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Recommendations for clinical implementation of blood-based biomarkers for Alzheimer's disease.
Mielke, Michelle M; Anderson, Matthew; Ashford, J Wesson; Jeromin, Andreas; Lin, Pei-Jung; Rosen, Allyson; Tyrone, Jamie; Vandevrede, Lawren; Willis, Deanna R; Hansson, Oskar; Khachaturian, Ara S; Schindler, Suzanne E; Weiss, Joan; Batrla, Richard; Bozeat, Sasha; Dwyer, John R; Holzapfel, Drew; Jones, Daryl Rhys; Murray, James F; Partrick, Katherine A; Scholler, Emily; Vradenburg, George; Young, Dylan; Braunstein, Joel B; Burnham, Samantha C; de Oliveira, Fabricio Ferreira; Hu, Yan Helen; Mattke, Soeren; Merali, Zul; Monane, Mark; Sabbagh, Marwan Noel; Shobin, Eli; Weiner, Michael; Udeh-Momoh, Chinedu T.
Affiliation
  • Mielke MM; Department of Epidemiology and Prevention, Wake Forest University School of Medicine, Winston-Salem, USA.
  • Anderson M; Atrium Health, Charlotte, North Carolina, USA.
  • Ashford JW; Department of Psychiatry and Behavioral Sciences, Stanford University School of Medicine, Stanford, California, USA.
  • Jeromin A; War Related Illness and Injury Study Center, VA Palo Alto Health Care System, Palo Alto, California, USA.
  • Lin PJ; ALZpath, Carlsbad, California, USA.
  • Rosen A; Center for the Evaluation of Value and Risk in Health Institute for Clinical Research and Health Policy Studies, Tufts Medical Center, Boston, Massachusetts, USA.
  • Tyrone J; Palo Alto Veterans Affairs Medical Center, Palo Alto, California, USA.
  • Vandevrede L; Stanford University School of Medicine, Stanford, California, USA.
  • Willis DR; Patient Advocate, Sacramento, California, USA.
  • Hansson O; Memory and Aging Center, Department of Neurology, University of California, San Francisco, California, USA.
  • Khachaturian AS; Department of Family Medicine, Indiana University School of Medicine, Indianapolis, Indiana, USA.
  • Schindler SE; Clinical Memory Research Unit, Department of Clinical Sciences Malmö, Lund University, Lund, Sweden.
  • Weiss J; Memory Clinic, Skåne University Hospital, Malmö, Sweden.
  • Batrla R; The Campaign to Prevent Alzheimer's Disease, Rockville, Maryland, USA.
  • Bozeat S; Department of Neurology, Knight Alzheimer's Disease Research Center, Washington University School of Medicine, St. Louis, Missouri, USA.
  • Dwyer JR; US Department of Health and Human Services, Health Resources and Services Administration, Bureau of Health Workforce, Rockville, Maryland, USA.
  • Holzapfel D; Eisai Inc, Nutley, New Jersey, USA.
  • Jones DR; F. Hoffman-La Roche AG, Basel, Switzerland.
  • Murray JF; Global Alzheimer's Platform Foundation, Washington, District of Columbia, USA.
  • Partrick KA; The Global CEO Initiative on Alzheimer's Disease, Philadelphia, Pennsylvania, USA.
  • Scholler E; Davos Alzheimer's Collaborative, Philadelphia, Pennsylvania, USA.
  • Vradenburg G; Eisai Inc, Nutley, New Jersey, USA.
  • Young D; Davos Alzheimer's Collaborative, Philadelphia, Pennsylvania, USA.
  • Braunstein JB; The Global CEO Initiative on Alzheimer's Disease, Philadelphia, Pennsylvania, USA.
  • Burnham SC; The Global CEO Initiative on Alzheimer's Disease, Philadelphia, Pennsylvania, USA.
  • de Oliveira FF; Davos Alzheimer's Collaborative, Philadelphia, Pennsylvania, USA.
  • Hu YH; The Global CEO Initiative on Alzheimer's Disease, Philadelphia, Pennsylvania, USA.
  • Mattke S; Davos Alzheimer's Collaborative, Philadelphia, Pennsylvania, USA.
  • Merali Z; Guidehouse, McLean, Virginia, USA.
  • Monane M; C2N Diagnostics, St. Louis, Missouri, USA.
  • Sabbagh MN; Eli Lilly & Co., Indianapolis, Indiana, USA.
  • Shobin E; Federal University of São Paulo, São Paulo, Brazil.
  • Weiner M; Eisai Inc, Nutley, New Jersey, USA.
  • Udeh-Momoh CT; The USC Brain Health Observatory, University of Southern California, Los Angeles, California, USA.
Alzheimers Dement ; 2024 Oct 01.
Article in En | MEDLINE | ID: mdl-39351838
ABSTRACT
Blood-based biomarkers (BBM) for Alzheimer's disease (AD) are being increasingly used in clinical practice to support an AD diagnosis. In contrast to traditional diagnostic modalities, such as amyloid positron emission tomography and cerebrospinal fluid biomarkers, BBMs offer a more accessible and lower cost alternative for AD biomarker testing. Their unique scalability addresses the anticipated surge in demand for biomarker testing with the emergence of disease-modifying treatments (DMTs) that require confirmation of amyloid pathology. To facilitate the uptake of BBMs in clinical practice, The Global CEO Initiative on Alzheimer's Disease convened a BBM Workgroup to provide recommendations for two clinical implementational pathways for BBMs one for current use for triaging and another for future use to confirm amyloid pathology. These pathways provide a standardized diagnostic approach with guidance on interpreting BBM test results. Integrating BBMs into clinical practice will simplify the diagnostic process and facilitate timely access to DMTs for eligible patients.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Alzheimers Dement Year: 2024 Document type: Article Affiliation country: United States Country of publication: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Alzheimers Dement Year: 2024 Document type: Article Affiliation country: United States Country of publication: United States