenerat Dis, Queen Sq, London, England
[12] UCL, UK Dementia Res Inst, London, England
[13] Hong Kong Ctr Neurodegenerat Dis, Clear Water Bay, Hong Kong, Peoples R China
[14] Vrije Univ, Amsterdam Univ Med Ctr, Dept Clin Chem, Neurochem,Amsterdam Neurosci, Amsterdam, Netherlands
关键词
Alzheimer's disease; appropriate use recommendations; blood-based biomarkers; diagnosis; prognosis; PLASMA NEUROFILAMENT LIGHT; FIBRILLARY ACIDIC PROTEIN; PHOSPHORYLATED TAU 181; AMYLOID-BETA; CLINICAL-DIAGNOSIS; DEMENTIA; ACCURACY; PREVALENCE; VALIDATION; PATHOLOGY;
D O I
10.1002/alz.12756
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Blood-based markers (BBMs) have recently shown promise to revolutionize the diagnostic and prognostic work-up of Alzheimer's disease (AD), as well as to improve the design of interventional trials. Here we discuss in detail further research needed to be performed before widespread use of BBMs. We already now recommend use of BBMs as (pre-)screeners to identify individuals likely to have AD pathological changes for inclusion in trials evaluating disease-modifying therapies, provided the AD status is confirmed with positron emission tomography (PET) or cerebrospinal fluid (CSF) testing. We also encourage studying longitudinal BBM changes in ongoing as well as future interventional trials. However, BBMs should not yet be used as primary endpoints in pivotal trials. Further, we recommend to cautiously start using BBMs in specialized memory clinics as part of the diagnostic work-up of patients with cognitive symptoms and the results should be confirmed whenever possible with CSF or PET. Additional data are needed before use of BBMs as stand-alone diagnostic AD markers, or before considering use in primary care.
引用
收藏
页码:2669 / 2686
页数:18
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