Use of flutemetamol F18-labeled positron emission tomography and other biomarkers to assess risk of clinical progression in patients with amnestic mild cognitive impairment

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Use of flutemetamol F18-labeled positron emission tomography and other biomarkers to assess risk of clinical progression in patients with amnestic mild cognitive impairment. / Wolk, David A.; Sadowsky, Carl; Safirstein, Beth; Rinne, Juha O.; Duara, Ranjan; Perry, Richard; Agronin, Marc; Gamez, Jose; Shi, Jiong; Ivanoiu, Adrian; Minthon, Lennart; Walker, Zuzana; Hasselbalch, Steen; Holmes, Clive; Sabbagh, Marwan; Albert, Marilyn; Fleisher, Adam; Loughlin, Paul; Triau, Eric; Frey, Kirk; Høgh, Peter; Bozoki, Andrea; Bullock, Roger; Salmon, Eric; Farrar, Gillian; Buckley, Christopher J.; Zanette, Michelle; Sherwin, Paul F.; Cherubini, Andrea; Inglis, Fraser.

In: JAMA Neurology, Vol. 75, No. 9, 2018, p. 1114-1123.

Research output: Contribution to journalArticle

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Wolk, DA, Sadowsky, C, Safirstein, B, Rinne, JO, Duara, R, Perry, R, Agronin, M, Gamez, J, Shi, J, Ivanoiu, A, Minthon, L, Walker, Z, Hasselbalch, S, Holmes, C, Sabbagh, M, Albert, M, Fleisher, A, Loughlin, P, Triau, E, Frey, K, Høgh, P, Bozoki, A, Bullock, R, Salmon, E, Farrar, G, Buckley, CJ, Zanette, M, Sherwin, PF, Cherubini, A & Inglis, F 2018, 'Use of flutemetamol F18-labeled positron emission tomography and other biomarkers to assess risk of clinical progression in patients with amnestic mild cognitive impairment', JAMA Neurology, vol. 75, no. 9, pp. 1114-1123. https://doi.org/10.1001/jamaneurol.2018.0894

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Wolk DA, Sadowsky C, Safirstein B, Rinne JO, Duara R, Perry R, Agronin M, Gamez J, Shi J, Ivanoiu A, Minthon L, Walker Z, Hasselbalch S, Holmes C, Sabbagh M, Albert M, Fleisher A, Loughlin P, Triau E, Frey K, Høgh P, Bozoki A, Bullock R, Salmon E, Farrar G, Buckley CJ, Zanette M, Sherwin PF, Cherubini A, Inglis F. 2018. Use of flutemetamol F18-labeled positron emission tomography and other biomarkers to assess risk of clinical progression in patients with amnestic mild cognitive impairment. JAMA Neurology. 75(9):1114-1123. https://doi.org/10.1001/jamaneurol.2018.0894

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Wolk, David A. ; Sadowsky, Carl ; Safirstein, Beth ; Rinne, Juha O. ; Duara, Ranjan ; Perry, Richard ; Agronin, Marc ; Gamez, Jose ; Shi, Jiong ; Ivanoiu, Adrian ; Minthon, Lennart ; Walker, Zuzana ; Hasselbalch, Steen ; Holmes, Clive ; Sabbagh, Marwan ; Albert, Marilyn ; Fleisher, Adam ; Loughlin, Paul ; Triau, Eric ; Frey, Kirk ; Høgh, Peter ; Bozoki, Andrea ; Bullock, Roger ; Salmon, Eric ; Farrar, Gillian ; Buckley, Christopher J. ; Zanette, Michelle ; Sherwin, Paul F. ; Cherubini, Andrea ; Inglis, Fraser. / Use of flutemetamol F18-labeled positron emission tomography and other biomarkers to assess risk of clinical progression in patients with amnestic mild cognitive impairment. In: JAMA Neurology. 2018 ; Vol. 75, No. 9. pp. 1114-1123.

RIS

TY - JOUR

T1 - Use of flutemetamol F18-labeled positron emission tomography and other biomarkers to assess risk of clinical progression in patients with amnestic mild cognitive impairment

AU - Wolk, David A.

AU - Sadowsky, Carl

AU - Safirstein, Beth

AU - Rinne, Juha O.

AU - Duara, Ranjan

AU - Perry, Richard

AU - Agronin, Marc

AU - Gamez, Jose

AU - Shi, Jiong

AU - Ivanoiu, Adrian

AU - Minthon, Lennart

AU - Walker, Zuzana

AU - Hasselbalch, Steen

AU - Holmes, Clive

AU - Sabbagh, Marwan

AU - Albert, Marilyn

AU - Fleisher, Adam

AU - Loughlin, Paul

AU - Triau, Eric

AU - Frey, Kirk

AU - Høgh, Peter

AU - Bozoki, Andrea

AU - Bullock, Roger

AU - Salmon, Eric

AU - Farrar, Gillian

AU - Buckley, Christopher J.

AU - Zanette, Michelle

AU - Sherwin, Paul F.

