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Sökning: WFRF:(Nazarenko Sergei) > Why Is Amyloid-β PE...

Why Is Amyloid-β PET Requested After Performing CSF Biomarkers?

Reimand, Juhan (författare)
Amsterdam UMC - Vrije Universiteit Amsterdam,Tallinn University of Technology
Groot, Colin (författare)
Vrije Universiteit Amsterdam,Amsterdam UMC - Vrije Universiteit Amsterdam
Teunissen, Charlotte E. (författare)
Amsterdam UMC - Vrije Universiteit Amsterdam,Vrije Universiteit Amsterdam
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Windhorst, Albert D. (författare)
Amsterdam UMC - Vrije Universiteit Amsterdam,Vrije Universiteit Amsterdam
Boellaard, Ronald (författare)
Amsterdam UMC - Vrije Universiteit Amsterdam,Vrije Universiteit Amsterdam
Barkhof, Frederik (författare)
University College London,Amsterdam UMC - Vrije Universiteit Amsterdam
Nazarenko, Sergei (författare)
Tallinn University of Technology
van der Flier, Wiesje M. (författare)
Amsterdam UMC - Vrije Universiteit Amsterdam,Vrije Universiteit Amsterdam
van Berckel, Bart N.M. (författare)
Vrije Universiteit Amsterdam,Amsterdam UMC - Vrije Universiteit Amsterdam
Scheltens, Philip (författare)
Amsterdam UMC - Vrije Universiteit Amsterdam,Vrije Universiteit Amsterdam
Ossenkoppele, Rik (författare)
Lund University,Lunds universitet,Klinisk minnesforskning,Forskargrupper vid Lunds universitet,Clinical Memory Research,Lund University Research Groups,Vrije Universiteit Amsterdam,Amsterdam UMC - Vrije Universiteit Amsterdam
Bouwman, Femke (författare)
Vrije Universiteit Amsterdam,Amsterdam UMC - Vrije Universiteit Amsterdam
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 (creator_code:org_t)
2020
2020
Engelska 11 s.
Ingår i: Journal of Alzheimer's disease : JAD. - 1387-2877. ; 73:2, s. 559-569
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • BACKGROUND: Amyloid-β positron emission tomography (PET) and cerebrospinal fluid (CSF) Aβ42 are considered interchangeable for clinical diagnosis of Alzheimer's disease. OBJECTIVE: To explore the clinical reasoning for requesting additional amyloid-β PET after performing CSF biomarkers. METHODS: We retrospectively identified 72 memory clinic patients who underwent amyloid-β PET after CSF biomarkers analysis for clinical diagnostic evaluation between 2011 and 2019. We performed patient chart reviews to identify factors which led to additional amyloid-β PET. Additionally, we assessed accordance with appropriate-use-criteria (AUC) for amyloid-β PET. RESULTS: Mean patient age was 62.0 (SD = 8.1) and mean Mini-Mental State Exam score was 23.6 (SD = 3.8). CSF analysis conflicting with the clinical diagnosis was the most frequent reason for requesting an amyloid-β PET scan (n = 53, 74%), followed by incongruent MRI (n = 16, 22%), unusual clinical presentation (n = 11, 15%) and young age (n = 8, 11%). An amyloid-β PET scan was rarely (n = 5, 7%) requested in patients with a CSF Aβ+/tau+ status. Fifteen (47%) patients with a post-PET diagnosis of AD had a predominantly non-amnestic presentation. In n = 11 (15%) cases, the reason that the clinician requested amyloid-β was not covered by AUC. This happened most often (n = 7) when previous CSF analysis did not support current clinical diagnosis, which led to requesting amyloid-β PET. CONCLUSION: In this single-center study, the main reason for requesting an amyloid-β PET scan after performing CSF biomarkers was the occurrence of a mismatch between the primary clinical diagnosis and CSF Aβ/tau results.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Neurologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Neurology (hsv//eng)

Nyckelord

Alzheimer’s disease
amyloid
cerebrospinal fluid
positron emission tomography
tau proteins

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art (ämneskategori)
ref (ämneskategori)

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