Clinical Effect of Early vs Late Amyloid Positron Emission Tomography in Memory Clinic Patients

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Bischof,Merçé Boada,Ronald Boellaard,Nenad Bogdanović,Ariane Bollack,Stéphanie Bombois, Stefan Borg, Anne Börjesson‐Hanson, Vladimir Boskov, Justine Boutantin,Claire Boutoleau-Brétonnière,Femke H. Bouwman,Laëtitia Breuilh, Eva Bringman, Baptiste Brunel,Marco Bucci,Chris Buckley,Mar Buendía, Santi Bullich,Anna Calvet, Laia Cañada, Marta Cañada,Camilla Caprioglio,M. Jorge Cardoso, Jasmine Carlier, E. Carré,Isabelle Carrié,Pascaline Cassagnaud, Emmanuelle Cassol,Miguel Castilla‐Martí, Elodie Cazalon, Tiphaine Chaarriau, Rachel Chaigeau, T. M. Chalmers, Marie-Thérèse Clerc,Montserrat Clerigué, Emmanuel Cognat, Nina Coll,Lyduine E. Collij, Peter Connely, Elodie Cordier, Corine Costes, C. Coulange, Hélène Courtemanche, E. Creisson, C. Crinquette, Rosario Cuevas, Marie-Noëlle Cufi, Sophie Dardenne, María Arriba, Chris R. Luis, Yvonne de Gier, D. De Verbizier Lonjon, Veronique Dekker, Bérengère Dekyndt, Xavier Delbeuck,Julien Delrieu,Jean‐François Démonet, Vincent Deramecourt, Françoise Desclaux, Carlos Díaz,Susana Diego, M. I. Djafar, Britta Dölle, Laura Doull,Laurence Dricot,Alexander Drzezga,Bruno Dubois, Julien Dumont, J P Dumur,Julien Dumurgier, Martin Dvořák, Mirian Ecay,Paul Edison, Claus Escher,Ainara Estanga, Ester Esteban, G Fanjaud,Gill Farrar,Karine Fauria, Marta Felez Sanchez, Paul Talla,Lisa Ford,Giovanni B. Frisoni, David Fuster,Audrey Gabelle,Valentina Garibotto, Sinead Gaubert, Cédric Gauci, Christine Geldhof,Jean Georges, Joseph Ghika,Rossella Gismondi,Juan Domingo Gispert, Elena Benito González, Valerie Goovaerts, D. Mariano Goulart, Caroline Grasselli,Oriol Grau‐Rivera,Katherine R. Gray, Martin Greensmith, Laure Grozn, Céline Guillemaud, Fiona Gunn, Prasad Guntur Ramkumar,Göran Hagman, Bernard Hansseuw,Fiona Heeman,Janine Hendriks, Jakob Himmelmann,Anne Hitzel, Florent Hives, Merle Hoenig, Claire Hourrègue, Justine Hudson, J. Huguet,Marta Ibarria, Ifrah Noor Iidow, Sandrine Indart,Silvia Ingala,Adrian Ivanoiu, Charlotte Jacquemont,Vesna Jelić,Frank Jessen,Jieqing Jiao, Sara Jofresa, Cathrine Jonsson, Dzmitry A. Kaliukhovich,Silke Kern,Miia Kivipelto, Iva Knezevic, Grégory Kuchcinski, Manon Laforce,Asunción Lafuente, Françoise Lala,Adriaan A. Lammertsma, Michelle Lax, Thibaud Lebouvier,Ho-Yun Lee, Lean Lee,Anna E. Leeuwis, Amandine Lefort, Jean‐François Legrand, Mélanie Leroy, Constance Lesoil Markowski, Marcel Lévy,Renaud Lhommel, Renaud Lopes,Isadora Lopes Alves,Luigi Lorenzini, Adrien Lorette, Emma S. Luckett, Mikael Lundin, Marie-Anne Mackowiak,Vincent Malotaux,Richard Manber, Nikolay V. Manyakov,Paweł Markiewicz, Paula Marne,Marta Marquié, E. 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Ritchie, Ernesto Suárez Rodríguez, Adeline Rollin,Olivier Rouaud, Simona Sacuiu,Laure Saint‐Aubert,Arianna Sala,Anne‐Sophie Salabert, Jon Saldias,Gemma Salvadó,Ángela Sanabria,Lena Sannemann, N. Sastre, D Savina,Irina Savitcheva,Jolien Schaeverbeke,Philip Scheltens, Carine Schildermans,Mark E. Schmidt,Michael Schöll, Jeroen Schuermans,Franck Semah,Mahnaz Shekari,Ingmar Skoog,Oscar Sotolongo‐Grau,Andrew Stephens, Tiffany M. Stewart, Jennyfer Stutzmann, Mary Tait,Lluís Tárraga,Juan Pablo Tartari, Ann-christine Tysen-backstrom,Sergi Valero,David Vállez García,Bart N.M. van Berckel, Marc van Essen,Koen Van Laere, Jeroen van Leur,Ingrid S. van Maurik,Rik Vandenberghe,Bruno Vellas, Jukka Virolinen,Pieter Jelle Visser,Zuzana Walker, Heike Walles, Elizabeth Wallin, Grant Whitelaw,Catriona Wimberley,Zarni Win,Alle Meije Wink,Robin Wolz, John Woodside,Maqsood Yaqub, Anna Zettergren, Philip Zeyen

