{"id":271164,"date":"2023-12-23T12:00:43","date_gmt":"2023-12-23T12:00:43","guid":{"rendered":"https:\/\/hamslivenews.com\/?p=271164"},"modified":"2023-12-27T10:34:51","modified_gmt":"2023-12-27T10:34:51","slug":"fujirebio-expands-its-alzheimers-disease-test-menu-with-the-much-awaited-and-fully-automated-lumipulse-g-ptau-217-plasma-assay-for-research-use-only-ruo","status":"publish","type":"post","link":"https:\/\/www.hamslive.com\/news\/2023\/12\/fujirebio-expands-its-alzheimers-disease-test-menu-with-the-much-awaited-and-fully-automated-lumipulse-g-ptau-217-plasma-assay-for-research-use-only-ruo\/","title":{"rendered":"Fujirebio Expands Its Alzheimer\u2019s Disease Test Menu With the Much Awaited and Fully Automated Lumipulse\u00ae G pTau 217 Plasma Assay for Research Use Only (RUO)"},"content":{"rendered":"

Business Wire India<\/b><\/p>\n

H.U. Group Holdings Inc. and its wholly-owned subsidiary Fujirebio today announced the availability of the Lumipulse G pTau 217 Plasma assay for the fully automated LUMIPULSE G immunoassay systems. This CLEIA (chemiluminescent enzyme immunoassay) assay allows for the quantitative measurement of Tau phosphorylated at threonine 217 (pTau 217) in human K2<\/sub>EDTA plasma within just 35 minutes.<\/p>\n

\u201cThe launch of the pTau 217 Plasma assay on our fully automated LUMIPULSE platform is an essential step in the efforts of Fujirebio to bring novel, innovative neurodegenerative biomarkers to laboratories and clinicians around the world,\u201d<\/i> said Goki Ishikawa, President and CEO of Fujirebio Holdings, Inc. \u201cExpectations are high for this new biomarker, and researchers and clinical research professionals can now study its clinical utility on a platform that has the required throughput and meets the regulatory requirements to support possible future routine use.\u201d<\/i><\/p>\n

About pTau 217 <\/b>
\nCurrent research indicates that plasma pTau, including pTau 217, is a predictor of amyloid status determined either by CSF1<\/sup> or PET2<\/sup>, and therefore able to differentiate between Alzheimer\u2019s disease (AD) and non-AD neurodegenerative diseases3,4<\/sup> and to predict progression to AD.5,6<\/sup> Blood-based biomarkers, such as plasma pTau, could potentially be used as inclusion criteria or to evaluate target engagement and treatment efficacy in clinical trials, and could further advance the development and implementation of disease-modifying treatments in the field of AD and related disorders.7<\/sup> This assay is designed to measure specifically the phosphorylation on position threonine 217 in human plasma.<\/p>\n

About Fujirebio <\/b>
\nFujirebio, a member of H.U. Group Holdings Inc., is a global leader in the field of high-quality in vitro diagnostics (IVD) testing. It has more than 50 years\u2019 accumulated experience in the conception, development, production, and worldwide commercialization of robust IVD products.<\/p>\n

Fujirebio was the first company to develop and market CSF biomarkers under the Innogenetics brand over 25 years ago. Fujirebio remains the only company with such a comprehensive line-up of manual and fully automated neurodegenerative disease assays and consistently partners with organizations and clinical experts across the world to develop new pathways for earlier, easier and more complete neurodegenerative diagnostic tools. More information can be found at www.fujirebio.com\/alzheimer<\/a>.<\/p>\n

References:<\/b><\/p>\n

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  1. Ashton N, et al. Plasma and CSF biomarkers in a memory clinic: head-to-head comparison of phosphorylated tau immunoassays. Alzheimers Dement, 19(5): 1913-1924, 2023.<\/li>\n
  2. Mielke M, et al. Performance of plasma phosphorylated tau 181 and 217 in the community. Nat Med, 28(7): 1398-1405, 2022.<\/li>\n
  3. Palmqvist S, et al. Discriminative accuracy of plasma phospho-tau 217 for Alzheimer\u2019s disease vs other neurodegenerative disorders. JAMA, 324(8): 772-781, 2020.<\/li>\n
  4. Thijssen E, et al. Plasma phosphorylated tau 217 and phosphorylated tau 181 as biomarkers in Alzheimer\u2019s disease and frontotemporal lobar degeneration: a retrospective diagnostic performance study. Lancet Neurol, 20(9): 739-752, 2021.<\/li>\n
  5. Jonaitis EM, et al. Plasma phosphorylated tau 217 in preclinical Alzheimer\u2019s disease. Brain Commun, 5(2): fcad057, 2023.<\/li>\n
  6. Mattsson-Carlgren N, et al. Prediction of longitudinal cognitive decline in preclinical Alzheimer disease using plasma biomarkers. JAMA Neurol, 80(4): 360-369, 2023.<\/li>\n
  7. Gonzalez-Ortiz F, et al. Plasma phospho-tau in Alzheimer\u2019s disease: towards diagnostic and therapeutic trial applications. Mol Neurodegener, 18(1): 18, 2023.<\/li>\n<\/ol>\n

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