AU - Cherubini, Andrea

AU - Inglis, Fraser

PY - 2018

Y1 - 2018

N2 - Importance: Patients with amnestic mild cognitive impairment (aMCI) may progress to clinical Alzheimer disease (AD), remain stable, or revert to normal. Earlier progression to AD among patients who were β-amyloid positive vs those who were β-amyloid negative has been previously observed. Current research now accepts that a combination of biomarkers could provide greater refinement in the assessment of risk for clinical progression. Objective: To evaluate the ability of flutemetamol F 18 and other biomarkers to assess the risk of progression from aMCI to probable AD. Design, Setting, and Participants: In this multicenter cohort study, from November 11, 2009, to January 16, 2014, patients with aMCI underwent positron emission tomography (PET) at baseline followed by local clinical assessments every 6 months for up to 3 years. Patients with aMCI (365 screened; 232 were eligible) were recruited from 28 clinical centers in Europe and the United States. Physicians remained strictly blinded to the results of PET, and the standard of truth was an independent clinical adjudication committee that confirmed or refuted local assessments. Flutemetamol F 18-labeled PET scans were read centrally as either negative or positive by 5 blinded readers with no knowledge of clinical status. Statistical analysis was conducted from February 19, 2014, to January 26, 2018. Interventions: Flutemetamol F 18-labeled PET at baseline followed by up to 6 clinical visits every 6 months, as well as magnetic resonance imaging and multiple cognitive measures. Main Outcomes and Measures: Time from PET to probable AD or last follow-upwas plotted as a Kaplan-Meier survival curve; PET scan results, age, hippocampal volume, and aMCI stage were entered into Cox proportional hazards logistic regression analyses to identify variables associated with progression to probable AD. Results: Of 232 patients with aMCI (118 women and 114 men; mean [SD] age, 71.1 [8.6] years), 98 (42.2%) had positive results detected on PET scan. By 36 months, the rates of progression to probable AD were 36.2% overall (81 of 224 patients), 53.6%(52 of 97) for patients with positive results detected on PET scan, and 22.8% (29 of 127) for patients with negative results detected on PET scan. Hazard ratios for association with progression were 2.51 (95% CI, 1.57-3.99; P < .001) for a positive β-amyloid scan alone (primary outcome measure), 5.60 (95%CI, 3.14-9.98; P < .001) with additional low hippocampal volume, and 8.45 (95%CI, 4.40-16.24; P < .001) when poorer cognitive status was added to the model. Conclusions and Relevance: A combination of positive results of flutemetamol F 18-labeled PET, low hippocampal volume, and cognitive status corresponded with a high probability of risk of progression from aMCI to probable AD within 36 months.

AB - Importance: Patients with amnestic mild cognitive impairment (aMCI) may progress to clinical Alzheimer disease (AD), remain stable, or revert to normal. Earlier progression to AD among patients who were β-amyloid positive vs those who were β-amyloid negative has been previously observed. Current research now accepts that a combination of biomarkers could provide greater refinement in the assessment of risk for clinical progression. Objective: To evaluate the ability of flutemetamol F 18 and other biomarkers to assess the risk of progression from aMCI to probable AD. Design, Setting, and Participants: In this multicenter cohort study, from November 11, 2009, to January 16, 2014, patients with aMCI underwent positron emission tomography (PET) at baseline followed by local clinical assessments every 6 months for up to 3 years. Patients with aMCI (365 screened; 232 were eligible) were recruited from 28 clinical centers in Europe and the United States. Physicians remained strictly blinded to the results of PET, and the standard of truth was an independent clinical adjudication committee that confirmed or refuted local assessments. Flutemetamol F 18-labeled PET scans were read centrally as either negative or positive by 5 blinded readers with no knowledge of clinical status. Statistical analysis was conducted from February 19, 2014, to January 26, 2018. Interventions: Flutemetamol F 18-labeled PET at baseline followed by up to 6 clinical visits every 6 months, as well as magnetic resonance imaging and multiple cognitive measures. Main Outcomes and Measures: Time from PET to probable AD or last follow-upwas plotted as a Kaplan-Meier survival curve; PET scan results, age, hippocampal volume, and aMCI stage were entered into Cox proportional hazards logistic regression analyses to identify variables associated with progression to probable AD. Results: Of 232 patients with aMCI (118 women and 114 men; mean [SD] age, 71.1 [8.6] years), 98 (42.2%) had positive results detected on PET scan. By 36 months, the rates of progression to probable AD were 36.2% overall (81 of 224 patients), 53.6%(52 of 97) for patients with positive results detected on PET scan, and 22.8% (29 of 127) for patients with negative results detected on PET scan. Hazard ratios for association with progression were 2.51 (95% CI, 1.57-3.99; P < .001) for a positive β-amyloid scan alone (primary outcome measure), 5.60 (95%CI, 3.14-9.98; P < .001) with additional low hippocampal volume, and 8.45 (95%CI, 4.40-16.24; P < .001) when poorer cognitive status was added to the model. Conclusions and Relevance: A combination of positive results of flutemetamol F 18-labeled PET, low hippocampal volume, and cognitive status corresponded with a high probability of risk of progression from aMCI to probable AD within 36 months.

U2 - 10.1001/jamaneurol.2018.0894

DO - 10.1001/jamaneurol.2018.0894

M3 - Article

VL - 75

SP - 1114

EP - 1123

JO - JAMA Neurology

JF - JAMA Neurology

SN - 2168-6157

IS - 9

ER -