JAMA Neurology(2023)

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摘要
Amyloid positron emission tomography (PET) allows the direct assessment of amyloid deposition, one of the main hallmarks of Alzheimer disease. However, this technique is currently not widely reimbursed because of the lack of appropriately designed studies demonstrating its clinical effect.To assess the clinical effect of amyloid PET in memory clinic patients.The AMYPAD-DPMS is a prospective randomized clinical trial in 8 European memory clinics. Participants were allocated (using a minimization method) to 3 study groups based on the performance of amyloid PET: arm 1, early in the diagnostic workup (within 1 month); arm 2, late in the diagnostic workup (after a mean [SD] 8 [2] months); or arm 3, if and when the managing physician chose. Participants were patients with subjective cognitive decline plus (SCD+; SCD plus clinical features increasing the likelihood of preclinical Alzheimer disease), mild cognitive impairment (MCI), or dementia; they were assessed at baseline and after 3 months. Recruitment took place between April 16, 2018, and October 30, 2020. Data analysis was performed from July 2022 to January 2023.Amyloid PET.The main outcome was the difference between arm 1 and arm 2 in the proportion of participants receiving an etiological diagnosis with a very high confidence (ie, ≥90% on a 50%-100% visual numeric scale) after 3 months.A total of 844 participants were screened, and 840 were enrolled (291 in arm 1, 271 in arm 2, 278 in arm 3). Baseline and 3-month visit data were available for 272 participants in arm 1 and 260 in arm 2 (median [IQR] age: 71 [65-77] and 71 [65-77] years; 150/272 male [55%] and 135/260 male [52%]; 122/272 female [45%] and 125/260 female [48%]; median [IQR] education: 12 [10-15] and 13 [10-16] years, respectively). After 3 months, 109 of 272 participants (40%) in arm 1 had a diagnosis with very high confidence vs 30 of 260 (11%) in arm 2 (P < .001). This was consistent across cognitive stages (SCD+: 25/84 [30%] vs 5/78 [6%]; P < .001; MCI: 45/108 [42%] vs 9/102 [9%]; P < .001; dementia: 39/80 [49%] vs 16/80 [20%]; P < .001).In this study, early amyloid PET allowed memory clinic patients to receive an etiological diagnosis with very high confidence after only 3 months compared with patients who had not undergone amyloid PET. These findings support the implementation of amyloid PET early in the diagnostic workup of memory clinic patients.EudraCT Number: 2017-002527-21.
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amyloid,patients,clinical effect
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