Longitudinal changes in Alzheimer's‐related plasma biomarkers and brain amyloid

Author:

Bilgel Murat1ORCID,An Yang1,Walker Keenan A.1,Moghekar Abhay R.2,Ashton Nicholas J.3456,Kac Przemysław R.3,Karikari Thomas K.3,Blennow Kaj37,Zetterberg Henrik378910,Jedynak Bruno M.11,Thambisetty Madhav1,Ferrucci Luigi12,Resnick Susan M.1

Affiliation:

1. Laboratory of Behavioral Neuroscience National Institute on Aging Baltimore Maryland USA

2. Department of Neurology Johns Hopkins University School of Medicine Baltimore Maryland USA

3. Department of Psychiatry and Neurochemistry Institute of Neuroscience and Physiology The Sahlgrenska Academy University of Gothenburg Mölndal Sweden

4. King's College London Institute of Psychiatry, Psychology and Neuroscience Maurice Wohl Clinical Neuroscience Institute London UK

5. NIHR Biomedical Research Centre for Mental Health and Biomedical Research Unit for Dementia at South London and Maudsley NHS Foundation London UK

6. Centre for Age‐Related Medicine Stavanger University Hospital Stavanger Norway

7. Clinical Neurochemistry Laboratory Sahlgrenska University Hospital Mölndal Sweden

8. Department of Neurodegenerative Disease UCL Institute of Neurology London UK

9. UK Dementia Research Institute at UCL London UK

10. Hong Kong Center for Neurodegenerative Diseases Clear Water Bay Hong Kong China

11. Department of Mathematics and Statistics Portland State University Portland Oregon USA

12. Translational Gerontology Branch National Institute on Aging Baltimore Maryland USA

Abstract

AbstractINTRODUCTIONUnderstanding longitudinal plasma biomarker trajectories relative to brain amyloid changes can help devise Alzheimer's progression assessment strategies.METHODSWe examined the temporal order of changes in plasma amyloid‐β ratio (), glial fibrillary acidic protein (GFAP), neurofilament light chain (NfL), and phosphorylated tau ratios (, ) relative to 11C‐Pittsburgh compound B (PiB) positron emission tomography (PET) cortical amyloid burden (PiB−/+). Participants (n = 199) were cognitively normal at index visit with a median 6.1‐year follow‐up.RESULTSPiB groups exhibited different rates of longitudinal change in . Change in brain amyloid correlated with change in GFAP (r = 0.5, 95% CI = [0.26, 0.68]). The greatest relative decline in (−1%/year) preceded brain amyloid positivity by 41 years (95% CI = [32, 53]).DISCUSSIONPlasma may begin declining decades prior to brain amyloid accumulation, whereas p‐tau ratios, GFAP, and NfL increase closer in time.HIGHLIGHTS Plasma declines over time among PiB− but does not change among PiB+. Phosphorylated‐tau to Aβ42 ratios increase over time among PiB+ but do not change among PiB−. Rate of change in brain amyloid is correlated with change in GFAP and neurofilament light chain. The greatest decline in may precede brain amyloid positivity by decades.

Funder

Vetenskapsrådet

Publisher

Wiley

Subject

Psychiatry and Mental health,Cellular and Molecular Neuroscience,Geriatrics and Gerontology,Neurology (clinical),Developmental Neuroscience,Health Policy,Epidemiology

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3