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FältnamnIndikatorerMetadata
00004313naa a2200409 4500
001oai:lup.lub.lu.se:37bec1ff-2e71-460d-88a5-2ca8b9fb4d79
003SwePub
008201112s2020 | |||||||||||000 ||eng|
024a https://lup.lub.lu.se/record/37bec1ff-2e71-460d-88a5-2ca8b9fb4d792 URI
024a https://doi.org/10.1002/acn3.511952 DOI
040 a (SwePub)lu
041 a engb eng
042 9 SwePub
072 7a art2 swepub-publicationtype
072 7a ref2 swepub-contenttype
100a Reimand, Juhanu North Estonia Medical Centre,Amsterdam UMC - Vrije Universiteit Amsterdam,Tallinn University of Technology,Vrije Universiteit Amsterdam4 aut
2451 0a Amyloid-β PET and CSF in an autopsy-confirmed cohort
264 c 2020-10-20
264 1b Wiley,c 2020
300 a 11 s.
520 a Objective: Accumulation of amyloid-β is among the earliest changes in Alzheimer’s disease (AD). Amyloid-β positron emission tomography (PET) and Aβ42 in cerebrospinal fluid (CSF) both assess amyloid-β pathology in-vivo, but 10–20% of cases show discordant (CSF+/PET− or CSF-/PET+) results. The neuropathological correspondence with amyloid-β CSF/PET discordance is unknown. Methods: We included 21 patients from our tertiary memory clinic who had undergone both CSF Aβ42 analysis and amyloid-β PET, and had neuropathological data available. Amyloid-β PET and CSF results were compared with neuropathological ABC scores (comprising of Thal (A), Braak (B), and CERAD (C) stage, all ranging from 0 [low] to 3 [high]) and neuropathological diagnosis. Results: Neuropathological diagnosis was AD in 11 (52%) patients. Amyloid-β PET was positive in all A3, C2, and C3 cases and in one of the two A2 cases. CSF Aβ42 was positive in 92% of ≥A2 and 90% of ≥C2 cases. PET and CSF were discordant in three of 21 (14%) cases: CSF+/PET− in a patient with granulomatosis with polyangiitis (A0B0C0), CSF+/PET− in a patient with FTLD-TDP type B (A2B1C1), and CSF-/PET+ in a patient with AD (A3B3C3). Two CSF+/PET+ cases had a non-AD neuropathological diagnosis, that is FTLD-TDP type E (A3B1C1) and adult-onset leukoencephalopathy with axonal spheroids (A1B1C0). Interpretation: Our study demonstrates neuropathological underpinnings of amyloid-β CSF/PET discordance. Furthermore, amyloid-β biomarker positivity on both PET and CSF did not invariably result in an AD diagnosis at autopsy, illustrating the importance of considering relevant comorbidities when evaluating amyloid-β biomarker results.
650 7a MEDICIN OCH HÄLSOVETENSKAPx Klinisk medicinx Neurologi0 (SwePub)302072 hsv//swe
650 7a MEDICAL AND HEALTH SCIENCESx Clinical Medicinex Neurology0 (SwePub)302072 hsv//eng
700a Boon, Baayla D.C.u Amsterdam UMC - Vrije Universiteit Amsterdam,Vrije Universiteit Amsterdam4 aut
700a Collij, Lyduine E.u Amsterdam UMC - Vrije Universiteit Amsterdam,Vrije Universiteit Amsterdam4 aut
700a Teunissen, Charlotte E.u Vrije Universiteit Amsterdam,Amsterdam UMC - Vrije Universiteit Amsterdam4 aut
700a Rozemuller, Annemieke J.M.u Amsterdam UMC - Vrije Universiteit Amsterdam,Vrije Universiteit Amsterdam4 aut
700a van Berckel, Bart N.M.u Vrije Universiteit Amsterdam,Amsterdam UMC - Vrije Universiteit Amsterdam4 aut
700a Scheltens, Philipu Amsterdam UMC - Vrije Universiteit Amsterdam,Vrije Universiteit Amsterdam4 aut
700a Ossenkoppele, Riku Lund University,Lunds universitet,Klinisk minnesforskning,Forskargrupper vid Lunds universitet,Clinical Memory Research,Lund University Research Groups,Amsterdam UMC - Vrije Universiteit Amsterdam,Vrije Universiteit Amsterdam4 aut0 (Swepub:lu)ri1513os
700a Bouwman, Femkeu Amsterdam UMC - Vrije Universiteit Amsterdam,Vrije Universiteit Amsterdam4 aut
710a North Estonia Medical Centreb Amsterdam UMC - Vrije Universiteit Amsterdam4 org
773t Annals of Clinical and Translational Neurologyd : Wileyg 7:11, s. 2150-2160q 7:11<2150-2160x 2328-9503
856u http://dx.doi.org/10.1002/acn3.51195x freey FULLTEXT
856u https://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/acn3.51195
8564 8u https://lup.lub.lu.se/record/37bec1ff-2e71-460d-88a5-2ca8b9fb4d79
8564 8u https://doi.org/10.1002/acn3.51195

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