Abstract
Original language | English |
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Journal | Alzheimer's and Dementia |
Early online date | 2021 |
DOIs | |
Publication status | E-pub ahead of print - 2021 |
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State-of-the-art of lumbar puncture and its place in the journey of patients with Alzheimer's disease. / Hampel, Harald; Shaw, Leslie M.; Aisen, Paul et al.
In: Alzheimer's and Dementia, 2021.Research output: Contribution to journal › Review article › Academic › peer-review
TY - JOUR
T1 - State-of-the-art of lumbar puncture and its place in the journey of patients with Alzheimer's disease
AU - Hampel, Harald
AU - Shaw, Leslie M.
AU - Aisen, Paul
AU - Chen, Christopher
AU - Lleó, Alberto
AU - Iwatsubo, Takeshi
AU - Iwata, Atsushi
AU - Yamada, Masahito
AU - Ikeuchi, Takeshi
AU - Jia, Jianping
AU - Wang, Huali
AU - Teunissen, Charlotte E.
AU - Peskind, Elaine
AU - Blennow, Kaj
AU - Cummings, Jeffrey
AU - Vergallo, Andrea
N1 - Funding Information: P. Aisen reports grants from Janssen, Eisai Inc., National Institute on Aging, Foundation for the National Institutes of Health, and the Alzheimer's Association; and consulting fees from Merck, Biogen, Roche, Lundbeck, and Immunobrain Checkpoint. C. Chen has provided consultation to Cerecin, Danone, Eisai Inc., Lundbeck, Moleac, and Senescence. A. Lleó has served as a consultant or on advisory boards for Fujirebio‐Europe, Roche, Biogen, and Nutricia. Dr. Lleó has received funding from the Fondo de Investigaciones Sanitario (FIS), Instituto de Salud Carlos III (AC19/00103), and the CIBERNED program (Program 1, Alzheimer Disease) partially funded by Fondo Europeo de Desarrollo Regional, Unión Europea, Una manera de hacer Europa. In addition, Dr. Lleó has patent WO2019175379 A1 Markers of synaptopathy in neurodegenerative disease. A. Iwata has received lecture and consultant fees from Eisai Inc. M. Yamada has received research grants from the Japan Society for the Promotion of Science (JSPS); the Ministry of Health, Labour and Welfare, Japan (MHLW); and the Japan Agency for Medical Research and Development (AMED). He has received scholarship grants from Astellas Pharma Inc.; Eisai Co., Ltd.; Otsuka Pharmaceutical Co., Ltd.; Kyowa Kirin Co., Ltd.; Shionogi Co., Ltd.; Daiichi Sankyo Healthcare Co., Ltd.; Takeda Pharmaceutical Co., Ltd.; Tsumura & Co.; Teijin Pharma, Ltd.; Nihon Medi‐Physics Co., Ltd.; Fujifilm Co.; Pfizer Japan Inc.; and Ricoh Co., Ltd. He received honoraria for sponsored lectures from Alnylam Japan K.K.; Alexion Pharma GK; Eisai Co., Ltd.; FP Pharmaceutical Co.; Otsuka Pharmaceutical Co., Ltd.; Ono Pharmaceutical Co., Ltd.; Sumitomo Dainippon Pharma Co., Ltd.; Daiichi Sankyo Healthcare Co., Ltd.; Takeda Pharmaceutical Co., Ltd.; Tsumura & Co.; Teijin Pharma, Ltd.; Nippon Chemiphar Co., Ltd.; Nihon Medi‐Physics Co., Ltd.; Nihon Pharmaceutical Co., Ltd.; Biogen Japan Ltd.; Fujifilm Co.; and Janssen Pharmaceutical K.K. T. Ikeuchi has provided consultation to Eisai Inc., Takeda, Janssen, Chugai, and Ono, and received lecture honoraria from Eisai Inc., Daiichi Sankyo, Novartis, Janssen, Takeda, Roche, and FUJIFILM RI Pharma. J. Jia has provided consultation to Eisai Inc., Novartis, Green Valley, Eli Lilly and Company, AstraZeneca, and CSPC‐NBP. H. Wang has provided consultation to Eisai Inc., Lundbeck, Roche, and Signant Health pharmaceutical and assessment companies. Dr. Wang owns the copyright of the individualized management system of neuropsychiatric symptoms (NPSIMS). C.E. Teunissen has a collaboration contract with ADx Neurosciences and Quanterix, and performed contract research for or received grants from Axon Neurosciences, Biogen, Boehringer Ingelheim, Brainstorm Therapeutics, Celgene, EIP Pharma, Eisai inc., Janssen Prevention Center, Roche, Toyama, and Vivoryon. K. Blennow has served as a consultant, on advisory boards, or data monitoring committees for Abcam, Axon Neurosciences, Biogen, JOMDD/Shimadzu, Julius Clinical, Eli Lilly and Company, MagQu, Novartis, Roche Diagnostics, and Siemens Healthineers, and is a co‐founder of Brain Biomarker Solutions in Gothenburg AB (BBS), which is part of the GU Ventures Incubator Program. J. Cummings has provided consultation to Acadia, Actinogen, Alkahest, Alzheon, Annovis, Avanir, Axsome, Biogen, Cassava, Cerecin, Cerevel, Cortexyme, Cytox, EIP Pharma, Eisai inc., Foresight, GemVax, Genentech, Green Valley, Grifols, Karuna, Merck, Novo Nordisk, Otsuka, Resverlogix, Roche, Samumed, Samus, Signant Health, Suven, and United Neuroscience pharmaceutical and assessment companies. Dr. Cummings has stock options in ADAMAS, AnnovisBio, MedAvante, and BiOasis. Dr. Cummings owns the copyright of the Neuropsychiatric