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      Independent study demonstrates amyloid probability score accurately indicates amyloid pathology

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          Abstract

          Background

          The amyloid probability score (APS) is the model read‐out of the analytically validated mass spectrometry‐based PrecivityAD ® blood test that incorporates the plasma Aβ42/40 ratio, ApoE proteotype, and age to identify the likelihood of brain amyloid plaques among cognitively impaired individuals being evaluated for Alzheimer's disease.

          Purpose

          This study aimed to provide additional independent evidence that the pre‐established APS algorithm, along with its cutoff values, discriminates between amyloid positive and negative individuals.

          Methods

          The diagnostic performance of the PrecivityAD test was analyzed in a cohort of 200 nonrandomly selected Australian Imaging, Biomarker & Lifestyle Flagship Study of Aging (AIBL) study participants, who were either cognitively impaired or healthy controls, and for whom a blood sample and amyloid PET imaging were available.

          Results

          In a subset of the dataset aligned with the Intended Use population (patients aged 60 and older with CDR ≥0.5), the pre‐established APS algorithm predicted amyloid PET with a sensitivity of 84.9% (CI: 72.9–92.1%) and specificity of 96% (CI: 80.5–99.3%), exclusive of 13 individuals for whom the test was inconclusive.

          Interpretation

          The study shows individuals with a high APS are more likely than those with a low APS to have abnormal amounts of amyloid plaques and be on an amyloid accumulation trajectory, a dynamic and evolving process characteristic of progressive AD pathology. Exploratory data suggest APS retains its diagnostic performance in healthy individuals, supporting further screening studies in the cognitively unimpaired.

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          Most cited references29

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          Clinical diagnosis of Alzheimer's disease: Report of the NINCDS-ADRDA Work Group* under the auspices of Department of Health and Human Services Task Force on Alzheimer's Disease

          Neurology, 34(7), 939-939
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            Lecanemab in Early Alzheimer’s Disease

            The accumulation of soluble and insoluble aggregated amyloid-beta (Aβ) may initiate or potentiate pathologic processes in Alzheimer's disease. Lecanemab, a humanized IgG1 monoclonal antibody that binds with high affinity to Aβ soluble protofibrils, is being tested in persons with early Alzheimer's disease.
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              Mild cognitive impairment--beyond controversies, towards a consensus: report of the International Working Group on Mild Cognitive Impairment.

              The First Key Symposium was held in Stockholm, Sweden, 2-5 September 2003. The aim of the symposium was to integrate clinical and epidemiological perspectives on the topic of Mild Cognitive Impairment (MCI). A multidisciplinary, international group of experts discussed the current status and future directions of MCI, with regard to clinical presentation, cognitive and functional assessment, and the role of neuroimaging, biomarkers and genetics. Agreement on new perspectives, as well as recommendations for management and future research were discussed by the international working group. The specific recommendations for the general MCI criteria include the following: (i) the person is neither normal nor demented; (ii) there is evidence of cognitive deterioration shown by either objectively measured decline over time and/or subjective report of decline by self and/or informant in conjunction with objective cognitive deficits; and (iii) activities of daily living are preserved and complex instrumental functions are either intact or minimally impaired.
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                Author and article information

                Contributors
                kyarasheski@c2n.com
                Journal
                Ann Clin Transl Neurol
                Ann Clin Transl Neurol
                10.1002/(ISSN)2328-9503
                ACN3
                Annals of Clinical and Translational Neurology
                John Wiley and Sons Inc. (Hoboken )
                2328-9503
                28 March 2023
                May 2023
                : 10
                : 5 ( doiID: 10.1002/acn3.v10.5 )
                : 765-778
                Affiliations
                [ 1 ] C2N Diagnostics St. Louis Missouri USA
                [ 2 ] Biogen Cambridge Massachusetts USA
                [ 3 ] Dept. of Neurology, Hope Center for Neurological Disorders, Knight Alzheimer's Disease Research Center, Tracey Family SILQ Center Washington University School of Medicine St. Louis Missouri USA
                [ 4 ] Stat4ward Pittsburgh Pennsylvania USA
                Author notes
                [*] [* ] Correspondence

                Kevin Yarasheski, C 2N Diagnostics, 4340 Duncan Ave, St. Louis, MO 63110, USA. Tel: +1‐314‐464‐0010; Fax: +1‐314‐499‐7080; E‐mail: kyarasheski@ 123456c2n.com

                Author information
                https://orcid.org/0000-0001-8550-7625
                https://orcid.org/0000-0002-3400-0856
                https://orcid.org/0000-0001-5436-2451
                Article
                ACN351763 ACN3-2023-01-0013.R1
                10.1002/acn3.51763
                10187729
                36975407
                d1f677aa-6b71-4f57-b53e-b6652f7756df
                © 2023 The Authors. Annals of Clinical and Translational Neurology published by Wiley Periodicals LLC on behalf of American Neurological Association.

                This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.

                History
                : 08 March 2023
                : 05 January 2023
                : 12 March 2023
                Page count
                Figures: 5, Tables: 4, Pages: 778, Words: 7956
                Funding
                Funded by: Biogen , doi 10.13039/100005614;
                This work was funded by Biogen , doi 10.13039/100005614; .
                Categories
                Research Article
                Research Articles
                Custom metadata
                2.0
                May 2023
                Converter:WILEY_ML3GV2_TO_JATSPMC version:6.2.8 mode:remove_FC converted:16.05.2023

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