Differences between blood and cerebrospinal fluid glial fibrillary Acidic protein levels: The effect of sample stability

被引:36
|
作者
Simren, Joel [1 ]
Weninger, Haley [1 ]
Brum, Wagner S. [1 ,2 ]
Khalil, Shilla [1 ]
Benedet, Andrea L. [1 ]
Blennow, Kaj [1 ,3 ]
Zetterberg, Henrik [1 ,3 ,4 ,5 ]
Ashton, Nicholas J. [1 ,6 ,7 ,8 ]
机构
[1] Univ Gothenburg, Sahlgrenska Univ Hosp, Sahlgrenska Acad,Dept Psychiat & Neurochem, Inst Neurosci & Physiol,Clin Neurochem Lab, Gothenburg, Sweden
[2] Univ Fed Rio Grande do Sul UFRGS, Grad Program Biol Sci Biochem, Porto Alegre, RS, Brazil
[3] Sahlgrens Univ Hosp, Clin Neurochem Lab, Gothenburg, Sweden
[4] UK Dementia Res Inst UCL, UCL Inst Neurol, Dept Neurodegenerat Dis, London, England
[5] Hong Kong Ctr Neurodegenerat Dis, Clear Water Bay, Hong Kong, Peoples R China
[6] Kings Coll London, Psychol & Neurosci, Maurice Wohl Clin Neurosci Inst, Inst Psychiat, London, England
[7] Maudsley NHS Fdn, Biomed Res Unit Dementia South London, NIHR Biomed Res Ctr Mental Hlth, London, England
[8] Stavanger Univ Hosp, Ctr Age Related Med, Stavanger, Norway
基金
美国国家卫生研究院; 欧洲研究理事会; 瑞典研究理事会;
关键词
MARKER; GFAP;
D O I
10.1002/alz.12806
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Introduction Recent evidence has shown that the marker of reactive astrogliosis, glial fibrillary acidic protein (GFAP), has a stronger relationship with cerebral amyloid beta (A beta) pathology in blood than in cerebrospinal fluid (CSF). This study investigates if pre-analytical treatment of blood and CSF contribute to these unexpected findings. Methods Paired CSF and serum samples from 49 individuals (A beta-negative = 28; A beta-positive = 21) underwent a series of seven freeze-thaw cycles (FTCs). All samples were analyzed for GFAP and neurofilament light (NfL) using single molecule array technology including a fresh unfrozen sample from each patient. Results FTC significantly affected CSF GFAP concentration (-188.12 pg/ml per FTC) but not serum GFAP. In the same samples, NfL remained stable. Serum GFAP had a higher discrimination of A beta burden than CSF GFAP, irrespective of FTC, which also included unfrozen samples. Discussion This study demonstrates large stability differences of GFAP in CSF and serum. However, this disparity does not seem to fully explain the stronger association of serum GFAP with A beta pathology. Further work should investigate mechanisms of GFAP release into the bloodstream under pathological conditions.
引用
收藏
页码:1988 / 1992
页数:5
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