Inventory. A. Vergallo is an employee of Eisai Inc. He has not received any fees or honoraria since November 2019. Before November 2019, he had received lecture honoraria from Roche, MagQu LLC, and Servier. E. Peskind has provided consultation to Acadia, Avanir, Eli Lilly and Company, and Takeda. Funding Information: L. Shaw is supported by NIH grants ADNI U19 AG024904; UPenn ADRC P30 AG010124; MJFox Foundation for Parkinson's Research MJFF‐005441. C. Chen is supported by the National Medical Research Council of Singapore. T. Ikeuchi is supported in part by AMED grants JP20dm0207073 and JP20dm0107143, and MHLW grants 19192257 and 20316440. J. Jia was supported by the Key Project of the National Natural Science Foundation of China (81530036); the National Key Scientific Instrument and Equipment Development Project (31627803); Beijing Scholars Program; Beijing Brain Initiative from Beijing Municipal Science & Technology Commission (Z201100005520016, Z201100005520017); Project for Outstanding Doctor with Combined Ability of Western and Chinese Medicine; and Beijing Municipal Commission of Health and Family Planning (PXM2019_026283_000003). H. Wang is supported by National Key Research and Development Project grant 2017YFC1311100. J. Cummings is supported by Keep Memory Alive (KMA); National Institute of General Medical Sciences grant P20GM109025; National Institute of Neurological Disorders and Stroke grant U01NS093334; and National Institute on Aging grant R01AG053798. Research of C.E. Teunissen is supported by the European Commission (Marie Curie International Training Network, Joint Programme – Neurodegenerative Disease), Health Holland, the Dutch Research Council (ZonMw), the Selfridges Group Foundation, Alzheimer Netherlands, and the Alzheimer Association. Medical writing support was provided by Paul O'Neill, PhD, of CMC AFFINITY, McCann Health Medical Communications, and was funded by Eisai. Publisher Copyright: © 2021 Eisai, Inc. Alzheimer's & Dementia published by Wiley Periodicals LLC on behalf of Alzheimer's Association. Copyright: Copyright 2021 Elsevier B.V., All rights reserved.
PY - 2021
Y1 - 2021
N2 - Recent advances in developing disease-modifying therapies (DMT) for Alzheimer's disease (AD), and the recognition that AD pathophysiology emerges decades before clinical symptoms, necessitate a paradigm shift of health-care systems toward biomarker-guided early detection, diagnosis, and therapeutic decision-making. Appropriate incorporation of cerebrospinal fluid biomarker analysis in clinical practice is an essential step toward system readiness for accommodating the demand of AD diagnosis and proper use of DMTs—once they become available. However, the use of lumbar puncture (LP) in individuals with suspected neurodegenerative diseases such as AD is inconsistent, and the perception of its utility and safety differs considerably among medical specialties as well as among regions and countries. This review describes the state-of-the-art evidence concerning the safety profile of LP in older adults, discusses the risk factors for LP-associated adverse events, and provides recommendations and an outlook for optimized use and global implementation of LP in individuals with suspected AD.
AB - Recent advances in developing disease-modifying therapies (DMT) for Alzheimer's disease (AD), and the recognition that AD pathophysiology emerges decades before clinical symptoms, necessitate a paradigm shift of health-care systems toward biomarker-guided early detection, diagnosis, and therapeutic decision-making. Appropriate incorporation of cerebrospinal fluid biomarker analysis in clinical practice is an essential step toward system readiness for accommodating the demand of AD diagnosis and proper use of DMTs—once they become available. However, the use of lumbar puncture (LP) in individuals with suspected neurodegenerative diseases such as AD is inconsistent, and the perception of its utility and safety differs considerably among medical specialties as well as among regions and countries. This review describes the state-of-the-art evidence concerning the safety profile of LP in older adults, discusses the risk factors for LP-associated adverse events, and provides recommendations and an outlook for optimized use and global implementation of LP in individuals with suspected AD.
KW - Alzheimer's disease
KW - biomarker
KW - cerebrospinal fluid
KW - diagnosis
KW - evidence-based guidelines
KW - lumbar puncture
KW - system readiness
UR - http://www.scopus.com/inward/record.url?scp=85106657164&partnerID=8YFLogxK
U2 - 10.1002/alz.12372
DO - 10.1002/alz.12372
M3 - Review article
C2 - 34043269
JO - Alzheimers & Dementia
JF - Alzheimers & Dementia
SN - 1552-5260
ER -